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面神经运动核中5-羟色胺受体的药理学特性:一项微量离子电泳研究。

Pharmacological characterization of serotonin receptors in the facial motor nucleus: a microiontophoretic study.

作者信息

McCall R B, Aghajanian G K

出版信息

Eur J Pharmacol. 1980 Jul 25;65(2-3):175-83. doi: 10.1016/0014-2999(80)90390-8.

Abstract

The effects of 'peripheral' serotonin (5-HT) antagonists on the facilitation of facial motoneuron excitation by 5-HT were investigated in the present study. Microiontophoretic application (5--10 aA) or intravenous administration of methysergide (0.5--1.0 mg/kg), cyproheptadine (0.5--1.0 mg/kg), cinanserin (0.5--1.0 mg/kg), or metergoline (50--100 micrograms/kg) antagonized the facilitating effect of 5-HT but not that of norepinephrine (NE) on facial motoneurons. Blockade developed within 1--2 min of the intravenous administration of methysergide, cyproheptadine and cinanserin and continued up to 30 min. The antagonism produced by intravenous metergoline took 8--15 min to develop and lasted for at least 6 h. Chronic administration of metergoline resulted in supersensitivity to 5-HT and NE in the facial nucleus. The putative 5-HT antagonists chlorpromazine, propranolol, and methiothepin failed to block the facilitating effect of 5-HT; however, methiothepin did block NE. The results are discussed in relation to a two-component model of the 5-HT mediated motor syndrome consisting of : (1) patterned excitatory inputs to motor nuclei; (2) 5-HT facilitation of these excitatory inputs. The 'peripheral' 5-HT antagonists appear to directly block the latter component.

摘要

本研究调查了“外周”5-羟色胺(5-HT)拮抗剂对5-HT促进面神经运动神经元兴奋作用的影响。微量离子电渗法给药(5-10纳安)或静脉注射麦角新碱(0.5-1.0毫克/千克)、赛庚啶(0.5-1.0毫克/千克)、辛那色林(0.5-1.0毫克/千克)或美替加林(50-100微克/千克)可拮抗5-HT对面神经运动神经元的促进作用,但不拮抗去甲肾上腺素(NE)的作用。静脉注射麦角新碱、赛庚啶和辛那色林后1-2分钟内出现阻断作用,并持续30分钟。静脉注射美替加林产生的拮抗作用需8-15分钟出现,并持续至少6小时。长期给予美替加林导致面神经核中对5-HT和NE超敏。公认的5-HT拮抗剂氯丙嗪、普萘洛尔和甲硫噻平未能阻断5-HT的促进作用;然而,甲硫噻平确实阻断了NE的作用。结合5-HT介导的运动综合征的双组分模型对结果进行了讨论,该模型包括:(1)对运动核的模式化兴奋性输入;(2)5-HT对这些兴奋性输入的促进作用。“外周”5-HT拮抗剂似乎直接阻断了后一组分。

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