Exp Mol Med.  2002 May;34(2):137-144.

Induction of hepatic inducible nitric oxide synthase by cholesterol in vivo and in vitro

• Kim JW
• Kang KW
• Oh GT
• Song J
• Kim ND
• Pak YK

Abstract

Cholesterol-rich diet impairs endothelial NO synthase (eNOS) and enhances inducible NOS (iNOS) expression. In this study, we investigated effects of cholesterol on iNOS expression in high-fat-fed rat models, HepG2 and RAW264.7 cells. The high-fat diet increased the plasma total cholesterol level 6-7 fold and low-density lipoprotein cholesterol level (LDL-C) approximately 70 fold and slightly increased the level of lipid peroxidation as determined by thiobarbituric acid-reactive substance assay. The high-fat diet also increased plasma nitric oxide (NO) concentrations up to 5 fold, and induced iNOS mRNA expression in liver. The contractile responses of the endothelium-denuded thoracic aortic rings to phenylephrine were significantly damaged in high-fat-fed rats when assessed by organ chamber study. Treatment with estrogen for 4 days failed to reduce iNOS expressions as well as aortic contractility, although it improved lipid profiles. In cultured HepG2 or murine macrophage RAW264.7 cells, 3 days treatment with either 25-hydroxycholesterol or 7-ketocholesterol induced iNOS mRNA expression, as determined by RT-PCR. Our data suggested that the chronic exposure of hepatocytes and macrophage cells to high concentration of cholesterol or oxysterols may induce iNOS expression and subsequent synthesis of NO, which may be important in the pathogenesis of atherosclerosis.

MeSH Terms

Animals
Cholesterol, Dietary/*pharmacology
Enzyme Induction
Estrogens/pharmacology
In Vitro
Liver/*enzymology
Male
Nitric Oxide/blood/metabolism
Nitric-Oxide Synthase/*biosynthesis/genetics
Potassium Chloride/metabolism
Rats
Rats, Sprague-Dawley
Receptors, Adrenergic, alpha-2/metabolism
Receptors, LDL/metabolism
Thiobarbituric Acid Reactive Substances/metabolism