AN INSIGHT OF FDA-APPROVED DRUGS FOR THE MANAGEMENT OF AGING-RELATED DISORDER - A IN SILICO STUDY

被引:0
|
作者
Yang, Tong-Jie [1 ]
Wan, Quan-Qing [1 ]
Wen, Peng-Peng [2 ]
机构
[1] Zhejiang Chinese Med Univ, Intervertebral Disc Dept, Affiliated Hosp 3, Hangzhou 310005, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Tradit Chinese Med Dept, Affiliated Hosp 1, Wenzhou 325000, Zhejiang, Peoples R China
来源
ACTA POLONIAE PHARMACEUTICA | 2022年 / 79卷 / 04期
关键词
molecular interaction; MD simulation; skeletal muscle; aging; drugs; SKELETAL-MUSCLE ATROPHY; MYOSTATIN;
D O I
10.32383/appdr/152839
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Skeletal muscle (SM) is the most complex and plastic tissue of the human body. Movement, postural support, breathing, and thermogenesis are important functions of SM. Muscle mass reduction is a common side effect of human aging. The growth factor myostatin (MSTN) appears to play a key role in aging-related muscle function decreases. Targeting MSTN might help people live longer by preventing SM alterations associated with aging. Therefore, in the present study, FDA-approved drugs were screened against MSTN to find the best drugs against MSTN for the management of the aging disease. In this re-gard, screening, docking, and molecular dynamics simulation were used. Based on structure-based vir-tual screening and free energy of bind, we select the top five drugs mentioned in this article. Two drugs were analyzed in-depth namely, Sonidegib and Revefenacin showing free energy of binding-10.95 and-12.03 kcal/mol respectively with MSTN. Further, these complex was forwarded for molecular dynamics simulation to check the structural stability during 100ns, which was found to be more stable. As a con-cluding remark, Sonidegib and Revefenacin can be considered for further designing of new drugs against MSTN for the treatment of aging-related disorders.
引用
收藏
页码:557 / 565
页数:9
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