Astragalus polysaccharides lowers plasma cholesterol through mechanisms distinct from statins

PLoS One. 2011;6(11):e27437. doi: 10.1371/journal.pone.0027437. Epub 2011 Nov 16.

Abstract

To determine the efficacy and underlying mechanism of Astragalus polysaccharides (APS) on plasma lipids in hypercholesterolemia hamsters. The effect of APS (0.25 g/kg/d) on plasma and liver lipids, fecal bile acids and neutral sterol, cholesterol absorption and synthesis, HMG-CoA reductase activity, and gene and protein expressions in the liver and small intestine was investigated in twenty-four hypercholesterolemia hamsters. Treatment periods lasted for three months. APS significantly lowered plasma total cholesterol by 45.8%, triglycerides by 30%, and low-density lipoprotein-cholesterol by 47.4%, comparable to simvastatin. Further examinations revealed that APS reduced total cholesterol and triglycerides in the liver, increased fecal bile acid and neutral sterol excretion, inhibited cholesterol absorption, and by contrast, increased hepatic cholesterol synthesis and HMG-CoA reductase activity. Plasma total cholesterol or low-density lipoprotein-cholesterol levels were significantly correlated with cholesterol absorption rates. APS up-regulated cholesterol-7α-hydroxylase and LDL-receptor gene expressions. These new findings identify APS as a potential natural cholesterol lowering agent, working through mechanisms distinct from statins.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astragalus Plant / chemistry*
  • Bile Acids and Salts / metabolism
  • Cholesterol / biosynthesis
  • Cholesterol / blood*
  • Cholesterol / metabolism
  • Cricetinae
  • Feces
  • Gene Expression Regulation / drug effects
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology*
  • Hyperlipidemias / blood
  • Hyperlipidemias / enzymology
  • Hyperlipidemias / metabolism
  • Hyperlipidemias / pathology
  • Intestinal Absorption / drug effects
  • Intestine, Small / drug effects
  • Intestine, Small / metabolism
  • Liver / drug effects
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Polysaccharides / pharmacology*
  • Receptors, LDL / genetics
  • Receptors, LDL / metabolism

Substances

  • Bile Acids and Salts
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Polysaccharides
  • Receptors, LDL
  • Cholesterol
  • Hydroxymethylglutaryl CoA Reductases