Triphala Ameliorates Nephropathy via Inhibition of TGF-β1 and Oxidative Stress in Diabetic Rats

被引:21
|
作者
Suryavanshi, Sachin, V [1 ]
Garud, Mayuresh S. [1 ]
Barve, Kalyani [1 ]
Addepalli, Veeranjaneyulu [1 ]
Utpat, Sachin, V [2 ]
Kulkarni, Yogesh A. [1 ]
机构
[1] SVKMs NMIMS, Shobhaben Pratapbhai Patel Sch Pharm & Technol Ma, VL Mehta Rd, Mumbai 400056, Maharashtra, India
[2] MES Ayurveda Mahavidyalaya, Tal Khed, Ratnagiri, India
关键词
Diabetic nephropathy; Triphala churna; Emblica officinalis; Terminalia belerica; Terminalia chebula; Diabetic complications; RENAL DAMAGE; COMPLICATIONS; APOPTOSIS;
D O I
10.1159/000508238
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Advanced glycation end products, oxidative stress, and TGF-beta expression play a crucial role in pathophysiology of diabetic nephropathy. Inhibition of oxidative stress and TGF-beta expression by natural traditional medicines may give an economic and safe alternative treatment option. Triphala churna, a traditional medicine, has been proved to have potent antioxidant activity, and individual components of it have shown significant antidiabetic activity. Hence, the present study was designed to study the effect of Triphala churna in diabetic nephropathy in rats. Methods: Diabetes was induced in rats by administration of streptozotocin (55 mg/kg i.p.). Four weeks after induction of diabetes, the animals were treated with Triphala churna at the doses of 250, 500, and 1,000 mg/kg for next 4 weeks. Various biochemical and urine parameters such as glucose, creatinine, blood urea nitrogen (BUN), total protein, and albumin were assessed at the end of study. Creatinine clearance, BUN clearance, and glomerular filtration rate were determined. Oxidative stress parameters such as malondialdehyde, catalase, reduced glutathione, and superoxide dismutase were determined in kidney tissues. TGF-beta 1 expression was measured with ELISA, immunohistochemistry, and western blot techniques. Histopathology study was carried out with haemotoxylin and eosin, periodic acid-Schiff, and Masson's trichrome staining to determine histological changes. Results: Treatment with Triphala churna significantly improved urine parameters. Triphala churna treatment also improved plasma proteins, albumin, creatinine, and BUN levels. The oxidative stress was reduced in the kidney with the treatment of Triphala churna. Histopathological studies revealed that Triphala churna reduced kidney damage. Immunohistochemistry, ELISA, and western blotting study revealed that treatment with Triphala decreased the expression of TGF-beta in kidney tissues. Conclusion: From the results, it can be concluded that Triphala churna has a significant nephroprotective effect because of its capability of inhibiting oxidative stress and TGF-beta in diabetes.
引用
收藏
页码:681 / 691
页数:11
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