Antroquinonol reduces oxidative stress by enhancing the Nrf2 signaling pathway and inhibits inflammation and sclerosis in focal segmental glomerulosclerosis mice

被引:99
作者
Tsai, Pei-Yi [2 ]
Ka, Shuk-Man [1 ]
Chao, Tai-Kuang
Chang, Jia-Ming [3 ]
Lin, Shih-Hua [4 ]
Li, Chen-Yun
Kuo, Mao-Tien [5 ]
Chen, Peini [5 ]
Chen, Ann [2 ]
机构
[1] Tri Serv Gen Hosp, Natl Def Med Ctr, Dept Pathol, Taipei, Taiwan
[2] Natl Def Med Ctr, Grad Inst Med Sci, Taipei, Taiwan
[3] Dev Ctr Biotechnol, Dept Anim Pharmacol, Taipei, Taiwan
[4] Tri Serv Gen Hosp, Div Nephrol, Dept Internal Med, Taipei, Taiwan
[5] Golden Biotechnol Corp, Taipei, Taiwan
关键词
Antroquinonol; Antrodia camphorata; Glomerular sclerosis; Epithelial hyperplasia lesion; Podocyte injury; Oxidative stress; Nuclear factor E2-related factor 2; Nuclear factor-kappa B; Transforming growth factor-beta 1; Free radicals; NADPH OXIDASE COMPONENTS; ANTRODIA-CAMPHORATA; PHASE-2; ENZYMES; ACTIVATION; EXPRESSION; FIBROSIS; PROTEIN; CELL; PATHOGENESIS; PROTECTION;
D O I
10.1016/j.freeradbiomed.2011.02.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Oxidative stress, inflammation, and fibrosis are involved in the development and progression of focal segmental glomerulosclerosis (FSGS), a common form of idiopathic nephrotic syndrome that represents a therapeutic challenge because it has a poor response to steroids. Antroquinonol (Antroq), a purified compound, is a major active component of a mushroom, namely Antrodia camphorata, that grows in the camphor tree in Taiwan, and it has inhibitory effects on nitric oxide production and inflammatory reactions. We hypothesized that Antroq might ameliorate FSGS renal lesions by modulating the pathogenic pathways of oxidative stress, inflammation, and glomerular sclerosis in the kidney. We demonstrate that Antroq significantly (1) attenuates proteinuria, renal dysfunction, and glomerulopathy, including epithelial hyperplasia lesions and podocyte injury; (2) reduces oxidative stress, leukocyte infiltration, and expression of fibrosis-related proteins in the kidney; (3) increases renal nuclear factor E2-related factor 2 (Nrf2) and glutathione peroxidase activity; and (4) inhibits renal nuclear factor-kappa B (NF-kappa B) activation and decreases levels of transforming growth factor (TGF)-beta 1 in serum and kidney tissue in a mouse FSGS model. Our data suggest that Antroq might be a potential therapeutic agent for FSGS, acting by boosting Nrf2 activation and suppressing NF-kappa B-dependent inflammatory and TGF-beta 1-mediated fibrosis pathways in the kidney. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1503 / 1516
页数:14
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