Chronic vitamin A-enriched diet feeding regulates hypercholesterolaemia through transcriptional regulation of reverse cholesterol transport pathway genes in obese rat model of WNIN/GR-Ob strain

Indian J Med Res. 2016 Aug;144(2):238-244. doi: 10.4103/0971-5916.195038.

Abstract

Background & objectives: Hepatic scavenger receptor class B1 (SR-B1), a high-density lipoprotein (HDL) receptor, is involved in the selective uptake of HDL-associated esterified cholesterol (EC), thereby regulates cholesterol homoeostasis and improves reverse cholesterol transport. Previously, we reported in euglycaemic obese rats (WNIN/Ob strain) that feeding of vitamin A-enriched diet normalized hypercholesterolaemia, possibly through hepatic SR-B1-mediated pathway. This study was aimed to test whether it would be possible to normalize hypercholesterolaemia in glucose-intolerant obese rat model (WNIN/GR/Ob) through similar mechanism by feeding identical vitamin A-enriched diet.

Methods: In this study, 30 wk old male lean and obese rats of WNIN/GR-Ob strain were divided into two groups and received either stock diet or vitamin A-enriched diet (2.6 mg or 129 mg vitamin A/kg diet) for 14 wk. Blood and other tissues were collected for various biochemical analyses.

Results: Chronic vitamin A-enriched diet feeding decreased hypercholesterolaemia and normalized abnormally elevated plasma HDL-cholesterol (HDL-C) levels in obese rats as compared to stock diet-fed obese groups. Further, decreased free cholesterol (FC) and increased esterified cholesterol (EC) contents of plasma cholesterol were observed, which were reflected in higher EC to FC ratio of vitamin A-enriched diet-fed obese rats. However, neither lecithin-cholesterol acyltransferase (LCAT) activity of plasma nor its expression (both gene and protein) in the liver were altered. On the contrary, hepatic cholesterol levels significantly increased in vitamin A-enriched diet fed obese rats. Hepatic SR-B1 expression (both mRNA and protein) remained unaltered among groups. Vitamin A-enriched diet fed obese rats showed a significant increase in hepatic low-density lipoprotein receptor mRNA levels, while the expression of genes involved in HDL synthesis, namely, ATP-binding cassette protein 1 (ABCA1) and apolipoprotein A-I, were downregulated. No such response was seen in vitamin A-supplemented lean rats as compared with their stock diet-fed lean counterparts.

Interpretation & conclusions: Chronic vitamin A-enriched diet feeding decreased hypercholesterolaemia and normalized HDL-C levels, possibly by regulating pathways involved in HDL synthesis and degradation, independent of hepatic SR-B1 in this glucose-intolerant obese rat model.

MeSH terms

  • ATP Binding Cassette Transporter 1 / biosynthesis
  • Animals
  • Apolipoprotein A-I / biosynthesis
  • Biological Transport / genetics
  • Cholesterol / blood*
  • Cholesterol / genetics
  • Cholesterol, HDL / biosynthesis
  • Cholesterol, HDL / blood
  • Diet
  • Disease Models, Animal
  • Gene Expression Regulation
  • Humans
  • Hypercholesterolemia / blood*
  • Hypercholesterolemia / diet therapy
  • Hypercholesterolemia / genetics
  • Liver / metabolism
  • Male
  • Metabolic Networks and Pathways / genetics
  • Obesity / blood*
  • Obesity / diet therapy
  • Obesity / genetics
  • Phosphatidylcholine-Sterol O-Acyltransferase / blood
  • Rats
  • Scavenger Receptors, Class B / biosynthesis*
  • Scavenger Receptors, Class B / genetics
  • Vitamin A / administration & dosage*
  • Vitamin A / metabolism

Substances

  • ABCA1 protein, rat
  • ATP Binding Cassette Transporter 1
  • Apolipoprotein A-I
  • Cholesterol, HDL
  • Scarb1 protein, rat
  • Scavenger Receptors, Class B
  • Vitamin A
  • Cholesterol
  • Phosphatidylcholine-Sterol O-Acyltransferase