Phycocyanin and phycocyanobilin from Spirulina platensis protect against diabetic nephropathy by inhibiting oxidative stress

被引:162
|
作者
Zheng, Jing [1 ]
Inoguchi, Toyoshi [1 ,2 ]
Sasaki, Shuji [1 ]
Maeda, Yasutaka [1 ]
McCarty, Mark F. [3 ]
Fujii, Masakazu [1 ]
Ikeda, Noriko [1 ]
Kobayashi, Kunihisa [1 ]
Sonoda, Noriyuki [1 ,2 ]
Takayanagi, Ryoichi [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Med & Bioregulatory Sci, Fukuoka 812, Japan
[2] Kyushu Univ, Innovat Ctr Med Redox Nav, Fukuoka 812, Japan
[3] NutriGuard Res Inc, Encinitas, CA USA
关键词
bilirubin; phycobilin; albuminuria; NAD(P)H oxidase; superoxide production; CORONARY-ARTERY-DISEASE; NAD(P)H OXIDASE; SERUM BILIRUBIN; VASCULAR COMPLICATIONS; C-PHYCOCYANIN; HEART-DISEASE; KIDNEY; RATS; EXPRESSION; ACTIVATION;
D O I
10.1152/ajpregu.00648.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Zheng J, Inoguchi T, Sasaki S, Maeda Y, McCarty MF, Fujii M, Ikeda N, Kobayashi K, Sonoda N, Takayanagi R. Phycocyanin and phycocyanobilin from Spirulina platensis protect against diabetic nephropathy by inhibiting oxidative stress. Am J Physiol Regul Integr Comp Physiol 304: R110-R120, 2013. First published October 31, 2012; doi:10.1152/ajpregu.00648.2011.-We and other investigators have reported that bilirubin and its precursor biliverdin may have beneficial effects on diabetic vascular complications, including nephropathy, via its antioxidant effects. Here, we investigated whether phycocyanin derived from Spirulina platensis, a blue-green algae, and its chromophore phycocyanobilin, which has a chemical structure similar to that of biliverdin, protect against oxidative stress and renal dysfunction in db/db mice, a rodent model for Type 2 diabetes. Oral administration of phycocyanin (300 mg/kg) for 10 wk protected against albuminuria and renal mesangial expansion in db/db mice, and normalized tumor growth factor-beta and fibronectin expression. Phycocyanin also normalized urinary and renal oxidative stress markers and the expression of NAD(P)H oxidase components. Similar antioxidant effects were observed following oral administration of phycocyanobilin (15 mg/kg) for 2 wk. Phycocyanobilin, bilirubin, and biliverdin also inhibited NADPH dependent superoxide production in cultured renal mesangial cells. In conclusion, oral administration of phycocyanin and phycocyanobilin may offer a novel and feasible therapeutic approach for preventing diabetic nephropathy.
引用
收藏
页码:R110 / R120
页数:11
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