Lipid Metabolism, Oxidative Stress and Cell Death Are Regulated by PKC Delta in a Dietary Model of Nonalcoholic SteatohepatitisReport as inadecuate




Lipid Metabolism, Oxidative Stress and Cell Death Are Regulated by PKC Delta in a Dietary Model of Nonalcoholic Steatohepatitis - Download this document for free, or read online. Document in PDF available to download.

Steatosis, oxidative stress, and apoptosis underlie the development of nonalcoholic steatohepatitis NASH. Protein kinase C delta PKCδ has been implicated in fatty liver disease and is activated in the methionine and choline-deficient MCD diet model of NASH, yet its pathophysiological importance towards steatohepatitis progression is uncertain. We therefore addressed the role of PKCδ in the development of steatosis, inflammation, oxidative stress, apoptosis, and fibrosis in an animal model of NASH. We fed PKCδ−-− mice and wildtype littermates a control or MCD diet. PKCδ−-− primary hepatocytes were used to evaluate the direct effects of fatty acids on hepatocyte lipid metabolism gene expression. A reduction in hepatic steatosis and triglyceride levels were observed between wildtype and PKCδ−-− mice fed the MCD diet. The hepatic expression of key regulators of β-oxidation and plasma triglyceride metabolism was significantly reduced in PKCδ−-− mice and changes in serum triglyceride were blocked in PKCδ−-− mice. MCD diet-induced hepatic oxidative stress and hepatocyte apoptosis were reduced in PKCδ−-− mice. MCD diet-induced NADPH oxidase activity and p47phox membrane translocation were blunted and blocked, respectively, in PKCδ−-− mice. Expression of pro-apoptotic genes and caspase 3 and 9 cleavage in the liver of MCD diet fed PKCδ−-− mice were blunted and blocked, respectively. Surprisingly, no differences in MCD diet-induced fibrosis or pro-fibrotic gene expression were observed in 8 week MCD diet fed PKCδ−-− mice. Our results suggest that PKCδ plays a role in key pathological features of fatty liver disease but not ultimately in fibrosis in the MCD diet model of NASH.



Author: Michael W. Greene , Christine M. Burrington, Darin T. Lynch, Samantha K. Davenport, Andrew K. Johnson, Melissa J. Horsman, Saleem

Source: http://plos.srce.hr/



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