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诺曼·麦卡利斯特·格雷格讲座。糖尿病视网膜病变的发病机制。

Norman MacAlister Gregg Lecture. The pathogenesis of diabetic retinopathy.

作者信息

Larkins R G, Dunlop M E, Johnson E I

机构信息

University of Melbourne, Department of Medicine, Royal Melbourne Hospital, Parkville, Victoria.

出版信息

Aust N Z J Ophthalmol. 1996 May;24(2):97-104. doi: 10.1111/j.1442-9071.1996.tb01561.x.

DOI:10.1111/j.1442-9071.1996.tb01561.x
PMID:9199738
Abstract

Diabetic retinopathy remains a major cause of loss of vision. The Diabetes Control and Complications Trial (DCCT) has implicated hyperglycaemia as a probable major direct causative factor in the pathogenesis of diabetic retinopathy. There are several plausible mechanisms by which high glucose concentrations could lead to the functional and later structural changes characterising diabetic retinopathy. These include increased activity of the aldose reductase pathway, increase de novo synthesis of diacylglycerol from glucose, causing protein kinase C activation, increased non-enzymatic glycation and increased oxidative damage. The demonstration of the potential roles of these pathways and the subsequent effects of growth factors in enhancing angiogenesis provide potential new approaches to the prevention and treatment of diabetic retinopathy.

摘要

糖尿病视网膜病变仍然是视力丧失的主要原因。糖尿病控制与并发症试验(DCCT)表明,高血糖可能是糖尿病视网膜病变发病机制中的一个主要直接致病因素。高血糖浓度可能通过几种合理的机制导致糖尿病视网膜病变的功能性改变以及随后的结构性改变。这些机制包括醛糖还原酶途径活性增加、葡萄糖从头合成二酰甘油增加导致蛋白激酶C激活、非酶糖基化增加以及氧化损伤增加。这些途径的潜在作用以及生长因子在促进血管生成方面的后续作用的证实,为糖尿病视网膜病变的预防和治疗提供了潜在的新方法。

相似文献

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Norman MacAlister Gregg Lecture. The pathogenesis of diabetic retinopathy.诺曼·麦卡利斯特·格雷格讲座。糖尿病视网膜病变的发病机制。
Aust N Z J Ophthalmol. 1996 May;24(2):97-104. doi: 10.1111/j.1442-9071.1996.tb01561.x.
2
Aldose reductase / polyol inhibitors for diabetic retinopathy.醛糖还原酶/多元醇抑制剂治疗糖尿病视网膜病变。
Curr Pharm Biotechnol. 2011 Mar 1;12(3):373-85. doi: 10.2174/138920111794480642.
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[What is the etiology of diabetic retinopathy?].[糖尿病视网膜病变的病因是什么?]
Ophthalmologe. 1993 Oct;90(5):426-33.
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Pathological Perturbations in Diabetic Retinopathy: Hyperglycemia, AGEs, Oxidative Stress and Inflammatory Pathways.糖尿病视网膜病变中的病理扰动:高血糖、晚期糖基化终末产物、氧化应激和炎症途径。
Curr Protein Pept Sci. 2019;20(1):92-110. doi: 10.2174/1389203719666180928123449.
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Recent advances in understanding the biochemical and molecular mechanism of diabetic retinopathy.糖尿病性视网膜病变的生化和分子机制的研究进展。
Biomed Pharmacother. 2015 Aug;74:145-7. doi: 10.1016/j.biopha.2015.08.002. Epub 2015 Aug 13.
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Role of advanced glycation end products (AGEs) and oxidative stress in diabetic retinopathy.晚期糖基化终末产物(AGEs)和氧化应激在糖尿病视网膜病变中的作用。
Curr Pharm Des. 2008;14(10):962-8. doi: 10.2174/138161208784139729.
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Update on the treatment of diabetic retinopathy.糖尿病视网膜病变治疗的最新进展。
ScientificWorldJournal. 2008 Feb 6;8:98-120. doi: 10.1100/tsw.2008.25.
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Oxidative stress and diabetic retinopathy: pathophysiological mechanisms and treatment perspectives.氧化应激与糖尿病视网膜病变:病理生理机制及治疗前景
Rev Endocr Metab Disord. 2008 Dec;9(4):315-27. doi: 10.1007/s11154-008-9090-4.
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On the pathogenesis of diabetic retinopathy.论糖尿病视网膜病变的发病机制。
Ophthalmology. 1984 Jun;91(6):626-34. doi: 10.1016/s0161-6420(84)34258-0.
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Diabetic retinopathy: is it a consequence of hyperglycaemia?糖尿病视网膜病变:它是高血糖的后果吗?
Diabet Med. 1985 May;2(3):200-3. doi: 10.1111/j.1464-5491.1985.tb00636.x.

引用本文的文献

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Ocular disease, knowledge and technology applications in patients with diabetes.眼部疾病、糖尿病患者的知识和技术应用。
Am J Med Sci. 2013 Apr;345(4):266-270. doi: 10.1097/MAJ.0b013e31828aa6fb.
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Immunohistochemical study of vascular endothelial growth factor (VEGF), tumor suppressor protein (p53) and intercellular adhesion molecule (ICAM-1) in the conjunctiva of diabetic patients.糖尿病患者结膜中血管内皮生长因子(VEGF)、肿瘤抑制蛋白(p53)和细胞间黏附分子(ICAM - 1)的免疫组织化学研究
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Diabetic neuropathies: features and mechanisms.
糖尿病性神经病变:特征与机制
Brain Pathol. 1999 Apr;9(2):369-91. doi: 10.1111/j.1750-3639.1999.tb00233.x.