| Literature DB >> 20175225 |
Jennifer Pfaffly1, Michael Michaelides, Gene-Jack Wang, Jeffrey E Pessin, Nora D Volkow, Panayotis K Thanos.
Abstract
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/ob mice but not in wild-type mice. Basal striatal D2R binding (measured with autoradiography [(3)H] 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.Entities:
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Year: 2010 PMID: 20175225 PMCID: PMC2873172 DOI: 10.1002/syn.20755
Source DB: PubMed Journal: Synapse ISSN: 0887-4476 Impact factor: 2.562