METHIONINE DEFICIENCY IN RATS FED SOY PROTEIN INDUCES HYPERCHOLESTEROLEMIA AND POTENTIATES LIPOPROTEIN SUSCEPTIBILITY TO PEROXIDATION

Citation
C. Moundras et al., METHIONINE DEFICIENCY IN RATS FED SOY PROTEIN INDUCES HYPERCHOLESTEROLEMIA AND POTENTIATES LIPOPROTEIN SUSCEPTIBILITY TO PEROXIDATION, Metabolism, clinical and experimental, 44(9), 1995, pp. 1146-1152
Citations number
49
Categorie Soggetti
Endocrynology & Metabolism
ISSN journal
00260495
Volume
44
Issue
9
Year of publication
1995
Pages
1146 - 1152
Database
ISI
SICI code
0026-0495(1995)44:9<1146:MDIRFS>2.0.ZU;2-H
Abstract
A number of studies have provided evidence that plant proteins, especi ally soy protein, have a cholesterol-lowering effect as compared with casein. However, dietary supply of sulfur amino acids may be deficient when soy protein is present in the diet at a suboptimal level, which could affect lipid metabolism. Accordingly, in rats fed 13% protein di ets, soy protein feeding resulted in a cholesterol-increasing effect ( +18%), which could be counteracted by methionine supplementation (0.4% ). In contrast, soy protein was effective in decreasing plasma triglyc eride, as compared with levels in rats fed casein; this triglyceride-l owering effect was entirely abolished by methionine supplementation. T he hypercholesterolemic effect of soy protein was characterized by a h igher cholesterol content in low-density lipoprotein (LDL) and high-de nsity lipoprotein 1 (HDL(1)) fractions, together with a marked inducti on of hepatic hydroxymethyl glutaryl coenzyme A (HMG CoA) reductase ac tivity and to a lesser extent cholesterol 7 alpha-hydroxylase. There w as practically no induction of these enzymes, as compared with levels in rats fed casein diets, when the soy protein diet was supplemented w ith methionine. Very-low-density lipoprotein (VLDL) plus LDL susceptib ility to peroxidation was higher in rats fed soy protein than in casei n-fed rats, which could reflect in part the lack of sulfur amino acid availability, since methionine supplementation led to a partial recove ry of lipoprotein resistance to peroxidation. These findings suggest t hat amino acid imbalance could be atherogenic by increasing circulatin g cholesterol and leading to a higher lipoprotein susceptibility to pe roxidation. Copyright (C) 1995 by W.B. Saunders Company