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和厚朴酚通过抑制氧化应激和炎症减轻脓毒症相关性急性肾损伤。

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

机构信息

Clinical Laboratory of Integrative Medicine, the First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China.

Department of Nephrology, The First Affiliated Hospital of Dalian Medical University, No.222 Zhongshan Road, Dalian, 116011, Liaoning, China.

出版信息

Inflammation. 2019 Jun;42(3):826-834. doi: 10.1007/s10753-018-0937-x.

Abstract

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-α, IL-1β, 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.

摘要

急性肾损伤(AKI)是脓毒症最常见的并发症之一,在很大程度上导致脓毒症的高死亡率。厚朴酚是一种来自传统中药厚朴的天然多酚,具有抗炎和抗氧化活性。在这里,分析了厚朴酚诱导改善脓毒症相关 AKI 的潜在机制。检查了氧化应激分子和 TLRs 介导的炎症途径的表达模式,以确定用脓毒症大鼠血清孵育的 NRK-52E 细胞对厚朴酚的反应。在脓毒症期间,NRK-52E 细胞中的 iNOS、NO 和髓过氧化物酶水平增加,厚朴酚可逆转这些增加。厚朴酚处理后,体内抗氧化剂 GSH 和 SOD 的产生增加。厚朴酚给药显著抑制了 AKI 诱导的 NRK-52E 细胞中 TLR2/4/MyD88 信号通路。此外,HO-1 抑制剂 ZnPPIX 减弱了厚朴酚介导的形态改善,以及 CLP 大鼠肾脏中 TNF-α、IL-1β 和 IL-6 的水平降低。最后,表明厚朴酚与 Nrf2-Keap1 维度相连。这些发现表明,厚朴酚通过抗氧化应激和炎症信号对脓毒症相关 AKI 发挥保护作用。

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