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自噬抑制减轻乙二醇诱导的肾结石大鼠模型中的晶体沉积和肾损伤

Inhibition of Autophagy Attenuated Ethylene Glycol Induced Crystals Deposition and Renal Injury in a Rat Model of Nephrolithiasis.

作者信息

Liu Yunlong, Liu Quan, Wang Xiang, He Ziqi, Li Derong, Guan Xiaofeng, Tao Zhiwei, Deng Yaoliang

机构信息

Department of Urology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Department of Urology, the Langdong Hospital of Guangxi Medical University, Nanning, China.

出版信息

Kidney Blood Press Res. 2018;43(1):246-255. doi: 10.1159/000487678. Epub 2018 Feb 22.

Abstract

BACKGROUND/AIMS: Nephrolithiasis is a common and frequently occurring disease, its exact pathogenesis is remains unclear. Emerging data suggest that autophagy plays a vital role in the pathophysiological processes of kidney diseases. Therefore, this study was designed to investigate the potential role of autophagy in the formation of calcium oxalate (CaOx) kidney stones in rat model.

METHODS

Thirty-two rats were randomly divided into four groups (eight rats/group): untreated control group, stone model group, rapamycin-treated group, chloroquine-treated group. Rat models of CaOx nephrolithiasis was administration of 0.75% ethylene glycol (EG) in their drinking water for 4 weeks. Western blot and transmission electron microscope (TEM) were used to detect the expression of autophagy related protein LC3-II, BECN1 and p62 and autophagic vacuoles respectively. Renal function was evaluated by measuring the levels of serum CRE and BUN. Renal tubular injury markers NGAL and Kim-1 was determined by ELISA kits. Von Kossa staining was used to assess crystal deposits and histological tissue injury. TUNEL staining was employed to assess apoptosis of the renal tubular cell.

RESULTS

Compare with the controls, the expression of autophagy related protein LC3-II, BECN1 and number of autophagic vacuoles were increased significantly, whereas the p62 protein level was decreased in the stone model group. The levels of apoptosis, serum CRE and BUN, NGAL and Kim-1 in the stone model group were increased compared with the control group and crystals deposition and renal injury were increased significantly. However, the levels of autophagy, kidney injury and crystal deposition were decreased by chloroquine but increased by rapamycin.

CONCLUSION

These findings suggested that rats were administration of ethylene glycol could lead to the formation of CaOx nephrolithiasis and autophagy activation. Inhibiting autophagy could be an effective therapeutic approach for decreasing the formation of nephrolithiasis.

摘要

背景/目的:肾结石是一种常见且多发的疾病,其确切发病机制尚不清楚。新出现的数据表明,自噬在肾脏疾病的病理生理过程中起着至关重要的作用。因此,本研究旨在探讨自噬在大鼠草酸钙(CaOx)肾结石形成中的潜在作用。

方法

32只大鼠随机分为四组(每组8只):未处理对照组、结石模型组、雷帕霉素处理组、氯喹处理组。通过在饮用水中给予0.75%乙二醇(EG)4周建立CaOx肾结石大鼠模型。采用蛋白质免疫印迹法和透射电子显微镜(TEM)分别检测自噬相关蛋白LC3-II、BECN1和p62的表达以及自噬泡。通过测量血清肌酐(CRE)和尿素氮(BUN)水平评估肾功能。采用酶联免疫吸附测定试剂盒测定肾小管损伤标志物中性粒细胞明胶酶相关脂质运载蛋白(NGAL)和肾损伤分子-1(Kim-1)。采用冯科萨染色评估晶体沉积和组织学损伤。采用末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)染色评估肾小管细胞凋亡。

结果

与对照组相比,结石模型组自噬相关蛋白LC3-II、BECN1的表达及自噬泡数量显著增加,而p62蛋白水平降低。结石模型组的凋亡水平、血清CRE和BUN、NGAL和Kim-1水平均高于对照组,晶体沉积和肾损伤显著增加。然而,氯喹可降低自噬水平、肾损伤和晶体沉积,而雷帕霉素则使其增加。

结论

这些研究结果表明,给予乙二醇可导致大鼠形成CaOx肾结石并激活自噬。抑制自噬可能是减少肾结石形成的一种有效治疗方法。

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