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眼部的前列腺素:功能、表达及其在青光眼中的作用

Prostaglandins in the eye: Function, expression, and roles in glaucoma.

作者信息

Doucette Lance P, Walter Michael A

机构信息

a Department of Medical Genetics, Faculty of Medicine and Dentistry , University of Alberta , Edmonton , Alberta , Canada.

出版信息

Ophthalmic Genet. 2017 Mar-Apr;38(2):108-116. doi: 10.3109/13816810.2016.1164193. Epub 2016 Apr 12.

Abstract

Prostaglandins are small pro-inflammatory molecules derived from arachidonic acid that play roles in a multitude of biological processes including, but not limited to, inflammation, pain modulation, allergies, and bone formation. Prostaglandin analogues are the front-line medications for the treatment of glaucoma, a condition resulting in blindness due to the death of retinal ganglion cells. These drugs act by lowering intraocular pressure (IOP), a major risk factor for glaucoma. The currently used prostaglandin analogues (latanoprost, bimatoprost, tafluprost, and travoprost) mimic PGF2 and target one of the prostaglandin receptors (FP), though research into harnessing the other receptors using compounds like Sulprostone (EP3 receptor), or Iloprost (IP receptor) are currently ongoing. In this review, we summarize the research into each of the prostaglandin molecules (PGD2, PGE2, PGF2, PGI2, TXA2) and their respective receptors (DP, EP1, 2, 3, 4, FP, IP). We examine the modes of action of each of these receptors, their expression, their role in aqueous humour production and outflow within the eye, as well as their roles as medications for the treatment of glaucoma.

摘要

前列腺素是一类由花生四烯酸衍生而来的小的促炎分子,在众多生物过程中发挥作用,包括但不限于炎症、疼痛调节、过敏和骨形成。前列腺素类似物是治疗青光眼的一线药物,青光眼是一种由于视网膜神经节细胞死亡导致失明的疾病。这些药物通过降低眼压起作用,眼压是青光眼的一个主要危险因素。目前使用的前列腺素类似物(拉坦前列素、比马前列素、他氟前列素和曲伏前列素)模拟前列腺素F2,并作用于一种前列腺素受体(FP),不过目前正在进行利用舒洛地特(EP3受体)或伊洛前列素(IP受体)等化合物作用于其他受体的研究。在本综述中,我们总结了对每种前列腺素分子(前列腺素D2、前列腺素E2、前列腺素F2、前列环素I2、血栓素A2)及其各自受体(DP、EP1、2、3、4、FP、IP)的研究。我们研究了这些受体的作用方式、它们的表达、它们在眼内房水生成和流出中的作用,以及它们作为治疗青光眼药物的作用。

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