N-acylphosphatidylethanolamine, a Gut-Derived Circulating Factor Induced by Fat Ingestion, Inhibits Food Intake

被引:115
作者
Gillum, Matthew P. [1 ,2 ,3 ]
Zhang, Dongyan [1 ]
Zhang, Xian-Man [2 ]
Erion, Derek M. [1 ,2 ,3 ]
Jamison, Rachel A. [1 ,2 ]
Choi, Cheolsoo [2 ]
Dong, Jianying [1 ]
Shanabrough, Marya [4 ]
Duenas, Hillary R. [4 ]
Frederick, David W. [2 ]
Hsiao, Jennifer J. [2 ]
Horvath, Tamas L. [4 ]
Lo, Chun Min [5 ]
Tso, Pat [5 ]
Cline, Gary W. [2 ]
Shulman, Gerald I. [1 ,2 ,3 ]
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Cellular & Mol Physiol, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Dept Comparat Med, New Haven, CT 06520 USA
[5] Univ Cincinnati, Dept Pathol, Cincinnati, OH 45627 USA
关键词
D O I
10.1016/j.cell.2008.10.043
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
N-acylphosphatidylethanolamines (NAPEs) are a relatively abundant group of plasma lipids of unknown physiological significance. Here, we show that NAPEs are secreted into circulation from the small intestine in response to ingested fat and that systemic administration of the most abundant circulating NAPE, at physiologic doses, decreases food intake in rats without causing conditioned taste aversion. Furthermore, C-14-radiolabeled NAPE enters the brain and is particularly concentrated in the hypothalamus, and intracerebroventricular infusions of nanomolar amounts of NAPE reduce food intake, collectively suggesting that its effects may be mediated through direct interactions with the central nervous system. Finally, chronic NAPE infusion results in a reduction of both food intake and body weight, suggesting that NAPE and long-acting NAPE analogs may be novel therapeutic targets for the treatment of obesity.
引用
收藏
页码:813 / 824
页数:12
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