In Silico Exploration of the Molecular Mechanism of Cassane Diterpenoids on Anti-inflammatory and Immunomodulatory Activity

被引:14
|
作者
Wang, Ying [1 ,2 ]
Hu, Baichun [1 ,3 ]
Peng, Yusheng [2 ]
Xiong, Xin [1 ,2 ]
Jing, Wenhua [1 ,2 ]
Wang, Jian [1 ,3 ]
Gao, Huiyuan [1 ,2 ]
机构
[1] Shenyang Pharmaceut Univ, Minist Educ, Key Lab Struct Based Drug Design & Discovery, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Shenyang 110016, Peoples R China
[3] Shenyang Pharmaceut Univ, Sch Pharmaceut Engn, Shenyang 110016, Peoples R China
基金
中国国家自然科学基金;
关键词
TOLL-LIKE RECEPTORS; CAESALPINIA-MINAX; RHEUMATOID-ARTHRITIS; TARGET PREDICTION; INFLAMMATION; SEEDS; FURANODITERPENES; NETWORKS; DISEASES; TNF;
D O I
10.1021/acs.jcim.8b00862
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cassane diterpenoids (CAs), recognized as main constituents of many medical plants of the genus Caesalpinia, exhibit diverse bioactivities, including anti-inflammatory and immunomodulatory activity, and also showed a therapeutic effect on rheumatoid arthritis (RA) according to previous work, including ours. In this study, 102 CA compounds were selected to explore the possible molecular mechanism of this class of natural products on anti-inflammatory and immunomodulatory activity using RA as a disease model through a series of in silico methods: chemical-similarity-based target prediction, molecular docking, and molecular dynamics (MD) simulation. As a consequence, four signaling pathways (TCR signaling pathway, TLR signaling pathway, VEGF signaling pathway, and osteoclast differentiation pathway) by which CAs exert their effect on inflammation and immunomodulation were identified. Furthermore, the binding modes of CAs complexing with several crucial targets, which were picked out by credible docking results and took part in these signaling pathways, were explored by MD simulations. This is the first time that the molecular mechanism of the anti-RA activity of natural CAs has been investigated with in silico methods, and these findings might explain the activity of CAs on anti-inflammation and immunomodulation, which could supply a valuable reference for drug design research on CAs.
引用
收藏
页码:2309 / 2323
页数:15
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