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陈皮在 LPS 刺激的 RAW264.7 巨噬细胞中的抗炎作用。

Anti-inflammatory effect of Citrus Unshiu peel in LPS-stimulated RAW 264.7 macrophage cells.

机构信息

Center for Herbal Medicine Improvement Research, Korea Institute of Oriental Medicine, Yuseong, Daejeon, Republic of Korea.

出版信息

Am J Chin Med. 2012;40(3):611-29. doi: 10.1142/S0192415X12500462.

Abstract

Citrus Unshiu peel (CUP) has been traditionally used in East Asia as a drug for the treatment of vomiting and dyspepsia. However, its effects on inflammation remain unknown. In this study, we investigated the effects of CUP on the production of pro-inflammatory mediators in lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. The research focused on determining whether CUP could inhibit the expression of inducible nitric oxide synthase (iNOS), cyclooxygenase (COX)-2 and the activation of nuclear factor (NF)-κB, mitogen-activated protein kinases (MAPKs), as well as the secretion of nitric oxide (NO), prostaglandin (PG) E(2), tumor necrosis factor-α (TNF-α) and interleukin (IL)-6 in LPS-stimulated RAW 264.7 cells. We found that CUP represses LPS-induced iNOS and COX-2 gene expression as well as NO, PGE(2), TNF-α and IL-6 production. Additionally, CUP inhibited the LPS-induced phosphorylation of extracellular signal-regulated kinase (ERK), p38, and c-Jun NH(2)-terminal kinase (JNK) MAPK, and suppressed IκBα degradation and nuclear translocation of NF-κB. Collectively, our results indicate that CUP inhibits the production of various inflammatory mediators via blockade of MAPK phosphorylation pursuant to the inhibition of IκBα degradation and the nuclear translocation of NF-κB. These findings are the first to clarify the mechanism underlying the anti-inflammatory effect exerted by CUP in RAW 264.7 macrophage cells stimulated by inflammatory agents.

摘要

柑橘果皮(CUP)在东亚传统上被用作治疗呕吐和消化不良的药物。然而,其对炎症的影响尚不清楚。在这项研究中,我们研究了 CUP 对脂多糖(LPS)刺激的 RAW 264.7 细胞中促炎介质产生的影响。研究重点是确定 CUP 是否可以抑制诱导型一氧化氮合酶(iNOS)、环氧化酶(COX)-2 的表达和核因子(NF)-κB、丝裂原激活蛋白激酶(MAPKs)的激活,以及抑制 LPS 刺激的 RAW 264.7 细胞中一氧化氮(NO)、前列腺素(PG)E(2)、肿瘤坏死因子-α(TNF-α)和白细胞介素(IL)-6 的分泌。我们发现 CUP 抑制 LPS 诱导的 iNOS 和 COX-2 基因表达以及 NO、PGE(2)、TNF-α和 IL-6 的产生。此外,CUP 抑制 LPS 诱导的细胞外信号调节激酶(ERK)、p38 和 c-Jun NH(2)-末端激酶(JNK)MAPK 的磷酸化,并抑制 IκBα降解和 NF-κB 的核转位。总之,我们的结果表明,CUP 通过抑制 IκBα 降解和 NF-κB 的核转位来抑制 MAPK 磷酸化,从而抑制各种炎症介质的产生。这些发现首次阐明了 CUP 在炎症介质刺激的 RAW 264.7 巨噬细胞中发挥抗炎作用的机制。

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