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通过整合网络药理学和体外实验洞察一种中药注射剂的分子机制。

Insight into the molecular mechanism of a herbal injection by integrating network pharmacology and in vitro.

作者信息

Ma Yi-Min, Zhang Xin-Zhuang, Su Zhen-Zhen, Li Na, Cao Liang, Ding Gang, Wang Zhen-Zhong, Xiao Wei

机构信息

State Key Laboratory of New-tech for Chinese Medicine Pharmaceutical Process, Kanion Pharmaceutical Corporation, NO. 58, Haichang Road Lianyungang, People's Republic of China.

State Key Laboratory of New-tech for Chinese Medicine Pharmaceutical Process, Kanion Pharmaceutical Corporation, NO. 58, Haichang Road Lianyungang, People's Republic of China.

出版信息

J Ethnopharmacol. 2015 Sep 15;173:91-9. doi: 10.1016/j.jep.2015.07.016. Epub 2015 Jul 17.

Abstract

Chinese medical herbs could treat complex diseases through the synergistic effect of multi-components, multi-targets and multi-channels. However, it was difficult to systematically investigate the pharmacological mechanisms of action due to the complex chemical composition and the lack of an effective research approach. Fortunately, network pharmacology as an integrated approach was proposed to systematically investigate and explain the underlying molecular mechanisms of Chinese medical herbs. Reduning injection (RDN) is one of the herbal injections for treatment of upper respiratory tract infections (URTIs). Previous studies revealed the molecular mechanism of RDN on URTIs through network pharmacology. In this work, the mechanism of RDN was verified by enzyme linked immunosorbent assay (ELISA), Western Blot, immunofluorescence assay and electrophoretic mobility shift assay (EMSA) in lipopolysaccharide (LPS)-induced RAW264.7 cells and enzyme assay. RDN dose-dependently suppressed the production of nitric oxide (NO), prostaglandin E2 (PGE2), interleukin-6 (IL-6) and interleukin-1β (IL-1β), and reduced the protein expression of inducible NO synthetase (iNOS) and cyclooxygenase-2 (COX-2), which could be related to its suppression on the phosphorylations of mitogen-activated protein (MAP) kinases, including extracellular signal-regulated kinase (ERK), c-jun NH2-terminal kinase(JNK) and p38, as well as the activation and translocation of nuclear factor-κB (NF-κB). In addition, the activity of RDN on PGE2 was also partly attributed to the inhibition of COX-2 enzyme. Therefore, it can be concluded that RDN inhibited the production of inflammatory mediators and the macrophage activation to treat URTIs via down-regulating the activation of MAPK and NF-κB signaling pathways, which might pave a way to illustrate the molecular mechanism of herbs.

摘要

中药可通过多成分、多靶点、多途径的协同作用治疗复杂疾病。然而,由于其化学成分复杂且缺乏有效的研究方法,难以系统地研究其药理作用机制。幸运的是,网络药理学作为一种综合方法被提出来系统地研究和解释中药的潜在分子机制。热毒宁注射液(RDN)是治疗上呼吸道感染(URTIs)的中药注射剂之一。以往的研究通过网络药理学揭示了RDN治疗URTIs的分子机制。在本研究中,通过酶联免疫吸附测定(ELISA)、蛋白质印迹法、免疫荧光测定法和电泳迁移率变动分析(EMSA),在脂多糖(LPS)诱导的RAW264.7细胞中以及酶活性测定中验证了RDN的作用机制。RDN剂量依赖性地抑制一氧化氮(NO)、前列腺素E2(PGE2)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β)的产生,并降低诱导型NO合酶(iNOS)和环氧化酶-2(COX-2)的蛋白表达,这可能与其对丝裂原活化蛋白(MAP)激酶磷酸化的抑制有关,包括细胞外信号调节激酶(ERK)、c-jun氨基末端激酶(JNK)和p38,以及核因子-κB(NF-κB)的激活和转位。此外,RDN对PGE2的作用活性也部分归因于对COX-2酶的抑制。因此,可以得出结论,RDN通过下调MAPK和NF-κB信号通路的激活来抑制炎症介质的产生和巨噬细胞的活化,从而治疗URTIs,这可能为阐明中药的分子机制铺平道路。

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