Department of Ophthalmology, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Department of Medical Life Sciences and Department of Biomedicine & Health Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Cell Death Dis. 2022 Apr 9;13(4):323. doi: 10.1038/s41419-022-04762-4.
The purpose of this study was to design an animal model mimicking glaucoma with hemodynamic instability and to identify involvement of angiotensin II (AngII) and associated changes of the retina. Systemic hypotension was induced in Sprague-Dawley rats by oral hydrochlorothiazide administration. Rats were sacrificed at 4, 8, and 12-week time points. AngII and receptor levels were examined in the serum and retina. To examine the relationship between glia activation and associated RGC death, biochemical analysis of GFAP, Iba-1, and necroptosis associated factors such as TNFα, receptor-interacting protein (RIP) 1, 3, and inactive caspase 8 were explored. To investigate the difference in RGC death mechanism, JNK inhibitor or RIP3 inhibitor were given intraperitoneally to rats with ocular hypertension and systemic hypotension both to identify the pathway mainly involved. AngII and receptors were increased in the serum and retina of systemic hypotensive rat. At 4, 8, and 12 weeks after hypotension induction, glial activation was increased as indicated by GFAP and Iba-1 staining. TNFα, RIP3 were elevated. and downregulation of inactive caspase 8 was apparent in the retina of hypotensive rat. Electron microscopy revealed that necroptosis of RGC was gradually increased after systemic hypotension. Following intraperitoneal JNK inhibitor or RIP3 inhibitor administration, RGC loss was attenuated in systemic hypotensive rats but not in ocular hypertensive rats. In conclusion, AngII is involved in glial activation and associated RGC necroptosis following systemic hypotension. This pathway represents a novel and distinct cell death mechanism when compared to that involved in elevated intraocular pressure.
本研究旨在设计一种模拟伴有血液动力学不稳定的青光眼的动物模型,并确定血管紧张素 II(AngII)的参与及其对视网膜的相关变化。通过口服氢氯噻嗪诱导 Sprague-Dawley 大鼠发生系统性低血压。在 4、8 和 12 周时间点处死大鼠。在血清和视网膜中检查 AngII 和受体水平。为了研究胶质细胞激活与相关 RGC 死亡之间的关系,探索了 GFAP、Iba-1 和与坏死性凋亡相关的因素,如 TNFα、受体相互作用蛋白(RIP)1、3 和无活性 caspase 8 的生化分析。为了研究 RGC 死亡机制的差异,向患有眼内压升高和系统性低血压的大鼠腹腔内给予 JNK 抑制剂或 RIP3 抑制剂,以确定主要涉及的途径。AngII 和受体在系统性低血压大鼠的血清和视网膜中增加。在低血压诱导后的 4、8 和 12 周,GFAP 和 Iba-1 染色表明胶质激活增加。TNFα、RIP3 升高,视网膜中无活性 caspase 8 的下调明显。电子显微镜显示,系统性低血压后 RGC 的坏死性凋亡逐渐增加。腹腔内给予 JNK 抑制剂或 RIP3 抑制剂后,系统性低血压大鼠的 RGC 损失减少,但眼内压升高大鼠的 RGC 损失没有减少。总之,AngII 参与系统性低血压后胶质激活和相关 RGC 坏死性凋亡。与涉及升高的眼内压的机制相比,该途径代表一种新的、独特的细胞死亡机制。