Inhibition of interleukin-12 and interferon-γ production in immune cells by tanshinones from Salvia miltiorrhiza

Immunopharmacology Pub Date : 2000-09-01 Epub Date: 2000-09-14 DOI:10.1016/S0162-3109(00)00256-3
Bok Yun Kang , Su Wol Chung , Seung Hyun Kim , Shi Yong Ryu , Tae Sung Kim
{"title":"Inhibition of interleukin-12 and interferon-γ production in immune cells by tanshinones from Salvia miltiorrhiza","authors":"Bok Yun Kang ,&nbsp;Su Wol Chung ,&nbsp;Seung Hyun Kim ,&nbsp;Shi Yong Ryu ,&nbsp;Tae Sung Kim","doi":"10.1016/S0162-3109(00)00256-3","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Pharmacological control of interleukin-12 (IL-12) and interferon-gamma (IFN-γ) production may be a key therapeutic strategy for modulating immunological diseases dominated by Th1-derived cytokine responses. In this study, we investigated the effects of three different </span>tanshinone pigments from </span><span><em>Salvia miltiorrhiza</em></span><span><span><span> (tanshinone I, dihydrotanshinone, and cryptotanshinone) on IL-12 production in mouse macrophages and on IFN-γ production in lymph node cells. All tested tanshinones significantly inhibited IL-12 production in </span>lipopolysaccharide (LPS)-activated macrophages and also IFN-γ production in </span>keyhole limpet hemocyanin<span> (KLH)-primed lymph node cells in a dose-dependent manner. Dihydrotanshinone was more effective than tanshinone I<span> or cryptotanshinone. Tanshinones significantly inhibited the expression of IL-12 p40 gene at the mRNA level. Furthermore, tanshinones potently inhibited the promoter activation of IL-12 p40 gene and nuclear factor (NF)-κB binding to the κB site, suggesting that tanshinones may negatively regulate IL-12 production at the transcription level. These results may explain some known biological activities of tanshinones including their anti-inflammatory effect, and suggest a possible use of tanshinones in the treatment of immunological diseases dominated by Th1-derived cytokine responses.</span></span></span></p></div>","PeriodicalId":13327,"journal":{"name":"Immunopharmacology","volume":"49 3","pages":"Pages 355-361"},"PeriodicalIF":0.0000,"publicationDate":"2000-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0162-3109(00)00256-3","citationCount":"135","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0162310900002563","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2000/9/14 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 135

Abstract

Pharmacological control of interleukin-12 (IL-12) and interferon-gamma (IFN-γ) production may be a key therapeutic strategy for modulating immunological diseases dominated by Th1-derived cytokine responses. In this study, we investigated the effects of three different tanshinone pigments from Salvia miltiorrhiza (tanshinone I, dihydrotanshinone, and cryptotanshinone) on IL-12 production in mouse macrophages and on IFN-γ production in lymph node cells. All tested tanshinones significantly inhibited IL-12 production in lipopolysaccharide (LPS)-activated macrophages and also IFN-γ production in keyhole limpet hemocyanin (KLH)-primed lymph node cells in a dose-dependent manner. Dihydrotanshinone was more effective than tanshinone I or cryptotanshinone. Tanshinones significantly inhibited the expression of IL-12 p40 gene at the mRNA level. Furthermore, tanshinones potently inhibited the promoter activation of IL-12 p40 gene and nuclear factor (NF)-κB binding to the κB site, suggesting that tanshinones may negatively regulate IL-12 production at the transcription level. These results may explain some known biological activities of tanshinones including their anti-inflammatory effect, and suggest a possible use of tanshinones in the treatment of immunological diseases dominated by Th1-derived cytokine responses.

丹参酮对免疫细胞白细胞介素-12和干扰素-γ产生的抑制作用
药理控制白介素-12 (IL-12)和干扰素-γ (IFN-γ)的产生可能是调节由th1来源的细胞因子反应主导的免疫性疾病的关键治疗策略。在这项研究中,我们研究了丹参酮三种不同的丹参酮色素(丹参酮I、二氢丹参酮和隐丹参酮)对小鼠巨噬细胞IL-12产生和淋巴结细胞IFN-γ产生的影响。所有测试的丹参酮均以剂量依赖性的方式显著抑制脂多糖(LPS)激活的巨噬细胞中IL-12的产生,以及锁孔帽贝血青素(KLH)引发的淋巴结细胞中IFN-γ的产生。二氢丹参酮比丹参酮I和隐丹参酮更有效。丹参酮在mRNA水平上显著抑制il - 12p40基因的表达。此外,丹参酮能有效抑制il - 12p40基因启动子的激活和NF -κB与κB位点的结合,提示丹参酮可能在转录水平负向调节IL-12的产生。这些结果可能解释了丹参酮的一些已知生物活性,包括其抗炎作用,并提示丹参酮可能用于治疗以th1来源的细胞因子反应为主的免疫性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书