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[糖尿病性视网膜病变——眼部新生血管形成机制及抗血管生成药物的研发]

[Diabetic retinopathy--the mechanisms of the ocular neovascularization and the development of anti-angiogenic drugs].

作者信息

Kuroki M, Kawakami M

机构信息

Jichi Medical School, Omiya Medical Center.

出版信息

Nihon Rinsho. 1999 Mar;57(3):584-9.

Abstract

Ocular neovascularization contributes to severe visual loss of the patients with diabetic retinopathy (DR) which is the leading cause of blindness on adults of working age. The mechanisms of ocular neovascularization are not fully understood. Several growth factors, particularly vascular endothelial growth factor (VEGF), vasoactive peptides such as angiotensin II and adhesion molecules such as integrins are considered to contribute to the ocular neovascularization. VEGF is believed to play the key role in the development of DR. Ischemic hypoxia of retina is well known to be the potent stimulus for the production of VEGF. In addition, we have reported that reactive oxygen intermediates, advanced glycation end products and insulin-like growth factor-1, also all, may participate in the pathogenesis of DR through their ability to increase VEGF production. The trials for anti-angiogenic drugs is developing now for the treatment of DR. VEGF may be the most suitable target for the inhibition of the ocular neovascularization.

摘要

眼部新生血管形成会导致糖尿病视网膜病变(DR)患者严重视力丧失,而糖尿病视网膜病变是工作年龄成年人失明的主要原因。眼部新生血管形成的机制尚未完全明确。几种生长因子,特别是血管内皮生长因子(VEGF)、血管活性肽如血管紧张素II以及黏附分子如整合素,被认为与眼部新生血管形成有关。VEGF被认为在糖尿病视网膜病变的发展中起关键作用。众所周知,视网膜缺血缺氧是VEGF产生的强大刺激因素。此外,我们曾报道,活性氧中间体、晚期糖基化终产物以及胰岛素样生长因子-1也都可能通过增加VEGF产生的能力参与糖尿病视网膜病变的发病机制。目前正在开展抗血管生成药物治疗糖尿病视网膜病变的试验。VEGF可能是抑制眼部新生血管形成的最合适靶点。

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