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兴奋性神经调质在呼吸神经元控制中的状态依赖相互作用。

State-dependent interactions between excitatory neuromodulators in the neuronal control of breathing.

机构信息

Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington 98101, USA.

出版信息

J Neurosci. 2010 Jun 16;30(24):8251-62. doi: 10.1523/JNEUROSCI.5361-09.2010.

Abstract

All neuronal networks are modulated by multiple neuropeptides and biogenic amines. Yet, few studies investigate how different modulators interact to regulate network activity. Here we explored the state-dependent functional interactions between three excitatory neuromodulators acting on neurokinin1 (NK1), alpha1 noradrenergic (alpha1 NE), and 5-HT2 serotonin receptors within the pre-Bötzinger complex (pre-BötC), an area critical for the generation of breathing. In anesthetized, in vivo mice, the reliance on endogenous NK1 activation depended on spontaneous breathing frequency and the modulatory state of the animal. Endogenous NK1 activation had no significant respiratory effect when stimulating raphe magnus and/or locus ceruleus, but became critical when alpha1 NE and 5-HT2 receptors were pharmacologically blocked. The dependence of the centrally generated respiratory rhythm on NK1 activation was blunted in the presence of alpha1 NE and 5-HT2 agonists as demonstrated in slices containing the pre-BötC. We conclude that a modulator's action is determined by the concurrent modulation and interaction with other neuromodulators. Deficiencies in one neuromodulator are immediately compensated by the action of other neuromodulators. This interplay could play a role in the state dependency of certain breathing disorders.

摘要

所有的神经网络都受到多种神经肽和生物胺的调节。然而,很少有研究调查不同的调节剂如何相互作用来调节网络活动。在这里,我们探索了三种兴奋性神经调节剂在预激复合体(pre-BötC)内作用于神经激肽 1(NK1)、α1 去甲肾上腺素能(α1 NE)和 5-羟色胺 2 受体(5-HT2)时的状态依赖性功能相互作用,pre-BötC 是呼吸产生的关键区域。在麻醉、体内的小鼠中,对内源性 NK1 激活的依赖取决于自发呼吸频率和动物的调节状态。当刺激中缝大核和/或蓝斑时,内源性 NK1 激活对呼吸没有显著的影响,但当α1 NE 和 5-HT2 受体被药理学阻断时,内源性 NK1 激活就变得至关重要。在含有 pre-BötC 的切片中,当存在α1 NE 和 5-HT2 激动剂时,中央产生的呼吸节律对 NK1 激活的依赖性减弱,这表明 NK1 激活的依赖性减弱。我们得出结论,调节剂的作用取决于其与其他调节剂的并发调节和相互作用。一种神经调节剂的缺陷会立即被其他神经调节剂的作用所补偿。这种相互作用可能在某些呼吸障碍的状态依赖性中发挥作用。

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