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In silico approach to explore the mechanism of bioactive ingredients from Belamcandae rhizoma against COVID-19
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作者 Zi-Wei Hu xun song +2 位作者 Jin-Hong Lin Xiao-Jian Li Zhen-Dan He 《Asian Toxicology Tesearch》 2020年第4期130-142,共13页
Background:To date,the epidemic of COVID-19,which result from newly discovered virus named SARS-CoV-2,has spawned a heavy economic loss and continued to claim tens of thousands of lives.It’s urgent now that develop a... Background:To date,the epidemic of COVID-19,which result from newly discovered virus named SARS-CoV-2,has spawned a heavy economic loss and continued to claim tens of thousands of lives.It’s urgent now that develop an ideal agent for suppressing the lifecycle of coronavirus while alleviate collateral severe inflammatory response.Belamcandae rhizoma,an herb which documented in various Chinese traditional medicine prescription,was reported to have effects of antiviral,anti-inflammatory and antipyretic.However,the relationship and related molecular mechanism between Belamcandae rhizoma and coronavirus are still unknown.Methods:Here,we achieved 14 kernel compounds from Belamcandae rhizoma and 261 validated“novel coronavirus pneumonia”correlative gene targets using a series of databases.Results:Subsequently,the pharmacology network and protein-protein interaction cluster,which constructed by the 20 overlapped genes targets between Belamcandae rhizoma and COVID-19,demonstrated that IL10,PTGS2,IL6,MAPK1,MAPK14 and CASP3 were as key targets in the treatment.The potential molecular mechanism involved IL-17,JAK-STAT and MAPK signaling pathways gained from gene enrichment analysis attract our attention.Molecular docking with 3CLpro of SARS-CoV-2 further suggested that luteolin and dinatin were the most bioactive compounds of Belamcandae rhizoma,among which luteolin connected with the maximum number of gene targets in above pharmacology network.Conclusion:Taken together,these findings provide deep insight into the putative therapeutic targets and underlying mechanism for COVID-19 treatment. 展开更多
关键词 Belamcandae rhizoma COVID-19 Network pharmacology MECHANISM Molecular docking
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Modulation of antiviral cytokine production and lung protection against influenza virus by the glycosides from Ligustrum purpurascens
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作者 Chen-Yang Li Xiao-Jun Zhong +7 位作者 Xiao-Peng Hu Qin-Chang Zhu Hai-Tao Xiao Peng Zhai Da-Hong Yao Muhammad Shahid Riaz Zhen-Dan He xun song 《Asian Toxicology Tesearch》 2021年第1期23-31,共9页
Ligustrum purpurascens has been used as a traditional herb for over 2,000 years in China.This study was design to investigate the modulation of antiviral cytokines and reduction in lung inflammation of virus-infected ... Ligustrum purpurascens has been used as a traditional herb for over 2,000 years in China.This study was design to investigate the modulation of antiviral cytokines and reduction in lung inflammation of virus-infected mice by the glycosides isolated from Ligustrum purpurascens.Methods:Ligustrum purpurascens glycosides(LPG)were isolated from the leaves of Ligustrum purpurascens.Proliferation of spleen lymphocytes were investigated after LPG treatment.The in vitro and in vivo cytokine modulation of LPG was studied.Furthermore,the anti-inflammatory and antiviral activities of LPG,with the potential to reduce inflammatory lung disorders,were investigated by influenza A virus infected mice.Results:LPG could significantly promote the proliferation,and also could stimulate the production of IFN-γby spleen lymphocytes in a dose-dependent manner.IFN-γexpression level was increased significantly compared to the control and presented a dose-dependent manner in vitro.Furthermore,LPG inhibit the expression of TNF-αand IL-10,which return to normal level in the cyclophosphamide-induced mice model in vivo.Besides,the histopathological analysis indicated LPG reduced acute lung injury in mice infected with influenza virus.Conclusion:This study suggested that LPG could increase the exression of IFN-γ,immunoregulation and decrease lung inflammation of virus-infected mice. 展开更多
关键词 Ligustrum purpurascens GLYCOSIDES CYTOKINES IMMUNOREGULATION ANTIVIRAL
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拓扑切换的集群系统分布式分组时变编队跟踪控制 被引量:11
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作者 田磊 王蒙一 +3 位作者 赵启伦 王晓东 宋勋 任章 《中国科学:信息科学》 CSCD 北大核心 2020年第3期408-423,共16页
分布式编队控制是集群智能控制重要的基础性研究课题之一.拒止环境和多任务需求对编队控制提出了新的挑战.本文研究了高阶线性集群系统在拓扑切换情况下的分布式分组时变编队跟踪控制问题.在本文所提出的集群系统模型架构中,智能体被分... 分布式编队控制是集群智能控制重要的基础性研究课题之一.拒止环境和多任务需求对编队控制提出了新的挑战.本文研究了高阶线性集群系统在拓扑切换情况下的分布式分组时变编队跟踪控制问题.在本文所提出的集群系统模型架构中,智能体被分为3类:虚拟领导者、分组领导者和跟随者.虚拟领导者为整个集群系统宏观运动提供参考轨迹或者跟踪指令.分组领导者一方面跟踪虚拟领导者所提供的轨迹或指令;另一方面通过与其他分组领导者之间的相互协作实现各分组之间的协同配合.跟随者实现对各自分组领导者的时变编队跟踪.在拓扑切换和外部扰动同时存在的情况下,基于智能体之间的局部有限邻居节点之间的相对信息反馈和滑模控制理论构造了分布式分组时变编队跟踪控制协议,并给出了控制协议中未知参数的求解算法,进而利用李雅普诺夫(Lyapunov)理论证明了集群系统在拓扑切换和外部扰动同时存在情况下的闭环稳定性.最后,数值仿真结果验证了本文提出的控制方法能够实现集群系统分组时变编队跟踪控制,并可应用在以无人机集群为代表的实际物理模型中. 展开更多
关键词 拒止环境 高阶线性集群系统 分组时变编队跟踪 拓扑切换 外部扰动
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