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Curcumin attenuates diabetic nephropathy by inhibiting PKC‐α and PKC‐β 1 activity in streptozotocin‐induced type I diabetic rats

2011; Wiley; Volume: 55; Issue: 11 Linguagem: Inglês

10.1002/mnfr.201100080

1613-4133

Vivian Soetikno, Kenichi Watanabe, Flori R. Sari, Meilei Harima, Rajarajan A. Thandavarayan, Punniyakoti T. Veeraveedu, Wawaimuli Arozal, Vijayakumar Sukumaran, Arun Prasath Lakshmanan, Somasundaram Arumugam, Kenji Suzuki,

Heme Oxygenase-1 and Carbon Monoxide

Abstract Scope : We hypothesized that curcumin, a potent anti‐oxidant, might be beneficial in ameliorating the development of diabetic nephropathy through inhibition of PKC‐α and PKC‐β1 activity‐ERK1/2 pathway. Methods and results : Diabetes was induced by a single intraperitoneal injection of streptozotocin (STZ) (55 mg/kg) in rats. Three weeks after STZ injection, rats were divided into three groups, namely, normal, diabetic and diabetic treated with curcumin at 100 mg/kg/day, p.o., for 8 wk. At 11 wk after STZ injection, diabetic rats exhibited renal dysfunction, as evidenced by reduced creatinine clearance, increased blood urea nitrogen (BUN) and proteinuria, marked increases in lipid peroxidation, NOX4 and p67phox and decrease in anti‐oxidant enzyme. All of these abnormalities were significantly reversed by curcumin. Furthermore, the high‐glucose‐induced PKC‐α and PKC‐β1 activities and phosphorylated ERK1/2 was significantly diminished by curcumin. Curcumin also attenuated the expression of TGF‐β1, CTGF, osteopontin, p300 and ECM proteins such as fibronectin and type IV collagen. The high‐glucose‐induced expression of VEGF and its receptor VEGF receptor II (flk‐1) was also ameliorated by curcumin. Conclusion : These results prove that curcumin produces dual blockade of both PKC‐α and PKC‐β1 activities, which suggests that curcumin is a potential adjuvant therapy for the prevention and treatment of diabetic nephropathy.