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α2受体阻断可增加蓝斑核神经元对兴奋性刺激的反应性。

Alpha-2 receptor blockade increases responsiveness of locus coeruleus neurons to excitatory stimulation.

作者信息

Simson P E, Weiss J M

出版信息

J Neurosci. 1987 Jun;7(6):1732-40. doi: 10.1523/JNEUROSCI.07-06-01732.1987.

Abstract

This study presents evidence that alpha 2-receptors in the locus coeruleus (LC) regulate the responsiveness of LC neurons to excitatory stimuli. In the first experiment, intravenous administration of the alpha 2-adrenergic antagonist idazoxan markedly potentiated the responses of LC neurons to the excitatory stimulus of contralateral hind paw compression (PC). Increased responsiveness of LC neurons to PC was seen with doses of idazoxan far below those that altered spontaneous activity of the LC. In the second experiment, increased responsiveness of LC neurons to PC was seen when low doses of idazoxan were infused directly into the LC, thereby indicating that increased responsiveness of LC neurons resulted from blockade of alpha 2-receptors in the LC region and not from greater stimulus input to the LC resulting from blockade of alpha 2-receptors elsewhere. In the third experiment, another alpha 2-adrenergic antagonist, yohimbine, also increased the responsiveness of LC neurons to PC. Finally, the response of the LC to another excitatory stimulus, peripheral injection of nicotine, was also found to be increased by idazoxan. Results obtained prior to these studies had indicated that alpha 2-receptors in the LC regulate the period of quiescence that follows a burst of LC firing. However, more recent studies suggest that this quiescence results primarily from changes in ionic conductance of the membrane following directly from depolarization. The present findings indicate that, in addition to whatever role alpha 2-receptors play in regulating postfiring quiescence, these receptors in the LC appear to play a major role in regulating the responsiveness of LC neurons to excitational influences.

摘要

本研究表明,蓝斑(LC)中的α2受体调节LC神经元对兴奋性刺激的反应性。在第一个实验中,静脉注射α2肾上腺素能拮抗剂咪唑克生显著增强了LC神经元对同侧后爪压迫(PC)这一兴奋性刺激的反应。在咪唑克生剂量远低于改变LC自发活动的剂量时,就观察到LC神经元对PC的反应性增加。在第二个实验中,当将低剂量的咪唑克生直接注入LC时,观察到LC神经元对PC的反应性增加,从而表明LC神经元反应性的增加是由于LC区域α2受体的阻断,而非其他部位α2受体阻断导致对LC的刺激输入增加所致。在第三个实验中,另一种α2肾上腺素能拮抗剂育亨宾也增加了LC神经元对PC的反应性。最后,还发现咪唑克生可增加LC对另一种兴奋性刺激——外周注射尼古丁的反应。在这些研究之前获得的结果表明,LC中的α2受体调节LC爆发式放电后的静息期。然而,最近的研究表明,这种静息主要是由直接去极化后膜离子电导的变化引起的。目前的研究结果表明,除了α2受体在调节放电后静息中所起的任何作用外,LC中的这些受体似乎在调节LC神经元对兴奋性影响的反应性方面起主要作用。

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