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在离体大鼠主动脉中,α-1肾上腺素能受体和5-羟色胺2受体同时激活所引发的收缩反应的相互作用放大效应。

Mutual-effect amplification of contractile responses elicited by simultaneous activation of alpha-1 adrenergic and 5-hydroxytryptamine2 receptors in isolated rat aorta.

作者信息

Christ G J, Jean-Jacques M

机构信息

Department of Urology, Albert Einstein College of Medicine, Bronx, New York.

出版信息

J Pharmacol Exp Ther. 1991 Feb;256(2):553-61.

PMID:1847200
Abstract

5-Hydroxytryptamine (5-HT), and the selective alpha-1 agonists phenylephrine (PE) and oxymetazoline (OXY), were used to study the effects of simultaneous coactivation of the 5-HT2 and alpha-1 adrenergic receptors, respectively, on the contractile responses of isolated rat aortic rings. Dissociation constants (KA) were determined for each of the agonists at their respective receptor subtypes. The KA values for PE and OXY at the alpha-1 receptor were 316 nM and 1.82 microM, respectively, while the KA for 5-HT at the 5-HT2 receptor was 478 nM. Concentration-response curves for each agonist were analyzed by the Black and Leff operational model of pharmacological agonism to determine efficacy (tau) and slope factor values. The estimated tau for PE (16.02) was much greater than the tau for either OXY (4.15) or 5-HT (2.95), which had similar efficacies. Using a previously described drug concentration paradigm, a mutual-effect amplification of the 5-HT-induced contractile response was observed with mixtures of 5-HT and PE, whereas mixtures of OXY and 5-HT elicited a mutual-effect amplification of the observed response to OXY alone. In both cases, the theoretical concentration-response curve constructed using the Poch and Holzmann method of equiactive substitution demonstrated that mutual-effect amplification was largely the result of simple additivity of agonist effects. In addition, estimates of tau and slope factor determined from the Black and Leff equation were substituted into the Leff model of mutual-effect amplification and used to accurately predict the location of the concentration-response curves elicited by mixtures of 5-HT and PE, as well as mixtures of OXY and 5-HT. This represents the first time a mathematical model has been used to accurately predict the outcome of coactivation of the alpha-1 and 5-HT2 receptors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用5-羟色胺(5-HT)以及选择性α-1激动剂去氧肾上腺素(PE)和羟甲唑啉(OXY),分别研究5-HT2和α-1肾上腺素能受体同时共激活对离体大鼠主动脉环收缩反应的影响。测定了每种激动剂在其各自受体亚型上的解离常数(KA)。PE和OXY在α-1受体上的KA值分别为316 nM和1.82 μM,而5-HT在5-HT2受体上的KA为478 nM。通过药理学激动作用的布莱克和莱夫操作模型分析每种激动剂的浓度-反应曲线,以确定效能(τ)和斜率因子值。PE的估计τ(16.02)远大于OXY(4.15)或5-HT(2.95)的τ,后两者具有相似的效能。使用先前描述的药物浓度范式,观察到5-HT与PE的混合物对5-HT诱导的收缩反应有相互效应放大作用,而OXY与5-HT的混合物对单独观察到的OXY反应有相互效应放大作用。在这两种情况下,使用波赫和霍尔兹曼等活性替代方法构建的理论浓度-反应曲线表明,相互效应放大在很大程度上是激动剂效应简单相加的结果。此外,将从布莱克和莱夫方程确定的τ和斜率因子估计值代入相互效应放大的莱夫模型,并用于准确预测5-HT与PE混合物以及OXY与5-HT混合物引发的浓度-反应曲线的位置。这是首次使用数学模型准确预测α-1和5-HT2受体共激活的结果。(摘要截断于250字)

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