Journal of Stress Physiology & Biochemistry, Vol. 9 No. 1 2013, pp. 96-105 ISSN 1997-0838
Original Text Copyright (cc) 2013 by  Sadeghi Niaraki, Nabavizadeh, Vaezi, Alizadeh, Nahrevanian, Moslehi and Azizian



ORIGINAL ARTICLE
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QueryDate : 2016-12-24
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Protective Effect of Ghrelin on Sodium Valproate-induced Liver Injury in Rat

Mandana Sadeghi Niaraki1, Fatemeh Nabavizadeh2*, Gholam H. Vaezi3, Ali M. Alizadeh4, Hossein Nahrevanian5, Azam Moslehi2, Saleh Azizian4

1 Department of biology, Damghan branch, Islamic Azad University, Damghan, Iran.
2 Department of physiology, Tehran University of Medicale Sciences and Health Services, Tehran, Iran.
3 Department of biology, Islamic Azad University, Damghan Branch, Semnan, Iran.
4 Cancer Research Center, Tehran University of medical sciences, Tehran, Iran.
5 Department of Parasitoligy, Pasteur Institute of Iran, Tehran 13164, Iran.

*E-Mail: nabavizadeh2000@yahoo.com


Received October 9, 2012


Ghrelin is a peptide that has protective effects on many tissues injury. It has anti-inflammatory and anti-oxidant effects. Sodium valproate is widely used anticonvuisant and anti-depression drug with hepatotoxic side effects. The aim of this study was to evaluated the protective role of ghrelin in liver toxicity due to sodium valproate overdose. Eighteen rats were used in this study and divided in to three groups, containing: control, sodium valproate, and sodium valproate and ghrelin groups. Nitric oxide (NO), prostaglandin E2 (PGE2) and hepatic enzymes AST (aspartate aminotransferase) and ALT (alanine aminotransferase), were assessed and histologic study of liver were performed as indicators of liver damage following sodium valproate toxicity. This study showed the ghrelin decreased ALT and AST to the normal level. Our results show that ghrelin significantly increased NO metabolites and decreased PGE2 level comparison with sodium valproate group, but had no significant change compared to the control group. we showed that ghrelin administration inhibited liver injury in rats due to sodium valproate toxicity.

Key words: Ghrelin, liver injury, nitric oxide(NO), prostaglandin E2(PGE2), sodium valproate

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