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诱导血红素加氧酶-1 减轻脂多糖诱导的小鼠乳腺炎中 NLRP3 炎性体的激活。

Induction of heme oxygenas-1 attenuates NLRP3 inflammasome activation in lipopolysaccharide-induced mastitis in mice.

机构信息

Department of Clinical Veterinary Medicine, College of Veterinary Medicine, Jilin University, Changchun, Jilin Province 130062, China.

College of Animal Sciences and Technology, Guangxi University, Nanning, Guangxi Province 530005, China.

出版信息

Int Immunopharmacol. 2017 Nov;52:185-190. doi: 10.1016/j.intimp.2017.09.007. Epub 2017 Sep 20.

Abstract

Mastitis is one of most prevalent production disease in dairy herds worldwide, and is responsible for enormous economic losses. Heme oxygenase-1 (HO-1) is a cytoprotective enzyme, which is involved in the response to oxidative stress and inflammatory response. The purpose of this study was to detect the protective effect of HO-1 on LPS-induced mastitis in mice. BALB/c mice were pretreated with hemin (HO-1 inducer) and zinc protoporphyrin (ZnPP; HO-1 inhibitor) at 2h before LPS stimulation. The results showed that the mammary gland damage, production of inflammatory cytokines IL-1β, and MPO activity in mammary gland tissues were significantly reduced after pretreated with hemin compared with the group of LPS stimulation only. However, ZnPP reversed the effects of hemin. Furthermore, we found that the levels of ROS and NLRP3 inflammasome were increased after LPS stimulation. The increases were inhibited by hemin and the inhibition of hemin on ROS production and NLRP3 inflammasome activation were blocked by ZnPP. In addition, the results showed that hemin reduced the expression of thioredoxin-interacting protein (TXNIP) induced by LPS, and ZnPP attenuated these changes. In conclusion, the results suggested that overproduction of HO-1 may inhibit the activation of NLRP3 inflammasome and the expression of TXNIP. Induction of HO-1 may be served as a promising method against mastitis induced by LPS.

摘要

乳腺炎是全球奶牛群中最常见的生产疾病之一,造成了巨大的经济损失。血红素加氧酶-1(HO-1)是一种细胞保护酶,参与氧化应激和炎症反应的反应。本研究旨在检测 HO-1 对 LPS 诱导的乳腺炎小鼠的保护作用。BALB/c 小鼠在 LPS 刺激前 2h 用血红素(HO-1 诱导剂)和锌原卟啉(ZnPP;HO-1 抑制剂)预处理。结果表明,与仅 LPS 刺激组相比,血红素预处理后乳腺损伤、炎症细胞因子 IL-1β的产生和乳腺组织中的 MPO 活性显著降低。然而,ZnPP 逆转了血红素的作用。此外,我们发现 LPS 刺激后 ROS 和 NLRP3 炎性体的水平增加。血红素抑制了这些增加,而 ZnPP 阻断了血红素对 ROS 产生和 NLRP3 炎性体激活的抑制作用。此外,结果表明血红素降低了 LPS 诱导的硫氧还蛋白相互作用蛋白(TXNIP)的表达,而 ZnPP 减弱了这些变化。总之,这些结果表明,HO-1 的过度产生可能抑制 NLRP3 炎性体的激活和 TXNIP 的表达。诱导 HO-1 可能成为对抗 LPS 诱导乳腺炎的一种有前途的方法。

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