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前列腺素E1在豚鼠结肠带肾上腺素能神经传递中的可能作用。

Possible role of prostaglandin E1 on adrenergic neurotransmission in the guinea-pig taenia coli.

作者信息

Sakato M, Shimo Y

出版信息

Eur J Pharmacol. 1976 Dec;40(2):209-14. doi: 10.1016/0014-2999(76)90054-6.

Abstract

The effects of prostaglandin (PG) E1 were investigated on the responses to adrenergic and non-adrenergic inhibitory nerve stimulation using the perivascular nerve-taenia preparation of the guinea pig. PGE1 caused a rapid and sustained contraction and markedly inhibited the response to adrenergic but not to non-adrenergic inhibitory nerve stimulation. It was also observed that PGE1 had some desensitizing action to exogenous noradrenaline on the postjunctional site. Although indomethacin decreased the tone of the preparation, it potentiated the response to adrenergic nerve stimulation without any effects on the response to non-adrenergic inhibitory nerve stimulation. From these observations, it was concluded that endogenous PGE1 may also play a regulatory role in adrenergic inhibitory neurotransmission, mainly by inhibitory action on noradrenaline release and partly by a similar action on the postjunctional site.

摘要

利用豚鼠的血管周围神经-绦虫制备物,研究了前列腺素(PG)E1对肾上腺素能和非肾上腺素能抑制性神经刺激反应的影响。PGE1引起快速且持续的收缩,并显著抑制对肾上腺素能神经刺激的反应,但不抑制对非肾上腺素能抑制性神经刺激的反应。还观察到PGE1对节后位点的外源性去甲肾上腺素具有一定的脱敏作用。尽管吲哚美辛降低了制备物的张力,但它增强了对肾上腺素能神经刺激的反应,而对非肾上腺素能抑制性神经刺激的反应没有任何影响。从这些观察结果得出结论,内源性PGE1可能在肾上腺素能抑制性神经传递中也发挥调节作用,主要是通过对去甲肾上腺素释放的抑制作用,部分是通过对节后位点的类似作用。

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