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大鼠丘脑运动核中神经元放电频率的胺能控制。

Aminergic control of neuronal firing rate in thalamic motor nuclei of the rat.

作者信息

Grasso C, Li Volsi G, Licata F, Ciranna L, Santangelo F

机构信息

Department of Physiological Sciences, University of Catania, Catania, Italy.

出版信息

Arch Ital Biol. 2006 Aug;144(3-4):173-96.

Abstract

The effects induced on neuronal firing by microiontophoretic application of the biological amines noradrenaline (NA) and 5-hydroxytryptamine (5-HT) were studied "in vivo" in ventral-anterior (VA) and ventrolateral (VL) thalamic motor nuclei of anaesthetized rats. In both nuclei the amines had a mostly depressive action on neuronal firing rate, the percentage of units responsive to NA application (88%) being higher than to 5-HT (72%). Short-lasting (less than 2 min) and long lasting (up to 20 min) inhibitory responses were recorded, the former mostly evoked by NA and the latter by 5-HT ejection. In some cases 5-HT application had no effect on the firing rate but modified the firing pattern. NA-evoked responses were significantly more intense in VL than in VA neurons. Short-lasting inhibitory responses similar to NA-induced effects were evoked by the alpha2 adrenergic receptor agonist clonidine and to a lesser extent by the beta adrenergic receptor agonist isoproterenol. Inhibitory responses to 5-HT were partially mimicked by application of the 5-HT(1A) receptor agonist 8-hydroxy-2(di-n-propylamino)tetralin (8-OH-DPAT) and of the 5-HT2 receptor agonist alpha-methyl-5-hydroxytryptamine (ALPHA-MET-5-HT). The latter evoked excitatory responses in some cases. Both 5-HT agonists were more effective on VA than on VL neurons. The effects evoked by agonists were at least partially blocked by respective antagonists. These results suggest that although both 5-HT and NA depress neuronal firing rate, their effects differ in time course and in the amount of inhibition; besides aminergic modulation is differently exerted on VA and VL.

摘要

在麻醉大鼠的腹前(VA)和腹外侧(VL)丘脑运动核中,以“体内”方式研究了通过微量离子电泳施加生物胺去甲肾上腺素(NA)和5-羟色胺(5-HT)对神经元放电的影响。在这两个核中,胺类物质对神经元放电频率大多具有抑制作用,对NA施加有反应的单位百分比(88%)高于对5-HT有反应的单位百分比(72%)。记录到了短暂(小于2分钟)和持久(长达20分钟)的抑制反应,前者大多由NA诱发,后者由5-HT喷射诱发。在某些情况下,5-HT施加对放电频率没有影响,但改变了放电模式。NA诱发的反应在VL神经元中比在VA神经元中明显更强。α2肾上腺素能受体激动剂可乐定诱发了类似于NA诱导效应的短暂抑制反应,β肾上腺素能受体激动剂异丙肾上腺素诱发的程度较小。对5-HT的抑制反应部分被5-HT(1A)受体激动剂8-羟基-2(二正丙基氨基)四氢萘(8-OH-DPAT)和5-HT2受体激动剂α-甲基-5-羟色胺(ALPHA-MET-5-HT)的应用所模拟。后者在某些情况下诱发了兴奋反应。两种5-HT激动剂对VA神经元的作用比对VL神经元更有效。激动剂诱发的效应至少部分被相应的拮抗剂阻断。这些结果表明,虽然5-HT和NA都降低神经元放电频率,但它们的效应在时间进程和抑制量上有所不同;此外,胺能调制在VA和VL上的作用方式也不同。

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