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人参皂苷Rg5、Rz1和Rk1的抗炎作用:抑制肿瘤坏死因子-α诱导的核因子-κB、环氧化酶-2和诱导型一氧化氮合酶的转录表达。

Anti-inflammatory effects of ginsenosides Rg5 , Rz1 , and Rk1 : inhibition of TNF-α-induced NF-κB, COX-2, and iNOS transcriptional expression.

作者信息

Lee Sang Myung

机构信息

Korea Ginseng Corp. Central Research Institute, Daejon, 305-805, Republic of Korea.

出版信息

Phytother Res. 2014 Dec;28(12):1893-6. doi: 10.1002/ptr.5203. Epub 2014 Jul 21.

Abstract

In the course of this experiment on the anti-inflammatory effect of ginsenosides, protopanaxdiol ginsenosides have shown inhibition activities in inflammatory responses: NF-κB, COX-2, and iNOS were induced by TNF-α. The responses of this experiment were evaluated by NF-κB-luciferase assay and RT-PCR experiment of COX-2 and iNOS genes. The NF-κB expressions were inhibited by ginsenosides Rd, Rg5 , Rz1 , and Rk1 in a dose-dependent manner. The IC50 values were 3.47, 0.61, 0.63, and 0.75 μM, respectively. Particularly, ginsenosides Rg5 , Rz1 , and Rk1 as converted ginsenosides from primary protopanaxdiol ginsenosidess significantly inhibited COX-2 and iNOS gene expression. These inhibition levels were similar to sulfasalazine as reference material.

摘要

在本次关于人参皂苷抗炎作用的实验过程中,原人参二醇型人参皂苷在炎症反应中表现出抑制活性:NF-κB、COX-2和iNOS由TNF-α诱导产生。本实验的反应通过NF-κB荧光素酶测定以及COX-2和iNOS基因的RT-PCR实验进行评估。人参皂苷Rd、Rg5、Rz1和Rk1以剂量依赖性方式抑制NF-κB表达。IC50值分别为3.47、0.61、0.63和0.75μM。特别地,作为由原人参二醇型人参皂苷转化而来的人参皂苷Rg5、Rz1和Rk1显著抑制COX-2和iNOS基因表达。这些抑制水平与作为参考物质的柳氮磺胺吡啶相似。

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