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从香附子根茎中分离得到的富吉地酸通过使RAW264.7巨噬细胞中的AP-1失活来抑制脂多糖诱导的诱导型一氧化氮合酶、环氧化酶-2、肿瘤坏死因子-α和白细胞介素-6的表达。

Fulgidic Acid Isolated from the Rhizomes of Cyperus rotundus Suppresses LPS-Induced iNOS, COX-2, TNF-α, and IL-6 Expression by AP-1 Inactivation in RAW264.7 Macrophages.

作者信息

Shin Ji-Sun, Hong Yujin, Lee Hwi-Ho, Ryu Byeol, Cho Young-Wuk, Kim Nam-Jung, Jang Dae Sik, Lee Kyung-Tae

机构信息

Department of Pharmaceutical Biochemistry, Kyung Hee University.

出版信息

Biol Pharm Bull. 2015;38(7):1081-6. doi: 10.1248/bpb.b15-00186.

Abstract

To identify bioactive natural products possessing anti-inflammatory activity, the potential of fulgidic acid from the rhizomes of Cyperus rotundus and the underlying mechanisms involved in its anti-inflammatory activity were evaluated in this study. Fulgidic acid reduced the production of nitric oxide (NO), prostaglandin E2 (PGE2), tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) in lipopolysaccharide (LPS)-induced RAW264.7 macrophages. Consistent with these findings, fulgidic acid suppressed the LPS-induced expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at the protein level, as well as iNOS, COX-2, TNF-α, and IL-6 at mRNA levels. Fulgidic acid suppressed the LPS-induced transcriptional activity of activator protein-1 (AP-1) as well as the phosphorylation of c-Fos and c-Jun. On the other hand, fulgidic acid did not show any effect on LPS-induced nuclear factor κB (NF-κB) activity. Taken together, these results suggest that the anti-inflammatory effect of fulgidic acid is associated with the suppression of iNOS, COX-2, TNF-α, and IL-6 expression through down-regulating AP-1 activation in LPS-induced RAW264.7 macrophages.

摘要

为了鉴定具有抗炎活性的生物活性天然产物,本研究评估了香附根茎中富吉地酸的潜力及其抗炎活性的潜在机制。富吉地酸可降低脂多糖(LPS)诱导的RAW264.7巨噬细胞中一氧化氮(NO)、前列腺素E2(PGE2)、肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的产生。与这些发现一致,富吉地酸在蛋白质水平上抑制了LPS诱导的诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达,以及在mRNA水平上抑制了iNOS、COX-2、TNF-α和IL-6的表达。富吉地酸抑制了LPS诱导的活化蛋白-1(AP-1)的转录活性以及c-Fos和c-Jun的磷酸化。另一方面,富吉地酸对LPS诱导的核因子κB(NF-κB)活性没有任何影响。综上所述,这些结果表明,富吉地酸的抗炎作用与通过下调LPS诱导的RAW264.7巨噬细胞中AP-1的活化来抑制iNOS、COX-2、TNF-α和IL-6的表达有关。

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