科研動態(tài)

為揭示黃芪防控豬繁殖與呼吸綜合征（PRRS）的物質(zhì)基礎及靶點信息，采用網(wǎng)絡藥理學方法，從中藥系統(tǒng)藥理學數(shù)據(jù)庫與分析平臺（TCMSP）篩選黃芪的潛在活性成分、作用靶點，同時從比較毒理基因組學數(shù)據(jù)庫（CTD）收集PRRS相關宿主基因，最后構建“活性成分-關鍵靶點”網(wǎng)絡、蛋白互作網(wǎng)絡，并進行GO功能和KEGG通路富集分析。結果顯示，從黃芪篩選出的17個潛在活性成分中，有14個潛在活性成分共計65個基因靶點與PRRS相關宿主基因交叉，其中槲皮素、山奈酚、刺芒柄花素、異鼠李素等潛在活性成分可能對治療PRRS有重要作用，TNF、IL8、TP53、IL6、IL10、IL1B、JUN等45個蛋白靶點間存在相互作用。此外，黃芪治療PRRS的作用機制可能涉及細胞外間隙和胞漿等組分，并可能與炎癥反應、細胞凋亡、T細胞受體信號通路等生物過程相關。本研究為臨床應用黃芪及其提取物治療PRRS奠定了理論基礎。

Analysis on the Material Basis and Drug Targets of Astragalus Membranaceus in Prevention and Control of PRRS Based on Network Pharmacology

In order to reveal the information concerning the material basis and drug targets of astragalus membranaceus acting on porcine reproductive and respiratory syndrome（PRRS），the potential active components and drug targets related to astragalus membranaceus were screened through traditional chinese medicine systems pharmacology database and analysis platform（TCMSP）by the network pharmacology. Meanwhile，the host genes related to PRRS were gathered from comparative toxicogenomics database（CTD）to construct the“active components-key targets”network and protein-protein interaction（PPI）network，and to analyze the GO functions and KEGG pathway enrichment. The results showed that 14 out of 17 potential active components including 65 gene targets crossed with the host genes related to PRRS，especially，quercetin，kaempferol，formononetin，isorhamnetin and other potential active components played an important role in fighting against PRRS，and 45 targets could interact with each other，including TNF，IL8，TP53，IL6，IL10，IL1B and JUN. In addition，the mechanism of astragalus membranaceus in fighting against PRRS might involve extracellular space and cytoplasmic components，and might be related to biological processes such as inflammatory response，apoptosis，and T cell receptor signaling pathway. Therefore，a theoretical foundation was laid for clinical application of astragalus membranaceus and its extract in fighting against PRRS.

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