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Cholesteryl ester species differently elevate plasma cholesterol in hamsters

  • Rui Jiao
  • , Jingnan Chen
  • , Cheng Peng
  • , Yintong Liang
  • , Ka Ying Ma
  • , Xiaobo Wang
  • , Yuwei Liu
  • , Lin Lei
  • , Yu Huang
  • , Zhen-Yu Chen

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

This study was to examine the effect of free cholesterol (C) and individual cholesteryl ester (CE) species, namely cholesteryl palmitate (CP), cholesteryl stearate (CS), cholesteryl oleate (CO), and cholesteryl linoleate (CL) on plasma total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), non-HDL-C, and triacylglycerols (TG) in hamsters. Results showed that addition of dietary CE species into diet at 0.1% differently raised plasma TC concentrations, with CO elevating plasma TC to 331 mg/dL, while CS raised plasma TC only to 220 mg/dL. It was found that CS was a poor substrate of pancreatic cholesterol esterase, while CO was a good substrate. The fecal analysis showed CS-fed hamsters had the highest fecal cholesterol concentration, while RT-PCR analysis found CS feeding was associated with down-regulations of intestinal Niemann-Pick C1 like 1 (NPC1L1) and acyl-CoA: cholesterol acyltransferase 2 (ACAT2) as well as microsomal triacylglycerol transport protein (MTP). It was therefore concluded that the plasma cholesterol-raising activity of CE species was partially governed by their hydrolysis rates in the intestine, and the relative low raising activity associated with CS was mediated by down-regulation of intestinal NPC1L1, ACAT2, and MTP. © 2013 American Chemical Society.
Original languageEnglish
Pages (from-to)11041-11047
JournalJournal of Agricultural and Food Chemistry
Volume61
Issue number46
DOIs
Publication statusPublished - 20 Nov 2013
Externally publishedYes

Bibliographical note

Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].

Research Keywords

  • ACAT 2
  • cholesterol
  • HDL cholesterol
  • HMG-CoA reductase
  • MTP
  • NPC1L1

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