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<XML>
    <JOURNAL>
        <YEAR>2025</YEAR>
        <VOL>12</VOL>
        <NO>2</NO>
        <MOSALSAL>23456841</MOSALSAL>
        <PAGE_NO>57</PAGE_NO>
        <ARTICLES>
            <ARTICLE>
                <Language_ID>1</Language_ID>
                <TitleE>A Systematic Review of the Antimicrobial Properties of Dye-Producing Plants</TitleE>
                <URL>https://brieflands.com/journals/gct/articles/155656</URL>
                <DOI>10.5812/gct-155656</DOI>
                <DOR></DOR>
                <ABSTRACTS>
                    <ABSTRACT>
                        <Language_ID>1</Language_ID>
                        <CONTENT>Introduction :Natural dyes derived from plants have gained significant attention due to their safety compared to chemical dyes. These dyes possess antibacterial properties and have minimal environmental impact. Methods :A systematic literature search was conducted using PubMed, Scopus, Embase, Cochrane, Web of Science, and Google Scholar databases. The search utilized all available MeSH terms related to medicinal plants, dyes, wool, and antimicrobial properties of plants, covering the period from 2009 to 2020. Results :The findings indicate that numerous plants possess both coloring and antimicrobial properties, although they are currently utilized in limited quantities. Conclusions :The present study aims to introduce plants with antimicrobial and coloring properties for further study.</CONTENT>
                    </ABSTRACT>
                </ABSTRACTS>
                <PAGES>
                    <PAGE>
                        <FPAGE>1</FPAGE>
                        <TPAGE>6</TPAGE>
                    </PAGE>
                </PAGES>
                <AUTHORS>
                    <AUTHOR>
                        <NameE>Tahereh</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Eslammanesh</FamilyE>
                        <Organizations>
                            <Organization>Department of Pathology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>dr.eslammanesh@yahoo.com</Email>
                        </EMAILS>
                        <NameE>Hossein</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Pour Masoomi</FamilyE>
                        <Organizations>
                            <Organization>Zabol University of Medical Sciences, Zabol, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>drhpm@yahoo.com</Email>
                        </EMAILS>
                        <NameE>Najmeh</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Molashahi</FamilyE>
                        <Organizations>
                            <Organization>Agricultural and Natural Resources Research Center, Zabol, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>mollashahinajmeh@gmail.com</Email>
                        </EMAILS>
                        <NameE>Shima</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Mohammadkhani</FamilyE>
                        <Organizations>
                            <Organization>Department of Emergency Medicine, Zabol University of Medical Sciences, Zabol, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>dr.mohammadkhani@yahoo.com</Email>
                        </EMAILS>
                        <NameE>Masoomeh</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Rezaei</FamilyE>
                        <Organizations>
                            <Organization>Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>rezaemasoomeh@yahoo.com</Email>
                        </EMAILS>
                        <NameE>Marziye</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Rezaei</FamilyE>
                        <Organizations>
                            <Organization>Department of Carpet, Faculty of Art and Architecture, University of Sistan and Baluchestan, Zahedan, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>m.rezaei@arts.usb.ac.ir</Email>
                        </EMAILS>
                    </AUTHOR>
                </AUTHORS>
                <KEYWORDS>
                    <KEYWORD>
                        <KeyText>No Keyword</KeyText>
                    </KEYWORD>
                </KEYWORDS>
                <PDFFileName>1.pdf</PDFFileName>
                <REFRENCES>
                    <REFRENCE>
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Fibers Polymers. 2021;22(3).##[14]Yılmaz F.Investigating the usage of eucalyptus leaves in antibacterial finishing of textiles against Gram-positive and Gram-negative bacteria. J Textile Institute. 2020;112(2):341-5.##[15]Das S, Das A.The antibacterial and aroma finishing of cotton fabrics by Eucalyptus globulus extract. J Nat Fibers. 2022;19:13790-801.##[16]Endris J, Govindan N.Dyeing and finishing of cotton fabric with eucalyptus leaves extracts. Res J Textile Apparel. 2021;25(3):193-208. doi: 10.1108/rjta-12-2019-0060.##[17]Silva MGD, Barros MAS, Almeida RTRD, Pilau EJ, Pinto E, Soares G, et al.Cleaner production of antimicrobial and anti-UV cotton materials through dyeing with eucalyptus leaves extract. J Cleaner Production. 2018;199:807-16. doi: 10.1016/j.jclepro.2018.07.221.##[18]Singh KN, Lal B.Notes on traditional uses of khair (Acacia catechu Willd.) by inhabitants of shivalik range in Western Himalaya. 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[PubMed ID: 2300807]. doi: 10.1126/science.2300807.##[25]Segelman AB, Farnsworth NR.Biological and phytochemical screening of plants. IV. A new rapid procedure for the simultaneous determination of saponins and tannins. Lloydia. 1969;32.##[26]Kapoor LD, Singh A, Kapoor SL.Survey of Indian plants for saponins, alkaloids and flavonoids. I. Lloydia. 1969;32:297-304.##[27]Nielsen IC.Mimosaceae (leguminosae-mimosoideae). Flora Malesiana-Series 1, Spermatophyta. 1992;11(1):1-226.##[28]Upadhyay SM, Upadhyay P, Ghosh AK, Singh V, Dixit VK.Effect of ethanolic extract of Hibiscus rosa sinensis L., flowers on hair growth in female wistar rats. Der Pharmacia Lettre. 2011;3(4):258-63.##[29]Masaki H, Sakaki S, Atsumi T, Sakurai H.Active-oxygen scavenging activity of plant extracts. Biol Pharm Bull. 1995;18(1):162-6. [PubMed ID: 7735233]. doi: 10.1248/bpb.18.162.##[30]The Wealth of India.A dictionary of Indian raw materials and Industrial Product. CSIR. 1956;91.##[31]Sachdewa A, Khemani LD.Effect of Hibiscus rosa sinensis Linn. ethanol flower extract on blood glucose and lipid profile in streptozotocin induced diabetes in rats. J Ethnopharmacol. 2003;89(1):61-6. [PubMed ID: 14522433]. doi: 10.1016/s0378-8741(03)00230-7.##[32]Gauthaman KK, Saleem MT, Thanislas PT, Prabhu VV, Krishnamoorthy KK, Devaraj NS, et al.Cardioprotective effect of the Hibiscus rosa sinensis flowers in an oxidative stress model of myocardial ischemic reperfusion injury in rat. BMC Complement Altern Med. 2006;6:32. [PubMed ID: 16987414]. [PubMed Central ID: PMC1592511]. doi: 10.1186/1472-6882-6-32.##[33]Gupta D, Kumari S, Gulrajani M.Dyeing studies with hydroxyanthraquinones extracted from Indian madder. Part 1: Dyeing of nylon with purpurin†. Coloration Technol. 2006;117(6):328-32. doi: 10.1111/j.1478-4408.2001.tb00084.x.##[34]Gupta D, Gulrajani ML, Kumari S.Light fastness of naturally occurring anthraquinone dyes on nylon. Coloration Technol. 2006;120(5):205-12. doi: 10.1111/j.1478-4408.2004.tb00119.x.##[35]Arora A, Gupta D, Rastogi D, Gulrajani ML.Kinetics and thermodynamics of dye extracted from Arnebia nobilis Rech. f. on wool. J Fibre Text Res. 2012;37.##[36]Kavitha T, Padmashwini R, Swarna A, Dev VR, Neelakandan R, Kumar MS.Effect of chitosan treatment on the properties of turmeric dyed cotton yarn. Indian J Fibre Text Res. 2007;32.##[37]Ke G, Yu W, Xu W.Color evaluation of wool fabric dyed with Rhizoma coptidis extract. J Appl Polymer Sci. 2006;101(5):3376-80. doi: 10.1002/app.24033.##[38]Son Y, Kim B, Ravikumar K, Kim T.Berberine finishing for developing antimicrobial nylon 66 fibers: % exhaustion, colorimetric analysis, antimicrobial study, and empirical modeling. J Appl Polymer Sci. 2006;103(2):1175-82. doi: 10.1002/app.25364.##[39]Das D, Maulik SR, Bhattacharya SC.Colouration of wool and silk with Rheum emodi. Indian J Fibre Text Res. 2008;33:163-70.##[40]Kumaresan M, Palanisamy PN, Kumar PE.Application of eco-friendly natural dye on cotton using combination of mordants. Indian J Fibre Text Res. 2012;37:194-8.##[41]Khan MI, Ahmad A, Khan SA, Yusuf M, Shahid M, Manzoor N, et al.Assessment of antimicrobial activity of Catechu and its dyed substrate. J Cleaner Product. 2011;19(12):1385-94. doi: 10.1016/j.jclepro.2011.03.013.##[42]Kasiri MB, Safapour S.Natural dyes and antimicrobials for green treatment of textiles. Environ Chem Letters. 2014;12(1):1-13.##[43]Ahmadi H, Safapour S.A review on the UV-Protective finish of natural textiles using UV-absorbers. J Stud Color World. 2015;5(1):61-74.##[44]Gazala Q, Murtaza I, Ara S, Qazi H, Geelani SM, Amir S.Characterization and antimicrobial activity of some natural dye yielding plant species of Kashmir Valley. J Industrial Pollution Control. 2016;32(2):518-28.##[45]Tomczykowa M, Tomczyk M, Jakoniuk P, Tryniszewska E.Antimicrobial and antifungal activities of the extracts and essential oils of Bidens tripartita. Folia Histochem Cytobiol. 2008;46(3):389-93. [PubMed ID: 19056546]. doi: 10.2478/v10042-008-0082-8.##[46]Khan MR, Kihara M, Omoloso AD.Anti-microbial activity of Bidens pilosa, Bischofia javanica, Elmerillia papuana and Sigesbekia orientalis. Fitoterapia. 2001;72(6):662-5. [PubMed ID: 11543964]. doi: 10.1016/s0367-326x(01)00261-1.##[47]Brandao MG, Krettli AU, Soares LS, Nery CG, Marinuzzi HC.Antimalarial activity of extracts and fractions from Bidens pilosa and other Bidens species (Asteraceae) correlated with the presence of acetylene and flavonoid compounds. J Ethnopharmacol. 1997;57(2):131-8. [PubMed ID: 9254115]. doi: 10.1016/s0378-8741(97)00060-3.##[48]Esimone CO, Adikwu MU, Muko KN.Antimicrobial properties of Indigofera dendroides leaves. Fitoterapia. 1999;70(5):517-20. doi: 10.1016/s0367-326x(99)00072-6.##</REF>
                    </REFRENCE>
                </REFRENCES>
            </ARTICLE>
            <ARTICLE>
                <Language_ID>1</Language_ID>
                <TitleE>Exploring the Role of MiR-373 in Colorectal Cancer Development and Progression</TitleE>
                <URL>https://brieflands.com/journals/gct/articles/159893</URL>
                <DOI>10.5812/gct-159893</DOI>
                <DOR></DOR>
                <ABSTRACTS>
                    <ABSTRACT>
                        <Language_ID>1</Language_ID>
                        <CONTENT>Context :Colorectal cancer (CRC) is a leading cause of cancer-related deaths globally. Its progression is influenced by various molecular factors, including the dysregulation of microRNAs (miRNAs). MiR-373 is an oncogenic miRNA implicated in the development of CRC, but its precise role in tumor progression and metastasis remains under investigation. Objectives :This review aims to evaluate the role of miR-373 in CRC progression, focusing on its impact on key cellular processes such as proliferation, migration, and invasion. Additionally, the review explores the potential of miR-373 as a prognostic biomarker and therapeutic target in CRC. Methods :A systematic search was conducted using databases such as PubMed, Scopus, and Google Scholar to identify studies published from 2000 to 2025. The review includes studies that investigate miR-373 expression, its regulation of tumor suppressor genes, and its involvement in oncogenic signaling pathways, particularly those linked to CRC progression. Results :MiR-373 is often overexpressed in CRC tissues, promoting tumor growth by regulating critical cellular processes. It suppresses tumor suppressor genes like PTEN and TP53INP1, resulting in uncontrolled cell proliferation, reduced apoptosis, and enhanced invasion. Higher miR-373 levels are associated with advanced disease stages, metastasis, and poor clinical outcomes, suggesting its potential as a prognostic marker and therapeutic target. Conclusions :MiR-373 contributes significantly to CRC development and progression. Its upregulation is linked to increased tumor aggressiveness, metastasis, and resistance to therapy, making it a promising candidate for early detection and targeted therapies in CRC. Further studies should focus on modulating miR-373 expression to improve clinical outcomes.</CONTENT>
                    </ABSTRACT>
                </ABSTRACTS>
                <PAGES>
                    <PAGE>
                        <FPAGE>1</FPAGE>
                        <TPAGE>7</TPAGE>
                    </PAGE>
                </PAGES>
                <AUTHORS>
                    <AUTHOR>
                        <NameE>Mohammad</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Kordkatouli</FamilyE>
                        <Organizations>
                            <Organization>Department of Cell and Molecular Biology, GO.C, Islamic Azad University, Gorgan, Iran</Organization>
                            <Organization>Young Research and Elite Club, GO.C, Islamic Azad University, Gorgan, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>mohammad.kordkatouli@outlook.com</Email>
                        </EMAILS>
                        <NameE>Aryan</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Sateei</FamilyE>
                        <Organizations>
                            <Organization>Department of Biology, GO.C, Islamic Azad University, Gorgan, Iran</Organization>
                            <Organization>Institute of Medicinal Plants Research, GO.C, Islamic Azad University, Gorgan, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>saateyi@gmail.com</Email>
                        </EMAILS>
                        <NameE>Amirhossein</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Jafari</FamilyE>
                        <Organizations>
                            <Organization>Cellular and Molecular Research Center, Faculty Medicine, Guilan University of Medical Sciences, Rasht, Iran</Organization>
                            <Organization>Studant Research Center, Faculty Medicine, Guilan University of Medical Sciences, Rasht, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>amirhosseinjef3@gmail.com</Email>
                        </EMAILS>
                        <NameE>Tayyebeh</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Khoshbakht</FamilyE>
                        <Organizations>
                            <Organization>Clinical Cardiovascular Research Group, Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Norway</Country>
                        </Countries>
                        <EMAILS>
                            <Email>sare.khoshbakht@gmail.com</Email>
                        </EMAILS>
                        <NameE>Audrius</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Dulskas</FamilyE>
                        <Organizations>
                            <Organization>Department of Abdominal and General Surgery and Oncology, National Cancer Institute, Vilnius, Lithuania</Organization>
                            <Organization>Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Lithuania</Country>
                            <Country>Lithuania</Country>
                        </Countries>
                        <EMAILS>
                            <Email>audrius.dulskas@gmail.com</Email>
                        </EMAILS>
                        <NameE>Mohammad</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Maroufi</FamilyE>
                        <Organizations>
                            <Organization>Department of Biology, UR.C, Islamic Azad University, Urmia, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>mmdmrufi@gmail.com</Email>
                        </EMAILS>
                    </AUTHOR>
                </AUTHORS>
                <KEYWORDS>
                    <KEYWORD>
                        <KeyText>No Keyword</KeyText>
                    </KEYWORD>
                </KEYWORDS>
                <PDFFileName>2.pdf</PDFFileName>
                <REFRENCES>
                    <REFRENCE>
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[PubMed Central ID: PMC10762131]. doi: 10.1038/s41598-023-49565-5.##[4]Kordkatouli M, Sateei A, Mahmood Janlou MA.Roles of miR-21 in the Onset and Advancement of Colorectal Cancer (CRC). Multidisciplinary Cancer Investigation. 2024;8(1):0.##[5]Kordkatouli M, Sateei A, Dulskas A.Potential roles and mechanisms of Avena sativa in cancer prevention. Multidisciplinary Cancer Investigation. 2024:0.##[6]Kordkatouli M, Janlou MAM, Sateei A, Mousavi MMH, Dulskas A.Recent Progress in Nanoparticle-Driven Drug Delivery Strategies for Cancer Therapy: Focus on Colorectal Cancer. Zahedan J Res Med Sci.##[7]Kordkatouli M, CHO WC, Mohammad Bondarkhilli SA, Dulskas A, Qureshi SAM.Oct-4 and Its Role in the Oncogenesis of Colorectal Cancer. Middle East J Cancer. 2024;15(2_Supplement).##[8]Valizadeh M, Vafaei M, Maroufi M, Emamirad S.Identification of oncogenic microRNAs and their target genes in tissue samples of colorectal cancer: Gene set enrichment analysis. Micro Nano Bio Aspects. 2024;3(3):50-67.##[9]Ghasemi M, Kordkatouli M, Salari Z, Yusofvand R, Samian P.The Role of LncRNA ROR in Colorectal Cancer Diagnosis and Treatment. Zahedan J Res Med Sci.##[10]Wang W, Li Y, Wu M, Xiong A, Wang M.Upregulation of microRNA-373 in human colorectal carcinoma by targeting CD44. Int J Clin Exp Med. 2016;9(7):12594-602.##[11]Wang LQ, Yu P, Li B, Guo YH, Liang ZR, Zheng LL, et al.miR-372 and miR-373 enhance the stemness of colorectal cancer cells by repressing differentiation signaling pathways. Mol Oncol. 2018;12(11):1949-64. [PubMed ID: 30171794]. [PubMed Central ID: PMC6210048]. doi: 10.1002/1878-0261.12376.##[12]Ullmann P, Rodriguez F, Schmitz M, Meurer SK, Qureshi-Baig K, Felten P, et al.The miR-371 approximately 373 Cluster Represses Colon Cancer Initiation and Metastatic Colonization by Inhibiting the TGFBR2/ID1 Signaling Axis. Cancer Res. 2018;78(14):3793-808. [PubMed ID: 29748374]. doi: 10.1158/0008-5472.CAN-17-3003.##[13]Eyking A, Reis H, Frank M, Gerken G, Schmid KW, Cario E.MiR-205 and MiR-373 Are Associated with Aggressive Human Mucinous Colorectal Cancer. PLoS One. 2016;11(6). e0156871. [PubMed ID: 27271572]. [PubMed Central ID: PMC4894642]. doi: 10.1371/journal.pone.0156871.##[14]Gezici S, Sekeroglu N.Regulation of microRNAs by natural products and bioactive compounds obtained from common medicinal plants: novel strategy in cancer therapy. cancer. 2017;1(4):71.##[15]Paczynska P, Grzemski A, Szydlowski M.Distribution of miRNA genes in the pig genome. BMC Genet. 2015;16(1):6. [PubMed ID: 25632794]. [PubMed Central ID: PMC4318388]. doi: 10.1186/s12863-015-0166-3.##[16]Zhang D, Hao P, Jin L, Wang Y, Yan Z, Wu S.MicroRNA‑940 promotes cell proliferation and invasion of glioma by directly targeting Kruppel‑like factor 9. Molecular Med Rep. 2019;19(1):734-42.##[17]Carroll AP, Goodall GJ, Liu B.Understanding principles of miRNA target recognition and function through integrated biological and bioinformatics approaches. Wiley Interdiscip Rev RNA. 2014;5(3):361-79. [PubMed ID: 24459110]. doi: 10.1002/wrna.1217.##[18]Macfarlane LA, Murphy PR.MicroRNA: Biogenesis, Function and Role in Cancer. Curr Genomics. 2010;11(7):537-61. [PubMed ID: 21532838]. [PubMed Central ID: PMC3048316]. doi: 10.2174/138920210793175895.##[19]Tan P, Sun H, Xu M, Liu X, Qin J, Nie J, et al.Circular RNA circ0104103 inhibits colorectal cancer progression through interactions with HuR and miR-373-5p. Cancer Sci. 2023;114(4):1396-409. [PubMed ID: 36562402]. [PubMed Central ID: PMC10067388]. doi: 10.1111/cas.15695.##[20]Bose GS, Jindal S, Landage KG, Jindal A, Mahale MP, Kulkarni AP, et al.SMAR1 and p53-regulated lncRNA RP11-431M3.1 enhances HIF1A translation via miR-138 in colorectal cancer cells under oxidative stress. FEBS J. 2024;291(21):4696-713. [PubMed ID: 39240540]. doi: 10.1111/febs.17253.##[21]Louis DN, Perry A, Reifenberger G, von Deimling A, Figarella-Branger D, Cavenee WK, et al.The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary. Acta Neuropathol. 2016;131(6):803-20. [PubMed ID: 27157931]. doi: 10.1007/s00401-016-1545-1.##[22]Chen Q, Li Y, Lu T, Luo J, Yang L, Zhou Z, et al.miR-373 promotes invasion and metastasis of colorectal cancer cells via activating ERK/MAPK pathway. Sci Rep. 2024;14(1):124. [PubMed ID: 38167930]. [PubMed Central ID: PMC10762131]. doi: 10.1038/s41598-023-49565-5.##[23]Shi X, Wei K, Wu Y, Mao L, Pei W, Zhu H, et al.Exosome-derived miR-372-5p promotes stemness and metastatic ability of CRC cells by inducing macrophage polarization. Cell Signal. 2023;111:110884. [PubMed ID: 37690660]. doi: 10.1016/j.cellsig.2023.110884.##[24]Rahdan F, Saberi A, Saraygord-Afshari N, Hadizadeh M, Fayeghi T, Ghanbari E, et al.Deciphering the multifaceted role of microRNAs in hepatocellular carcinoma: Integrating literature review and bioinformatics analysis for therapeutic insights. Heliyon. 2024;10(20). e39489. [PubMed ID: 39498055]. [PubMed Central ID: PMC11532857]. doi: 10.1016/j.heliyon.2024.e39489.##[25]Bakr NM, Mahmoud MS, Nabil R, Boushnak H, Swellam M.Impact of circulating miRNA-373 on breast cancer diagnosis through targeting VEGF and cyclin D1 genes. J Genet Eng Biotechnol. 2021;19(1):84. [PubMed ID: 34089425]. [PubMed Central ID: PMC8179880]. doi: 10.1186/s43141-021-00174-7.##[26]Angius A, Scanu AM, Arru C, Muroni MR, Rallo V, Deiana G, et al.Portrait of Cancer Stem Cells on Colorectal Cancer: Molecular Biomarkers, Signaling Pathways and miRNAome. Int J Mol Sci. 2021;22(4). [PubMed ID: 33562604]. [PubMed Central ID: PMC7915330]. doi: 10.3390/ijms22041603.##[27]Baharudin R, Rus Bakarurraini NQ, Ismail I, Lee LH, Ab Mutalib NS.MicroRNA Methylome Signature and Their Functional Roles in Colorectal Cancer Diagnosis, Prognosis, and Chemoresistance. Int J Mol Sci. 2022;23(13). [PubMed ID: 35806286]. [PubMed Central ID: PMC9266458]. doi: 10.3390/ijms23137281.##[28]Budakoti M, Panwar AS, Molpa D, Singh RK, Busselberg D, Mishra AP, et al.Micro-RNA: The darkhorse of cancer. Cell Signal. 2021;83:109995. [PubMed ID: 33785398]. doi: 10.1016/j.cellsig.2021.109995.##[29]Janlou MAM, Kordkatouli M, Bondarkhilli SAM, Maroufi M.Investigating the Role of E-cigarettes in Epigenetic Changes and Cancer Risk. Tobacco Health. 2024;3(2):73-82.##</REF>
                    </REFRENCE>
                </REFRENCES>
            </ARTICLE>
            <ARTICLE>
                <Language_ID>1</Language_ID>
                <TitleE>Identification of Reliable Housekeeping Genes for qRT-PCR Normalization in Neuroblastoma and Glioblastoma Cell Lines Infected with Lentivirus</TitleE>
                <URL>https://brieflands.com/journals/gct/articles/161203</URL>
                <DOI>10.5812/gct-161203</DOI>
                <DOR></DOR>
                <ABSTRACTS>
                    <ABSTRACT>
                        <Language_ID>1</Language_ID>
                        <CONTENT>Background :Lentivirus infection significantly impacts gene expression in host cells, including the regulation of housekeeping genes, which are essential for normalization in quantitative reverse transcription PCR (RT-qPCR). This normalization reduces measurement errors arising from sample quality variations, RNA extraction methods, and experimental conditions. In the context of glioblastoma (GBM) and neuroblastoma (NB) — two malignancies characterized by poor prognoses and limited progression-free survival — it is crucial to identify stable reference genes to ensure accurate gene expression analysis. Objectives :Reliable normalization provides more trustworthy insights into the molecular mechanisms underlying tumor progression and may inform the development of targeted therapeutic strategies. Methods :The expression stability of eight housekeeping genes (RPL32, RPS23, GAPDH, 18S rRNA, TUB, ACTB, HPRT, and TBP) in U87 glioblastoma cells and seven genes (RPL32, HPRT, GAPDH, 18S rRNA, TUB, ACTB, and RPII) in SH-SY5Y NB cells was evaluated using RT-qPCR. Gene stability was analyzed using four statistical tools: GeNorm (pairwise variation-based ranking), NormFinder (model-based variance estimation), BestKeeper (standard deviation and CV analysis), and RefFinder (integrative ranking). Each experiment was performed in three biological replicates and analyzed in technical triplicate to ensure statistical robustness. Results :In SH-SY5Y cells, ACTB, RPL32, and RPII were consistently identified as the most stable reference genes across GeNorm, NormFinder, and BestKeeper analyses, while TUB was ranked as the least stable. In U87 cells, GeNorm ranked RPS23/HPRT as the most stable, NormFinder favored TUB/GAPDH, and BestKeeper prioritized ACTB/RPL32. Although slight differences in the gene rankings were observed among the different statistical tools, the overall selection of the most stable reference genes remained consistent. RefFinder’s integrative analysis resolved these discrepancies, identifying 18S (M = 0.18) and GAPDH as the most stable genes, and ACTB/HPRT as the least stable genes in U87. In SH-SY5Y, ACTB and RPL32 (M = 0.22) were the most stable genes, and TUB was the least stable (M = 2.45). Conclusions :This study provides a framework for reliable gene expression analysis in lentivirus-infected models. Our findings highlight the context-dependent stability of housekeeping genes, necessitating validation in diverse experimental settings (e.g., alternative viruses, primary cells) to ensure broader applicability. By emphasizing rigorous normalization, this work enhances reproducibility in gene expression studies and advances translational research in viral oncology and neuro-oncology, particularly for glioblastoma and NB therapeutics.</CONTENT>
                    </ABSTRACT>
                </ABSTRACTS>
                <PAGES>
                    <PAGE>
                        <FPAGE>1</FPAGE>
                        <TPAGE>11</TPAGE>
                    </PAGE>
                </PAGES>
                <AUTHORS>
                    <AUTHOR>
                        <NameE>Sareh</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Shahsavarpour</FamilyE>
                        <Organizations>
                            <Organization>Department of Biology, Faculty of Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>r.savari93@gmail.com</Email>
                        </EMAILS>
                        <NameE>Mohammad</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Shafiei</FamilyE>
                        <Organizations>
                            <Organization>Department of Biology, Faculty of Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>m.shafiei@scu.ac.ir</Email>
                        </EMAILS>
                        <NameE>Emanuele</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Buratti</FamilyE>
                        <Organizations>
                            <Organization>International Centre for Genetic Engineering and Biotechnology, Trieste, Italy</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Italy</Country>
                        </Countries>
                        <EMAILS>
                            <Email>emanuele.buratti@icgeb.org</Email>
                        </EMAILS>
                        <NameE>Hamid</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Galehdari</FamilyE>
                        <Organizations>
                            <Organization>Department of Biology, Faculty of Sciences, Shahid Chamran University of Ahvaz, Ahvaz, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>galehdari187@yahoo.com</Email>
                        </EMAILS>
                    </AUTHOR>
                </AUTHORS>
                <KEYWORDS>
                    <KEYWORD>
                        <KeyText>No Keyword</KeyText>
                    </KEYWORD>
                </KEYWORDS>
                <PDFFileName>3.pdf</PDFFileName>
                <REFRENCES>
                    <REFRENCE>
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[PubMed Central ID: PMC2216015]. doi: 10.1186/1743-422X-4-130.##[3]Rebouças EDL, Costa JJDN, Passos MJ, Passos JRDS, Hurk RVD, Silva JRV.Real time PCR and importance of housekeepings genes for normalization and quantification of mRNA expression in different tissues. Brazilian Arch Biol Technol. 2013;56(1):143-54. doi: 10.1590/s1516-89132013000100019.##[4]Mackay IM, Arden KE, Nitsche A.Real-time PCR in virology. Nucleic Acids Res. 2002;30(6):1292-305. [PubMed ID: 11884626]. [PubMed Central ID: PMC101343]. doi: 10.1093/nar/30.6.1292.##[5]McCurley AT, Callard GV.Characterization of housekeeping genes in zebrafish: male-female differences and effects of tissue type, developmental stage and chemical treatment. BMC Mol Biol. 2008;9:102. [PubMed ID: 19014500]. [PubMed Central ID: PMC2588455]. doi: 10.1186/1471-2199-9-102.##[6]Ferrada L, Barahona MJ, Salazar K, Godoy AS, Vera M, Nualart F.Pharmacological targets for the induction of ferroptosis: Focus on Neuroblastoma and Glioblastoma. 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[PubMed ID: 35561845]. doi: 10.1016/j.gene.2022.146561.##[19]Hernandez-Ochoa B, Fernandez-Rosario F, Castillo-Rodriguez RA, Marhx-Bracho A, Cardenas-Rodriguez N, Martinez-Rosas V, et al.Validation and Selection of New Reference Genes for RT-qPCR Analysis in Pediatric Glioma of Different Grades. Genes (Basel). 2021;12(9). [PubMed ID: 34573317]. [PubMed Central ID: PMC8468898]. doi: 10.3390/genes12091335.##[20]Kuchipudi SV, Tellabati M, Nelli RK, White GA, Perez BB, Sebastian S, et al.18S rRNA is a reliable normalisation gene for real time PCR based on influenza virus infected cells. Virol J. 2012;9:230. [PubMed ID: 23043930]. [PubMed Central ID: PMC3499178]. doi: 10.1186/1743-422X-9-230.##[21]Tan SC, Carr CA, Yeoh KK, Schofield CJ, Davies KE, Clarke K.Identification of valid housekeeping genes for quantitative RT-PCR analysis of cardiosphere-derived cells preconditioned under hypoxia or with prolyl-4-hydroxylase inhibitors. Mol Biol Rep. 2012;39(4):4857-67. [PubMed ID: 22065248]. [PubMed Central ID: PMC3294216]. doi: 10.1007/s11033-011-1281-5.##[22]Barber RD, Harmer DW, Coleman RA, Clark BJ.GAPDH as a housekeeping gene: analysis of GAPDH mRNA expression in a panel of 72 human tissues. Physiol Genomics. 2005;21(3):389-95. [PubMed ID: 15769908]. doi: 10.1152/physiolgenomics.00025.2005.##[23]da Conceicao Braga L, Goncalves BOP, Coelho PL, da Silva Filho AL, Silva LM.Identification of best housekeeping genes for the normalization of RT-qPCR in human cell lines. Acta Histochem. 2022;124(1):151821. [PubMed ID: 34861601]. doi: 10.1016/j.acthis.2021.151821.##[24]Pessoa F, Viana VBJ, de Oliveira MB, Nogueira BMD, Ribeiro RM, Oliveira DS, et al.Validation of Endogenous Control Genes by Real-Time Quantitative Reverse Transcriptase Polymerase Chain Reaction for Acute Leukemia Gene Expression Studies. Genes (Basel). 2024;15(2). [PubMed ID: 38397141]. [PubMed Central ID: PMC10887733]. doi: 10.3390/genes15020151.##[25]Valceckiene V, Kontenyte R, Jakubauskas A, Griskevicius L.Selection of reference genes for quantitative polymerase chain reaction studies in purified B cells from B cell chronic lymphocytic leukaemia patients. Br J Haematol. 2010;151(3):232-8. [PubMed ID: 20813001]. doi: 10.1111/j.1365-2141.2010.08363.x.##[26]Bednarz-Misa I, Neubauer K, Zacharska E, Kapturkiewicz B, Krzystek-Korpacka M.Whole blood ACTB, B2M and GAPDH expression reflects activity of inflammatory bowel disease, advancement of colorectal cancer, and correlates with circulating inflammatory and angiogenic factors: Relevance for real-time quantitative PCR. Adv Clin Exp Med. 2020;29(5):547-56. [PubMed ID: 32424999]. doi: 10.17219/acem/118845.##[27]Zhang S, Jiang Y, Cheng Q, Zhong Y, Qin Y, Chen M.Inclusion Body Fusion of Human Parainfluenza Virus Type 3 Regulated by Acetylated alpha-Tubulin Enhances Viral Replication. J Virol. 2017;91(3). [PubMed ID: 27881643]. [PubMed Central ID: PMC5244348]. doi: 10.1128/JVI.01802-16.##[28]Wang L, Yang C, Liu Q, Zhang X, Mei X, Zhang T, et al.Validation and Evaluation of Reference Genes for Quantitative Real-Time PCR Analysis in Mythimna loreyi (Lepidoptera: Noctuidae). Insects. 2024;15(3). [PubMed ID: 38535380]. [PubMed Central ID: PMC10970824]. doi: 10.3390/insects15030185.##[29]Freitas FCP, Depintor TS, Agostini LT, Luna-Lucena D, Nunes FMF, Bitondi MMG, et al.Evaluation of reference genes for gene expression analysis by real-time quantitative PCR (qPCR) in three stingless bee species (Hymenoptera: Apidae: Meliponini). Sci Rep. 2019;9(1):17692. [PubMed ID: 31776359]. [PubMed Central ID: PMC6881334]. doi: 10.1038/s41598-019-53544-0.##[30]Wang Z, Meng Q, Zhu X, Sun S, Gao S, Gou Y, et al.Evaluation and Validation of Reference Genes for Quantitative Real-Time PCR in Helopeltis theivora Waterhouse (Hemiptera: Miridae). Sci Rep. 2019;9(1):13291. [PubMed ID: 31527603]. [PubMed Central ID: PMC6746731]. doi: 10.1038/s41598-019-49479-1.##[31]Kriegova E, Arakelyan A, Fillerova R, Zatloukal J, Mrazek F, Navratilova Z, et al.PSMB2 and RPL32 are suitable denominators to normalize gene expression profiles in bronchoalveolar cells. BMC Mol Biol. 2008;9:69. [PubMed ID: 18671841]. [PubMed Central ID: PMC2529339]. doi: 10.1186/1471-2199-9-69.##[32]Majidzadeh AK, Esmaeili R, Abdoli N.TFRC and ACTB as the best reference genes to quantify Urokinase Plasminogen Activator in breast cancer. BMC Res Notes. 2011;4:215. [PubMed ID: 21702980]. [PubMed Central ID: PMC3141519]. doi: 10.1186/1756-0500-4-215.##[33]Liu LL, Zhao H, Ma TF, Ge F, Chen CS, Zhang YP.Identification of valid reference genes for the normalization of RT-qPCR expression studies in human breast cancer cell lines treated with and without transient transfection. PLoS One. 2015;10(1). e0117058. [PubMed ID: 25617865]. [PubMed Central ID: PMC4305315]. doi: 10.1371/journal.pone.0117058.##[34]Paula Maria N, Jonas F, Veronika M, Carsten T, Sarah S.Validation of a Suitable Housekeeping Gene in Human Neuroblastoma SHSY-5Y Cell-Line Treated with Steroid Hormones Progesterone and Testosterone. Int J Neurol Neurother. 2023;10(2). doi: 10.23937/2378-3001/1410125.##</REF>
                    </REFRENCE>
                </REFRENCES>
            </ARTICLE>
            <ARTICLE>
                <Language_ID>1</Language_ID>
                <TitleE>Evaluation of Antifungal Effects of Various Extracts of Indigo (&lt;i&gt;Indigofera tinctoria&lt;/i&gt;) on &lt;i&gt;Phytophthora&lt;/i&gt; Fungus In Vitro</TitleE>
                <URL>https://brieflands.com/journals/gct/articles/162066</URL>
                <DOI>10.5812/gct-162066</DOI>
                <DOR></DOR>
                <ABSTRACTS>
                    <ABSTRACT>
                        <Language_ID>1</Language_ID>
                        <CONTENT>Background :The damage to agricultural products caused by fungal diseases accounts for approximately 12% of global production, with a higher impact in developing countries. One particularly destructive disease that inflicts significant damage on vegetable crops and greenhouses annually is seedling death and bush dieback disease, caused by the Phytophthora fungus. Currently, producers often rely heavily on chemical fertilizers and pesticides to enhance productivity and product quality. However, the use of some synthetic pesticides has recently been banned due to their high toxicity and long preharvest interval (PHI) periods. Biological control of plant diseases and pests is the optimal solution to mitigate the damages caused by synthetic pesticides. Objectives :This study aimed to evaluate the in vitro antifungal efficacy of different extracts derived from the aerial shoot of Indigofera tinctoria against plant pathogenic fungi. Methods :The aerial shoots of the Indigo plant were collected during the flowering stage from the medicinal plants collection of the Institute of Agricultural Research, Agriculture Institute Research, Institute of Zabol, Zabol, Iran. Ethanolic, methanolic, n-hexane, and acetone extracts were prepared by cold maceration with a ratio of 1:10. The antifungal effects of these extracts were investigated by measuring the diameter of halo growth inhibition under in vitro conditions. The LSD test was used to compare data means. Results :Our results showed that the best growth-inhibiting effect was observed with the ethanolic extract at a concentration of 300 μg/mL (2 mm) after 24 hours of incubation, whereas the diameter of colonies in the control was 27 mm, confirming a 92.5% inhibition of fungal growth. After 48 hours of incubation, the growth of Phytophthora drechsleri mycelium was clearly evident. In fact, the growth rate nearly doubled within 48 hours, but then at 73 hours, the mycelium grew at a slower rate. The inhibitory effect of the indigo extract was dose-dependent; as the extract concentration increased, the inhibitory effect became stronger. Conclusions :According to these results, the in vitro treatments were more significant when the plant extract concentration was higher. These findings could be promising for the production of natural fungicides.</CONTENT>
                    </ABSTRACT>
                </ABSTRACTS>
                <PAGES>
                    <PAGE>
                        <FPAGE>1</FPAGE>
                        <TPAGE>5</TPAGE>
                    </PAGE>
                </PAGES>
                <AUTHORS>
                    <AUTHOR>
                        <NameE>Zeynab</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Mohkami</FamilyE>
                        <Organizations>
                            <Organization>Department of Agriculture and Plant Breeding, Agriculture Institute, Research Institute of Zabol, Zabol, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>zaynabmohkami@uoz.ac.ir</Email>
                        </EMAILS>
                        <NameE>Fatemeh</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Bidarnamani</FamilyE>
                        <Organizations>
                            <Organization>Department of Agriculture and Plant Breeding, Agriculture Institute, Research Institute of Zabol, Zabol, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>f.bidarnamani@uoz.ac.ir</Email>
                        </EMAILS>
                        <NameE>Yasub</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Shiri</FamilyE>
                        <Organizations>
                            <Organization>Department of Agriculture and Plant Breeding, Agriculture Institute, Research Institute of Zabol, Zabol, Iran</Organization>
                            <Organization>Horticulture Department, Faculty of Agriculture and Natural Resources, Mohaghegh Ardabili University, Ardabil, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>yasub.shiri@gmail.com</Email>
                        </EMAILS>
                        <NameE>Dariush</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Ramezan</FamilyE>
                        <Organizations>
                            <Organization>Department of Horticultural Sciences and Green Space, Faculty of Agriculture, University of Zabol,Zabol,Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>drhorticul@uoz.ac.ir</Email>
                        </EMAILS>
                        <NameE>Yusuf</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Farrokhzad</FamilyE>
                        <Organizations>
                            <Organization>Department of Horticultural Sciences, Faculty of Agriculture, Shahid Chamran University of Ahvaz, Ahvaz, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>farrokhzadyusuf@gmail.com</Email>
                        </EMAILS>
                    </AUTHOR>
                </AUTHORS>
                <KEYWORDS>
                    <KEYWORD>
                        <KeyText>No Keyword</KeyText>
                    </KEYWORD>
                </KEYWORDS>
                <PDFFileName>4.pdf</PDFFileName>
                <REFRENCES>
                    <REFRENCE>
                        <REF>[0]Bajpai VK.In Vitro and In Vivo Inhibition of Plant Pathogenic Fungi by Essential Oil and Extracts of Magnolia liliflora Desr. Journal of Agricultural Science and Technology. 2012;14(4):845-56.##[1]Sitara U, Niaz I, Naseem J, Sultana N.Antifungal effect of essential oils on in vitro growth of pathogenic fungi. Pakistan Journal of Botany. 2008;40(1):409.##[2]Etebarian HR.[Diseases of vegetable and cucurbit and their control]. Univ Tehran. 2012;40(1):600.FA.##[3]Pal KK, McSpadden Gardener B.Biological Control of Plant Pathogens. The Plant Health Instructor. 2006. doi: 10.1094/phi-a-2006-1117-02.##[4]Soković M, van Griensven LJ.Antimicrobial activity of essential oils and their components against the three major pathogens of the cultivated button mushroom, Agaricus bisporus. European Journal of Plant Pathology. 2006;116(3):211-24. doi: 10.1007/s10658-006-9053-0.##[5]Rasooli I, Moosavi ML, Rezaee MB, Jaimand K.Susceptibility of microorganisms to Myrtus communis L. essential oil and its chemical composition. Agriculture Science Technol. 2018;(4):127-33.##[6]Cowan MM.Plant products as antimicrobial agents. Clin Microbiol Rev. 1999;12(4):564-82. [PubMed ID: 10515903]. [PubMed Central ID: PMC88925]. doi: 10.1128/CMR.12.4.564.##[7]Amini M, Safaie N, Salmani MJ, Shams-Bakhsh M.Antifungal activity of three medicinal plant essential oils against some phytopathogenic fungi. Trakia J Sci. 2012;10(1):1-8.##[8]Meazza G, Dayan FE, Wedge DE.Activity of quinones on colletotrichum species. J Agric Food Chem. 2003;51(13):3824-8. [PubMed ID: 12797750]. doi: 10.1021/jf0343229.##[9]Oliveira I, Sousa A, Ferreira IC, Bento A, Estevinho L, Pereira JA.Total phenols, antioxidant potential and antimicrobial activity of walnut (Juglans regia L.) green husks. Food Chem Toxicol. 2008;46(7):2326-31. [PubMed ID: 18448225]. doi: 10.1016/j.fct.2008.03.017.##[10]Fernández-Agulló A, Pereira E, Freire MS, Valentão P, Andrade PB, González-Álvarez J, et al.Influence of solvent on the antioxidant and antimicrobial properties of walnut (Juglans regia L.) green husk extracts. Industrial Crops and Products. 2013;42:126-32. doi: 10.1016/j.indcrop.2012.05.021.##[11]Stampar F, Solar A, Hudina M, Veberic R, Colaric M.Traditional walnut liqueur – cocktail of phenolics. Food Chemistry. 2006;95(4):627-31. doi: 10.1016/j.foodchem.2005.01.035.##[12]Mikulic-Petkovsek M, Slatnar A, Veberic R, Stampar F, Solar A.Phenolic response in green walnut husk after the infection with bacteria Xanthomonas arboricola pv. juglandis. Physiological and Molecular Plant Pathology. 2011;76(3-4):159-65. doi: 10.1016/j.pmpp.2011.09.006.##[13]Satish S, Raveesha KA, Janardhana GR.Antibacterial activity of plant extracts on phytopathogenic Xanthomonas campestris pathovars. Letters in Applied Microbiology. 2002;28(2):145-7. doi: 10.1046/j.1365-2672.1999.00479.x.##[14]Guleria S, Tiku AK.Botanicals in Pest Management: Current Status and Future Perspectives. Integrated Pest Management: Innovation-Development Process. 2009. p. 317-29. doi: 10.1007/978-1-4020-8992-3_12.##[15]Xu Y, Wu M, Feng XZ, Yin XB, He XW, Zhang YK.Reduced carbon dots versus oxidized carbon dots: photo- and electrochemiluminescence investigations for selected applications. Chemistry. 2013;19(20):6282-8. [PubMed ID: 23526652]. doi: 10.1002/chem.201204372.##[16]V SS, S GK, N MD.GC-MS Analysis and Phytochemical Screening of Indigofera tinctoria (Linn.) Leaf Extract Characterizing its Medicinal Use. International Journal of Ayurvedic Medicine. 2020;11(2):289-99. doi: 10.47552/ijam.v11i2.1540.##[17]Riccioni L, Orzali L.Activity of Tea Tree (Melaleuca alternifolia, Cheel) and thyme (Thymus vulgaris, Linnaeus.) Essential Oils against Some Pathogenic Seed Borne Fungi. Journal of Essential Oil Research. 2011;23(6):43-7. doi: 10.1080/10412905.2011.9712280.##[18]Colak M, Göktaş O, Özen E, Koca I, Cetin T.Research on the usage of antifungal and antibacterial properties of indigo (indigofera tinctoria l.) colorant used as a wood preservative. Wood Res. 2015;60(6):953-62.##[19]Bhat SA, Zargar MI, Wani SUD, Mohiuddin I, Masoodi MH, Shakeel F, et al.In-vitro evaluation of Indigofera heterantha extracts for antibacterial, antifungal and anthelmintic activities. J Pharm Health Care Sci. 2024;10(1):7. [PubMed ID: 38268049]. [PubMed Central ID: PMC10809583]. doi: 10.1186/s40780-024-00328-y.##</REF>
                    </REFRENCE>
                </REFRENCES>
            </ARTICLE>
            <ARTICLE>
                <Language_ID>1</Language_ID>
                <TitleE>Optimization of In Vitro Maturation in Ovine Oocytes: A Comparative Study of Maturation Media</TitleE>
                <URL>https://brieflands.com/journals/gct/articles/160506</URL>
                <DOI>10.5812/gct-160506</DOI>
                <DOR></DOR>
                <ABSTRACTS>
                    <ABSTRACT>
                        <Language_ID>1</Language_ID>
                        <CONTENT>Background :One of the most common techniques in assisted reproductive technologies (ART) is in vitro embryo production (IVEP), the success of which depends on the intrinsic quality of oocytes and the composition of the culture medium. Objectives :This study investigates the effects of gonadotropin hormones (such as eCG and hCG) along with the antioxidant quercetin on the maturation of ovine oocytes, as well as the impact of different media on the expression of Bcl2 and Bax genes in blastocysts. Methods :After washing the oocytes, cumulus-oocyte complexes (COCs) that exhibited three or more layers of cells and homogeneous cytoplasm were selected and matured in BO-IVM, TCM (TCM-199 + 10% FBS + 10% ovine follicular fluid + 5 mg/mL FSH + 1 mg/mL estradiol-17β + 0.81 mM sodium pyruvate + 50 mg/mL gentamicin sulfate), and TCM+ (TCM + 20 µg/mL eCG + 5 µg/mL hCG + 15 µg/mL quercetin) media for 24 hours at 38.5°C, 20% O2, and 5% CO2. After maturation, oocytes were fertilized with frozen ram semen, and presumed zygotes were cultured in BO-IVC under uniform conditions. Embryo development occurred at 38.5°C in a humid atmosphere with 5% CO2, 5% O2, and 90% N2. Results :The results indicated that the BO-IVM medium had a significantly higher mean percentage of zygotes, morulae, blastocysts, and hatched blastocysts compared to TCM+ and TCM (P &lt; 0.05). Moreover, blastocyst formation and hatched blastocysts were significantly more frequent in TCM+ than in TCM (P &lt; 0.05). However, the BO-IVM medium demonstrated a significant improvement compared to other maturation media. Gene expression analysis showed no significant difference in Bcl2 expression among the groups, while Bax expression was significantly higher in TCM (P &lt; 0.05). Overall, the BO-IVM medium was identified as the best option for optimizing oocyte maturation and producing high-quality blastocysts in ovine, with TCM+ yielding better results than the TCM medium without hormonal and antioxidant compounds. Conclusions :The results of this study showed that the addition of the antioxidant quercetin and the growth factors eCG and hCG improved the performance of the TCM medium. However, further research is needed to enhance the performance of the TCM maturation medium compared to the commercial BO-IVM medium.</CONTENT>
                    </ABSTRACT>
                </ABSTRACTS>
                <PAGES>
                    <PAGE>
                        <FPAGE>1</FPAGE>
                        <TPAGE>8</TPAGE>
                    </PAGE>
                </PAGES>
                <AUTHORS>
                    <AUTHOR>
                        <NameE>Abbas</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Darzi Nia</FamilyE>
                        <Organizations>
                            <Organization>Department of Agriculture, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>a1darzinia@gmail.com</Email>
                        </EMAILS>
                        <NameE>Mohammad</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Zandi</FamilyE>
                        <Organizations>
                            <Organization>Department of Agriculture, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>mz1075@yahoo.com</Email>
                        </EMAILS>
                        <NameE>Annahita</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Ghaedrahmati</FamilyE>
                        <Organizations>
                            <Organization>Department of Animal Science, Agricultural Sciences and Natural Resources University of Khuzestan, Khuzestan, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>rahmati.annahita1372@yahoo.com</Email>
                        </EMAILS>
                    </AUTHOR>
                </AUTHORS>
                <KEYWORDS>
                    <KEYWORD>
                        <KeyText>No Keyword</KeyText>
                    </KEYWORD>
                </KEYWORDS>
                <PDFFileName>5.pdf</PDFFileName>
                <REFRENCES>
                    <REFRENCE>
                        <REF>[0]Musapoor S, Davoodian N, Kadivar A, Ahmadi E, Nazari H.Media Supplementation With Gamma-Oryzanol Improves the Outcome of Ovine Oocyte Maturation In Vitro. Vet Med Sci. 2025;11(1). e70134. [PubMed ID: 39688528]. [PubMed Central ID: PMC11651092]. doi: 10.1002/vms3.70134.##[1]Podda A, Dujickova L, Ariu F, Leoni GG, Izquierdo D, Paramio MT, et al.Effect of Liquid Marble 3D Culture System on In Vitro Maturation and Embryo Development of Prepubertal Goat Oocytes. Animals (Basel). 2025;15(2). [PubMed ID: 39858188]. [PubMed Central ID: PMC11758309]. doi: 10.3390/ani15020188.##[2]Bahrami M, Cottee PA.Culture conditions for in vitro maturation of oocytes–A review. Reproduct Breed. 2022;2(2):31-6.##[3]Bilal M, Ashraf MK, Ashraf T, Yaseen M, Husnain A, Bin Majeed MB, et al.Effect of human chorionic gonadotropin on oocyte maturation and developmental competence in buffalo. Theriogenology. 2025;235:56-63. [PubMed ID: 39787661]. doi: 10.1016/j.theriogenology.2024.12.029.##[4]Farag IM, Girgis SM, Khalil WKB, Hassan NHA, Sakr AAM, Abd Allah SM, et al.Effect of hormones, culture media and oocyte quality on in vitro maturation of Egyptian Sheep oocytes. J Appl Biosci. 2009;24:1520-34.##[5]Wei SC, Gong ZD, Zhao HW, Liang HQ, Lai LJ, Deng YY.Equine chorionic gonadotropin influence on sheep oocyte in vitro maturation, apoptosis, and follicle-stimulating hormone receptor and luteinizing hormone receptor expression. Genet Mol Res. 2016;15(4):1-12.##[6]Zhu J, Moawad AR, Wang CY, Li HF, Ren JY, Dai YF.Advances in in vitro production of sheep embryos. Int J Vet Sci Med. 2018;6(Suppl):S15-26. [PubMed ID: 30761316]. [PubMed Central ID: PMC6161858]. doi: 10.1016/j.ijvsm.2018.02.003.##[7]Bastos BDM, da Silva MNP, Gonçalves PR, Cândido AECM, Barberino RDS, do Monte APO, et al.Effect of different gonadotropins on in vitro maturation of sheep oocytes. Semina: Cienc. 2022;43(6).##[8]Russell DL, Gilchrist RB, Brown HM, Thompson JG.Bidirectional communication between cumulus cells and the oocyte: Old hands and new players? Theriogenology. 2016;86(1):62-8. [PubMed ID: 27160446]. doi: 10.1016/j.theriogenology.2016.04.019.##[9]Chandra V, Sharma GT.In vitro strategies to enhance oocyte developmental competence. Front Biosci (Schol Ed). 2020;12(1):116-36. [PubMed ID: 32114451]. doi: 10.2741/S543.##[10]Karami Shabankareh H, Sarsaifi K, Mehrannia T.In vitro maturation of ovine oocytes using different maturation media: effect of human menopausal serum. J Assist Reprod Genet. 2011;28(6):531-7. [PubMed ID: 21152965]. [PubMed Central ID: PMC3158248]. doi: 10.1007/s10815-010-9523-3.##[11]Gupta PS, Nandi S, Ravindranatha BM, Sarma PV.Effect of commercially available PMSG on maturation, fertilization and embryo development of buffalo oocytes in vitro. Reprod Fertil Dev. 2001;13(5-6):355-60. [PubMed ID: 11833930]. doi: 10.1071/rd01026.##[12]Di Berardino C, Peserico A, Capacchietti G, Crociati M, Monaci M, Tosi U, et al.Equine Chorionic Gonadotropin as an Effective FSH Replacement for In Vitro Ovine Follicle and Oocyte Development. Int J Mol Sci. 2021;22(22). [PubMed ID: 34830304]. [PubMed Central ID: PMC8619287]. doi: 10.3390/ijms222212422.##[13]Mingoti GZ, Garcia JM, Rosa-e-Silva AA.Steroidogenesis in cumulus cells of bovine cumulus-oocyte-complexes matured in vitro with BSA and different concentrations of steroids. Anim Reprod Sci. 2002;69(3-4):175-86. [PubMed ID: 11812628]. doi: 10.1016/s0378-4320(01)00187-7.##[14]Baiomy FM, Kamel AM, Hussein AF, Hassanin SH.The Impact of Maturation Medium Supplemented with PMSG and HCG Hormones on In vitro Maturation of Ovine Oocytes. J Appl Veterinary Sci. 2025;10(1):81-91.##[15]Kang JT, Kwon DK, Park SJ, Kim SJ, Moon JH, Koo OJ, et al.Quercetin improves the in vitro development of porcine oocytes by decreasing reactive oxygen species levels. J Vet Sci. 2013;14(1):15-20. [PubMed ID: 23388446]. [PubMed Central ID: PMC3615227]. doi: 10.4142/jvs.2013.14.1.15.##[16]Davoodian N, Kadivar A, Ahmadi E, Nazari H, Mehrban H.Quercetin effect on the efficiency of ovine oocyte vitrification at GV stage. Theriogenology. 2021;174:53-9. [PubMed ID: 34418772]. doi: 10.1016/j.theriogenology.2021.07.027.##[17]Cao Y, Zhao H, Wang Z, Zhang C, Bian Y, Liu X, et al.Quercetin promotes in vitro maturation of oocytes from humans and aged mice. Cell Death Dis. 2020;11(11):965. [PubMed ID: 33177495]. [PubMed Central ID: PMC7658351]. doi: 10.1038/s41419-020-03183-5.##[18]Davoodian N, Kadivar A, Davoodian N, Ahmadi E, Nazari H, Mehrban H.The effect of quercetin in the maturation media on cumulus-granulosa cells and the developmental competence of bovine oocytes. Theriogenology. 2022;189:262-9. [PubMed ID: 35809360]. doi: 10.1016/j.theriogenology.2022.06.026.##[19]Khadr AH, El-Sherbiny AM, Abdoon ASS.Effect of Culture Media, Gonadotropins, Proteins, Growth Factors and Hyaluronic Acid on In-Vitro Maturation of Buffalo Oocytes. J Animal Poultry Pro. 2022;13(7):91-7.##[20]Farag IM, Girgis SM, Zowail ME, El-Hafez MAMA.In vitro maturation of camel (Camelus dromedarius) cumulus-denuded oocytes. World Appl Sci J. 2013;26(3):352-9.##[21]Hegab AO, Montasser AE, Hammam AM, El-Naga E, Zaabel SM.Improving in vitro maturation and cleavage rates of buffalo oocytes. Animal Repro. 2018;6(2):416-21.##[22]Mogas T, Izquierdo D, Palomo MJ, Paramio MT.Effect of hormones, serum source and culture system on the IMV and IVF of prepubertal goat oocytes and subsequent embryo development. Theriogenology. 1995;(43):284.##[23]Leisinger C, Coffman E, Coutinho da Silva M, Forshey B, Pinto C.Factors affecting in vitro maturation of alpaca (Lama paco) oocytes. Anim Reprod Sci. 2014;150(1-2):70-5. [PubMed ID: 25261077]. doi: 10.1016/j.anireprosci.2014.08.011.##[24]Quispe-Gutiérrez US, Olivera-Marocho LV, Ccopa-Ccallata J, Pahuara-Farfan LE, Barragán-Condori M, Berndtson JL.Effect of FSH and eCG on alpaca (Vicugna pacos) oocyte maturation in vitro. J Vet Sci. 2021;10(3).##[25]Kang JT, Moon JH, Choi JY, Park SJ, Kim SJ, Saadeldin IM, et al.Effect of Antioxidant Flavonoids (Quercetin and Taxifolin) on In vitro Maturation of Porcine Oocytes. Asian-Australas J Anim Sci. 2016;29(3):352-8. [PubMed ID: 26950865]. [PubMed Central ID: PMC4811785]. doi: 10.5713/ajas.15.0341.##[26]Yu S, Long H, Lyu QF, Zhang QH, Yan ZG, Liang HX, et al.Protective effect of quercetin on the development of preimplantation mouse embryos against hydrogen peroxide-induced oxidative injury. PLoS One. 2014;9(2). e89520. [PubMed ID: 24586844]. [PubMed Central ID: PMC3931787]. doi: 10.1371/journal.pone.0089520.##[27]Karimian M, Zandi M, Sanjabi MR, Masoumian M, Ofoghi H.Effects of grape seed extract, quercetin and vitamin C on ovine oocyte maturation and subsequent embryonic development. Cell Mol Biol (Noisy-le-grand). 2018;64(4):98-102. [PubMed ID: 29631690].##[28]Wang H, Jo YJ, Oh JS, Kim NH.Quercetin delays postovulatory aging of mouse oocytes by regulating SIRT expression and MPF activity. Oncotarget. 2017;8(24):38631-41. [PubMed ID: 28418847]. [PubMed Central ID: PMC5503559]. doi: 10.18632/oncotarget.16219.##[29]Silva AAA, Silva MNP, Figueiredo LBF, Goncalves JD, Silva MJS, Loiola MLG, et al.Quercetin influences in vitro maturation, apoptosis and metabolically active mitochondria of goat oocytes. Zygote. 2018;26(6):465-70. [PubMed ID: 30767819]. doi: 10.1017/S0967199418000485.##[30]Banihosseini SZ, Novin MG, Nazarian H, Piryaei A, Parvardeh S, Eini F.Quercetin improves developmental competence of mouse oocytes by reducing oxidative stress during in vitro maturation. Ann Animal Sci. 2018;18(1).##[31]Rashidi Z, Aleyasin A, Eslami M, Nekoonam S, Zendedel A, Bahramrezaie M, et al.Quercetin protects human granulosa cells against oxidative stress via thioredoxin system. Reprod Biol. 2019;19(3):245-54. [PubMed ID: 31383475]. doi: 10.1016/j.repbio.2019.07.002.##[32]Yang W, Liu R, Sun Q, Huang X, Zhang J, Huang L, et al.Quercetin Alleviates Endoplasmic Reticulum Stress-Induced Apoptosis in Buffalo Ovarian Granulosa Cells. Animals (Basel). 2022;12(6). [PubMed ID: 35327186]. [PubMed Central ID: PMC8944572]. doi: 10.3390/ani12060787.##[33]Wang J, Qian X, Gao Q, Lv C, Xu J, Jin H, et al.Quercetin increases the antioxidant capacity of the ovary in menopausal rats and in ovarian granulosa cell culture in vitro. J Ovarian Res. 2018;11(1):51. [PubMed ID: 29929541]. [PubMed Central ID: PMC6013856]. doi: 10.1186/s13048-018-0421-0.##[34]Chelenga M, Yanagawa Y, Katagiri S, Nagano M.Pre-maturational culture promotes the developmental competence of bovine oocytes derived from an 8-day in vitro growth culture system. J Reprod Dev. 2023;69(4):214-7. [PubMed ID: 37197977]. [PubMed Central ID: PMC10435529]. doi: 10.1262/jrd.2023-022.##[35]Bunderson I, Liu Y, Polejaeva I.215 Effects of serum-free maturation medium and resveratrol supplementation on ovine oocyte maturation and quality. Repro Fertility Develop. 2023;36(2):263.##[36]Prochowska S, Nizanski W, Partyka A, Kochan J, Mlodawska W, Nowak A, et al.The use of human and bovine commercial media for oocyte maturation and embryo development in the domestic cat (Felis catus). Reprod Domest Anim. 2019;54(4):719-26. [PubMed ID: 30786066]. doi: 10.1111/rda.13418.##[37]Pryor JH, Hasler JF, Strøbech L, Avery B, Hashem N, Menges S, et al.86 improved bovine embryo production using novel in vitro culture systems. Repro Fertility Develop. 2016;28(2):172.##[38]Ratchamak R, Authaida S, Koedkanmark T, Boonkum W, Chankitisakul V.Coenzyme Q10 Supplementation Effects on In Vitro Oocyte Maturation, Lipid Peroxidation, and Embryonic Development in Prepubertal and Aging Thai-Holstein Cows. Animals (Basel). 2024;15(1). [PubMed ID: 39794960]. [PubMed Central ID: PMC11718854]. doi: 10.3390/ani15010018.##[39]Ghaedrahmati A, Mamouei M, Zandi M.Low Serum Concentration in Ovine Embryo Culture Media. Gene, Cell and Tissue. 2024;11(3).##[40]Kale SD, Pawshe CH, Birade HS, Ingawale MV, Deshmukh SG, Harkal SB, et al.Effect of maturation media on early embryonic development of goat immature oocytes. J Entomol Zool Stud. 2020;8(1):1345-8.##</REF>
                    </REFRENCE>
                </REFRENCES>
            </ARTICLE>
            <ARTICLE>
                <Language_ID>1</Language_ID>
                <TitleE>Aerobic Exercise and Celastrol: A Promising Combination for Achilles Tendon Regeneration</TitleE>
                <URL>https://brieflands.com/journals/gct/articles/160515</URL>
                <DOI>10.5812/gct-160515</DOI>
                <DOR></DOR>
                <ABSTRACTS>
                    <ABSTRACT>
                        <Language_ID>1</Language_ID>
                        <CONTENT>Background :Tendons are subjected to mechanical stress and strain during daily activities and physical exercise, which makes them susceptible to injury. Objectives :This randomized trial evaluated the effects of a 4-week combination of training and celastrol on the healing of Achilles tendon ruptures in rats. It assessed cytokine levels, gene expression, and histological changes. Methods :Rats with Achilles tendon ruptures were randomly assigned to several treatment groups: Sham, negative control, training, celastrol, and a combination of training and celastrol. Eligibility criteria included age, weight, and the absence of pre-existing tendon injuries. The assessments included enzyme-linked immunosorbent assay (ELISA) to measure cytokine levels [bFGF, IGF1, cyclooxygenase 2 (COX2)], real-time polymerase chain reaction (RT-PCR) to analyze gene expression (scleraxis, periostin, MMP9, collagen I), and histological analysis using Masson's trichrome staining to evaluate collagen organization. Results :The training-celastrol group exhibited the highest levels of bFGF, IGF1, and COX2, indicating a synergistic effect on tendon healing compared to the sham and negative control groups, with effect sizes of 0.85 (95% CI: 0.70 - 1.00). Additionally, RT-PCR results showed that the training-celastrol group had the highest expression of scleraxis, periostin, MMP9, and collagen I, suggesting enhanced tendon repair and remodeling. Histological analysis revealed that the training-celastrol group displayed the most organized collagen fibers, whereas the sham group showed regular organization, and the negative control group exhibited disorganized fibers. Conclusions :The study concluded that combining aerobic training and celastrol significantly enhances tendon healing by improving cytokine levels, gene expression, and collagen organization. Outcome measures were assessed at baseline, mid-treatment (week 2), and post-treatment (week 4) to evaluate temporal changes. These findings highlight the effectiveness of these therapeutic strategies in promoting tendon repair and maintaining structural integrity.</CONTENT>
                    </ABSTRACT>
                </ABSTRACTS>
                <PAGES>
                    <PAGE>
                        <FPAGE>1</FPAGE>
                        <TPAGE>12</TPAGE>
                    </PAGE>
                </PAGES>
                <AUTHORS>
                    <AUTHOR>
                        <NameE>Arash</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Bagherzadeh</FamilyE>
                        <Organizations>
                            <Organization>Department of Sports Physiology, Islamic Azad University, Islamshahr Branch, Islamshahr, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>arashbagherzadeh@live.com</Email>
                        </EMAILS>
                        <NameE>Yaser</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Kazemzadeh</FamilyE>
                        <Organizations>
                            <Organization>Department of Sports Physiology, Islamic Azad University, Islamshahr Branch, Islamshahr, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>yaser.kazemzadeh@yahoo.com</Email>
                        </EMAILS>
                        <NameE>Arash</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Abdolmaleki</FamilyE>
                        <Organizations>
                            <Organization>Department of Biophysics, Faculty of Advanced Technologies, University of Mohaghegh Ardabili, Namin, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>abdolmalekiarash1364@gmail.com</Email>
                        </EMAILS>
                        <NameE>Zohreh</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Afsharmand</FamilyE>
                        <Organizations>
                            <Organization>Department of Physical Education and Sport Sciences, Islamic Azad University, Islamshahr Branch, Tehran, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>afsharmandz231@gmail.com</Email>
                        </EMAILS>
                    </AUTHOR>
                </AUTHORS>
                <KEYWORDS>
                    <KEYWORD>
                        <KeyText>No Keyword</KeyText>
                    </KEYWORD>
                </KEYWORDS>
                <PDFFileName>6.pdf</PDFFileName>
                <REFRENCES>
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[PubMed ID: 19793213]. doi: 10.1111/j.1600-0838.2009.00949.x.##[19]Chen H, Li S, Xiao H, Wu B, Zhou L, Hu J, et al.Effect of Exercise Intensity on the Healing of the Bone-Tendon Interface: A Mouse Rotator Cuff Injury Model Study. Am J Sports Med. 2021;49(8):2064-73. [PubMed ID: 33989078]. doi: 10.1177/03635465211011751.##[20]Gao Q, Qin H, Zhu L, Li D, Hao X.Celastrol attenuates collagen-induced arthritis via inhibiting oxidative stress in rats. Int Immunopharmacol. 2020;84:106527. [PubMed ID: 32402948]. doi: 10.1016/j.intimp.2020.106527.##[21]Zhang J, Wang R, Cheng L, Xu H.Celastrol inhibit the proliferation, invasion and migration of human cervical HeLa cancer cells through down-regulation of MMP-2 and MMP-9. J Cell Mol Med. 2021;25(11):5335-8. [PubMed ID: 33945201]. [PubMed Central ID: PMC8178258]. doi: 10.1111/jcmm.16488.##[22]Wang W, Ha C, Lin T, Wang D, Wang Y, Gong M.Celastrol attenuates pain and cartilage damage via SDF-1/CXCR4 signalling pathway in osteoarthritis rats. 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                    </REFRENCE>
                </REFRENCES>
            </ARTICLE>
            <ARTICLE>
                <Language_ID>1</Language_ID>
                <TitleE>The Effect of Branched-Chain Amino Acids (L-Valine, L-Leucine and L-Isoleucine) on Intestinal Morphology and IGF-1 Gene Expression in Broiler Chickens</TitleE>
                <URL>https://brieflands.com/journals/gct/articles/157575</URL>
                <DOI>10.5812/gct-157575</DOI>
                <DOR></DOR>
                <ABSTRACTS>
                    <ABSTRACT>
                        <Language_ID>1</Language_ID>
                        <CONTENT>Background :Insulin-like growth factor 1 (IGF-1) is an important regulator of growth, amino acid (AA) elongation, glucose metabolism, DNA synthesis, protein synthesis, and the proliferation and differentiation of various cell types. Therefore, IGF-1 may affect intestinal morphology by increasing nutrient uptake into intestinal enterocytes and promoting cell proliferation. Objectives :The present study aimed to evaluate the effects of different levels of branched-chain amino acids (BCAAs) (L-valine, L-leucine, and L-isoleucine) in low crude protein (CP) diets on intestinal morphology and IGF-1 gene expression in broiler chickens. Methods :A total of 480 one-day-old male and female broilers of the Ross 308 strain, with an average weight of 42.75 ± 0.47 g, were used. This experiment was carried out as a 3 × 2 factorial in the form of a completely randomized design with 6 treatments and 4 replications. The experimental diets included three levels of BCAA (0%, 10%, and 20% higher than the standard) and two levels of CP (standard or 10% lower than the standard). Results :Using 20% BCAA in the diet increased the villus height to crypt depth (VH/CD) ratio in the duodenum, jejunum, and ileum compared to the standard level of BCAA (P &lt; 0.05). Reducing CP by 10% significantly lowered the VH/CD ratio in the duodenum, jejunum, and ileum (P &lt; 0.05). The expression of IGF-1 mRNA in liver tissue was higher in the groups containing 10% BCAA than in the standard BCAA groups, regardless of the CP level. Conclusions :In general, BCAA supplementation could be beneficial for improving intestinal morphology and IGF-1 gene expression in broiler chickens on low CP diets.</CONTENT>
                    </ABSTRACT>
                </ABSTRACTS>
                <PAGES>
                    <PAGE>
                        <FPAGE>1</FPAGE>
                        <TPAGE>8</TPAGE>
                    </PAGE>
                </PAGES>
                <AUTHORS>
                    <AUTHOR>
                        <NameE>Shahriyar</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Khalilzadeh</FamilyE>
                        <Organizations>
                            <Organization>Department of Animal Science, Karaj Branch, Islamic Azad University, Karaj, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>1980shahriyar@gmail.com</Email>
                        </EMAILS>
                        <NameE>Abolfazl</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Zarei</FamilyE>
                        <Organizations>
                            <Organization>Department of Animal Science, Karaj Branch, Islamic Azad University, Karaj, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>a-zarei@kiau.ac.ir</Email>
                        </EMAILS>
                        <NameE>Nima</NameE>
                        <MidNameE></MidNameE>
                        <FamilyE>Eila</FamilyE>
                        <Organizations>
                            <Organization>Department of Animal Science, Karaj Branch, Islamic Azad University, Karaj, Iran</Organization>
                        </Organizations>
                        <Universities>
                            <University></University>
                        </Universities>
                        <Countries>
                            <Country>Iran</Country>
                        </Countries>
                        <EMAILS>
                            <Email>nima.eila@kiau.ac.ir</Email>
                        </EMAILS>
                    </AUTHOR>
                </AUTHORS>
                <KEYWORDS>
                    <KEYWORD>
                        <KeyText>No Keyword</KeyText>
                    </KEYWORD>
                </KEYWORDS>
                <PDFFileName>7.pdf</PDFFileName>
                <REFRENCES>
                    <REFRENCE>
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                    </REFRENCE>
                </REFRENCES>
            </ARTICLE>
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