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腹侧被盖区中瘦素与胰淀素信号之间的协同相互作用对食物摄入的控制。

Cooperative interaction between leptin and amylin signaling in the ventral tegmental area for the control of food intake.

作者信息

Mietlicki-Baase Elizabeth G, Olivos Diana R, Jeffrey Brianne A, Hayes Matthew R

机构信息

Translational Neuroscience Program, Department of Psychiatry, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania

Translational Neuroscience Program, Department of Psychiatry, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Am J Physiol Endocrinol Metab. 2015 Jun 15;308(12):E1116-22. doi: 10.1152/ajpendo.00087.2015. Epub 2015 Apr 21.

Abstract

Peripheral coadministration of amylin and leptin produces enhanced suppression of food intake and body weight, but the central nuclei mediating these effects remain unclear. Because each of these peptides controls feeding via actions at the ventral tegmental area (VTA), we tested the hypothesis that the VTA is a site of action for the cooperative effects of leptin and amylin on energy balance control. First, we show that intra-VTA injection of amylin and leptin at doses of each peptide that are effective in reducing food intake and body weight when administered separately produces an enhanced suppression of feeding when administered in combination. We also demonstrate that subthreshold doses of both amylin and leptin cause significant hypophagia and body weight loss when coadministered into the VTA. Additionally, we provide evidence that VTA amylin receptor blockade significantly attenuates the ability of intra-VTA leptin to reduce feeding and body weight gain. Together, these data provide the first evidence that the VTA mediates the interaction of amylin and leptin to cooperatively promote negative energy balance.

摘要

胰淀素和瘦素外周联合给药可增强对食物摄入和体重的抑制作用,但介导这些效应的中枢核团仍不清楚。由于这些肽类均通过作用于腹侧被盖区(VTA)来控制进食,我们检验了如下假设:VTA是瘦素和胰淀素对能量平衡控制产生协同作用的作用位点。首先,我们发现,当单独给药时,以有效减少食物摄入和体重的剂量向VTA内注射胰淀素和瘦素,联合给药时对进食的抑制作用增强。我们还证明,阈下剂量的胰淀素和瘦素共同注入VTA时会导致显著的摄食减少和体重减轻。此外,我们提供的证据表明,VTA内胰淀素受体阻断可显著减弱VTA内注射瘦素减少进食和体重增加的能力。这些数据共同提供了首个证据,即VTA介导胰淀素和瘦素的相互作用,以协同促进负能量平衡。

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