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肾上腺素能药物对箭毒化大鼠膈半膈肌神经刺激诱发的肌肉抽搐的促进作用。

Facilitatory action of adrenergic drugs on muscle twitch evoked by nerve stimulation in the curarized rat phrenic hemidiaphragm.

作者信息

Baños J, Badia A, Janè F

机构信息

Departament de Farmacologia i Psiquiatria, Facultat de Medicina, Universidad Autónoma de Barcelona, Campus de Bellaterra, Spain.

出版信息

Arch Int Pharmacodyn Ther. 1988 May-Jun;293:219-27.

PMID:3421779
Abstract

The facilitatory effects of alpha-adrenergic drugs on neuromuscular transmission has been studied in the curarized rat phrenic-hemidiaphragm. The reversal effect of blocking action of (+)-tubocurarine on indirectly-induced twitch by alpha-adrenergic agents was higher with noradrenaline (EC50 = 6.51 +/- 0.18 microM) compared with adrenaline (EC50 = 11.80 +/- 1.06 microM) or phenylephrine (EC50 = 17.36 +/- 1.02 microM). Methoxamine, clonidine and azepexol showed no effect. The action of noradrenaline was blocked by prazosin (IC50 = 3.96 +/- 0.76 nM) and tolazoline (IC50 = 10.30 +/- 0.5 nM) but not by yohimbine at the concentration range 0.01-0.1 microM. From these results it could be concluded that an alpha 1-adrenergic mechanism might be involved in the facilitatory action of alpha-adrenergic agents at the level of motor nerve terminals.

摘要

已在箭毒化的大鼠膈神经-半膈肌标本上研究了α-肾上腺素能药物对神经肌肉传递的易化作用。与肾上腺素(EC50 = 11.80 ± 1.06 μM)或去氧肾上腺素(EC50 = 17.36 ± 1.02 μM)相比,去甲肾上腺素(EC50 = 6.51 ± 0.18 μM)对(+)-筒箭毒碱间接诱发抽搐的阻断作用的逆转效果更高。甲氧明、可乐定和阿泽哌醇无作用。在0.01 - 0.1 μM浓度范围内,去甲肾上腺素的作用被哌唑嗪(IC50 = 3.96 ± 0.76 nM)和妥拉唑啉(IC50 = 10.30 ± 0.5 nM)阻断,但未被育亨宾阻断。从这些结果可以得出结论,α1-肾上腺素能机制可能参与了α-肾上腺素能药物在运动神经末梢水平的易化作用。

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