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体内电生理证据表明,内源性去甲肾上腺素对大鼠海马体中5-羟色胺终端的α2-肾上腺素能受体有持续性激活作用。

In vivo electrophysiological evidence for tonic activation by endogenous noradrenaline of alpha 2-adrenoceptors on 5-hydroxytryptamine terminals in the rat hippocampus.

作者信息

Mongeau R, Blier P, de Montigny C

机构信息

Department of Psychiatry, McGill University, Montréal, Québec, Canada.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1993 Mar;347(3):266-72. doi: 10.1007/BF00167444.

Abstract

The activation of alpha 2-adrenergic heteroreceptors was studied by comparing the effectiveness of the electrical stimulation of the ascending 5-HT pathway in suppressing the firing activity of CA3 dorsal hippocampus pyramidal neurons prior to, and following, the intravenous administration of noradrenergic agents. Desipramine (2 mg/kg), a selective noradrenaline reuptake blocker, reduced the efficacy of the stimulation; this effect was reversed by the alpha 2-adrenoceptor antagonists yohimbine (0.5 mg/kg) and (-)mianserin (0.5 mg/kg), but not by idazoxan (0.5 mg/kg), an adrenoceptor antagonist with preferential affinity for the imidazoline recognition sites. Low doses of the alpha 2-adrenoceptor agonist clonidine (2 and 10 micrograms/kg) enhanced the efficacy of the stimulation, while high doses (100 and 400 micrograms/kg) reduced it. These incremental and decremental effects of clonidine were reversed by 0.1 and 1 mg/kg of yohimbine, respectively. The enhancing effect of the low dose of clonidine (10 micrograms/kg) was abolished in rats pretreated with the noradrenaline neurotoxin 6-hydroxydopamine. However, the inhibitory effect of a high dose of clonidine (100 micrograms/kg) was unaltered by this pretreatment. These results indicate that low doses of clonidine preferentially activate alpha 2-adrenergic autoreceptors on the noradrenaline neurons resulting in a reduction of the tonic inhibitory effect of endogenous noradrenaline on 5-HT neurotransmission, while higher doses of clonidine would decrease 5-HT neurotransmission through the direct activation of alpha 2-adrenergic heteroreceptors on 5-HT terminals. Furthermore, the selective alpha 2-adrenergic heteroreceptors antagonist (-)mianserin (0.5 mg/kg) increased by itself the efficacy of 5-HT neurotransmission, an effect not observed with yohimbine and idazoxan.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过比较静脉注射去甲肾上腺素能药物前后,电刺激5-羟色胺(5-HT)上行通路对抑制CA3背侧海马锥体神经元放电活动的效果,研究了α2-肾上腺素能异受体的激活情况。去甲丙咪嗪(2毫克/千克),一种选择性去甲肾上腺素再摄取阻滞剂,降低了刺激的效果;α2-肾上腺素能受体拮抗剂育亨宾(0.5毫克/千克)和(-)米安色林(0.5毫克/千克)可逆转这种效应,但对咪唑啉识别位点具有优先亲和力的肾上腺素能受体拮抗剂伊达唑胺(0.5毫克/千克)则不能。低剂量的α2-肾上腺素能受体激动剂可乐定(2和10微克/千克)增强了刺激的效果,而高剂量(100和400微克/千克)则降低了该效果。可乐定的这些增强和减弱效应分别被0.1和1毫克/千克的育亨宾逆转。低剂量可乐定(10微克/千克)的增强作用在用去甲肾上腺素神经毒素6-羟基多巴胺预处理的大鼠中被消除。然而,高剂量可乐定(100微克/千克)的抑制作用不受该预处理的影响。这些结果表明,低剂量可乐定优先激活去甲肾上腺素能神经元上的α2-肾上腺素能自身受体,导致内源性去甲肾上腺素对5-HT神经传递的紧张性抑制作用减弱,而高剂量可乐定则通过直接激活5-HT终末上的α2-肾上腺素能异受体来减少5-HT神经传递。此外,选择性α2-肾上腺素能异受体拮抗剂(-)米安色林(0.5毫克/千克)自身增加了5-HT神经传递的效果,育亨宾和伊达唑胺未观察到这种效应。(摘要截短至250字)

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