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白杨素通过干扰脂多糖诱导的乳腺炎中 Toll 样受体 4/核因子 kappa B 信号通路来减轻炎症反应。

Alpinetin attenuates inflammatory responses by interfering toll-like receptor 4/nuclear factor kappa B signaling pathway in lipopolysaccharide-induced mastitis in mice.

机构信息

Department of General Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou 510280, Guangdong Province, China.

出版信息

Int Immunopharmacol. 2013 Sep;17(1):26-32. doi: 10.1016/j.intimp.2013.04.030. Epub 2013 May 10.

DOI:10.1016/j.intimp.2013.04.030
PMID:23669335
Abstract

Alpinetin, a novel plant flavonoid derived from Alpinia katsumadai Hayata, has been reported to exhibit anti-inflammatory properties. However, the effect of alpinetin on mastitis has not been investigated. The aim of this study was to investigate the protective effect of alpinetin against lipopolysaccharide (LPS)-induced mastitis and to clarify the possible mechanism. In the present study, primary mouse mammary epithelial cells and an LPS-induced mouse mastitis model were used to investigate the effect of alpinetin on mastitis and the possible mechanism. In vivo, we observed that alpinetin significantly attenuated the infiltration of neutrophilic granulocytes, and the activation of myeloperoxidase; down-regulated the level of pro-inflammatory cytokines, including TNF-α, IL-1β and IL-6; inhibited the phosphorylation of IκB-α, NF-κB p65 and the expression of TLR4, caused by LPS. In vitro, we also observed that alpinetin inhibited the expression of TLR4 and the production of TNF-α, IL-1β and IL-6 in LPS-stimulated primary mouse mammary epithelial cells. However, alpinetin could not inhibit the production of IL-1β and IL-6 in TNF-α-stimulated primary mouse mammary epithelial cells. In conclusion, our results suggest that the anti-inflammatory effects of alpinetin against LPS-induced mastitis may be due to its ability to inhibit TLR4-mediated NF-κB signaling pathways. Alpinetin may be a promising potential therapeutic reagent for mastitis treatment.

摘要

山姜素,一种从益智中提取的新型植物类黄酮,已被报道具有抗炎作用。然而,山姜素对乳腺炎的作用尚未被研究过。本研究旨在探讨山姜素对脂多糖(LPS)诱导的乳腺炎的保护作用,并阐明可能的机制。在本研究中,使用原代小鼠乳腺上皮细胞和 LPS 诱导的小鼠乳腺炎模型来研究山姜素对乳腺炎的作用及其可能的机制。在体内,我们观察到山姜素显著减轻了嗜中性粒细胞的浸润和髓过氧化物酶的激活;下调了 LPS 诱导的 TNF-α、IL-1β 和 IL-6 等促炎细胞因子的水平;抑制了 LPS 诱导的 IκB-α、NF-κB p65 和 TLR4 的磷酸化。在体外,我们还观察到山姜素抑制了 LPS 刺激的原代小鼠乳腺上皮细胞中 TLR4 的表达和 TNF-α、IL-1β 和 IL-6 的产生。然而,山姜素不能抑制 TNF-α刺激的原代小鼠乳腺上皮细胞中 IL-1β 和 IL-6 的产生。综上所述,我们的结果表明,山姜素对 LPS 诱导的乳腺炎的抗炎作用可能与其抑制 TLR4 介导的 NF-κB 信号通路的能力有关。山姜素可能是一种有前途的乳腺炎治疗潜在治疗试剂。

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