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觉醒相关神经元中峰电位诱发钙瞬变的递质调制:毒蕈碱对SNX - 482敏感钙内流的抑制作用

Transmitter modulation of spike-evoked calcium transients in arousal related neurons: muscarinic inhibition of SNX-482-sensitive calcium influx.

作者信息

Kohlmeier Kristi A, Leonard Christopher S

机构信息

Department of Physiology, New York Medical College, Valhalla, NY 10595, USA.

出版信息

Eur J Neurosci. 2006 Mar;23(5):1151-62. doi: 10.1111/j.1460-9568.2006.04640.x.

Abstract

Nitric oxide synthase (NOS)-containing cholinergic neurons in the laterodorsal tegmentum (LDT) influence behavioral and motivational states through their projections to the thalamus, ventral tegmental area and a brainstem 'rapid eye movement (REM)-induction' site. Action potential-evoked intracellular calcium transients dampen excitability and stimulate NO production in these neurons. In this study, we investigated the action of several arousal-related neurotransmitters and the role of specific calcium channels in these LDT Ca(2+)-transients by simultaneous whole-cell recording and calcium imaging in mouse (P14-P30) brain slices. Carbachol, noradrenaline and adenosine inhibited spike-evoked Ca(2+)-transients, while histamine, t-ACPD, a metabotropic glutamate receptor agonist, and orexin-A did not. Carbachol inhibition was blocked by atropine, was insensitive to blockade of G-protein-coupled inward rectifier (GIRK) channels and was not inhibited by nifedipine, omega-conotoxin GVIA or omega-agatoxin IVA, which block L-, N- and P/Q-type calcium channels, respectively. In contrast, SNX-482 (100 nm), a selective antagonist of R-type calcium channels containing the alpha1E (Cav2.3) subunit, attenuated carbachol inhibition of the somatic spike-evoked calcium transient. To our knowledge, this is the first demonstration of muscarinic inhibition of native SNX-482-sensitive R-channels. Our findings indicate that muscarinic modulation of these channels plays an important role in the feedback control of cholinergic LDT neurons and that inhibition of spike-evoked Ca(2+)-transients is a common action of neurotransmitters that also activate GIRK channels in these neurons. Because spike-evoked calcium influx dampens excitability, our findings suggest that these 'inhibitory' transmitters could boost firing rate and enhance responsiveness to excitatory inputs during states of high firing, such as waking and REM sleep.

摘要

外侧背盖区(LDT)中含一氧化氮合酶(NOS)的胆碱能神经元通过其向丘脑、腹侧被盖区和脑干“快速眼动(REM)诱导”位点的投射来影响行为和动机状态。动作电位诱发的细胞内钙瞬变会抑制这些神经元的兴奋性并刺激一氧化氮的产生。在本研究中,我们通过在小鼠(P14 - P30)脑片上同时进行全细胞记录和钙成像,研究了几种与觉醒相关的神经递质的作用以及特定钙通道在这些LDT钙瞬变中的作用。卡巴胆碱、去甲肾上腺素和腺苷抑制了动作电位诱发的钙瞬变,而组胺、反式 - ACPD(一种代谢型谷氨酸受体激动剂)和食欲素 - A则没有。卡巴胆碱的抑制作用被阿托品阻断,对G蛋白偶联内向整流(GIRK)通道的阻断不敏感,且不受分别阻断L型、N型和P/Q型钙通道的硝苯地平、ω - 芋螺毒素GVIA或ω - 阿加毒素IVA的抑制。相反,含有α1E(Cav2.3)亚基的R型钙通道的选择性拮抗剂SNX - 482(100 nM)减弱了卡巴胆碱对体细胞动作电位诱发的钙瞬变的抑制作用。据我们所知,这是首次证明毒蕈碱对天然SNX - 482敏感的R通道的抑制作用。我们的研究结果表明,这些通道的毒蕈碱调节在胆碱能LDT神经元的反馈控制中起重要作用,并且动作电位诱发的钙瞬变的抑制是这些神经元中也激活GIRK通道的神经递质的共同作用。由于动作电位诱发的钙内流会抑制兴奋性,我们的研究结果表明,这些 “抑制性” 递质在高放电状态(如清醒和REM睡眠)期间可以提高放电频率并增强对兴奋性输入的反应性。

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