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Effect of Lecithin and silymarin on D-galactosamine induced toxicity in isolated hepatocytes and rats. | LitMetric

Effect of Lecithin and silymarin on D-galactosamine induced toxicity in isolated hepatocytes and rats.

Indian J Clin Biochem

Manipal College of Pharmaceutical Sciences, Manipal University, Manipal, 576104 Karnataka India.

Published: April 2010

AI Article Synopsis

  • The study examined the hepatoprotective effects of Lecithin against toxicity induced by D-galactosamine (D-GalN) in rat liver cells and live animal models.
  • Lecithin significantly reduced liver damage in isolated rat hepatocytes at a concentration of 100 μg/ml and showed similar protective effects as the standard treatment, silymarin.
  • In live rat models, Lecithin administered at 100 mg/kg body weight effectively normalized altered biochemical levels due to D-galactosamine-induced liver damage, comparable to the effects of silymarin.

Article Abstract

To investigate Lecithin for its hepatoprotective activity against D-galactosamine (D-GalN) induced toxicity in freshly isolated rat hepatocytes and animal models. Freshly isolated rat hepatocytes were exposed to Dgalactosamine (30 mM) along with/without lecithin (100 μg/ml) and the levels of selected liver enzymes were measured. Thirty six Wistar strain albino rats were used for the in vivo investigations. Lecithin 50 and 100 mg/kg.b.wt were administered for one week by oral route. Liver damage was induced by intra peritoneal administration of 400 mg/kg b.wt D-galactosamine. The antihepatotoxic effect of lecithin was observed in freshly isolated rat hepatocytes at concentration 100 μg/ml and was found to be similar to that of the standard silymarin used. Its in vivo hepatoprotective effect at 100 mg/kg b.wt was comparable with that of the standard silymarin at 100 mg/kg body weight. Lecithin was able to normalise the biochemical levels which were altered due to D-galactosamine intoxication in freshly isolated rat hepatocytes and also in animal models.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3453104PMC
http://dx.doi.org/10.1007/s12291-010-0031-0DOI Listing

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