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Melanin concentrating hormone depresses synaptic activity of glutamate and GABA neurons from rat lateral hypothalamus

机译:黑色素浓缩激素抑制大鼠下丘脑外侧谷氨酸和GABA神经元的突触活性

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摘要

class="enumerated" style="list-style-type:decimal">The neuropeptide melanin concentrating hormone (MCH) is synthesised only by neurons of the lateral hypothalamic (LH) area in the CNS. MCH cells project widely throughout the brain. Despite the growing interest in this peptide, in part related to its role in feeding, little has been done to characterise its physiological effects in neurons. Using whole-cell recording with current and voltage clamp, we examined the cellular actions in neurons from the LH.MCH induced a consistent decrease in the frequency of action potentials and reduced synaptic activity. Most fast synaptic activity in the hypothalamus is mediated by GABA or glutamate. MCH inhibited the synaptic activity of both glutamatergic and GABAergic LH neurons, each tested independently.MCH reduced the amplitude of glutamate-evoked currents and reduced the amplitude of miniature excitatory currents, indicating an inhibitory modulation of postsynaptic glutamate receptors.In the presence of tetrodotoxin to block action potentials, MCH caused a depression in the frequency of miniature glutamate-mediated postsynaptic currents, suggesting a presynaptic site of receptor expression.In voltage clamp experiments, MCH depressed the amplitude of calcium currents, suggesting that a mechanism of inhibition may involve a reduced calcium-dependent release of amino acid transmitter.Previous reports have suggested that MCH activated potassium channels in non-neuronal cells transfected with the MCH receptor gene. We found no effect of MCH on voltage-dependent potassium channels in LH neurons. Baclofen, a GABAB receptor agonist, activated G-protein gated inwardly rectifying potassium (GIRK)-type channels; in the same neurons, MCH had no effect on GIRK channels. MCH showed no modulation of sodium currents.Blockade of the Gi/Go protein with pertussis toxin eliminated the actions of MCH.The inhibitory actions of MCH on both excitatory and inhibitory synaptic events, coupled with opposing excitatory actions of hypocretin, another LH peptide that projects to many of the same loci, suggest a substantial level of complexity in neuropeptide modulation of LH actions.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 神经肽黑色素浓缩激素(MCH)仅由CNS中下丘脑(LH)区域的神经元合成。 MCH细胞广泛分布于整个大脑。尽管人们对该肽的兴趣日益增长,部分与它在饲料中的作用有关,但几乎没有任何表征其在神经元中的生理作用的研究。使用带有电流和电压钳位的全细胞记录,我们检查了LH神经元中的细胞动作。 MCH导致动作电位频率持续降低并降低了突触活动。下丘脑中最快速的突触活性是由GABA或谷氨酸介导的。 MCH抑制分别测试的谷氨酸能和GABA能LH神经元的突触活性。 在存在河豚毒素以阻断动作电位的情况下,MCH导致微型谷氨酸介导的突触后电流频率降低,表明受体表达处于突触前。 电压在钳位实验中,MCH降低了钙电流的幅度,表明这种抑制机制可能涉及减少钙依赖性氨基酸递质的释放。 以前的报道表明,MCH激活了非神经元中的钾通道。 MCH受体基因转染的细胞。我们发现MCH对LH神经元的电压依赖性钾通道没有影响。 GABAB受体激动剂巴氯芬激活G蛋白门控的内向整流钾(GIRK)型通道。在相同的神经元中,MCH对GIRK通道没有影响。 MCH没有显示出对钠电流的调节。 用百日咳毒素封锁Gi / Go蛋白消除了MCH的作用。 MCH对兴奋性和抑制性突触事件的抑制作用,再加上相反的促胰高血糖素的兴奋作用,hypocretin是投射到许多相同基因座的另一种LH肽,提示LH动作的神经肽调节具有相当大的复杂性。

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