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Prevention of leukostasis and vascular leakage in streptozotocin-induced diabetic retinopathy via intercellular adhesion molecule-1 inhibition

机译:通过抑制细胞间粘附分子-1预防链脲佐菌素诱导的糖尿病性视网膜病变的白细胞停滞和血管渗漏

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摘要

Diabetic retinopathy is a leading cause of adult vision loss and blindness. Much of the retinal damage that characterizes the disease results from retinal vascular leakage and nonperfusion. This study shows that diabetic retinal vascular leakage and nonperfusion are temporally and spatially associated with retinal leukocyte stasis (leukostasis) in the rat model of streptozotocin-induced diabetes. Retinal leukostasis increases within days of developing diabetes and correlates with the increased expression of retinal intercellular adhesion molecule-1 (ICAM-1). ICAM-1 blockade with a mAb prevents diabetic retinal leukostasis and vascular leakage by 48.5% and 85.6%, respectively. These data identify the causal role of leukocytes in the pathogenesis of diabetic retinopathy and establish the potential utility of ICAM-1 inhibition as a therapeutic strategy for the prevention of diabetic retinopathy.
机译:糖尿病性视网膜病是成人视力丧失和失明的主要原因。表征该疾病的大部分视网膜损伤是由于视网膜血管渗漏和未灌注引起的。这项研究表明,在链脲佐菌素诱发的糖尿病大鼠模型中,糖尿病性视网膜血管渗漏和非灌注在时间和空间上与视网膜白细胞停滞(白细胞停滞)有关。在发展成糖尿病的数天内,视网膜白细胞增多会增加,并与视网膜细胞间粘附分子1(ICAM-1)的表达增加有关。用mAb阻断ICAM-1可使糖尿病性视网膜白细胞减少和血管渗漏分别减少48.5%和85.6%。这些数据确定了白细胞在糖尿病性视网膜病的发病机理中的因果作用,并建立了ICAM-1抑制作为预防糖尿病性视网膜病的治疗策略的潜在效用。

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