糖尿病样大鼠视网膜微血管增殖的放射生物学研究

X. Mao, P. Archambeau, Waheed Baqai, S. Larsen, J. Archambeau
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引用次数: 0

摘要

糖尿病视网膜病变视网膜血管的进展演变导致每年多达8000例患者失明。本研究的主要目的是确定高乳糖血症诱导的糖尿病样视网膜病变大鼠模型中视网膜血管的质子辐射剂量反应,并了解质子放疗在糖尿病视网膜病变控制中的可能作用。在诱导高半乳糖血症4个月后,对每只大鼠的一只眼睛进行单剂量范围的质子辐射(8、14和20 Gy)。每只大鼠未照射的对侧眼显示视网膜病变的正常进展。立体技术被用于在视网膜消化准备中原位量化组织参数,使血管畅通无阻。在50%半乳糖饮食后15个月,未照射的眼睛出现了视网膜病变的特征性组织病理学病变,如毛细血管内皮细胞增殖、毛细血管闭合、毛细血管微动脉瘤、周细胞丢失。50%半乳糖组大鼠内皮细胞密度显著高于对照组(p<0.05)。质子辐照在14Gy至20Gy剂量范围内显著抑制内皮细胞增殖(p<0.05),但在当前剂量范围内未减少周细胞损失。这些发现表明质子辐射对高半乳糖血症引起的糖尿病样视网膜病变有有益的作用。我们的研究应该对进一步优化糖尿病视网膜病变放射治疗策略的研究产生影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiobiological Study of Retinal Microvessel Proliferation in Diabetic-like Rat Model
Progressive evolution of retinal vascular in diabetic retinopathy leads to blindness in up to 8,000 patients yearly. The major purpose of this investigation was to determine proton radiation dose response of the eye's retinal vascu- lature in the hypergalactosemia induced rat model of diabetic-like retinopathy and gain insight of possible role of proton radiotherapy in controlling diabetic retinopathy. A single dose range of proton radiation (8, 14, and 20 Gy) was delivered to one eye of each rat at 4 months following induction of hypergalactosemia. The opposite eye of each rat, which was not irradiated, showed normal progression of retinopathy. Stereologic techniques were used to quantify tissue parameters in situ in a retinal digest preparation that allowed unobstructed access to the vasculature. 15 months following 50% galactose diet, characteristic histopathological lesions of retinopathy such as capillary endothelial cell proliferation, capillary clo- sure, capillary microaneurysms, pericyte loss developed in non-irradiated eyes. The endothelial cell densities for rat re- ceiving 50% galactose diet were significantly higher than that of control (p<0.05). Proton irradiation inhibited significant endothelial cell proliferation at dose from 14Gy to 20Gy (p<0.05), yet not diminished pericyte loss at current dose sched- ule. These findings indicated beneficial effects of proton radiation on hypergalactosemia induced diabetic-like retinopa- thy. Our study should have an impact on further studies to optimize radiation treatment strategies for diabetic retinopathy.
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