Dietary polyenylphosphatidylcholine decreases cholesterolemia in hypercholesterolemic rabbits: role of the hepato-biliary axis

Life Sci. 2000 Oct 13;67(21):2563-76. doi: 10.1016/s0024-3205(00)00840-7.

Abstract

The aim of this work was to study the cholesterol-lowering mechanisms induced by dietary soybean lecithin in hypercholesterolemic rabbits. Male New Zealand white rabbits (n = 6 in each group) were fed for 10 weeks either a low-fat control C diet, containing 27 g fat/kg, or high-fat diets enriched with 2 g cholesterol/kg and 77 g fat/kg. The high-fat diets contained 50 g lard (L), 50 g soybean triacylglycerol (SO), or 50 g pure soybean phosphatidylcholine (PLE). PLE diet decreased by 30% beta-VLDL-cholesterol, compared with SO diet. HDL2-, HDL3- and LDL-lipid contents were unchanged in the L, SO and PLE groups. In gallbladder bile, amounts of phospholipids, bile salts and cholesterol were significantly increased in PLE group by respectively 45%, 11% and 44%, in comparison with SO group. Intestinal and hepatic Hydroxy Methyl Glutaryl Coenzyme A reductase activities were not increased by PLE diet. Triacylglycerol hepatic content was lower in PLE group than in L or SO groups. Compared with triacylglycerol enriched diet, phosphatidylcholine enriched diet developed significant higher cholesterol- and triacylglycerol-lowering effects by a two-step mechanism: i) by reducing the beta-VLDLs, ii) by enhancing the secretion of bile cholesterol. Such results constitute promising effects of soybean phosphatidylcholine at the hepato-biliary level, in the treatment or prevention of hyperlipidemia and related atherosclerosis.

Publication types

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

MeSH terms

  • Animals
  • Bile Acids and Salts / metabolism
  • Cholesterol / blood*
  • Cholesterol, Dietary / administration & dosage
  • Diet*
  • Gallbladder / metabolism*
  • Gallbladder / pathology
  • Hydroxymethylglutaryl CoA Reductases / metabolism
  • Hypercholesterolemia / blood
  • Hypercholesterolemia / diet therapy*
  • Hypercholesterolemia / pathology
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Microsomes, Liver / enzymology
  • Phosphatidylcholines / administration & dosage*
  • Phospholipids / metabolism
  • Rabbits

Substances

  • Bile Acids and Salts
  • Cholesterol, Dietary
  • Phosphatidylcholines
  • Phospholipids
  • lipostabil
  • Cholesterol
  • Hydroxymethylglutaryl CoA Reductases