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蓝斑作为大鼠主动呼气和吸气的警觉中心。

Locus Coeruleus as a vigilance centre for active inspiration and expiration in rats.

机构信息

School of Medicine of Ribeirão Preto, Department of Physiology, University of São Paulo, Ribeirão Preto, SP, Brazil.

School of Physiology, Pharmacology and Neuroscience, Biomedical Sciences, University of Bristol, Bristol, UK.

出版信息

Sci Rep. 2018 Oct 23;8(1):15654. doi: 10.1038/s41598-018-34047-w.

Abstract

At rest, inspiration is an active process while expiration is passive. However, high chemical drive (hypercapnia or hypoxia) activates central and peripheral chemoreceptors triggering reflex increases in inspiration and active expiration. The Locus Coeruleus contains noradrenergic neurons (A6 neurons) that increase their firing frequency when exposed to hypercapnia and hypoxia. Using recently developed neuronal hyperpolarising technology in conscious rats, we tested the hypothesis that A6 neurons are a part of a vigilance centre for controlling breathing under high chemical drive and that this includes recruitment of active inspiration and expiration in readiness for flight or fight. Pharmacogenetic inhibition of A6 neurons was without effect on resting and on peripheral chemoreceptors-evoked inspiratory, expiratory and ventilatory responses. On the other hand, the number of sighs evoked by systemic hypoxia was reduced. In the absence of peripheral chemoreceptors, inhibition of A6 neurons during hypercapnia did not affect sighing, but reduced both the magnitude and incidence of active expiration, and the frequency and amplitude of inspiration. These changes reduced pulmonary ventilation. Our data indicated that A6 neurons exert a CO-dependent modulation of expiratory drive. The data also demonstrate that A6 neurons contribute to the CO-evoked increases in the inspiratory motor output and hypoxia-evoked sighing.

摘要

在休息时,吸气是一个主动过程,而呼气是被动过程。然而,高化学驱动力(高碳酸血症或缺氧)会激活中枢和外周化学感受器,引发吸气和主动呼气的反射性增加。蓝斑含有去甲肾上腺素能神经元(A6 神经元),当暴露于高碳酸血症和缺氧时,其放电频率会增加。在清醒大鼠中使用最近开发的神经元超极化技术,我们测试了这样一个假设,即 A6 神经元是控制高化学驱动力下呼吸的警戒中心的一部分,这包括为飞行或战斗做准备而募集主动吸气和呼气。A6 神经元的药理学抑制对静息状态和外周化学感受器诱发的吸气、呼气和通气反应均无影响。另一方面,全身缺氧引起的叹息次数减少。在外周化学感受器不存在的情况下,高碳酸血症期间 A6 神经元的抑制并不影响叹息,但减少了主动呼气的幅度和发生率,以及吸气的频率和幅度。这些变化降低了肺通气。我们的数据表明,A6 神经元对呼气驱动力产生 CO 依赖性调制。这些数据还表明,A6 神经元有助于 CO 诱发的吸气运动输出增加和缺氧诱发的叹息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9744/6199338/18cfded85df6/41598_2018_34047_Fig1_HTML.jpg

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