Frequent cholesterol intake up-regulates intestinal NPC1L1, ACAT2, and MTP
Publication in refereed journal


摘要Dietary cholesterol elevates plasma total cholesterol (TC) level. However, no study to date has examined how cholesterol intake frequency interacts with the gene of sterol transporters, receptors, and enzymes involved in cholesterol metabolism. Thirty-three hamsters were divided into three groups with the control hamsters being given daily 9 mg of cholesterol in the diet (CD), whereas the second group being gavage-administered 3 mg of cholesterol three times per day (C-3) and the third group being gavage-administered 9 mg of cholesterol one time per day (C-1). The experiment lasted for 6 weeks. The hamsters were killed under carbon dioxide suffocation. Data demonstrated that plasma TC, non-high-density lipoprotein cholesterol, and triacylglycerols were elevated with the increasing cholesterol intake frequency. Western blotting analyses revealed that the intake frequency had no effect on protein mass of hepatic sterol regulatory element binding protein-2, liver X receptor-α, 3-hydroxy-3-methylglutaryl-CoA reductase, LDL receptor, and cholesterol- 7α-hydroxylase. However, the frequent cholesterol intake down-regulated the mRNA level of hepatic LDL receptor. In contrast, the frequent cholesterol intake up-regulated the mRNA levels of intestinal Niemann-Pick C1-like 1 (NPC1L1), acyl coenzyme A:cholesterol acyltransferase 2 (ACAT2), and microsomal triacylglycerol transport protein (MTP). It was concluded that the cholesterol intake frequency-induced elevation in plasma TC was associated with greater cholesterol absorption, possibly mediated by up-regulation of NPC1L1, ACAT2, and MTP. © 2010 American Chemical Society.
著者Jiao R., Guan L., Yang N., Peng C., Liang Y., Ma K.Y., Huang Y., Chen Z.-Y.
期刊名稱Journal of Agricultural and Food Chemistry
詳細描述To ORKTS: doi: 10.1021/jf100879y
出版社American Chemical Society
出版地United States
頁次5851 - 5857
關鍵詞ABCG5, ACAT2, Cholesterol, Consumption frequency, CYP7A1, HMG CoA reductase, LDL receptor, Liver X receptor, MTP, NPC1L1, SREBP

上次更新時間 2022-14-01 於 23:45