Department of Nephrology, Faculty of Medicine, Saitama Medical University, 38 Moro-hongo Moroyama, Iruma, Saitama 350-0495, Japan.
Diabetologia. 2011 Aug;54(8):2192-201. doi: 10.1007/s00125-011-2175-8. Epub 2011 May 15.
AIMS/HYPOTHESIS: We examined the link between altered gap junctional communication and renal haemodynamic abnormalities in diabetes in studies performed on Zucker lean (ZL) and the Zucker diabetic fatty (ZDF) rat model of type 2 diabetes.
The abundance of connexin (Cx) 37, 40 and 43 was assessed by western blot and immunohistochemistry. Renal haemodynamics was characterised with GAP peptides, which are Cx mimetics, to inhibit gap junctions as a probe in both strains.
ZDF rats exhibited higher plasma glucose, 8-epi-prostaglandin F2α excretion, renal plasma flow and GFR than ZL rats. In ZDF rat kidney phosphorylation of Cx43 was enhanced compared with that in ZL rats. Immunohistochemical study revealed that the density of abundance of Cx37 in renin-secreting cells was significantly reduced in ZDF rats. Although renal autoregulation was markedly impaired in ZDF rats, it was preserved in ZL rats. GAP27 for Cx37,43 and for Cx40 impaired renal autoregulation in ZL rats, but failed to induce further alterations in renal autoregulation in ZDF rats.
CONCLUSIONS/INTERPRETATION: Our findings indicate that ZDF rats have glomerular hyperfiltration with impaired autoregulation. They also demonstrate enhanced phosphorylation of Cxs and reduced production of Cxs in ZDF rat kidney, especially of Cx37 in renin-secreting cells. Finally, our data suggest that an impairment of gap junctional communication in juxtaglomerular apparatus plays a role in altered renal autoregulation in diabetes.
目的/假设:我们研究了缝隙连接通讯改变与糖尿病肾血流动力学异常之间的联系,研究对象为 Zucker 瘦(ZL)和 Zucker 糖尿病肥胖(ZDF)大鼠 2 型糖尿病模型。
通过 Western blot 和免疫组织化学检测连接蛋白(Cx)37、40 和 43 的丰度。用 GAP 肽作为探针,抑制缝隙连接,以研究两种品系的肾血流动力学。
与 ZL 大鼠相比,ZDF 大鼠的血浆葡萄糖、8-epi-前列腺素 F2α 排泄、肾血浆流量和 GFR 更高。与 ZL 大鼠相比,ZDF 大鼠肾脏中 Cx43 的磷酸化增强。免疫组织化学研究显示,ZDF 大鼠肾素分泌细胞中 Cx37 的丰度密度明显降低。尽管 ZDF 大鼠的肾自身调节明显受损,但 ZL 大鼠的肾自身调节得以保留。GAP27 对 Cx37、43 和 Cx40 的作用可损害 ZL 大鼠的肾自身调节,但不能在 ZDF 大鼠中引起进一步的改变。
结论/解释:我们的研究结果表明,ZDF 大鼠存在肾小球高滤过伴自身调节受损。它们还表明,ZDF 大鼠肾脏中 Cxs 的磷酸化增强,Cxs 的产生减少,尤其是肾素分泌细胞中的 Cx37。最后,我们的数据表明,肾小球旁器中缝隙连接通讯的受损在糖尿病中改变的肾自身调节中起作用。