首页> 外文期刊>Investigative ophthalmology & visual science >Aquaporin Changes during Diabetic Retinopathy in Rats Are Accelerated by Systemic Hypertension and Are Linked to the Renin-Angiotensin System
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Aquaporin Changes during Diabetic Retinopathy in Rats Are Accelerated by Systemic Hypertension and Are Linked to the Renin-Angiotensin System

机译:系统性高血压会加速大鼠糖尿病性视网膜病变中水通道蛋白的变化,并与肾素-血管紧张素系统相关

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Purpose.: We explored the relationship between the renin-angiotensin system (RAS) and aquaporins (AQP1 and AQP4 in M??ller glia and astrocytes) in diabetic retinopathy (DR) with and without systemic hypertension. Methods.: Diabetes was induced in spontaneously hypertensive rats (SHR) and normotensive control Wistar Kyoto (WKY) rats by intraperitoneal injections of streptozotocin. The diabetic and control non-diabetic rats were assigned randomly to receive no anti-hypertension treatment, or to be treated with the angiotensin II receptor blocker (ARB), valsartan (40 mg/kg/d) or the beta-blocker, metoprolol (50 mg/kg/day). Eight weeks later, retinas were evaluated by immunohistochemistry and Western blot to detect changes in the expression of AQP1, AQP4, and glial fibrillary acidic protein (GFAP). Results.: Hypertension increased expression of glial GFAP and AQP4 (P 0.01), but not AQP1 (P 0.05) in diabetic rats. Valsartan and metoprolol decreased GFAP, AQP1, and AQP4 expression in diabetic SHR rats (P 0.01). Valsartan decreased GFAP and AQP1 expression in diabetic WKY rats (P 0.01), while metoprolol did not. Conclusions.: Activation of M??ller glia and astrocytes was involved in the mechanism by which systemic hypertension affects DR. AQPs and macroglia were linked to changes in the RAS in DR. Changes in aquaporin expression in DR were increased by hypertension. This provides additional support for the early use of an ARB in the treatment of DR, especially in cases with retinal edema.
机译:目的:我们探讨了糖尿病性视网膜病变(DR)伴或不伴全身性高血压的肾素-血管紧张素系统(RAS)与水通道蛋白(M?ller胶质细胞和星形胶质细胞中的AQP1和AQP4)之间的关系。方法:通过腹膜内注射链脲佐菌素在自发性高血压大鼠(SHR)和血压正常的Wistar Kyoto(WKY)大鼠中诱发糖尿病。糖尿病和对照非糖尿病大鼠被随机分配为不接受抗高血压治疗,或接受血管紧张素II受体阻滞剂(ARB),缬沙坦(40 mg / kg / d)或β受体阻滞剂美托洛尔( 50 mg / kg /天)。八周后,通过免疫组织化学和蛋白质印迹评估视网膜,以检测AQP1,AQP4和神经胶质纤维酸性蛋白(GFAP)表达的变化。结果:在糖尿病大鼠中,高血压增加了神经胶质GFAP和AQP4的表达(P <0.01),但不增加AQP1(P> 0.05)。缬沙坦和美托洛尔降低了糖尿病SHR大鼠的GFAP,AQP1和AQP4表达(P <0.01)。缬沙坦可降低糖尿病WKY大鼠的GFAP和AQP1表达(P <0.01),而美托洛尔则不。结论:M?ller胶质细胞和星形胶质细胞的激活参与系统性高血压影响DR的机制。 AQP和大胶质细胞与DR中RAS的变化有关。高血压增加了DR中水通道蛋白表达的变化。这为早期使用ARB治疗DR提供了额外的支持,特别是在视网膜水肿的情况下。

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