期刊
SYNAPSE
卷 64, 期 7, 页码 503-510出版社
WILEY
DOI: 10.1002/syn.20755
关键词
obesity; food; insulin; autoradiography; reward; beta-Imager
资金
- NIAAA [AA 11034, AA07574, AA07611]
Peripheral and central leptin administration have been shown to mediate central dopamine (DA) signaling. Leptin-receptor deficient rodents show decreased DA D2 receptor (D2R) binding in striatum and unique DA profiles compared to controls. Leptin-deficient mice show increased DA activity in reward-related brain regions. The objective of this study was to examine whether basal D2R-binding differences contribute to the phenotypic behaviors of leptin-deficient ob/ob mice, and whether D2R binding is altered in response to peripheral leptin treatment in these mice. Leptin decreased body weight, food intake, and plasma insulin concentration in ob lob mice but not in wild-type mice. Basal striatal D2R binding (measured with autoradiography [H-3] spiperone) did not differ between ob/ob and wild-type mice but the response to leptin did. In wild-type mice, leptin decreased striatal D2R binding, whereas, in ob/ob mice, leptin increased D2R binding. Our findings provide further evidence that leptin modulates D2R expression in striatum and that these effects are genotype/phenotype dependent. Synapse 64:503-510, 2010. (C) 2010 Wiley-Liss, Inc.
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