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动情间期豚鼠环形子宫肌层的α1和α2肾上腺素能受体

Alpha 1-and alpha 2-adrenoceptors of the circular myometrium from the dioestrous guinea-pig.

作者信息

Haynes J, Pennefather J N

机构信息

Department of Pharmacology, Monash University, Clayton, Victoria, Australia.

出版信息

Clin Exp Pharmacol Physiol. 1988 Sep;15(9):695-701. doi: 10.1111/j.1440-1681.1988.tb01129.x.

Abstract
  1. In order to investigate the nature of the alpha-adrenoceptors mediating contraction of circular myometrium from dioestrous guinea-pigs, the effects of several adrenoceptor antagonists upon log concentration curves to noradrenaline and phenylephrine have been examined. 2. In the presence of ICI 118,551 and nisoxetine both phenylephrine and noradrenaline produced concentration-dependent contractures of circular myometrium from virgin dioestrous guinea-pigs. Noradrenaline was the more potent and produced larger maximal contractions. Indomethacin (1 mumol/l) decreased the maximum effects of phenylephrine but not those of noradrenaline. Xylazine produced indomethacin-sensitive contractions which were not dose-related and which never exceeded 40% of those evoked by noradrenaline. Responses to xylazine and to noradrenaline, but not those to phenylephrine, were reduced in a low calcium solution. 3. Prazosin produced competitive antagonism of the effects of phenylephrine upon preparations of circular myometrium from virgin and parous dioestrous animals; pA2 values were both 8.1. Phentolamine also competitively antagonized the effects of phenylephrine (virgin animals, pA2=7.7). 4. Both prazosin and phentolamine antagonized the effects of noradrenaline upon preparations from virgin dioestrous animals, however, Schild plot analysis did not indicate a simple bimolecular interaction between agonist and receptors. In the presence of prazosin the alpha 2-adrenoceptor antagonist idazoxan produced dose-dependent parallel shifts in the positions of the log concentration-response curves to noradrenaline; the pA2 was 7.7. In the presence of idazoxan or of indomethacin prazosin competitively antagonized the effects of noradrenaline; the pA2 values were 8.5 and 8.2 respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 为了研究介导动情间期豚鼠环形子宫肌层收缩的α-肾上腺素能受体的性质,已检测了几种肾上腺素能受体拮抗剂对去甲肾上腺素和苯肾上腺素对数浓度曲线的影响。2. 在ICI 118,551和尼索西汀存在的情况下,苯肾上腺素和去甲肾上腺素均引起动情间期未孕豚鼠环形子宫肌层浓度依赖性挛缩。去甲肾上腺素作用更强,产生的最大收缩幅度更大。吲哚美辛(1 μmol/L)降低了苯肾上腺素的最大效应,但未降低去甲肾上腺素的最大效应。赛拉嗪产生吲哚美辛敏感的收缩,其与剂量无关,且从未超过去甲肾上腺素诱发收缩的40%。在低钙溶液中,对赛拉嗪和去甲肾上腺素的反应降低,但对苯肾上腺素的反应未降低。3. 哌唑嗪对动情间期未孕和经产动物的环形子宫肌层制剂中苯肾上腺素的作用产生竞争性拮抗作用;pA2值均为8.1。酚妥拉明也竞争性拮抗苯肾上腺素的作用(未孕动物,pA2 = 7.7)。4. 哌唑嗪和酚妥拉明均拮抗去甲肾上腺素对动情间期未孕动物制剂的作用,然而,希尔德分析并未表明激动剂与受体之间存在简单的双分子相互作用。在哌唑嗪存在的情况下,α2-肾上腺素能受体拮抗剂咪唑克生使去甲肾上腺素对数浓度-反应曲线的位置产生剂量依赖性平行移动;pA2为7.7。在咪唑克生或吲哚美辛存在的情况下,哌唑嗪竞争性拮抗去甲肾上腺素的作用;pA2值分别为8.5和8.2。(摘要截断于250字)

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