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Hyperhexosemia-Induced Retinal Vascular Pathology in a Novel Primate Model of Diabetic Retinopathy

机译:糖尿病视网膜病变的新型灵长类动物模型中的高血血症诱导的视网膜血管病理学。

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摘要

The paucity of animal models exhibiting full pathology of diabetic retinopathy (DR) has impeded understanding of the pathogenesis of DR and the development of therapeutic interventions. Here, we investigated whether hyperhexosemic marmosets (Callithrix jacchus) develop characteristic retinal vascular lesions including macular edema (ME), a leading cause of vision loss in DR. Marmosets maintained on 30% galactose (gal)-rich diet for 2 years were monitored for retinal vascular permeability, development of ME, and morphological characteristics including acellular capillaries (AC) and pericyte loss (PL), vessel tortuosity, and capillary basement membrane (BM) thickness. Excess vascular permeability, increased number of AC and PL, vascular BM thickening, and increased vessel tortuosity were observed in the retinas of gal-fed marmosets. Optical coherence tomography (OCT) images revealed significant thickening of the retinal foveal and the juxtafoveal area, and histological analysis showed incipient microaneurysms in retinas of gal-fed marmosets. Findings from this study indicate that hyperhexosemia can trigger retinal vascular changes similar to those seen in human DR including ME and microaneurysms. The striking similarities between the marmoset retina and the human retina, and the exceptionally small size of the monkey, offer significant advantages to this primate model of DR.
机译:缺乏完整的糖尿病性视网膜病(DR)病理模型的动物模型阻碍了对DR发病机理和治疗干预措施的了解。在这里,我们调查了高糖血症mar猴(Callithrix jacchus)是否发展出包括黄斑水肿(ME)在内的特征性视网膜血管病变,黄斑水肿(DR)是导致视力丧失的主要原因。监测保持30%富含半乳糖(gal)饮食2年的mos猴的视网膜血管通透性,ME的发展以及形态特征,包括无细胞毛细血管(AC)和周细胞丢失(PL),血管曲折和毛细血管基底膜( BM)厚度。在喂食mos猴的视网膜中观察到过度的血管通透性,AC和PL数量增加,血管BM增厚以及血管曲折性增加。光学相干断层扫描(OCT)图像显示视网膜中央凹和近凹凹区域明显增厚,组织学分析显示,gal喂养的mos猴的视网膜出现初期的微动脉瘤。这项研究的结果表明,高血血症可以触发视网膜血管变化,类似于在人类DR中所见的包括ME和微动脉瘤的变化。 mar猴视网膜和人类视网膜之间惊人的相似性,以及猴子异常小的体型,为这种灵长类DR模型提供了显着优势。

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