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前列腺素F2α对子宫肌层运动的体外作用。与肾上腺素能和胆碱能受体的相互作用。

In vitro effect of prostaglandine F2alpha on the motility of the myometrium. Interactions with adrenergic and cholinergic receptors.

作者信息

Milenov K, Chernaeva L

出版信息

Acta Physiol Pharmacol Bulg. 1976;2(1):63-71.

PMID:1015304
Abstract

The in vitro effects of prostaglandine F2alpha(PGF2alpha) on the spontaneous contractile activity of the myometrium of rat, guinea-pig and rabbit and its interactions with adrenergic and cholinergic receptors were studied. All animals were with oestrogen domination. One myometral strip of each animal species was placed under identical conditions in a common bath with Krebbs solution. Each strip was connected to a strain gauge for the recording of the contractile activity. L-Noradrenaline (N) and Adrenaline (A) in doses of 10(-6) g/ml inhibit the contractile activity of rat myometrium (stimulation of the beta-receptors) and this effect is antagonized by beta-blocking agents. Conversely, N and A stimulate the myometrium of guinea-pigs and rabbits (stimulation of the alpha-receptors) and this effect is antagonized by the alpha-blocking agents. Unlike N and A, PGF2alpha stimulates the contractile myometral activity in all three species and its effect is not antagonized either by adrenergic or by cholinergic blocking agents. The stimulating effect of PGF2alpha antagonizes the inhibitory effect of N and A on rat myometrium and potentiates their stimulating effect on the myometrium of guinea-pigs and rabbits with a noncompetitive mechanism.

摘要

研究了前列腺素F2α(PGF2α)对大鼠、豚鼠和家兔子宫肌层自发收缩活性的体外作用及其与肾上腺素能和胆碱能受体的相互作用。所有动物均处于雌激素占优势状态。将每种动物的一条子宫肌条置于相同条件下的含有 Krebs 溶液的共同浴槽中。每条肌条连接到一个应变片以记录收缩活性。剂量为10(-6) g/ml 的左旋去甲肾上腺素(N)和肾上腺素(A)抑制大鼠子宫肌层的收缩活性(刺激β受体),且这种作用被β受体阻滞剂拮抗。相反,N 和 A 刺激豚鼠和家兔的子宫肌层(刺激α受体),且这种作用被α受体阻滞剂拮抗。与 N 和 A 不同,PGF2α刺激所有三种动物的子宫肌层收缩活性,且其作用既不被肾上腺素能也不被胆碱能阻滞剂拮抗。PGF2α的刺激作用拮抗 N 和 A 对大鼠子宫肌层的抑制作用,并以非竞争性机制增强它们对豚鼠和家兔子宫肌层的刺激作用。

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