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Effect of l-ornithine l-aspartate against thioacetamide-induced hepatic damage in rats

OBJECTIVE: To investigate the hepatoprotective activity of L-ornithine-L-aspartate against thioacetamide (TAA)-induced hepataopathy in rats. MATERIALS AND METHODS: The hepatoprotective activity of L-ornithine-L-aspartate (OA) at a dose of 2 g/kg, p.o. for 10 days was evaluated against TAA (250 mg/kg...

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Detalles Bibliográficos
Autores principales: Najmi, Abul K., Pillai, K.K., Pal, S.N., Akhtar, M., Aqil, M., Sharma, M.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991698/
https://www.ncbi.nlm.nih.gov/pubmed/21189911
http://dx.doi.org/10.4103/0253-7613.71926
Descripción
Sumario:OBJECTIVE: To investigate the hepatoprotective activity of L-ornithine-L-aspartate against thioacetamide (TAA)-induced hepataopathy in rats. MATERIALS AND METHODS: The hepatoprotective activity of L-ornithine-L-aspartate (OA) at a dose of 2 g/kg, p.o. for 10 days was evaluated against TAA (250 mg/kg, i.p. for 2 days) induced hepatopathy in rats. Biochemical parameters such as serum aspartate transaminase, alanine transaminase, alkaline phosphatase, bilirubin and glutathione, thiobarbituric acid reactive substances, and protein in liver tissues were estimated to assess the liver function. RESULTS: TAA-induced pathogenic changes in the levels of the above indices were significantly (P < 0.01) reversed by the OA treatment. OA treatment also exhibited significant restoration of the hepatic architecture and lobular structure in histological evaluation of the rat liver sections. CONCLUSION: Ornithine aspartate exhibited significant hepatoprotective activity against TAA-induced hepatic damage in rats.