瘦素通过局部紧凑旁-网状旁回路激活黑质中的多巴胺和 GABA 神经元。

IF 4.4 2区 医学 Q1 NEUROSCIENCES
Maria Mancini, Takuya Hikima, Paul Witkovsky, Jyoti C Patel, Dominic W Stone, Alison H Affinati, Margaret E Rice
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引用次数: 0

摘要

脂肪源性瘦素通过平衡食物摄入和运动输出来促进能量平衡,但人们对瘦素如何作用于大脑运动中枢仍知之甚少。我们研究了瘦素对两个参与运动控制的基底神经节核团(黑质紧密旁(SNc)和网状旁(SNr))神经元活动的影响。我们利用小鼠报告基因来识别表达瘦素受体(LepRs)的细胞,发现在两性中,大多数黑质多巴胺神经元都表达高水平的 LepR。在雄性野生型小鼠的体外中脑切片中进行的全细胞记录显示,瘦素能直接激活SNc多巴胺神经元并增加体支多巴胺的释放。虽然在SNr GABA输出神经元中LepR表达较低,但瘦素也能激活这些细胞。其他实验表明,瘦素对SNr神经元的影响是间接的,涉及D1多巴胺受体和TRPC3通道。给雄性小鼠注射瘦素可增加运动活动,这与激活SNc中的多巴胺神经元以及之前报道的瘦素在纹状体切片中放大轴突多巴胺释放的结果一致。这些研究结果表明,瘦素除了作为饱腹感激素管理能量平衡外,还能促进轴突和体支多巴胺的释放,从而影响运动输出。我们在此研究表明,瘦素可直接增加黑质(SN)紧实旁多巴胺神经元的活性,从而增强躯体树突多巴胺的释放。瘦素还能提高黑质网状结构旁的GABA能神经元的活性,但这是通过被局部释放的多巴胺激活的D1多巴胺受体间接实现的。与黑质多巴胺神经元活性的增加以及之前显示瘦素能放大纹状体多巴胺释放的证据相一致,全身性瘦素能增加运动行为。运动活动的增加补充了瘦素对食物摄入的抑制作用,为这种激素调节能量平衡增添了一个新的维度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leptin activates dopamine and GABA neurons in the substantia nigra via a local pars compacta-pars reticulata circuit.

Adipose-derived leptin contributes to energy homeostasis by balancing food intake and motor output, but how leptin acts in brain motor centers remains poorly understood. We investigated the influence of leptin on neuronal activity in two basal ganglia nuclei involved in motor control: the substantia nigra pars compacta (SNc) and pars reticulata (SNr). Using a mouse reporter line to identify cells expressing leptin receptors (LepRs), we found that in both sexes, a majority of SNc dopamine neurons express a high level of LepR. Whole-cell recording in ex vivo midbrain slices from male wild-type mice showed that leptin activates SNc dopamine neurons directly and increases somatodendritic dopamine release. Although LepR expression in SNr GABA output neurons was low, leptin also activated these cells. Additional experiments showed that the influence of leptin on SNr neurons is indirect and involves D1 dopamine receptors and TRPC3 channels. Administration of leptin to male mice increased locomotor activity, consistent with activation of dopamine neurons in the SNc coupled to previously reported amplification of axonal dopamine release by leptin in striatal slices. These findings indicate that in addition to managing energy homeostasis through its actions as a satiety hormone, leptin also promotes axonal and somatodendritic dopamine release that can influence motor output.Significance statement Dopamine neurons regulate motivated behaviors, but how they are influenced by metabolic hormones, like leptin, is incompletely understood. We show here that leptin increases the activity of substantia nigra (SN) pars compacta dopamine neurons directly, and that this enhances somatodendritic dopamine release. Leptin also increases the activity of GABAergic neurons in the SN pars reticulata, but does so indirectly via D1 dopamine receptors activated by locally released dopamine. Consistent with increased nigral dopamine neuron activity and previous evidence showing that leptin amplifies striatal dopamine release, systemic leptin increases locomotor behavior. This increase in motor activity complements the well-established inhibitory effect of leptin on food intake and adds an additional dimension to the regulation of energy balance by this hormone.

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来源期刊
Journal of Neuroscience
Journal of Neuroscience 医学-神经科学
CiteScore
9.30
自引率
3.80%
发文量
1164
审稿时长
12 months
期刊介绍: JNeurosci (ISSN 0270-6474) is an official journal of the Society for Neuroscience. It is published weekly by the Society, fifty weeks a year, one volume a year. JNeurosci publishes papers on a broad range of topics of general interest to those working on the nervous system. Authors now have an Open Choice option for their published articles
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