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多巴胺对豚鼠肠系膜动脉神经肌肉传递的影响。

Effects of dopamine on neuromuscular transmission in the guinea-pig mesenteric artery.

作者信息

Fujisawa K

出版信息

Eur J Pharmacol. 1983 Aug 19;92(1-2):105-12. doi: 10.1016/0014-2999(83)90114-0.

Abstract

The effects of dopamine on neuromuscular transmission in the guinea-pig mesenteric artery were investigated using a microelectrode method. Dopamine did not modify the membrane potential or the membrane resistance of the smooth muscle, but did reduce the amplitude of excitatory junction potentials (e.j.p.) and enhance the facilitation of e.j.p. produced by repetitive stimulation. Phentolamine (10(-7) M) enhanced the amplitude and the facilitation of the e.j.p., and with the addition of dopamine (10(-6) M) there was a reduction in the amplitude of e.j.p. but not in the facilitation. Haloperidol and sulpiride (greater than 10(-6) M) increased the amplitude of e.j.p. without altering the postjunctional membrane properties. Haloperidol and sulpiride did not increase the facilitation of e.j.p. produced by repetitive stimulation. In the presence of haloperidol or sulpiride (10(-5) M), dopamine (10(-6) M) did not suppress the amplitude of the e.j.p. These results indicate that in the guinea-pig mesenteric artery, dopamine inhibits the release of transmitter at the presynaptic membrane.

摘要

采用微电极方法研究了多巴胺对豚鼠肠系膜动脉神经肌肉传递的影响。多巴胺并未改变平滑肌的膜电位或膜电阻,但确实降低了兴奋性接头电位(e.j.p.)的幅度,并增强了重复刺激所产生的e.j.p.的易化作用。酚妥拉明(10^(-7) M)增强了e.j.p.的幅度和易化作用,加入多巴胺(10^(-6) M)后,e.j.p.的幅度降低,但易化作用未受影响。氟哌啶醇和舒必利(大于10^(-6) M)增加了e.j.p.的幅度,而未改变接头后膜特性。氟哌啶醇和舒必利并未增加重复刺激所产生的e.j.p.的易化作用。在存在氟哌啶醇或舒必利(10^(-5) M)的情况下,多巴胺(10^(-6) M)并未抑制e.j.p.的幅度。这些结果表明,在豚鼠肠系膜动脉中,多巴胺抑制突触前膜递质的释放。

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