肾素-血管紧张素系统双重阻断对糖尿病高血压大鼠肾脏和血管内皮生长因子-A表达的影响

Q4 Pharmacology, Toxicology and Pharmaceutics
Asmaa Hussien Elsayed Mobarak, N. E. Sayed, Y. Maklad, S. Kenawy
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引用次数: 0

摘要

研究了血管紧张素转换酶(ACE)抑制剂赖诺普利和/或血管紧张素受体阻断剂缬沙坦早期阻断肾素-血管紧张素系统(RAS)对糖尿病高血压大鼠肾脏nephrin和血管内皮生长因子(VEGF)-A基因表达的影响。成年Wistar大鼠连续4天使用链脲佐菌素(45mg/kg,i.p.)和Nω-硝基-L-精氨酸甲酯(60mg/kg/12h)诱导糖尿病和高血压。实验动物被分为六组(n=6):正常对照组、糖尿病对照组、高血压对照组和赖诺普利、缬沙坦和联合治疗的糖尿病高血压组(5mg/kg/药物/天,口服,持续21天)。每周测量并记录血糖、血压、体重、肾重体重比、血清白蛋白、肌酐、总蛋白和尿素。Nephrin和VEGF-A基因表达采用实时聚合酶链反应进行测定。用ELISA法和nephrin免疫染色法测定肾脏nephrin蛋白。所有治疗组的血压均显著下降(P≤0.05),血清白蛋白和尿素均正常化。血清肌酐显著降低,而总蛋白显著升高(P≤0.05)。糖尿病高血压大鼠的Nephrin基因表达无显著降低,但随着个体治疗的进行,其表达在统计学上增加(P≤0.05%),并在联合治疗中正常化。糖尿病性高血压大鼠肾脏nephrin蛋白显著降低,赖诺普利使其正常化,缬沙坦和联合治疗使其显著增加(P≤0.05)。糖尿病高血压大鼠VEGF-A的表达显著增加,赖诺普利和缬沙坦单药治疗使其明显降低,联合治疗使VEGF-A正常化(P≤0.05%)。nephrin的免疫染色在联合治疗的情况下也显示出明显增加。糖尿病高血压大鼠早期双重阻断RAS可保护其免受肾损伤,并改善肾蛋白和VEGF-A基因表达以及肾蛋白表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of dual blockade of renin-angiotensin system on renal nephrin and vascular endothelial growth factor – A expression in diabetic-hypertensive rats
The effects of early renin-angiotensin system (RAS) blockade using angiotensin-converting enzyme (ACE) inhibitor lisinopril and/or angiotensin receptor blocker valsartan on renal nephrin and vascular endothelial growth factor (VEGF)-A gene expression were investigated in diabetic-hypertensive rats. Diabetes and hypertension were induced in adult Wistar rats using streptozotocin (45 mg/kg, i.p.) and Nω-nitro-L-arginine methyl ester (60 mg/kg/12 h) for 4 consecutive days. Experimental animals were allocated into six groups (n = 6): normal control, diabetic control, diabetic-hypertensive control and lisinopril-, valsartan- and combination-treated diabetic-hypertensive groups (5 mg/kg/drug/day, p.o., for 21 days). Blood glucose, blood pressure, body weight, kidney weight to body weight ratio, serum albumin, creatinine, total protein and urea were measured and recorded every week. Nephrin and VEGF-A gene expression were measured using real-time polymerase chain reaction. Renal nephrin protein was measured using ELISA as well as nephrin immunostaining. Blood pressure was significantly decreased by all treatments (P ≤ 0.05). All treatments normalised serum albumin and urea. Serum creatinine significantly decreased, while total protein significantly increased (P ≤ 0.05). Nephrin gene expression had a non-significant decrease in diabetic-hypertensive rats, yet it was statistically increased with individual treatments (P ≤ 0.05) and normalised with combined treatment. Renal nephrin protein significantly decreased in diabetic-hypertensive rats, normalised by lisinopril and significantly increased by valsartan and combined treatments (P ≤ 0.05). VEGF-A expression significantly increased in diabetic-hypertensive rats and significantly decreased with lisinopril and valsartan monotherapy and normalised with combined treatment (P ≤ 0.05). Immunostaining of nephrin also showed an obvious increase in the case of combined treatment. Early dual blockade of RAS in diabetic-hypertensive rats protected against renal damage and improved renal nephrin and VEGF-A gene expression as well as renal nephrin protein expression.
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来源期刊
Indian journal of physiology and pharmacology
Indian journal of physiology and pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.50
自引率
0.00%
发文量
35
期刊介绍: Indian Journal of Physiology and Pharmacology (IJPP) welcomes original manuscripts based upon research in physiological, pharmacological and allied sciences from any part of the world.
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