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Science.
2006 May 12;312(5775):927-30.
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Comment in:
Science. 2006 May 12;312(5775):861-4.
Science. 2006 Sep 1;313(5791):1236-8; author reply 1236-8.
Hypothalamic mTOR signaling regulates food intake.
Cota D
,
Proulx K
,
Smith KA
,
Kozma SC
,
Thomas G
,
Woods SC
,
Seeley RJ
.
Department of Psychiatry, University of Cincinnati, Genome Research Institute, 2170 East Galbraith Road, Cincinnati, OH 45237, USA.
The mammalian Target of Rapamycin (mTOR) protein is a serine-threonine kinase that regulates cell-cycle progression and growth by sensing changes in energy status. We demonstrated that mTOR signaling plays a role in the brain mechanisms that respond to nutrient availability, regulating energy balance. In the rat, mTOR signaling is controlled by energy status in specific regions of the hypothalamus and colocalizes with neuropeptide Y and proopiomelanocortin neurons in the arcuate nucleus. Central administration of leucine increases hypothalamic mTOR signaling and decreases food intake and body weight. The hormone leptin increases hypothalamic mTOR activity, and the inhibition of mTOR signaling blunts leptin's anorectic effect. Thus, mTOR is a cellular fuel sensor whose hypothalamic activity is directly tied to the regulation of energy intake.
Publication Types:
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
PMID: 16690869 [PubMed - indexed for MEDLINE]
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