Cover image of the article: Hepatoprotective effect of ethanolic extract of Crocus sativus L. (Saffron) stigma in comparison with silymarin against rifampin induced hepatotoxicity in rats

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Hepatoprotective effect of ethanolic extract of Crocus sativus L. (Saffron) stigma in comparison with silymarin against rifampin induced hepatotoxicity in rats

Authors

Daryoush Mohajeri1,*, Yousef Doustar2, Ali Rezaei3, Mehran Mesgari-Abbasi4
1Associate Professor of Pathobiology, School of Veterinary Medicine, Islamic Azad University, Tabriz Branch, Tabriz, Iran
2Assistant Professor of Pathobiology, School of Veterinary Medicine, Islamic Azad University, Tabriz Branch, Tabriz, Iran.
3Associate Professor of Clinical Science, School of Veterinary Medicine, Islamic Azad University, Tabriz Branch, Tabriz, Iran.
4Assistant Professor of Veterinary, Drug Resistant Research Center, Tabriz Medical University and Health Services, , Tabriz, Iran.
*Corresponding Author: Associate Professor of Pathobiology, School of Veterinary Medicine, Islamic Azad University, Tabriz Branch, Tabriz, Iran Email: daryoushmohajeri@iaut.ac.ir.com

Zahedan Journal of Research in Medical Sciences:Vol. 12, issue 5; e94102
Published online:Nov 19, 2010
Article type:Research Article
Received:Jun 21, 2010
Accepted:Sep 16, 2010
How to Cite:Mohajeri D, Doustar Y, Rezaei A, Mesgari-Abbasi M. Hepatoprotective effect of ethanolic extract of Crocus sativus L. (Saffron) stigma in comparison with silymarin against rifampin induced hepatotoxicity in rats. Zahedan J Res Med Sci. 2011;12(5):e94102. doi:

Abstract

  Background : Anti-tuberculous drug Rifampin is a potent hepatotoxicant. The aim of the present study was to evaluate the protective effect of ethanolic extract of Crocus sativus L. stigma (EECSL.S) in comparison with standard drug silimarin against rifampin-induced hepatotoxicity in the rats.

  Materials and Method : 40 male Wistar rats with the mean body weight of 200 ± 20 gr and age of 10 weeks were randomly assigned into 5 groups of 8 animals and kept in specific cages with 12/12 h light/dark cycle at 21 ± 2 ο C . Group I as normal control received normal saline (10 ml/kg) and group II as toxicant control received rifampin (500 mg/kg). Group Ш as positive control received silymarin plus rifampin (500 mg/kg) and groups IV and V (50 mg/kg) received EECSL.S at 40 mg/kg and 80 mg/kg plus rifampin, respectively. All the treatments were carried out through the gavage dissolving in 10 ml/kg normal saline daily for 1 month. At the end of experiment, levels of liver function marker enzymes (Aspartate aminotransferase, Alanine aminotransferase and Alkaline Phosphatase), total bilirubin, albumin and total proteins were assessed in serum of the rats. Moreover, histopathological observation was assayed at the degree of hepatic injury.

  Results : In rifampin-treated rats, silymarin and EECSL.S (40 and 80 mg/kg) significantly decreased the levels of serum biomarker of hepathic injury and total bilirubin and elevated the levels of albumin and total proteins. Histopathologically, silymarin and EECSL.S ameliorated rifampin induced hepatic injury. Histopathological changes were in agreement with biochemical findings.

  Conclusion : Results indicated that EECSL.S (80 mg/kg) equals with silymarin as standard drug , point of view hepatoprotective effects against rifampin-induced hepatotoxicity

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© 2011, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

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