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Hypothalamic melanocortin neurons integrate signals of energy state.

机译:下丘脑的黑皮质素神经元整合了能量状态信号。

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Neurons of the arcuate nucleus of the hypothalamus appear to be sites of convergence of central and peripheral signals of energy stores, and profoundly modulate activity of the melanocortin circuits, providing strong rationale for pursuing these circuits as therapeutic targets for disorders of energy homeostasis. Recent studies in our lab and those of our collaborators have shown that leptin modulates different populations of hypothalamic cells in different ways. In this report, we outline an integrated model of leptin's action in the arcuate nucleus, derived from our electrophysiological studies of brain slice preparations taken from transgenic mice bred to express a variety of fluorescent proteins in specific cell types. We also discuss the recently withdrawn obesity drug fenfluramine, which appears to act on proopiomelanocortin neurons via serotonin (2C) receptors. Finally, we review current inquiries into the ability of the hormone ghrelin to stimulate appetite by its activation of neuropeptide Y neurons and inhibition of proopiomelanocortin neurons.
机译:下丘脑弓状核的神经元似乎是能量储存中心和周边信号会聚的部位,并深刻调节黑皮质素回路的活性,为将这些回路作为能量稳态障碍的治疗靶点提供了有力的依据。我们实验室和合作者最近的研究表明,瘦素以不同的方式调节不同的下丘脑细胞群。在本报告中,我们概述了瘦蛋白在弓形核中作用的整合模型,该模型源于我们对脑切片制品的电生理研究,该切片取自转基因小鼠,在特定的细胞类型中表达了多种荧光蛋白。我们还讨论了最近撤消的肥胖药芬氟拉明,它似乎通过5-羟色胺(2C)受体作用于原黑皮层皮质素神经元。最后,我们回顾了关于ghrelin激素通过激活神经肽Y神经元和抑制​​proopiomelanocortin神经元刺激食欲的能力的最新研究。

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