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首页> 外文期刊>Neuropharmacology >Muscarinic M 4 receptors regulate GABAergic transmission in rat tuberomammillary nucleus neurons
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Muscarinic M 4 receptors regulate GABAergic transmission in rat tuberomammillary nucleus neurons

机译:毒蕈碱型M 4受体调节大鼠结核性乳头状核神经元的GABA能传递

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Histaminergic neurons within the tuberomammillary nucleus (TMN) play an important role in sleep-wakefulness regulation. Here, we report the muscarinic modulation of GABAergic spontaneous miniature inhibitory postsynaptic currents (mIPSCs) in mechanically dissociated rat histaminergic neurons using a conventional whole-cell patch clamp technique. Muscarine, a nonselective muscarinic acetylcholine (mACh) receptor agonist, reversibly decreased mIPSC frequency without affecting the current amplitude, indicating that muscarine acts presynaptically to decrease the probability of spontaneous GABA release. The muscarine action on GABAergic mIPSC frequency was completely blocked by atropine, a nonselective mACh receptor antagonist, and tropicamide, an M 4 receptor antagonist. The muscarine-induced decrease in mIPSC frequency was completely occluded in the presence of Cd 2+, a general voltage-dependent Ca 2+ channel blocker, or in a Ca 2+-free external solution. However, pharmacological agents affecting adenylyl cyclase or G-protein coupled inwardly rectifying K + channel activity did not prevent the inhibitory action of muscarine on GABAergic mIPSCs. These results suggest that muscarine acts on M 4 receptors on GABAergic nerve terminals projecting to histaminergic neurons to inhibit spontaneous GABA release via the inhibition of Ca 2+ influx from the extracellular space. Muscarine also inhibited action potential-dependent GABA release by activating presynaptic M 4 receptors in more physiological conditions. The M 4 receptor-mediated modulation of GABAergic transmission onto TMN neurons may contribute to the regulation of sleep-wakefulness. Highlights: Muscarine acted presynaptically to decrease GABAergic mIPSC frequency in TMN neurons. Tropicamide, an M 4 receptor antagonist, blocked the inhibitory action of muscarine on GABAergic mIPSCs. Muscarine decreased spontaneous GABA release by inhibiting Ca 2+ influx from the extracellular space. M 4 receptor activation decreased GABA release evoked by the electrical stimulation of the preoptic area.
机译:结核母核(TMN)内的组胺能神经元在睡眠-清醒调节中起重要作用。在这里,我们报告使用传统的全细胞膜片钳技术机械解离的大鼠组胺能神经元中的GABA能自发微型抑制突触后电流(mIPSCs)的毒蕈碱调节。毒蕈碱是一种非选择性毒蕈碱乙酰胆碱(mACh)受体激动剂,可逆地降低mIPSC频率,而不会影响电流幅度,表明毒蕈碱会先突触地降低自发GABA释放的可能性。毒蕈碱对GABA能mIPSC频率的作用完全被非选择性mACh受体拮抗剂阿托品和M 4受体拮抗剂tropicamide完全阻断。毒蕈碱诱导的mIPSC频率降低在Cd 2+,一种一般的电压依赖性Ca 2+通道阻滞剂或无Ca 2+的外部溶液中完全被阻止。但是,影响腺苷酸环化酶或G蛋白偶联向内整流K +通道活性的药理药物并不能阻止毒蕈碱对GABA能mIPSC的抑制作用。这些结果表明毒蕈碱对投射到组胺能神经元的GABA能神经末梢的M 4受体起作用,以通过抑制来自细胞外空间的Ca 2+流入来抑制自发性GABA释放。毒蕈碱还可以通过在更多生理条件下激活突触前M 4受体来抑制动作电位依赖性GABA的释放。 M 4受体介导的GABA能传递到TMN神经元上的调节可能有助于调节睡眠-清醒状态。重点:毒蕈碱可先天性地降低TMN神经元中GABA能的mIPSC频率。 Tropicamide是一种M 4受体拮抗剂,可阻断毒蕈碱对GABA能mIPSC的抑制作用。毒蕈碱通过抑制来自细胞外空间的Ca 2+流入而减少了自发GABA的释放。 M 4受体激活减少了视前区的电刺激引起的GABA释放。

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