Department of Psychiatry, Ribicoff Research Facilities, Yale University School of Medicine, New Haven, Connecticut 06508, USA.
J Neurosci. 2010 Jun 16;30(24):8263-73. doi: 10.1523/JNEUROSCI.5858-09.2010.
The lateral hypothalamus and the nucleus accumbens shell (AcbSh) are brain regions important for food intake. The AcbSh contains high levels of receptor for melanin-concentrating hormone (MCH), a lateral hypothalamic peptide critical for feeding and metabolism. MCH receptor (MCHR1) activation in the AcbSh increases food intake, while AcbSh MCHR1 blockade reduces feeding. Here biochemical and cellular mechanisms of MCH action in the rodent AcbSh are described. A reduction of phosphorylation of GluR1 at serine 845 (pSer(845)) is shown to occur after both pharmacological and genetic manipulations of MCHR1 activity. These changes depend upon signaling through G(i/o), and result in decreased surface expression of GluR1-containing AMPA receptors (AMPARs). Electrophysiological analysis of medium spiny neurons (MSNs) in the AcbSh revealed decreased amplitude of AMPAR-mediated synaptic events (mEPSCs) with MCH treatment. In addition, MCH suppressed action potential firing MSNs through K(+) channel activation. Finally, in vivo recordings confirmed that MCH reduces neuronal cell firing in the AcbSh in freely moving animals. The ability of MCH to reduce cell firing in the AcbSh is consistent with a general model from other pharmacological and electrophysiological studies whereby reduced AcbSh neuronal firing leads to food intake. The current work integrates the hypothalamus into this model, providing biochemical and cellular mechanisms whereby metabolic and limbic signals converge to regulate food intake.
外侧下丘脑和伏隔核壳(AcbSh)是与摄食有关的重要脑区。AcbSh 富含黑色素浓缩激素受体(MCHR),MCH 是一种促进摄食和代谢的关键性外侧下丘脑肽。AcbSh 中 MCH 受体(MCHR1)的激活会增加食物摄入,而 AcbSh 中 MCHR1 的阻断则会减少摄食。本文描述了 MCH 在啮齿动物 AcbSh 中的生化和细胞作用机制。研究表明,MCHR1 活性的药理学和遗传操作后,谷氨酸受体 1(GluR1)丝氨酸 845 位(pSer(845))的磷酸化减少。这些变化依赖于 G(i/o)信号转导,导致包含 GluR1 的 AMPA 受体(AMPAR)的表面表达减少。对 AcbSh 中的中间神经元(MSNs)进行电生理分析显示,MCH 处理后 AMPAR 介导的突触事件(mEPSC)的幅度减小。此外,MCH 通过激活 K(+)通道抑制 MSN 的动作电位放电。最后,在体记录证实,MCH 减少了自由活动动物 AcbSh 中的神经元放电。MCH 能够减少 AcbSh 中的细胞放电,这与其他药理学和电生理学研究的一般模型一致,即 AcbSh 神经元放电减少导致食物摄入增加。目前的工作将下丘脑纳入这一模型,提供了生化和细胞机制,使代谢和边缘信号能够汇聚以调节食物摄入。