Department of Anatomy, Faculty of Medicine and Health, Bosch Institute, University of Sydney, Camperdown, New South Wales, Australia.
Department of Anatomy, Faculty of Medicine and Health, Bosch Institute, University of Sydney, Camperdown, New South Wales, Australia; Department of Ophthalmology and Visual Sciences, University of Alabama, Birmingham, Alabama.
Am J Pathol. 2023 Nov;193(11):1789-1808. doi: 10.1016/j.ajpath.2023.02.019. Epub 2023 Mar 23.
This study investigated retinal changes in a Western diet (WD)-induced nonhuman primate model of type 2 diabetes. Rhesus nonhuman primates, aged 15 to 17 years, were fed a high-fat diet (n = 7) for >5 years reflective of the traditional WD. Age-matched controls (n = 6) were fed a standard laboratory primate diet. Retinal fundus photography, optical coherence tomography, autofluorescence imaging, and fluorescein angiography were performed before euthanasia. To assess diabetic retinopathy (DR), eyes were examined using trypsin digests, lipofuscin autofluorescence, and multimarker immunofluorescence on cross-sections and whole mounts. Retinal imaging showed venous engorgement and tortuosity, aneurysms, macular exudates, dot and blot hemorrhages, and a marked increase in fundus autofluorescence. Post-mortem changes included the following: decreased CD31 blood vessel density (P < 0.05); increased acellular capillaries (P < 0.05); increased density of ionized calcium-binding adaptor molecule expressing amoeboid microglia/macrophage; loss of regular distribution in stratum and spacing typical of ramified microglia; and increased immunoreactivity of aquaporin 4 and glial fibrillary acidic protein (P < 0.05). However, rhodopsin immunoreactivity (P < 0.05) in rods and neuronal nuclei antibody-positive neuronal density of 50% (P < 0.05) were decreased. This is the first report of a primate model of DR solely induced by a WD that replicates key features of human DR.
本研究调查了西方饮食(WD)诱导的 2 型糖尿病非人灵长类动物模型中的视网膜变化。15 至 17 岁的恒河猴被喂食高脂肪饮食(n = 7)超过 5 年,以反映传统的 WD。年龄匹配的对照组(n = 6)喂食标准实验室灵长类动物饮食。在安乐死前进行视网膜眼底照相、光学相干断层扫描、自发荧光成像和荧光素血管造影。为了评估糖尿病视网膜病变(DR),使用胰蛋白酶消化、脂褐素自发荧光和多标记免疫荧光在切片和全片中检查眼睛。视网膜成像显示静脉充血和扭曲、动脉瘤、黄斑渗出、点和斑状出血以及眼底自发荧光明显增加。死后变化包括以下内容:CD31 血管密度降低(P < 0.05);无细胞毛细血管增加(P < 0.05);表达阿米巴样小胶质细胞/巨噬细胞的离子钙结合接头分子表达密度增加;树突状小胶质细胞的分层和间隔典型的规则分布丧失;水通道蛋白 4 和神经胶质纤维酸性蛋白的免疫反应性增加(P < 0.05)。然而,杆状细胞的视紫红质免疫反应性(P < 0.05)和神经元核抗体阳性神经元密度的 50%(P < 0.05)降低。这是首次报道仅由 WD 诱导的 DR 灵长类动物模型,复制了人类 DR 的关键特征。