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远志酸 D 通过激活 LPS 刺激的原代牛乳腺上皮细胞中的 LXRα 来抑制 LPS 诱导的炎症反应。

Platycodin D suppressed LPS-induced inflammatory response by activating LXRα in LPS-stimulated primary bovine mammary epithelial cells.

机构信息

College of Veterinary Medicine, Jilin University, Changchun, Jilin 130062, People's Republic of China.

College of Animal Science and Technology, Jilin Agricultural University, Changchun, People's Republic of China.

出版信息

Eur J Pharmacol. 2017 Nov 5;814:138-143. doi: 10.1016/j.ejphar.2017.07.037. Epub 2017 Jul 20.

DOI:10.1016/j.ejphar.2017.07.037
PMID:28736281
Abstract

Platycodin D (PLD), a triterpenoid saponin derived from the root of Platycodon grandiflorum, has been reported to possess anti-inflammatory activity. However, the protective effect of PLD on mastitis has not been reported. In the present study, we aim to investigate the anti-inflammatory feature of PLD on the primary bovine mammary epithelial cells (bMEC) challenged with LPS. The cell viability of bMEC was measured by MTT assay. The quantitative real-time polymerase chain reaction (qRT-PCR) was conducted to detect the gene expression of pro-inflammatory cytokines and western blotting was carried out to measure the expression of LXRα and NF-κB. The results showed that PLD inhibited LPS-induced TNF-α, IL-1β, and IL-6 expression in LPS-stimulated bEMC. Meanwhile, PLD suppressed LPS-induced NF-κB activation. Furthermore, PLD was found to up-regulate the expression of LXRα. The inhibition of PLD on NF-κB activation and inflammatory cytokines production were reversed by GGPP, the inhibitor of LXRα. In conclusion, our results suggested that PLD inhibited LPS-induced inflammatory response in bMEC by activating LXRα. PLD may be a potential therapeutic drug for mastitis.

摘要

远志酸(PLD)是一种来源于桔梗的三萜皂苷,具有抗炎活性。然而,PLD 对乳腺炎的保护作用尚未见报道。在本研究中,我们旨在研究 PLD 对脂多糖刺激的原代牛乳腺上皮细胞(bMEC)的抗炎作用。通过 MTT 法测定 bMEC 的细胞活力。采用定量实时聚合酶链反应(qRT-PCR)检测促炎细胞因子的基因表达,采用 Western blot 检测 LXRα 和 NF-κB 的表达。结果表明,PLD 抑制 LPS 刺激的 bEMC 中 TNF-α、IL-1β 和 IL-6 的表达。同时,PLD 抑制 LPS 诱导的 NF-κB 激活。此外,还发现 PLD 可上调 LXRα 的表达。LXRα 的抑制剂 GGPP 逆转了 PLD 对 NF-κB 激活和炎症细胞因子产生的抑制作用。综上所述,我们的研究结果表明,PLD 通过激活 LXRα 抑制 bMEC 中 LPS 诱导的炎症反应。PLD 可能是乳腺炎的一种潜在治疗药物。

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