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2 型糖尿病大鼠模型在眼前段重现了人类疾病。

Rat Model of Type 2 Diabetes Mellitus Recapitulates Human Disease in the Anterior Segment of the Eye.

机构信息

Department of Ophthalmology and Visual Sciences, Carver College of Medicine, University of Iowa, Iowa City, Iowa.

Department of Ophthalmology and Visual Sciences, Carver College of Medicine, University of Iowa, Iowa City, Iowa; Iowa Lions Eye Bank, Coralville, Iowa.

出版信息

Am J Pathol. 2024 Jun;194(6):1090-1105. doi: 10.1016/j.ajpath.2024.02.004. Epub 2024 Feb 24.

Abstract

Changes in the anterior segment of the eye due to type 2 diabetes mellitus (T2DM) are not well-characterized, in part due to the lack of a reliable animal model. This study evaluated changes in the anterior segment, including crystalline lens health, corneal endothelial cell density, aqueous humor metabolites, and ciliary body vasculature, in a rat model of T2DM compared with human eyes. Male Sprague-Dawley rats were fed a high-fat diet (45% fat) or normal diet, and rats fed the high-fat diet were injected with streptozotocin intraperitoneally to generate a model of T2DM. Cataract formation and corneal endothelial cell density were assessed using microscopic analysis. Diabetes-related rat aqueous humor alterations were assessed using metabolomics screening. Transmission electron microscopy was used to assess qualitative ultrastructural changes ciliary process microvessels at the site of aqueous formation in the eyes of diabetic rats and humans. Eyes from the diabetic rats demonstrated cataracts, lower corneal endothelial cell densities, altered aqueous metabolites, and ciliary body ultrastructural changes, including vascular endothelial cell activation, pericyte degeneration, perivascular edema, and basement membrane reduplication. These findings recapitulated diabetic changes in human eyes. These results support the use of this model for studying ocular manifestations of T2DM and support a hypothesis postulating blood-aqueous barrier breakdown and vascular leakage at the ciliary body as a mechanism for diabetic anterior segment pathology.

摘要

由于缺乏可靠的动物模型,2 型糖尿病(T2DM)引起的眼前节变化尚不清楚。本研究评估了 T2DM 大鼠模型与人类眼睛相比,眼前节的变化,包括晶状体健康、角膜内皮细胞密度、房水代谢物和睫状体血管。雄性 Sprague-Dawley 大鼠给予高脂肪饮食(45%脂肪)或正常饮食,给予高脂肪饮食的大鼠腹腔内注射链脲佐菌素以生成 T2DM 模型。使用显微镜分析评估白内障形成和角膜内皮细胞密度。使用代谢组学筛选评估与糖尿病相关的大鼠房水改变。使用透射电子显微镜评估在糖尿病大鼠和人类眼房水形成部位睫状体的微观结构变化。糖尿病大鼠的眼睛表现出白内障、较低的角膜内皮细胞密度、改变的房水代谢物和睫状体超微结构变化,包括血管内皮细胞激活、周细胞退化、血管周围水肿和基底膜重复。这些发现重现了人类眼睛的糖尿病变化。这些结果支持该模型用于研究 T2DM 的眼部表现,并支持一种假说,即血房水屏障破裂和睫状体的血管渗漏是糖尿病前节病理学的一种机制。

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