Abstract
Keywords
Introduction
Free radicals, along with oxidative stress reactions can lead to damage biological molecules like DNA, proteins, and lipids (1, 2). Therefore, oxidative stress has been involved in pathogenesis of various diseases including cancers, atherosclerosis, and neurodegenerative disorders such as Alzheimer’disease (AD) (3, 4). Pathophysiology of AD is relevant to oxidative stress and evacuation of neurotransmitter acetylcholine by acetylcholinesterases (5). A prevalent method for treating AD is to increase the ACh level in the brain utilization AChE inhibitors (6). The chemical medicines have limitations associated with side-effects. The search for discovering strong new AChE inhibitors from natural origins without side effects is great attention (7). Currently, a number of treatments are applied against Alzheimer’s disease too to answer the effect of oxidative stress. These consist of the use of acetylcholinesterase inhibitors (AChEIs) and large amount of antioxidant (5).
Plants supply a valuable resource, functional as leads to the extension of therapeutic compounds (8). Regular consumption of numerous plant species as daily diet and use of natural health products (NHPs) as medication urged the scientists to conduct extensive research on the antioxidant and AChE inhibitory effects of phenolic compounds in the treatment of AD (9).
The genus Leutea is represented by 11 taxa widespread throughout central Asia and Iran (10). Recently, this genus has been categorized as Ferula group (Ferula, Dorema, and Leutea) (11, 12). Since Dorema and Ferula genera have strong antioxidant activity, this study was conducted on Leutea avicenniae for the first time (12, 13).
The extracts and diastereoisomers of Ferula lutea were examined for antioxidant activity and AChE inhibitory effects. The ethyl acetate extract had the strongest antioxidant activity (IC50 = 12.8 ± 1.29 µg/mL) (13). Another investigation reported antioxidant and anti-hemolytic activities of Ferula gummosa Boiss.and its extract exerted moderate antioxidant activity (IC50 = 579.6 ± 19.4 µg/mL) which was comparable with vitamin C (14).
In a study, antioxidant effects and AChE inhibitory effects of quercetin and astragalin isolated from Gossypium herbaceum were examined showing strong antioxidant effects (IC50=0.84 µg/mL) and acetylcholinesterase inhibitory (IC50 = 50.99 µg/mL) (15).
In this study, we report the results of the antioxidant and AChE inhibitory effects of L. avicennia extract and it’s identified compounds isolated from the methanol fraction.
Experimental
Chemicals
Acetylcholinesterase (AChE) and Acetylthiocholin iodide (ATCI) was purchased from Sigma (Germany). 5, 5′-dithiobis-(2-nitrobenzoic acid) (DTNB) and other chemicals and solvents were provided from Merck (Germany).
Plant material
Aerial parts of L. avicennia were collected during flowering period from Kaboudarahang Mountain (2200 m) in Hamadan Province (West Iran), in August 2012 and identified by botanist Majid Aghaahmadi. The voucher specimen of the plant (Voucher No. 6761-TEH) was kept in the Herbarium of the Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Methods
Extraction and fractionation
700g of the air dried aerial parts of plant was macerated with 80% methanol (4 L ×5) at room temperature and was concentrated with an evaporator in low temperature (40 °C). The crude extract (160 g) was sequentially fractionated with petroleum ether, chloroform, ethyl acetate, and methanol (each 4 L) respectively, to obtain four fractions.
Acetylcholinestrase (AChE) inhibitory activity of Fractions
AChE inhibitory effect of petroleum ether, chloroform, ethyl acetate, and methanol fractions were carried out by the Ellman′s method (16). Galantamine was used as a positive control and distilled water as negative control.
In this method, 100 µL of 0.1 mM sodium phosphate buffer (pH = 8.0), 20 µL DTNB (5,5′-Dithiobis (2-nitrobenzoic acid) 20 µL of sample solution, 2 µL of AChE solution were added into 96 micro plates and were incubated for 15 min at 25 °C and then acetylcholine iodide (100 µL of 0.05 mM water solution) was added as substrate. Acetylcholinestrase activity was evaluated by measuring the absorbance at 412 nm by an ELISA plate reader for 3.0 min at 25 °C. The concentration of the compound which inhibited 50% of acetylcholinestrase activity (IC50) was calculated (Table 1).
Antioxidant Activity and AChE Inhibitory effects of extract, fractions and isolated compounds of L.avicennia
| Samples | Antioxidant Activity IC50 ± SD | AChE Inhibitory IC50 ± SD* |
|---|---|---|
| Crude extract | 125.20±1.0 | - |
| Petroleum ether fraction | 253.40±2.2 | - |
| Chloroform fraction | 106.70±4.8 | - |
| Ethyl acetate fraction | 85.40±4.3 | - |
| Methanol fraction | 49.80±7.0 | 205.10±3.3 |
| Quercetin | 10.24±1.3 | 66.50±2.4 |
| Astragalin | 26.92±3.5 | 72.80±1.8 |
| Caffeic acid | 11.41±6.0 | 12.06±2.0 |
| Salicylic acid | 114.57±1.0 | - |
| p-Coumaric acid | 110.33±1.2 | - |
| BHT | 19.50±2.8 | ND |
| Galantamine | ND | 6.24±2.2 |
DPPH radical scavenging activity
The DPPH method is based on the free radical scavenging activity (17). briefly, 2 mL of DPPH solution in methanol (4×10-5 g/mL) was prepared and added to 1 mL of different concentrations of sample solution in methanol (0.1, 0.5 and 1.0 mg/mL). The mixture was kept in the dark for 30 min at room temperature. The antioxidant activity was measured by Shimadzu, UV/VIS model 160A spectrophotometer at 517 nm.
All the measurements were done in triplicate. The IC50 values were calculated as means ± SD and butylated hydroxytoluene (BHT) was used as positive control.
Isolation and identification of compounds
The potent methanol fraction (20 g) was subjected to Sephadex LH-20 (Fluka, Switzerland) column chromatography using 100% methanol as eluent. This was followed by increasing water up to 50% resulting in 3 fractions (M1-M2-M3). Fraction M1 (1.5g) was re-chromatographed over a Sephadex LH-20 and eluted with MeOH-H2O (6:4) to collect compound 1 (8 mg). Fraction M2 (700 mg) was run on a C18 reversed-phase (230-400 mesh, fully end capped, Fluka, Switzerland) column chromatography using MeOH-H2O (8:2) as eluent, and compound 2 (11 mg) was achieved.
Compounds 3, 4, 5 were isolated from M3 fraction using paper chromatography (PC, Whatman No.1) and solvent system BAW (butanol: acetic acid: water, 4:1:5). For further purification the subfractions were subjected to PC on Whatman No.1 with 15% acetic acid, then, they were re-chromatographed over sephadex LH-20 to earn compound 3 (12 mg, Rf = 0.4, blue before and after using NH3 vapor at 366 nm), compound 4 (9 mg, Rf = 0.59, yellow before and after using NH3 under 366 nm), and compound 5 (250 mg, Rf = 0.34, dark blue before and after using NH3 under 366 nm) (18, 19).The isolated compounds were identified with different spectroscopic methods (1H-NMR, 13C-NMR and UV) as quercetin, astragalin, caffeic acid, salicylic acid and p-coumric acid (Figure1).
Acetylcholinestrase inhibitory and antioxidant activity of isolated compounds
AChE inhibitory and antioxidant effects of isolated compounds: quercetin, astragalin, caffeic acid, p-coumaric acid and salicylic acid were examined by the Ellman′s and DPPH methods respectively for determination of effective compounds (Table 1).
Results and Discussion
L. avicennia is an endemic plant of Iran and the purpose of this study was evaluation of antioxidant and AchE inhibitory effects of the plant extract, fractions, and isolated compounds. According to the antioxidant test, methanol fraction exerted strong free radical scavenging activity (IC50 = 49.8 ± 7.0 µg/mL) compared to the other fractions. Quercetin exhibited the highest free radical scavenging activity with IC50 = 10.24 ± 1.3 µg/mL compared to BHT as positive control (IC50=19.5 ± 2.8 µg/mL) while the lowest activity belonged to salicylic acid (IC50=114.57 ± 1.0 µg/mL). Regarding the inhibition of acethylcholinestrase, methanol fraction showed inhibitory activity (205.10 ± 3.3 µg/mL) among other fraction and caffeic acid (IC50 = 12.06 ± 2.01 µg/mL) was stronger than other isolated compounds.
The antioxidant activity and AChE inhibitory assay of the total extract, fractions, and compounds are listed in the Table 1.
Isolation and purification of compounds from methanol fraction, has been done by various chromatographic techniques, including PC, and column chromatography (LH 20, normal and reversed–phase silicagel). Finally, five compounds were isolated and identified with different spectroscopic methods (1H- NMR, 13C-NMR, and UV) and were compared with the reported data, including quercetin (20, 21, 22), astragalin (20, 23), caffeic acid (24, 25), salicylic acid (26) and p-coumric acid (27, 28, 29) (Figure1).
In previous study, quercetin(IC50=19.8 µg/mL). and 3-methoxy quercetin (IC50=37.9 µg/mL) isolated from Agrimonia had remarkable AChE inhibitory effect (16). Also, effect of quercetin on triple transgenic mice of Alzheimer’s disease model has been studied and protective effects on performance, emotional and cognitive behavior have been confirmed on brain cells (30). In another study conducted in 2015, pharmacokinetics and mechanism of neuroprotective effect of quercetin was studied in mice representing strong protective effects of this compound on the brain cells (31).
Conclusion
This study was conducted for the first time on Leutea avicennia, and showed this plant is rich of phenolic compounds that exhibited appropriate antioxidant and anti- acetylcholinesterase properties. Caffeic acid is one of the substances which showed potent activity in both assays, therefore methanol fraction of L.avicennia and their components probably could be used in treatment of neurodegenerative disease, so in-vivo animal model is worthwhile and recommended.
Acknowledgements
References
-
1.
Grassi D, Desideri G, Croce G, Tiberti S, Aggio A, Ferri C. Flavonoids, vascular function and cardiovascular protection. Curr. Pharm. Des. 2009;15:1072-84. [PubMed ID: 19355949].
-
2.
Stocker R, Keaney JF. Role of Oxidative Modifications in Atherosclerosis. J. Physiol. Rev. 2004;84:1381-478.
-
3.
Madamanchi NR, Vendrov A, Runge MS. Oxidative Stress and Vascular Disease Arterioscler. Thromb. Vasc. Biol. 2005;25:29-38.
-
4.
Ji HF, Zhang HY. Theoretical evaluation of flavonoids as multipotent agents to combat Alzheimer›s disease. J. Mol. Struct. Theochem. 2006;767:3-9.
-
5.
Ghribia L, Ghouilaa H, Omrib L, Besbesb M, Ben Janneta H. Antioxidant and anti-acetylcholinesterase activities of extracts and secondary metabolites from Acacia cyanophylla. J. Asian Pac. Trop. Biomed. 2014;4:417-23.
-
6.
Ramassamy C. Emerging role of polyphenolic compounds in the treatment of neurodegenerative diseases: A review of their intracellular targets. Eur. J. Pharmacol. 2006;545:51-64. [PubMed ID: 16904103].
-
7.
Heo HJ, Kim MJ, Lee JM, Choi SJ, Cho HY, Hong B, Kim HK, Kim E and Shin DH. Naringenin from Citrus junos has an inhibitory effect on acetylcholinesterase and a mitigating effect on amnesia. Dement Geriatr Cogn Disord. . 2004;17:151-7. [PubMed ID: 14739537].
-
8.
Gurib-Fakim A. Medicinal plants: traditions of yesterday and drugs of tomorrow. J. Mol. Aspects Med. 2006;27:1-93.
-
9.
Orhan IE, Yilmaz BS, Altun ML, Saltan G, Sener B. Anti-Acetylcholinesterase and Antioxidant Appraisal of the Bulb Extracts of Five Sternbergia Species. Rec. Nat. Prod. 2011;5:193-201.
-
10.
Mozaffarian V. Flora of Iran, No.54: Umbelliferae. Research Institute of Forests and Rangelands. 2007. p. 439-42.
-
11.
Ajani Y, Ajani A, Cordes JM, Watson MF, Downie SR. Phylogenetic analysis of nrDNAITS sequences reveals relationships within five groups of Iranian Apiaceae subfamily Apioideae. TAXON. 2008;57:383-401.
-
12.
Kurzyna-Młynik R, Oskolski A, Downie SR, Kopacz R, Wojewódzka A, Spalik k. Phylogenetic position of the genus Ferula (Apiaceae) and its placement in tribe Scandiceae as inferred from nrDNA ITS sequence variation. Plant Sys. Evol. 2008;274:47.
-
13.
Znati M, Jannet HB, Cazaux S, Bouajila J. Chemical Composition, Biological and Cytotoxic Activities of Plant Extracts and Compounds Isolated from Ferula lutea. J. Molecules. 2014;19:2733-47.
-
14.
Ebeahimizadeh MA, Nabavi SM, Nabavi SF, Dehpour AA. Antioxidant activity of hydroalcholic extract of Ferula gummosa Boiss roots. J. Eur. Rev. Med. Pharmacol. Sci. 2011;15:658-64.
-
15.
Zhao Y, Dou J, Wu T, Aisa HA. Investigating the Antioxidant and Acetylcholinesterase Inhibition Activities of Gossypium herbaceam. J. Molecules. 2013;18:951-62.
-
16.
Jung M, Park M. Acetylcholinesterase Inhibition by Flavonoids from Agrimonia pilosa. J. Molecules. 2007;12:2130-9.
-
17.
Tofighi Z, Alipour F, Hadavinia H, Abdollahi M, Hadjiakhoondi A, Yassa N. Effective antidiabetic and antioxidant fractions of Otostegia persica extract and their constituents. J. Pharm. Biol. 2014;8:961-6.
-
18.
Galloway KR, Bretz SL, Novak M. Paper Chromatography and UV–Vis Spectroscopy To Characterize Anthocyanins and Investigate Antioxidant Properties in the Organic Teaching Laboratory. J. Chem. Educ. 2015;92:183-8.
-
19.
Yassa N, Saeidnia S, Pirouzi R, Akbaripour M, Shafiee A. Three phenolic glycosides and immunological properties of Achillea millefolium from Iran, population of Golestan. DARU. 2007;15:49-52.
-
20.
Yin J, Si CL, Wang MH. Antioxidant activity of flavanoids and their glucosides from Sonchus oleraceus L. J. Appl. Biol. Chem. 2008;51:57-60.
-
21.
Selvaraj K, Chowdhury R, Bhattacharjee C. Isolation and structural elucidation of flavonoid from aquatic fern Azolla microphylla and evaluation of free radical scavenging activity. Int.J. Pharm. Pharm Sci. (IJPPS). 2013;5:743-9.
-
22.
Huang w, Wan C, Zhou S. Quercetin - A Flavonoid Compound from Sarcopyra misbodinieri var delicate with Potential Apoptotic Activity in HepG2 Liver Cancer Cells. Res. J. Trop. Pharm. 2013;4:529-33.
-
23.
Wei Y, Xie Q, Fisher D, Sutherland IA. Separation of patuletin-3-O-glucoside, astragalin, quercetin, kaempferol and isorhamnetin from Flaveria bidentis (L) Kuntze by elution-pump-out high-performance counter-current chromatography. J. Chromatogr. A. 2011;36:6206-11.
-
24.
Jeong CH, Jeong HR, Choi GN, Kim DO, Lee UK, Heo HJ. Neuroprotective and anti-oxidant effects of caffeic acid isolated from Erigeron annuus leaf. J. Med. 2011;6:25.
-
25.
Bhatt B. Chemical constituents of Solanum xantho carpum. J. Chem. Pharm. Res. 2011;3:176-81.
-
26.
Jadrijevi M, Taka M, Topic DV, Govorcinovic T. FT-IR and NMR spectroscopic studies of salicylic acid derivatives I Gentisamide – a metabolite of salicylamide. J. Acta Pharm. 2004;54:177-91.
-
27.
Durust N, Ozden S, Umur E, Durust Y, Kucukislamoglu M. The Isolation of Carboxylic Acids from the Flowers of Delphinium formosum. Turk. J. Chem. 2001;25:93-7.
-
28.
Karthikeyan R, Devadasu C, Babu PS. Isolation, Characterization, and RP-HPLC Estimation of P-Coumaric Acid from Methanolic Extract of Durva Grass (Cynodon dactylon Linn). Int.J. Anal. Chem. 2015;10:20-7.
-
29.
Yi B, Hu L, Mei W, Zhou K, Wang H, Luo Y, Wei X, Dai H. Antioxidant Phenolic Compounds of Cassava (Manihot esculenta) from Hainan. J. Molecules. 2010;16:10157-67.
-
30.
Sabogal-Guaqueta AM, Muñoz-Manco JI, Ramírez-Pineda JR, Lamprea-Rodriguez M, Osorio E, Cardona-Gomez GP. The flavonoid quercetin ameliorates Alzheimer’s disease pathology and protects cognitive and emotional function in aged triple transgenic Alzheimer’s disease model mice. J. Neuropharm. 2015;93:134-45.
-
31.
Lei X, Chao H, Zhang Z, Lv J, Li S, Wei H, Xue R, Li F, Li Z. Neuroprotective effects of quercetin in a mouse model of brain ischemic/reperfusion injury via antiapoptotic mechanisms based on the Akt pathway. Mol. Med. Rep. 2015;12:3688-96. [PubMed ID: 26016839].