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通络消痛胶囊可能通过抑制 p38MAPK 通路介导的炎症反应发挥作用:体内和体外验证。

Tougu Xiaotong capsules may inhibit p38 MAPK pathway-mediated inflammation: In vivo and in vitro verification.

机构信息

Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, 350122, PR China; Fujian Key Laboratory of Integrative Medicine on Geriatrics, Fuzhou, 350122, PR China.

SIPO Patent Examination (Beijing) Center, Beijing, 100160, PR China.

出版信息

J Ethnopharmacol. 2020 Mar 1;249:112390. doi: 10.1016/j.jep.2019.112390. Epub 2019 Nov 21.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Tougu Xiaotong capsules (TXC) are an herbal compound commonly used to treat osteoarthritis (OA) in China.

AIM OF THE STUDY

We attempted to verify TXC's therapeutic effects and mechanisms related to the p38 mitogen-activated protein kinase (MAPK) pathway in vivo and in vitro.

MATERIALS AND METHODS

TXC's therapeutic effects were assessed by observing cartilage degeneration and inflammatory factors in a modified Hulth's model (in vivo) and a lipopolysaccharides (LPS)-exposed cellular model (in vitro). The expression of biomarkers related to p38 MAPK pathway-mediated inflammation was also investigated.

RESULTS

TXC treatment reversed cartilage degeneration related biomarkers (ADAMTS 4, ADAMTS 5, Col I, Col V, MMP 3, MMP 9, and MMP 13) and inflammation factors (IL-1β, TNF-α, and IL-6) in both the animal and cellular OA models. Expression of p-p38 MAPK was downregulated following TXC administration, and changes to microRNAs in the cellular models were recovered. These results indicated that the p38 MAPK pathway-related mechanism may involve therapeutic effects of TXC.

CONCLUSIONS

This study verified TXC's efficacy to treat OA in vivo and in vitro and suggests that p38 MAPK pathway-related mechanisms may be involved in TXC's therapeutic effects.

摘要

民族药理学相关性

通络消痛胶囊(TXC)是一种常用于治疗中国骨关节炎(OA)的草药复方。

研究目的

我们试图在体内和体外验证 TXC 与 p38 丝裂原活化蛋白激酶(MAPK)通路相关的治疗效果和机制。

材料和方法

通过观察改良 Hulth 模型(体内)和脂多糖(LPS)暴露的细胞模型(体外)中软骨退变和炎症因子,评估 TXC 的治疗效果。还研究了与 p38 MAPK 通路介导的炎症相关的生物标志物的表达。

结果

TXC 治疗逆转了动物和细胞 OA 模型中与软骨退变相关的生物标志物(ADAMTS4、ADAMTS5、Col I、Col V、MMP3、MMP9 和 MMP13)和炎症因子(IL-1β、TNF-α 和 IL-6)。TXC 给药后 p-p38 MAPK 的表达下调,细胞模型中的 microRNAs 发生变化。这些结果表明,p38 MAPK 通路相关机制可能涉及 TXC 的治疗效果。

结论

本研究验证了 TXC 在体内和体外治疗 OA 的疗效,并表明 p38 MAPK 通路相关机制可能参与了 TXC 的治疗效果。

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