| Literature DB >> 25640749 |
Fei Wang1, Alison B Kohan2, Chun-Min Lo1, Min Liu1, Philip Howles1, Patrick Tso1.
Abstract
The purpose of this review is to summarize our current understanding of the physiological roles of apoA-IV in metabolism, and to underscore the potential for apoA-IV to be a focus for new therapies aimed at the treatment of diabetes and obesity-related disorders. ApoA-IV is primarily synthesized by the small intestine, attached to chylomicrons by enterocytes, and secreted into intestinal lymph during fat absorption. In circulation, apoA-IV is associated with HDL and chylomicron remnants, but a large portion is lipoprotein free. Due to its anti-oxidative and anti-inflammatory properties, and because it can mediate reverse-cholesterol transport, proposed functions of circulating apoA-IV have been related to protection from cardiovascular disease. This review, however, focuses primarily on several properties of apoA-IV that impact other metabolic functions related to food intake, obesity, and diabetes. In addition to participating in triglyceride absorption, apoA-IV can act as an acute satiation factor through both peripheral and central routes of action. It also modulates glucose homeostasis through incretin-like effects on insulin secretion, and by moderating hepatic glucose production. While apoA-IV receptors remain to be conclusively identified, the latter modes of action suggest that this protein holds therapeutic promise for treating metabolic disease.Entities:
Keywords: chylomicron; diabetes; glucose tolerance; incretins; intestinal lipid transport; lymph fistula mouse model; obesity
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Year: 2015 PMID: 25640749 PMCID: PMC4513983 DOI: 10.1194/jlr.R052753
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922