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2 型糖尿病大鼠肾脏发育过程中肾内肾素-血管紧张素系统的异常激活。

Aberrant activation of the intrarenal renin-angiotensin system in the developing kidneys of type 2 diabetic rats.

机构信息

Department of Traditional Chinese Medicine, Beijing Tongren Hospital, Capital Medical University, Beijing, PR China.

出版信息

Horm Metab Res. 2013 May;45(5):338-43. doi: 10.1055/s-0032-1331256. Epub 2013 Jan 15.

Abstract

We have previously reported that intrarenal angiotensin II (Ang II) levels are increased long before diabetes becomes apparent in obese Otsuka-Long-Evans-Tokushima-Fatty (OLETF) rats, a model of type 2 diabetes. In this study, we examined the changes in intrarenal renin-angiotensin system (RAS) activity in the developing kidneys of OLETF rats. Ang II contents and mRNA levels of RAS components were measured in male OLETF and control Long-Evans Tokushima (LETO) rats at postnatal days (PND) 1, 5, and 15, and at 4-30 weeks of age. In both LETO and OLETF rats, kidney Ang II levels peaked at PND 1, then decreased during the pre- and post-weaning periods. However, Ang II levels and gene expression of RAS components, including angiotensinogen (AGT), renin, and angiotensin-converting enzyme (ACE), were not significantly different between LETO and OLETF rats. Intrarenal Ang IIcontents further decreased during puberty (from 7 to 11 weeks of age) in LETO rats, bur not in OLETF rats. At 11 weeks of age, kidney Ang II levels, urinary AGT excretion, and mRNA levels of AGT and renin were higher in OLETF rats than in LETO rats, while blood glucose levels were not significantly different between these groups of rats. These data indicate that continued intrarenal expression of Ang II during pubescence contributes to the increases in intrarenal Ang II levels in prediabetic OLETF rats, and is associated with increased intrarenal AGT and renin expression. Inappropriate activation of the intrarenal RAS in the prediabetic stage may facilitate the onset and development of diabetic nephropathy in later life.

摘要

我们之前曾报道过,在肥胖型 Otsuka-Long-Evans-Tokushima-Fatty(OLETF)大鼠(2 型糖尿病模型)出现糖尿病之前,肾脏内血管紧张素 II(Ang II)水平就已经升高了。在这项研究中,我们检测了 OLETF 大鼠肾脏发育过程中肾素-血管紧张素系统(RAS)活性的变化。在雄性 OLETF 和对照 Long-Evans Tokushima(LETO)大鼠的出生后第 1、5 和 15 天以及 4-30 周龄时,测量了 Ang II 含量和 RAS 成分的 mRNA 水平。在 LETO 和 OLETF 大鼠中,肾脏 Ang II 水平在出生后第 1 天达到峰值,然后在断奶前和断奶后期间下降。然而,LETO 和 OLETF 大鼠之间 Ang II 水平和 RAS 成分的基因表达(包括血管紧张素原(AGT)、肾素和血管紧张素转换酶(ACE))没有显著差异。在 LETO 大鼠中,青春期(7-11 周龄)期间肾脏内 Ang II 含量进一步下降,但在 OLETF 大鼠中没有。在 11 周龄时,OLETF 大鼠的肾脏 Ang II 水平、尿 AGT 排泄量以及 AGT 和肾素的 mRNA 水平均高于 LETO 大鼠,而两组大鼠的血糖水平无显著差异。这些数据表明,青春期持续的肾脏内 Ang II 表达导致糖尿病前期 OLETF 大鼠肾脏内 Ang II 水平升高,并与肾脏内 AGT 和肾素表达增加有关。在糖尿病前期阶段,肾内 RAS 的不适当激活可能促进糖尿病肾病的发生和发展。

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