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N,N-二乙基-2-(1-吡啶基)乙胺,豚鼠回肠中组胺受体的部分激动剂。

N,N-Diethyl-2-(1-pyridyl)ethylamine, a partial agonist for the histamine receptor in guinea pig ileum.

作者信息

Kenakin T P, Cook D A

出版信息

Can J Physiol Pharmacol. 1980 Nov;58(11):1307-10. doi: 10.1139/y80-198.

Abstract

N,N-Diethyl-2-(1-pyridyl)ethylamine (E-2-P) produced 59 +/- 7% of the maximal response to histamine in guinea pig ileal longitudinal smooth muscle and antagonized the responses of this tissue to histamine. The estimated binding constant of E-2-P for the histamine receptor predicted a binding curve nearly coincident with the agonist concentration-response curve indicating no receptor reserve for this partial agonist. Diphenhydramine (30 nM) produced competitive antagonism of response to E-2-P (pKB = 8.3 +/- 0.13). Triprolidine (0.3 nM), a slower acting antihistamine, produced a depression of the maximal responses to E-2-P. This effect was analyzed in terms of a "hemi-equilibrium" hypothesis which approximates a pseudoirreversible antagonism of histamine receptors by triprolidine with respect to E-2-P. All data are consistent with the classification of E-2-P as a simple partial agonist for the histamine receptor of guinea pig ileum.

摘要

N,N - 二乙基 - 2 -(1 - 吡啶基)乙胺(E - 2 - P)在豚鼠回肠纵行平滑肌中产生了组胺最大反应的59±7%,并拮抗了该组织对组胺的反应。E - 2 - P对组胺受体的估计结合常数预测其结合曲线几乎与激动剂浓度 - 反应曲线重合,表明该部分激动剂不存在受体储备。苯海拉明(30 nM)对E - 2 - P的反应产生竞争性拮抗作用(pKB = 8.3±0.13)。曲普利啶(0.3 nM),一种起效较慢的抗组胺药,使对E - 2 - P的最大反应降低。根据“半平衡”假说对该效应进行了分析,该假说近似于曲普利啶对组胺受体相对于E - 2 - P的拟不可逆拮抗作用。所有数据均与将E - 2 - P归类为豚鼠回肠组胺受体的简单部分激动剂一致。

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