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积雪草酸通过抑制 LPS 诱导的 RAW264.7 巨噬细胞细胞中 NF-κB 通路发挥抗炎作用。

Anti-inflammatory effects of madecassic acid via the suppression of NF-kappaB pathway in LPS-induced RAW 264.7 macrophage cells.

机构信息

College of Pharmacy, Kyung-Hee University, Hoegi-Dong, Seoul, Republic of Korea.

出版信息

Planta Med. 2010 Feb;76(3):251-7. doi: 10.1055/s-0029-1186142. Epub 2009 Sep 11.

Abstract

We have investigated the anti-inflammatory effects of madecassic acid and madecassoside isolated from Centella asiatica (Umbelliferae) on lipopolysaccharide (LPS)-stimulated RAW 264.7 murine macrophage cells. Both madecassic acid and madecassoside inhibited the production of nitric oxide (NO), prostaglandin E(2) (PGE(2)), tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1beta), and IL-6. However, madecassic acid more potently suppressed these inflammatory mediators than did madecassoside. Consistent with these observations, madecassic acid inhibited the LPS-induced expression of iNOS and COX-2 at the protein level and of iNOS, COX-2, TNF-alpha, IL-1beta, and IL-6 at the mRNA level in RAW 264.7 macrophage cells, as determined by Western blotting and RT-PCR, respectively. Furthermore, madecassic acid suppressed the LPS-induced activation of nuclear factor-kappaB (NF-kappaB), and this was associated with the abrogation of inhibitory kappa B-alpha (IkappaB-alpha) degradation and with the subsequent blocking of p65 protein translocation to the nucleus. These results suggest that the anti-inflammatory properties of madecassic acid are caused by iNOS, COX-2, TNF-alpha, IL-1beta, and IL-6 inhibition via the downregulation of NF-kappaB activation in RAW 264.7 macrophage cells.

摘要

我们研究了从积雪草(伞形科)中分离得到的积雪草酸和积雪草苷对脂多糖(LPS)刺激的 RAW 264.7 鼠巨噬细胞的抗炎作用。积雪草酸和积雪草苷均可抑制一氧化氮(NO)、前列腺素 E2(PGE2)、肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的产生。然而,积雪草酸比积雪草苷更能抑制这些炎症介质的产生。与这些观察结果一致,积雪草酸通过 Western blot 和 RT-PCR 分别抑制 LPS 诱导的 RAW 264.7 巨噬细胞中 iNOS 和 COX-2 的蛋白表达以及 iNOS、COX-2、TNF-α、IL-1β和 IL-6 的 mRNA 表达。此外,积雪草酸抑制 LPS 诱导的核因子-κB(NF-κB)激活,这与抑制κB-α(IkappaB-α)降解和随后阻止 p65 蛋白向核内转位有关。这些结果表明,积雪草酸的抗炎特性是通过下调 RAW 264.7 巨噬细胞中 NF-κB 的激活,从而抑制 iNOS、COX-2、TNF-α、IL-1β和 IL-6 的表达而产生的。

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