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HMG-CoA reductase, cholesterol 7alpha-hydroxylase, LDL receptor, SR-B1, and ACAT in diet-induced syndrome X.

AbstractBACKGROUND:
Long-term consumption of Western diets can lead to acquired syndrome X, which presents with obesity, insulin resistance, hypertension, hyperlipidemia, and risk of atherosclerotic cardiovascular disease. While plasma lipid abnormalities in syndrome X have been well characterized, their molecular basis remains unclear. This study explored potential mechanisms of hypercholesterolemia in diet-induced syndrome X.
METHODS:
Female Fischer rats were fed a high-fat, refined-carbohydrate (sucrose) diet (HFS) or standard rat chow (low-fat, complex carbohydrate, LFCC) for 20 months. Plasma lipids and hepatic tissue mRNA, protein, and/or activities of the key enzymes and receptors involved in cholesterol metabolism were determined.
RESULTS:
The HFS group exhibited hypertension, hyperlipidemia, insulin resistance, obesity, significant down-regulation of hepatic cholesterol 7alpha-hydroxylase (the rate-limiting step in cholesterol catabolism) and low-density lipoprotein (LDL) receptor (LDL-R, the primary pathway of LDL clearance). In contrast, hepatic tissue acyl-coenzyme A:cholesterol acyltransferase (ACAT-2, the primary enzyme involved in intracellular esterification of cholesterol) and scavenger-receptor class B, type 1 (SR-B1 or HDL receptor) were up-regulated. While 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase mRNA expression was increased, its protein abundance and activity were unchanged, and HMG-CoA reductase-to-cholesterol 7alpha-hydroxylase ratio was increased in HFS-fed animals.
CONCLUSION:
Hypercholesterolemia in diet-induced syndrome X is associated with depressed cholesterol 7alpha-hydroxylase, diminished LDL-R, elevated ACAT, and increased HMG-CoA reductase-to-cholesterol 7alpha-hydroxylase ratio. These findings point to impaired hepatic catabolism and uptake of cholesterol and inappropriate cholesterol production capacity as the underlying causes of hypercholesterolemia in rats with diet-induced syndrome X.
AuthorsChristian K Roberts, Kaihui Liang, R James Barnard, Choong H Kim, Nosratola D Vaziri
JournalKidney international (Kidney Int) Vol. 66 Issue 4 Pg. 1503-11 (Oct 2004) ISSN: 0085-2538 [Print] United States
PMID15458444 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Dietary Sucrose
  • Receptors, Immunologic
  • Receptors, LDL
  • Receptors, Scavenger
  • Scarb1 protein, rat
  • Scavenger Receptors, Class B
  • Hydroxymethylglutaryl CoA Reductases
  • Cholesterol 7-alpha-Hydroxylase
  • Sterol O-Acyltransferase
  • sterol O-acyltransferase 2
Topics
  • Animal Feed
  • Animals
  • Cholesterol 7-alpha-Hydroxylase (metabolism)
  • Dietary Sucrose (pharmacology)
  • Female
  • Hydroxymethylglutaryl CoA Reductases (metabolism)
  • Hyperlipidemias (metabolism)
  • Liver (enzymology)
  • Metabolic Syndrome (metabolism)
  • Obesity (metabolism)
  • Rats
  • Rats, Inbred F344
  • Receptors, Immunologic (metabolism)
  • Receptors, LDL (metabolism)
  • Receptors, Scavenger
  • Scavenger Receptors, Class B
  • Sterol O-Acyltransferase (metabolism)

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