首页> 外文期刊>International journal of biological sciences >Detailed Localization of Augmented Angiotensinogen mRNA and Protein in Proximal Tubule Segments of Diabetic Kidneys in Rats and Humans
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Detailed Localization of Augmented Angiotensinogen mRNA and Protein in Proximal Tubule Segments of Diabetic Kidneys in Rats and Humans

机译:增强的血管紧张素原mRNA和蛋白在大鼠和人类糖尿病肾近端小管节中的详细定位

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In the intrarenal renin-angiotensin system, angiotensinogen levels are well known to be increased in diabetes, and these enhanced intrarenal angiotensinogen levels may initiate the development and accelerate the progression of diabetic nephropathy. However, the specific localization of the augmented angiotensinogen in proximal tubule segments in diabetes is still unknown. We investigated the detailed localization of angiotensinogen in 3 proximal tubule segments in the diabetic Otsuka Long-Evans Tokushima fatty (OLETF) rats and the control Long-Evans Tokushima Otsuka (LETO) rats. We also prepared OLETF rats treated with angiotensin II type 1 receptor blocker, olmesartan or with a combination of vasodilator agents. Moreover, biopsied samples of human kidney cortex were used to confirm the results of animal studies. We examined the co-localization of angiotensinogen with segment-specific markers by double staining using fluorescence in situ hybridization and/or immunofluorescence. Angiotensinogen mRNA expression was barely detectable in segment 1. In segment 3, the area of angiotensinogen mRNA expression was augmented in the OLETF rats compared with the LETO rats. Angiotensinogen protein expression areas in segments 1 and 3 were also increased in the OLETF rats compared with the LETO rats. Chronic treatment with olmesartan ameliorated these areas of augmented angiotensinogen expression. Biopsied human kidney samples showed similar results. These data suggest that the augmented angiotensinogen mRNA levels in segment 3 and angiotensinogen protein levels in segments 1 and 3 may contribute to the progression of diabetic nephropathy.
机译:在肾内肾素-血管紧张素系统中,众所周知血管紧张素原水平在糖尿病中升高,并且这些升高的肾内血管紧张素原水平可能启动糖尿病性肾病的发展并加速其进展。但是,糖尿病患者近端小管节段中血管紧张素原的特异性定位仍是未知的。我们调查了血管紧张素原在糖尿病的大冢长岛伊万德岛肥胖(OLETF)大鼠和对照长岛长岛伊万岛大冢(LETO)大鼠的3个近端小管节中的详细定位。我们还准备了用血管紧张素II 1型受体阻滞剂,奥美沙坦或血管扩张剂联合治疗的OLETF大鼠。此外,使用人肾皮质活检样本来证实动物研究的结果。我们使用荧光原位杂交和/或免疫荧光技术通过双重染色检查了血管紧张素原与节段特异性标记的共定位。在区段1中几乎检测不到血管紧张素原mRNA表达。在区段3中,与LETO大鼠相比,OLETF大鼠中血管紧张素原mRNA表达的面积增加。与LETO大鼠相比,OLETF大鼠中第1段和第3段的血管紧张素原蛋白表达面积也增加了。奥美沙坦的长期治疗改善了血管紧张素原表达增加的这些区域。活检的人肾脏样品显示出相似的结果。这些数据表明,第3节中血管紧张素原mRNA水平的增加以及第1节和第3节中血管紧张素原蛋白水平的升高可能有助于糖尿病性肾病的进展。

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