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  • 标题:Soy protein reduces hepatic lipotoxicity in hyperinsulinemic obese Zucker fa/fa rats
  • 本地全文:下载
  • 作者:Tovar, Armando R. ; Torre-Villalvazo, Ivan ; Ochoa, Melissa
  • 期刊名称:JLR Papers In Press
  • 印刷版ISSN:0022-2275
  • 电子版ISSN:1539-7262
  • 出版年度:2005
  • 卷号:46
  • 期号:09
  • 页码:1823-1832
  • DOI:10.1194/jlr.M500067-JLR200
  • 出版社:American Society for Biochemistry and Molecular Biology
  • 摘要:Hepatic steatosis is commonly present during the development of insulin resistance, and it is a clear sign of lipotoxicity attributable in part to an accelerated lipogenesis. There is evidence that a soy protein diet prevents the overexpression of hepatic sterol-regulatory element binding protein-1 (SREBP-1), decreasing lipid accumulation. Therefore, the aim of the present work was to study whether a soy protein diet may prevent the development of fatty liver through the regulation of transcription factors involved in lipid metabolism in hyperinsulinemic and hyperleptinemic Zucker obese fa/fa rats. Serum and hepatic cholesterol and triglyceride levels, as well as VLDL-triglyceride and LDL-cholesterol, were significantly lower in rats fed soy protein than in rats fed a casein diet for 160 days. The reduction in hepatic cholesterol was associated with a low expression of liver X receptor-{alpha} and its target genes, 7-{alpha} hydroxylase and ABCA1. Soy protein also decreased the expression of SREBP-1 and several of its target genes, FAS, stearoyl-CoA desaturase-1, and {Delta}5 and {Delta}6 desaturases, decreasing lipogenesis even in the presence of hyperinsulinemia. Reduction in SREBP-1 was not associated with the presence of soy isoflavones. Finally, soy protein reduced SREBP-1 expression in adipocytes, preventing hypertrophy, which also helps prevent the development of hepatic lipotoxicity. Supplementary key words steatosis • liver • liver X receptor-{alpha} • sterol-regulatory element binding protein-1
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