Honokiol Attenuates Sepsis-Associated Acute Kidney Injury via the Inhibition of Oxidative Stress and Inflammation

被引:68
|
作者
Xia, Shilin [1 ]
Lin, Hongli [2 ]
Liu, Han [3 ]
Lu, Zhidan [4 ]
Wang, Hui [4 ]
Fan, Songtao [5 ]
Li, Nan [4 ]
机构
[1] Dalian Med Univ, Affiliated Hosp 1, Clin Lab Integrat Med, 222 Zhongshan Rd, Dalian 116011, Liaoning, Peoples R China
[2] Dalian Med Univ, Affiliated Hosp 1, Dept Nephrol, 222 Zhongshan Rd, Dalian 116011, Liaoning, Peoples R China
[3] Dalian Med Univ, Dept Oral Pathol, 9 West Sect Lvshun South Rd, Dalian 116044, Liaoning, Peoples R China
[4] Dalian Med Univ, Affiliated Hosp 1, Intens Care Unit, 222 Zhongshan Rd, Dalian 116011, Liaoning, Peoples R China
[5] Dalian Med Univ, Affiliated Hosp 1, Dept Ophthalmol, 222 Zhongshan Rd, Dalian 116011, Liaoning, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
AKI; honokiol; oxidative stress; inflammation; NF-KAPPA-B; NITRIC-OXIDE; NRF2; PATHWAY; MYELOPEROXIDASE; ISCHEMIA; OXYGEN; RATS; ACTIVATION; MECHANISMS; LEUKOCYTES;
D O I
10.1007/s10753-018-0937-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Acute kidney injury (AKI) is one of the most common complications of sepsis, which largely contributes to the high mortality rate of sepsis. Honokiol, a natural polyphenol from the traditional Chinese herb Magnolia officinalis, is known to possess anti-inflammatory and antioxidant activity. Here, the underlying mechanism of honokiol-induced amelioration of sepsis-associated AKI was analyzed. The expression patterns of oxidative stress moleculars and TLRs-mediated inflammation pathway were examined to identify the response of NRK-52E cells incubated with septic rats' serum to honokiol. The levels of iNOS, NO, and myeloperoxidase in NRK-52E cells were increased during sepsis, which could be reversed by honokiol. The production of GSH and SOD as in vivo antioxidant was increased after honokiol treatment. The administration of honokiol significantly inhibited TLR2/4/MyD88 signaling pathway in AKI-induced NRK-52E cells. Furthermore, ZnPPIX, the HO-1 inhibitor, weakened honokiol-mediated morphological amelioration, and the reduced level of TNF-, IL-1, and IL-6 in kidneys of rats subjected to CLP. Finally, Honokiol was shown to connect with the Nrf2-Keap1 dimensionally. These findings suggest that honokiol plays its protective role on sepsis-associated AKI against oxidative stress and inflammatory signals.
引用
收藏
页码:826 / 834
页数:9
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