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桦木酸通过 Nrf2 信号通路减轻氧化应激和炎症反应保护 T-2 毒素诱导的小鼠肾损伤。

Betulinic acid protects against renal damage by attenuation of oxidative stress and inflammation via Nrf2 signaling pathway in T-2 toxin-induced mice.

机构信息

Hunan Engineering Research Center of Livestock and Poultry Health Care, College of Veterinary Medicine, Hunan Agricultural University, Changsha City 410128, China.

Hunan Engineering Research Center of Livestock and Poultry Health Care, College of Veterinary Medicine, Hunan Agricultural University, Changsha City 410128, China.

出版信息

Int Immunopharmacol. 2021 Dec;101(Pt B):108210. doi: 10.1016/j.intimp.2021.108210. Epub 2021 Oct 7.

Abstract

Betulinic acid (BA) is a pentacyclic triterpenoid compound with potential antioxidant and anti-inflammatory effects. In this study, T-2 toxin was injected intraperitoneally in mice to establish kidney damage model and to evaluate the protective effects of BA and further reveal the molecular mechanism. BA pretreatment inhibited the T-2 toxin-stimulated increase in serum Crea, but showed no significant effect on serum Urea. BA pretreatment alleviated excessive glomerular hemorrhage and inflammatory cell infiltration in kidneys caused by T-2 toxin. Moreover, pretreatment with BA mitigated T-2 toxin-induced renal oxidative damage by up-regulating the activities of SOD and CAT, and the content of GSH, while down-regulating the accumulation of ROS and MDA. Meanwhile, BA pretreatment markedly attenuated T-2 toxin-induced renal inflammatory response by decreasing the mRNA expression of IL-1β, TNF-α and IL-10, and increasing IL-6 mRNA expression. Furthermore, mechanism research found that pretreatment with BA could activate Nrf2 signaling pathway. It was suggested that BA ameliorated the oxidative stress and inflammatory response of T-2 toxin-triggered renal damage by activating the Nrf2 signaling pathway.

摘要

白桦脂酸(BA)是一种五环三萜类化合物,具有潜在的抗氧化和抗炎作用。在本研究中,通过腹腔注射 T-2 毒素建立小鼠肾脏损伤模型,评估 BA 的保护作用,并进一步揭示其分子机制。BA 预处理抑制了 T-2 毒素刺激引起的血清 Crea 升高,但对血清 Urea 无明显影响。BA 预处理减轻了 T-2 毒素引起的肾小球出血和炎症细胞浸润。此外,BA 通过上调 SOD 和 CAT 的活性以及 GSH 的含量,同时下调 ROS 和 MDA 的积累,减轻了 T-2 毒素诱导的肾脏氧化损伤。同时,BA 预处理通过降低 IL-1β、TNF-α 和 IL-10 的 mRNA 表达,增加 IL-6 mRNA 表达,显著减轻 T-2 毒素诱导的肾脏炎症反应。此外,机制研究发现,BA 预处理可以激活 Nrf2 信号通路。提示 BA 通过激活 Nrf2 信号通路改善 T-2 毒素诱导的肾脏损伤的氧化应激和炎症反应。

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