Qiwei granules alleviates podocyte lesion in kidney of diabetic KK-Ay mice

• Published in: BMC complementary and alternative medicine 2015-03, Vol.15 (1), p.97-97, Article 97
• Main Authors: Zhou, Jingxin, Sun, Wen, Yoshitomi, Hisae, Li, Linyi, Qin, Lingling, Guo, Xiangyu, Wu, Lili, Zhang, Yan, Wu, Xinli, Xu, Tunhai, Gao, Ming, Liu, Tonghua
• Format: Article
• Language: English
• Subjects: Adaptor Proteins, Signal Transducing - metabolism; Analysis; Animal experimentation; Animals; Biomarkers - metabolism; Body Weight; Care and treatment; Caspase 3 - metabolism; Cellular signal transduction; Cytoskeletal Proteins - metabolism; Diabetic nephropathies; Diabetic Nephropathies - drug therapy; Diabetic Nephropathies - metabolism; Diabetic Nephropathies - pathology; Diagnosis; Drugs, Chinese Herbal - pharmacology; Drugs, Chinese Herbal - therapeutic use; Health aspects; Integrin alpha3beta1 - metabolism; Integrins; Kidney - drug effects; Kidney - metabolism; Kidney - pathology; Magnoliopsida; Male; Membrane Proteins - metabolism; Mice; Mice, Inbred C57BL; Phytotherapy; Podocytes - drug effects; Podocytes - pathology; Protective Agents - pharmacology; Signal Transduction - drug effects
• ISSN: 1472-6882; 1472-6882
• DOI: 10.1186/s12906-015-0603-x

Chinese medicine comprised of all natural herbs is widespread used in the treatment of diabetic nephropathy (DN). Podocyte contributes to the integrity of glomerular filtration barrier whose injury plays an important role in the initiation and progression of DN. Our study aimed to investigate the effect of Qiwei granules on podocyte lesion in diabetic KK-A(y) mice kidney and its underlying mechanism. Twelve-week-old male KK-A(y) mice were randomly divided in vehicle group and Qiwei granules group, while C57BL/6J mice were used as normal control. The mice were gavage with 1.37 g/kg/day Qiwei granules or water for 10 weeks. We measured water, food intake and body weight (BW) and fasting blood glucose (FBG) every 2 weeks, and urine protein every 4 weeks. At the end of the experiment, all surviving mice were sacrificed. The kidney weight and serum renal parameters were measured, and the renal morphology was observed. To search the underlying mechanism, we examined the podocyte positive marker, slit diaphragm protein expression and some involved cell signal pathway. Qiwei granules treatment significantly improved the metabolic parameters, alleviated the urinary protein, and protected renal function in KK-A(y) mice. In addition, the glomerular injuries and podocyte lesions were mitigated with Qiwei granules treatment. Furthermore, Qiwei granules increased expression of nephrin, CD2AP, and integrin alpha3beta1 in the podocytes of KK-A(y) mice. Qiwei granules improved the phosphoration of Akt and inhibited cleaved caspase-3 protein expression. These finding suggest that Qiwei granules protects the podocyte from the development of DN via improving slit diaphragm (SD) molecules expression and likely activating Akt signaling pathway in KK-A(y) mice.