Nozako Masanori, Koyama Takashi, Nagano Chifumi, Sato Makoto, Matsumoto Satoshi, Mitani Kiminobu, Yasufuku Reiko, Kohashi Masayuki, Yoshikawa Tomohiro
Free Radical Research Project, Otsuka Pharmaceutical Co., Ltd., Tokushima, Tokushima, Japan.
Department of Toxicology, Drug Safety Research Center, Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd., Tokushima, Tokushima, Japan.
PLoS One. 2015 Nov 25;10(11):e0143979. doi: 10.1371/journal.pone.0143979. eCollection 2015.
Diabetic nephropathy develops in association with hyperglycemia, is aggravated by atherogenic factors such as dyslipidemia, and is sometimes initiated before obvious hyperglycemia is seen. However, the precise mechanisms of progression are still unclear. In this study, we investigated the influence of an atherogenic Paigen diet (PD) on the progression of nephropathy in spontaneous type 2 diabetic OLETF rats. Feeding PD to male OLETF rats for 12 weeks caused an extensive increase in excretion of urinary albumin and markers of tubular injury such as KIM-1 and L-FABP, accompanied by mesangial expansion and tubular atrophy. PD significantly increased plasma total cholesterol concentration, which correlates well with increases in urine albumin excretion and mesangial expansion. Conversely, PD did not change plasma glucose and free fatty acid concentrations. PD enhanced renal levels of mRNA for inflammatory molecules such as KIM-1, MCP-1, TLR4 and TNF-α and promoted macrophage infiltration and lipid accumulation in the tubulointerstitium and glomeruli in OLETF rats. Intriguingly, PD had little effect on urine albumin excretion and renal morphology in normal control LETO rats. This model may be useful in studying the complex mechanisms that aggravate diabetic nephropathy in an atherogenic environment.
糖尿病肾病与高血糖相关,会因血脂异常等致动脉粥样硬化因素而加重,有时在出现明显高血糖之前就已发病。然而,其确切的进展机制仍不清楚。在本研究中,我们调查了致动脉粥样硬化的派金饮食(PD)对自发性2型糖尿病OLETF大鼠肾病进展的影响。给雄性OLETF大鼠喂食PD 12周导致尿白蛋白排泄以及KIM-1和L-FABP等肾小管损伤标志物大量增加,同时伴有系膜扩张和肾小管萎缩。PD显著提高了血浆总胆固醇浓度,这与尿白蛋白排泄增加和系膜扩张密切相关。相反,PD并未改变血浆葡萄糖和游离脂肪酸浓度。PD提高了肾内KIM-1、MCP-1、TLR4和TNF-α等炎症分子的mRNA水平,并促进了OLETF大鼠肾小管间质和肾小球中的巨噬细胞浸润及脂质蓄积。有趣的是,PD对正常对照LETO大鼠的尿白蛋白排泄和肾脏形态几乎没有影响。该模型可能有助于研究在致动脉粥样硬化环境中加重糖尿病肾病的复杂机制。