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没有证据表明兔肺动脉中存在不止一种类型的α1 -肾上腺素能受体。

No evidence for more than one type of alpha 1-adrenoreceptor in rabbit pulmonary artery.

作者信息

Docherty J R

机构信息

Department of Clinical Pharmacology, Royal College of Surgeons in Ireland, Dublin.

出版信息

J Auton Pharmacol. 1988 Dec;8(4):327-32. doi: 10.1111/j.1474-8673.1988.tb00576.x.

DOI:10.1111/j.1474-8673.1988.tb00576.x
PMID:2908113
Abstract
  1. The effects of the alpha-adrenoreceptor antagonists, prazosin and yohimbine, have been examined on the isometric contraction of the rabbit pulmonary artery produced by alpha 1-adrenoreceptor agonists. Cocaine, corticosterone and propranolol were present throughout and either a single or two concentration-response curve method was used. 2. Prazosin and yohimbine competitively antagonized the responses to agonists but did not reveal differences between agonists. 3. Using the single concentration-response curve method, prazosin had pA2 values of 9.06 against clonidine and 8.76 against methoxamine. 4. Using the two concentration-response curve method the absolute pA2 values of prazosin (8.65 against phenylephrine, 8.78 against clonidine) and yohimbine (5.73 against phenylephrine, 5.72 against clonidine), as well as the relative potencies of the two antagonists (prazosin approximately 1000 times more potent than yohimbine), suggest that both agonists act on alpha 1-adrenoreceptors. 5. There is no evidence from this study to support the suggestion that the rabbit pulmonary artery contains two subtypes of alpha 1-adrenoreceptor.
摘要
  1. 研究了α-肾上腺素能受体拮抗剂哌唑嗪和育亨宾对α1-肾上腺素能受体激动剂所致兔肺动脉等长收缩的影响。实验全程使用了可卡因、皮质酮和普萘洛尔,采用单浓度-反应曲线法或双浓度-反应曲线法。2. 哌唑嗪和育亨宾竞争性拮抗激动剂的反应,但未揭示激动剂之间的差异。3. 使用单浓度-反应曲线法时,哌唑嗪对可乐定的pA2值为9.06,对甲氧明的pA2值为8.76。4. 使用双浓度-反应曲线法时,哌唑嗪(对去氧肾上腺素的pA2值为8.65,对可乐定的pA2值为8.78)和育亨宾(对去氧肾上腺素的pA2值为5.73,对可乐定的pA2值为5.72)的绝对pA2值,以及两种拮抗剂的相对效价(哌唑嗪的效力约为育亨宾的1000倍),表明两种激动剂均作用于α1-肾上腺素能受体。5. 本研究没有证据支持兔肺动脉含有两种α1-肾上腺素能受体亚型这一观点。

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