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在2型糖尿病大鼠模型中,血管紧张素II依赖的血管内皮生长因子基因表达通过NADPH氧化酶参与视网膜病变。

Involvement of angiotensin II-dependent vascular endothelial growth factor gene expression via NADPH oxidase in the retina in a type 2 diabetic rat model.

作者信息

Fukumoto Masanori, Takai Shinji, Ishizaki Eisuke, Sugiyama Tetsuya, Oku Hidehiro, Jin Denan, Sakaguchi Masato, Sakonjo Hiroshi, Ikeda Tsunehiko, Miyazaki Mizuo

机构信息

Department of Pharmacology, Osaka Medical College, Osaka, Japan.

出版信息

Curr Eye Res. 2008 Oct;33(10):885-91. doi: 10.1080/02713680802389851.

Abstract

PURPOSE

To clarify the involvement of angiotensin II-dependent vascular endothelial growth factor (VEGF) via NADPH oxidase in the retina in spontaneously diabetic Torii (SDT) rats, a type 2 diabetic rat model. In SDT rats, the plasma glucose level and angiotensin-converting enzyme (ACE) levels were measured, and effects of angiotensin II receptor blocker (ARB) and angiotensin II were also studied.

MATERIALS AND METHODS

We evaluated the age-dependent changes in the peripheral and ocular angiotensin II-forming systems in SDT rats at 15 (n = 8), 20 (n = 8), 30 (n = 7), and 50 weeks of age (n = 8). We also evaluated the effect of an ARB (2.5 mg/kg/day candesartan) or angiotensin II (500 ng/kg/min) on retinal gene expressions of VEGF and p22phox, a subunit of NADPH oxidase.

RESULTS

The plasma glucose level was significantly increased from 20 weeks of age. No significant changes in ACE activities in the plasma, aorta, and eye were observed until 30 weeks of age. At 50 weeks, ACE activity in the eyes was significantly increased, whereas ACE activities in the plasma and aorta were not. At 50 weeks, significant increases in VEGF and p22phox, an NADPH oxidase subunit, were significantly reduced by candesartan. Angiotensin II infusion resulted in significant increases in VEGF and p22phox levels.

CONCLUSIONS

Angiotensin II is involved in the gene expression of VEGF via NADPH oxidase in the retina of SDT rats.

摘要

目的

在2型糖尿病大鼠模型——自发性糖尿病Torii(SDT)大鼠中,阐明血管紧张素II通过NADPH氧化酶介导的血管内皮生长因子(VEGF)在视网膜中的作用。测定了SDT大鼠的血糖水平和血管紧张素转换酶(ACE)水平,并研究了血管紧张素II受体阻滞剂(ARB)和血管紧张素II的作用。

材料与方法

我们评估了15周龄(n = 8)、20周龄(n = 8)、30周龄(n = 7)和50周龄(n = 8)的SDT大鼠外周和眼部血管紧张素II生成系统的年龄依赖性变化。我们还评估了ARB(坎地沙坦2.5 mg/kg/天)或血管紧张素II(500 ng/kg/分钟)对视网膜VEGF和NADPH氧化酶亚基p22phox基因表达的影响。

结果

血糖水平从20周龄开始显著升高。直到30周龄,血浆、主动脉和眼部的ACE活性均未观察到显著变化。在50周时,眼部的ACE活性显著增加,而血浆和主动脉中的ACE活性没有增加。在50周时,VEGF和NADPH氧化酶亚基p22phox显著增加,坎地沙坦可使其显著降低。输注血管紧张素II导致VEGF和p22phox水平显著增加。

结论

血管紧张素II通过NADPH氧化酶参与SDT大鼠视网膜中VEGF的基因表达。

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