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大鼠下丘脑后区通过 A7 儿茶酚胺细胞群对伤害感受发挥相反的作用。

The posterior hypothalamus exerts opposing effects on nociception via the A7 catecholamine cell group in rats.

机构信息

College of Nursing Science, Kyung Hee University, 26 Kyunghee-daero, Dongdaemun-gu, Seoul 130-701, Korea.

出版信息

Neuroscience. 2012 Dec 27;227:144-53. doi: 10.1016/j.neuroscience.2012.09.058. Epub 2012 Oct 2.

Abstract

Stimulation of the posterior hypothalamic area (PH) produces antinociception in rats and humans, but the precise mechanisms are unknown. The PH forms anatomical connections with the parabrachial area, which contains the pontine A7 catecholamine cell group, a group of spinally projecting noradrenergic neurons known to produce antinociception in the dorsal horn. The aim of the present study was to determine whether PH-induced antinociception is mediated in part through connections with the A7 cell group in female Sprague-Dawley rats, as measured by the tail flick and foot withdrawal latency. Stimulation of the PH with the cholinergic agonist carbachol (125 nmol) produced antinociception that was blocked by pretreatment with atropine sulfate. Intrathecal injection of the α(2)-adrenoceptor antagonist yohimbine reversed PH-induced antinociception, but the α(1)-adrenoceptor antagonist WB4101 facilitated antinociception. Intrathecal injection of normal saline had no effect. In a separate experiment, cobalt chloride, which reversibly arrests synaptic activity, was microinjected into the A7 cell group and blocked PH-induced antinociception. These findings provide evidence that the PH modulates nociception in part through connections with the A7 catecholamine cell group through opposing effects. Antinociception occurs from actions at α(2)-adrenoceptors in the dorsal horn, while concurrent hyperalgesia occurs from actions of norepinephrine at α(1)-adrenoceptors. This hyperalgesic response likely attenuates antinociception from PH stimulation.

摘要

刺激下丘脑后区 (PH) 可在大鼠和人类中产生镇痛作用,但确切的机制尚不清楚。PH 与臂旁区形成解剖连接,臂旁区包含含有脑桥 A7 儿茶酚胺细胞群,该细胞群是一组向脊髓投射的去甲肾上腺素能神经元,已知其在背角产生镇痛作用。本研究的目的是确定 PH 诱导的镇痛是否部分通过与 A7 细胞群的连接来介导,如尾部闪烁和足部退缩潜伏期所示。用胆碱能激动剂 carbachol(125 nmol)刺激 PH 可产生镇痛作用,该作用可被硫酸阿托品预处理所阻断。鞘内注射α(2)-肾上腺素能受体拮抗剂育亨宾可逆转 PH 诱导的镇痛,但α(1)-肾上腺素能受体拮抗剂 WB4101 促进镇痛。鞘内注射生理盐水无影响。在另一个实验中,可逆性阻断突触活动的氯化钴被微注射到 A7 细胞群中,阻断了 PH 诱导的镇痛。这些发现提供了证据,表明 PH 通过与 A7 儿茶酚胺细胞群的连接,通过相反的作用来调节痛觉。镇痛作用是通过背角的α(2)-肾上腺素能受体的作用产生的,而同时发生的痛觉过敏是通过去甲肾上腺素在α(1)-肾上腺素能受体上的作用产生的。这种痛觉过敏反应可能会减弱 PH 刺激引起的镇痛作用。

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