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彩虹蜥蜴(变色蜥)离体直肠对拟交感神经药的反应。

Responses of the isolated rectum of the rainbow lizard (Agama agama) to sympathomimetics.

作者信息

Inyang A L, Okpako D T

机构信息

Department of Pharmacology, College of Medical Sciences, University of Calabar, Nigeria.

出版信息

Can J Physiol Pharmacol. 1989 Jan;67(1):68-71. doi: 10.1139/y89-011.

Abstract

The relaxant effects of isoprenaline, noradrenaline, and adrenaline on the isolated rectum of the rainbow lizard (Agama agama) were studied. Responses were measured as a reduction of carbachol-induced contractions for each sympathomimetic agent. Isoprenaline, adrenaline, noradrenaline produced a dose-dependent relaxation of this preparation and the order of potency was as given. The pD2 value of 8.15 +/- 1.88 obtained for isoprenaline was significantly different (p less than 0.05) from those for adrenaline (5.80 +/- 0.90) and noradrenaline (5.25 +/- 1.18). H35/25, propranolol, and practolol competitively antagonized the relaxant effects of isoprenaline on the isolated lizard rectum. The pA2 values for these beta-adrenoceptor antagonists did not differ significantly (at p less than 0.05). alpha-Adrenoceptor antagonists, phentolamine and phenoxybenzamine, failed to alter the relaxant responses of these sympathometics to any appreciable extent. These results are interpreted to suggest that the relaxant effect produced by these sympathomimetics are mediated predominantly by beta-adrenoceptors that are not significantly differentiated into subtypes. alpha-Adrenoceptors in this preparation contribute minimally to the observed inhibitory response following sympathomimetic stimulation.

摘要

研究了异丙肾上腺素、去甲肾上腺素和肾上腺素对彩虹蜥蜴(鬃狮蜥)离体直肠的松弛作用。以每种拟交感神经药对卡巴胆碱诱导的收缩的抑制作用来衡量反应。异丙肾上腺素、肾上腺素、去甲肾上腺素对该标本产生剂量依赖性松弛,其效价顺序如下。异丙肾上腺素的pD2值为8.15±1.88,与肾上腺素(5.80±0.90)和去甲肾上腺素(5.25±1.18)的pD2值有显著差异(p<0.05)。H35/25、普萘洛尔和美托洛尔竞争性拮抗异丙肾上腺素对离体蜥蜴直肠的松弛作用。这些β-肾上腺素能受体拮抗剂的pA2值无显著差异(p<0.05)。α-肾上腺素能受体拮抗剂酚妥拉明和酚苄明未能在任何显著程度上改变这些拟交感神经药的松弛反应。这些结果表明,这些拟交感神经药产生的松弛作用主要由未显著分化为亚型的β-肾上腺素能受体介导。该标本中的α-肾上腺素能受体对拟交感神经刺激后观察到的抑制反应贡献最小。

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