4.7 Article

Downregulation of GPR83 in the hypothalamic preoptic area reduces core body temperature and elevates circulating levels of adiponectin

期刊

METABOLISM-CLINICAL AND EXPERIMENTAL
卷 61, 期 10, 页码 1486-1493

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.metabol.2012.03.015

关键词

Lentivirus; RNAi; shRNA; Knockdown; Warm sensitive neurons; Preoptic area; G-protein coupled receptor 83; Thermoregulation; Body temperature; Adiponectin; Leptin; Insulin; IGF-1

资金

  1. Ellison Medical Foundation, NIH [AG028040]

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The G protein-coupled receptor 83 (GPR83) was recently demonstrated in warm sensitive neurons (WSN) of the hypothalamic preoptic area (POA) that participate in temperature homeostasis. Thus, we investigated whether GPR83 may have a role in regulating core body temperature (CBT) by reducing its expression in the POA. Dissipation of energy in the form of heat is the primary mode of energy expenditure in mammals and can ultimately affect energy homeostasis. Thus, we also measured the level of important regulators of metabolism. Downregulation of GPR83 was obtained by lentiviral short-hairpin RNAs (shGPR83) vectors designed and selected for their ability to reduce GPR83 levels in vitro. Mice received POA injection of shGPR83 or non-silencing vectors and were monitored for CBT, motor activity, food intake body weight and circulating levels of IGF-1, insulin, leptin and adiponectin. Down-regulation of GPR83 in the POA resulted in a small (0.15 degrees C) but significant reduction of CBT during the dark/active cycle of the day. Temperature reduction was followed by increased body weight gain independent of caloric intake. shGPR83 mice also had increased level of circulating adiponectin (31916 +/- 952 pg/mL vs. 23474 +/- 1507 pg/mL, P<.01) while no change was observed for insulin, IGF-1 or leptin. GPR83 may participate in central therrnoregulation and the central control of circulating adiponectin. Further work is required to determine how GPR83 can affect POA WSN and what are the long term metabolic consequences of its down-regulation. (C) 2012 Elsevier Inc. All rights reserved.

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