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突触后α-肾上腺素能受体储备以及由不可逆性α-肾上腺素能拮抗剂酚苄明引起的浓度-反应曲线右移。

Postsynaptic alpha-adrenoceptor reserve and the shift of the concentration-response curves to the right, as caused by the irreversible alpha-adrenoceptor antagonist phenoxybenzamine.

作者信息

Guimarães S, Paiva M Q

机构信息

Department of Pharmacology, Faculty of Medicine, Porto, Portugal.

出版信息

Br J Pharmacol. 1987 Nov;92(3):505-12. doi: 10.1111/j.1476-5381.1987.tb11350.x.

Abstract
  1. The effect of different concentrations of phenoxybenzamine (0.1, 0.3, 1, 3, 10 and 30 nmoll -1) on the concentration-response curves to phenylephrine (a selective alpha 1-adrenoceptor agonist) and noradrenaline (a mixed alpha 1- and alpha 2-adrenoceptor agonist) was compared in two kinds of vascular tissue: dog saphenous vein (has both postsynaptic alpha 1- and alpha 2-adrenoceptors) and dog mesenteric and renal arteries--where only postsynaptic alpha 1-adrenoceptors have been shown to exist. 2. In the saphenous vein, where both alpha 1- and alpha 2-adrenoceptors coexist, at only one concentration of phenoxybenzamine, 3 nmoll -1, the concentration-response curve of noradrenaline was shifted to the right without a reduction of the maximum; and this shift was small (by 0.4 log units). 3. In tissues where only alpha 1-adrenoceptors exist postsynaptically (mesenteric and renal arteries) phenoxybenzamine never caused any shift of the noradrenaline concentration-response curves to the right without depressing the maximum effect. 4. In none of the tissues did phenoxybenzamine at any concentration shift the concentration-response curve of phenylephrine to the right without depressing its maximum. 5. All these results indicate that in the dog saphenous vein there is a 'false' alpha-adrenoceptor reserve for noradrenaline, since two kinds of receptors participate in the response to this amine. 6. The calculation of the occupancy-response relationship for the renal artery showed that 24% of the maximal response occurs when only 2% of alpha 1-adrenoceptors are activated and 50% of maximum at 9% occupation. However, for 95% of the maximal response an 83% occupancy is required. Similar values were calculated for the mesenteric artery. 7. Thus, the surplus alpha-adrenoceptors which is very large for a half-maximal response becomes smaller and smaller as the magnitude of the response increases and probably disappears at the 100% response level. 8. If we retain the original definition of 'spare receptors' - receptors in 'excess' of those required to produce a maximal response, we conclude, that there is no receptor reserve in the dog mesenteric and renal arteries.
摘要
  1. 在两种血管组织中比较了不同浓度的酚苄明(0.1、0.3、1、3、10和30 nmol/L)对去氧肾上腺素(一种选择性α1肾上腺素能受体激动剂)和去甲肾上腺素(一种α1和α2肾上腺素能受体混合型激动剂)浓度-反应曲线的影响:犬大隐静脉(同时具有突触后α1和α2肾上腺素能受体)以及犬肠系膜动脉和肾动脉——已证实仅存在突触后α1肾上腺素能受体。2. 在同时存在α1和α2肾上腺素能受体的大隐静脉中,仅在一种酚苄明浓度(3 nmol/L)下,去甲肾上腺素的浓度-反应曲线向右移动且最大反应未降低;并且这种移动较小(0.4个对数单位)。3. 在仅突触后存在α1肾上腺素能受体的组织(肠系膜动脉和肾动脉)中,酚苄明从未使去甲肾上腺素浓度-反应曲线向右移动而不降低最大效应。4. 在任何组织中,酚苄明在任何浓度下均未使去氧肾上腺素浓度-反应曲线向右移动而不降低其最大效应。5. 所有这些结果表明,在犬大隐静脉中,对于去甲肾上腺素存在一种“假性”α肾上腺素能受体储备,因为两种受体参与了对该胺类的反应。6. 肾动脉的占有率-反应关系计算表明,当仅2%的α1肾上腺素能受体被激活时,出现最大反应的24%,占有率为9%时出现最大反应的50%。然而,对于最大反应的95%,需要83%的占有率。对肠系膜动脉计算得到类似值。7. 因此,对于半数最大反应而言非常大的多余α肾上腺素能受体,随着反应幅度增加变得越来越小,并且可能在100%反应水平时消失。8. 如果我们保留“备用受体”的原始定义——产生最大反应所需受体数量“多余”的受体,我们得出结论,犬肠系膜动脉和肾动脉中不存在受体储备。

相似文献

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Alpha-adrenoceptor reserve in the canine cephalic vein.犬头静脉中的α-肾上腺素能受体储备
Eur J Pharmacol. 1990 Apr 10;179(1-2):9-16. doi: 10.1016/0014-2999(90)90396-n.

本文引用的文献

1
A modification of receptor theory.受体理论的一种修正。
Br J Pharmacol Chemother. 1956 Dec;11(4):379-93. doi: 10.1111/j.1476-5381.1956.tb00006.x.
2
Alpha-adrenoceptor subclassification.α-肾上腺素能受体亚分类
Rev Physiol Biochem Pharmacol. 1981;88:199-236.

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