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白藜芦醇通过激活 Nrf2 信号通路缓解无乳链球菌感染引起的氧化应激。

Resveratrol alleviates oxidative stress caused by Streptococcus uberis infection via activating the Nrf2 signaling pathway.

机构信息

MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.

MOE Joint International Research Laboratory of Animal Health and Food Safety, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.

出版信息

Int Immunopharmacol. 2020 Dec;89(Pt A):107076. doi: 10.1016/j.intimp.2020.107076. Epub 2020 Oct 9.

Abstract

Due to its antioxidant properties, resveratrol may relieve the cellular oxidative injury induced by Streptococcus uberis (S. uberis) infection. However, the underlying molecular mechanisms remain unknown. Herein, we used S. uberis to challenge C57BL/6 mice or a mouse mammary epithelial cell line (EpH-Ev), and the regulatory molecular mechanism of resveratrol on hosts' oxidative injury were investigated. The results showed that gavage of resveratrol alleviate the inflammatory responses and oxidative injury of mammary gland tissues induced by S. uberis infection via activating Nrf2 signaling pathways. To further understand the molecular mechanism, inhibitor of Nrf2 (ML385) and siRNA targeting p62 were used in mammary epithelial cells. The findings indicated that resveratrol mediates Keap1 degradation by activating p62, induces the expression of Nrf2 and its downstream antioxidant signaling pathways, and ameliorates oxidative damage during S. uberis infection. Collectively, these outcomes suggested that resveratrol can function as an activator of the p62-Keap1/Nrf2 signaling pathway to improve oxidative injury caused by S. uberis in mammary glands as well as in EpH-Ev cells. Therefore, resveratrol may be useful to prevent and control S. uberis-induced bovine mastitis by relieving oxidative stress.

摘要

由于其抗氧化特性,白藜芦醇可能减轻无乳链球菌(S. uberis)感染引起的细胞氧化损伤。然而,其潜在的分子机制尚不清楚。在此,我们使用 S. uberis 来挑战 C57BL/6 小鼠或小鼠乳腺上皮细胞系(EpH-Ev),并研究了白藜芦醇对宿主氧化损伤的调节分子机制。结果表明,灌胃白藜芦醇通过激活 Nrf2 信号通路,缓解 S. uberis 感染引起的乳腺组织的炎症反应和氧化损伤。为了进一步了解分子机制,我们在乳腺上皮细胞中使用了 Nrf2 抑制剂(ML385)和靶向 p62 的 siRNA。研究结果表明,白藜芦醇通过激活 p62 介导 Keap1 的降解,诱导 Nrf2 及其下游抗氧化信号通路的表达,并在 S. uberis 感染期间减轻氧化损伤。综上所述,这些结果表明,白藜芦醇可以作为 p62-Keap1/Nrf2 信号通路的激活剂,改善 S. uberis 引起的乳腺以及 EpH-Ev 细胞的氧化损伤。因此,白藜芦醇可能通过缓解氧化应激来预防和控制由 S. uberis 引起的奶牛乳腺炎。

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