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在兔离体耳静脉中介导平滑肌收缩的接头后肾上腺素能受体群体主要为α₂型的证据。

Evidence that the population of postjunctional-adrenoceptors mediating contraction of smooth muscle in the rabbit isolated ear vein is predominantly alpha 2.

作者信息

Daly C J, McGrath J C, Wilson V G

机构信息

Autonomic Physiology Unit, University of Glasgow, Scotland.

出版信息

Br J Pharmacol. 1988 Aug;94(4):1085-90. doi: 10.1111/j.1476-5381.1988.tb11626.x.

Abstract
  1. Noradrenaline (NA), phenylephrine and UK-14304 elicited concentration-dependent contractions of the rabbit isolated ear vein of similar maximal magnitude. The rank order of potency, UK-14304 greater than noradrenaline greater than phenylephrine, is consistent with that of an effect mediated through an alpha 2-subtype. 2. The potent and highly selective alpha 1-adrenoceptor antagonists prazosin and YM-12617, at concentrations as high as 1 microM, produced less than a 4 fold rightward displacement of the NA concentration-response curve. 3. The selective alpha 2-adrenoceptor antagonists rauwolscine, Wy-26703 and CH-38083 antagonized responses to noradrenaline in a competitive manner. For all three antagonists, the pA2 values were consistent with an effect at alpha 2-adrenoceptors. However, 0.1 microM YM-12617 increased the potency of rauwolscine 2 fold indicating the presence of a small population of postjunctional alpha 1-adrenoceptors. 4. The relative antagonist potency of the yohimbine diastereoisomers rauwolscine and corynanthine against noradrenaline (rauwolscine 30 fold greater than corynanthine) is also consistent with an effect at alpha 2-adrenoceptors. 5. Contractions elicited by noradrenaline in the rabbit isolated ear vein appear to be mediated predominantly by postjunctional alpha 2-adrenoceptors.
摘要
  1. 去甲肾上腺素(NA)、去氧肾上腺素和UK-14304均可引起兔离体耳静脉浓度依赖性收缩,最大收缩幅度相似。效价顺序为UK-14304大于去甲肾上腺素大于去氧肾上腺素,这与通过α2亚型介导的效应一致。2. 强效且高度选择性的α1肾上腺素能受体拮抗剂哌唑嗪和YM-12617,在高达1μM的浓度下,使NA浓度-反应曲线向右位移不到4倍。3. 选择性α2肾上腺素能受体拮抗剂育亨宾、Wy-26703和CH-38083以竞争性方式拮抗对去甲肾上腺素的反应。对于所有三种拮抗剂,pA2值与α2肾上腺素能受体的效应一致。然而,0.1μM的YM-12617使育亨宾的效价增加了2倍,表明存在少量的节后α1肾上腺素能受体。4. 育亨宾非对映异构体育亨宾和柯楠因对去甲肾上腺素的相对拮抗剂效价(育亨宾比对柯楠因大30倍)也与α2肾上腺素能受体的效应一致。5. 去甲肾上腺素在兔离体耳静脉中引起的收缩似乎主要由节后α2肾上腺素能受体介导。

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