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Evaluation of Hepatoprotective Potential of Hesa-A (A Marine Compound) Pretreatment Against Thioacetamide-Induced Hepatic Damage in Rabbits Pubmed



Ahmadi A1 ; Naderi GA2, 3, 4 ; Asgary S2
Authors
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Authors Affiliations
  1. 1. Cancer Research Center, Tehran University of Medical Science, Tehran, Iran
  2. 2. Isfahan Cardiovasc. Research Center, Isfahan Univ. of Medical Sciences, Isfahan, Iran
  3. 3. Isfahan Cardiovasc. Research Center, WHO Collaborating Center, Sedigheh Tahereh Hospital, Isfahan, Khorram St., Iran
  4. 4. Isfahan, P. O. Box: 81465-1148, Iran

Source: Drugs under Experimental and Clinical Research Published:2005


Abstract

HESA-A, a marine compound, has been shown to exhibit antihepatic cancer, antitumor and anti-Parkinson effects. The hepatoprotective potential of HESA-A pretreatment at doses of 125 mg and 250 mg per day orally for a period of 40 days was evaluated against thioacetamide-induced liver damage in rabbits. Biochemical parameters such as serum glutamate oxaloacetate transaminase and lactate dehydrogenase in serum were estimated to assess liver function and lipid peroxidation products (malondialdehyde [MDA]) and the antierythrocyte lysis effect of plasma for measurement of antioxidant potential capacity. Data on the hepatic biochemical parameters revealed the hepatoprotective potential of HESA-A pretreatment against thioacetamide-induced hepatotoxicity in rabbits. There was an increase in total antioxidant and antierythrocyte lysis and a decrease in MDA in plasma after HESA-A treatment. These results strongly suggest that HESA-A has a protective action against preoperative damage to biomembranes. © 2005 Bioscience Ediprint Inc.
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