Studies on prostanoid receptors in ocular tissues.

P Bhattacherjee, C A Paterson
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引用次数: 15

Abstract

Cyclooxygenase products of arachidonic acid, for example prostaglandins (PGs), prostacyclin, and thromboxane A2, mediate a wide range of physiological actions. Vasodilation, increased vascular permeability, platelet aggregation and its inhibition, and immunomodulation are some of the important biological actions of cyclooxygenase products (1). Depending on type and dose, PGs cause vasodilation, increase or decrease intraocular pressure, and disrupt the blood-aqueous barrier (2, 3). These actions also vary qualitatively and quantitatively with the animal species. Prostaglandins, like any biological molecule, must act by binding with their specific receptors. Coleman and coworkers (4, 5), from a series of studies with PG agonists and antagonists in vascular and non-vascular smooth muscle preparations, classified PG receptors. This classification led to a greater appreciation of the relationship between PG actions and specific PG receptors in various tissues. Ocular actions of PGs linked with specific PG receptors are far from being clear. In this communication we will review our work on PG binding sites in ocular tissues and PG receptors coupled to adenylyl cyclase or phosphoinositidase C signal transduction pathways in ocular tissues of various animal species.

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眼组织中前列腺素受体的研究。
花生四烯酸的环加氧酶产物,如前列腺素(pg)、前列环素和血栓素A2,介导广泛的生理作用。血管舒张、血管通透性增加、血小板聚集及其抑制和免疫调节是环加氧酶产物的一些重要生物作用(1)。根据类型和剂量的不同,PGs可引起血管舒张、升高或降低眼压、破坏血水屏障(2,3)。这些作用在动物种类上也存在定性和定量上的差异。前列腺素,像任何生物分子一样,必须通过与特定受体结合来起作用。Coleman和同事(4,5)通过对血管和非血管平滑肌制剂中PG激动剂和拮抗剂的一系列研究,对PG受体进行了分类。这种分类使人们对PG作用与不同组织中特定PG受体之间的关系有了更深入的了解。与特定PG受体相关的PG的眼部作用尚不清楚。在这篇文章中,我们将回顾我们在眼组织中PG结合位点和不同动物眼组织中PG受体与腺苷酸环化酶或磷酸肌醇酶C信号转导通路的研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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