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肾上腺素能受体机制在人类子宫颈收缩活动调节中的作用

Adrenoceptor mechanisms in the regulation of contractile activity in the human cervix.

作者信息

Bryman I, Lindblom B, Norström A, Sahni S

出版信息

Obstet Gynecol. 1984 Sep;64(3):363-7.

PMID:6146956
Abstract

The effects of adrenoceptor agonists and antagonists on the contractile activity of cervical strips from early pregnant and nonpregnant women were studied. Noradrenaline and the alpha-adrenoceptor agonist, phenylephrine, had a stimulatory effect on smooth muscle activity. This response could be blocked totally by the alpha-adrenoceptor antagonist, phenoxybenzamine. Isoprenaline, known to be a beta-adrenoceptor agonist with some alpha-adrenoceptor activity, had stimulatory and inhibitory effects, whereas the beta 2-adrenoceptor agonist, terbutaline, exhibited a pure inhibitory action. The inhibitory effects of isoprenaline and terbutaline were totally blocked by the beta-adrenoceptor antagonist propranolol. In pregnant patients, the sensitivity to noradrenaline was significantly higher, and the inhibitory action of terbutaline was less pronounced, which indicated the predominance of alpha-receptor activity in the uterine cervix during pregnancy.

摘要

研究了肾上腺素能受体激动剂和拮抗剂对早孕和未孕妇女宫颈条收缩活性的影响。去甲肾上腺素和α-肾上腺素能受体激动剂苯肾上腺素对平滑肌活性有刺激作用。这种反应可被α-肾上腺素能受体拮抗剂酚苄明完全阻断。异丙肾上腺素是一种已知具有一定α-肾上腺素能受体活性的β-肾上腺素能受体激动剂,具有刺激和抑制作用,而β2-肾上腺素能受体激动剂特布他林则表现出单纯的抑制作用。异丙肾上腺素和特布他林的抑制作用被β-肾上腺素能受体拮抗剂普萘洛尔完全阻断。在孕妇中,对去甲肾上腺素的敏感性显著更高,特布他林的抑制作用则不太明显,这表明孕期子宫颈中α-受体活性占主导地位。

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