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眼部α2肾上腺素能受体异质性的药理学证据。

Pharmacological evidence for heterogeneity of ocular alpha 2 adrenoceptors.

作者信息

Crosson C E, Heath A R, DeVries G W, Potter D E

机构信息

Center for Biotechnology, Baylor College of Medicine, The Woodlands, TX.

出版信息

Curr Eye Res. 1992 Oct;11(10):963-70. doi: 10.3109/02713689209033494.

Abstract

Previous studies have shown that ocular alpha 2 adrenoceptors are located prejunctionally on sympathetic neurons and postjunctionally on cells in the iris/ciliary body. While the activation of alpha 2 adrenoceptors at each site has been postulated to alter aqueous humor dynamics, little is known about the pharmacological characteristics of these receptors or their role in the modulation of anterior segment function. The purpose of the current study was to determine the possible heterogeneity of ocular alpha 2 adrenoceptors using relatively selective alpha 2 adrenoceptor agonists and antagonists to examine ocular pre- and postjunctional alpha 2 adrenoceptors. Prejunctional alpha 2 effects were evaluated by means of the cat nictitating membrane (CNM) preparation. Postjunctional alpha 2 effects were evaluated by means of the cAMP assay in rabbit iris root/ciliary body. In the CNM, the administration of UK-14, 304 (UK) produced a dose-related inhibition of neuronally mediated contractions. Pretreatment with the alpha 2 antagonist rauwolscine caused a 1 to 2 log unit right shift in the dose-response curve of UK in the CNM. However, pretreatment with alpha 2 antagonist SKF 104078 had no demonstrable effect on UK-induced inhibition of neuronally mediated contractions of the CNM. In the rabbit iris root/ciliary body, UK produced a concentration-dependent inhibition of cAMP accumulation on isoproterenol- and VIP-induced cAMP production. Pretreatment of iris root/ciliary bodies with SKF 104078 or rauwolscine reversed the inhibitory effect of UK on isoproterenol- and VIP-induced accumulation of cAMP. These data provide the first evidence that the pre- and postjunctional alpha 2 adrenoceptors represent pharmacologically distinct subpopulations of receptors in the eye.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

以往研究表明,眼部α2肾上腺素能受体位于交感神经元的突触前以及虹膜/睫状体细胞的突触后。虽然推测在每个位点激活α2肾上腺素能受体会改变房水动力学,但对于这些受体的药理学特性或其在调节眼前节功能中的作用知之甚少。本研究的目的是使用相对选择性的α2肾上腺素能受体激动剂和拮抗剂来检测眼部突触前和突触后的α2肾上腺素能受体,以确定眼部α2肾上腺素能受体可能存在的异质性。通过猫瞬膜(CNM)制备来评估突触前α2效应。通过兔虹膜根部/睫状体的cAMP检测来评估突触后α2效应。在CNM中,给予UK-14,304(UK)可产生与剂量相关的对神经介导收缩的抑制作用。用α2拮抗剂育亨宾预处理可使CNM中UK的剂量-反应曲线右移1至2个对数单位。然而,用α2拮抗剂SKF 104078预处理对UK诱导的CNM神经介导收缩的抑制作用没有明显影响。在兔虹膜根部/睫状体中,UK对异丙肾上腺素和血管活性肠肽诱导的cAMP产生具有浓度依赖性的抑制作用。用SKF 104078或育亨宾预处理虹膜根部/睫状体可逆转UK对异丙肾上腺素和血管活性肠肽诱导的cAMP积累的抑制作用。这些数据首次证明,突触前和突触后的α2肾上腺素能受体代表了眼中药理学上不同的受体亚群。(摘要截短于250字)

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