Critical review of acylation-stimulating protein physiology in humans and rodents

被引:275
作者
Cianflone, K
Xia, ZN
Chen, LY
机构
[1] McGill Univ, Royal Victoria Hosp, Montreal, PQ H3A 1A1, Canada
[2] Fu Wei Hosp, Beijing, Peoples R China
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2003年 / 1609卷 / 02期
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
C3adesArg; complement c3; obesity; CAD; diabetes;
D O I
10.1016/S0005-2736(02)00686-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the last few years, there has been increasing interest in the physiological role of acylation-stimulating protein (ASP). Recent studies in rats and mice, in particular in C3 ( - / -) mice that are ASP deficient, have advanced our understanding of the role of ASP. Of note, the background strain of the mice influences the phenotype of delayed postprandial triglyceride clearance in ASP-deficient mice. Administration of ASP in all types of lean and obese mice studied to date, however, enhances postprandial triglyceride clearance. On the other hand, regardless of the background strain, ASP-deficient mice demonstrate reduced body weight, reduced leptin and reduced adipose tissue mass, suggesting that ASP deficiency results in protection against development of obesity. In humans, a number of studies have examined the relationship between ASP, obesity, diabetes and dyslipidemia as well as the influence of diet, exercise and pharmacological therapy. While many of these studies have small subject numbers, interesting observations may help us to better understand the parameters that may influence ASP production and ASP action. The aim of the present review is to provide a comprehensive overview of the recent literature on ASP, with particular emphasis on those studies carried out in rodents and humans. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:127 / 143
页数:17
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