Sophora flavescens , which was first recorded in Shen Nong s Herbal Classic , has the functions of clearing away heat, drying dampness, killing parasites and promoting urination. In its long-term application, traditio...Sophora flavescens , which was first recorded in Shen Nong s Herbal Classic , has the functions of clearing away heat, drying dampness, killing parasites and promoting urination. In its long-term application, traditional Chinese medicine has gradually deepened its understanding of the origin and efficacy of S. flavescens . In order to explore changes in the origin and efficacy of traditional Chinese herb S. flavescens in the history of China and Japan, in this paper, the origin and development of S. flavescens in China and Japan were compared from three aspects: the origin, medicinal efficacy, and processing methods of S. flavescens in China and Japan, hoping to provide clear understanding of the medicinal plant S. flavescens .展开更多
[Objectives]This study was conducted to screen lavandulyl flavonoids with anti-inflammatory activity from Sophora flavescens.[Methods]35 compounds were screened from traditional Chinese medicine S.flavescens using the...[Objectives]This study was conducted to screen lavandulyl flavonoids with anti-inflammatory activity from Sophora flavescens.[Methods]35 compounds were screened from traditional Chinese medicine S.flavescens using the nitric oxide(NO)anti-inflammatory activity model.[Results]Five components,8(xanthohumol),13(kurarinol),27(4-methoxysalicylic acid),28(b-resorcic acid)and 30(b-resorcic acid),exhibited significant anti-inflammatory activity,with IC 50 values of 5.99,4.76,6.96,3.41 and 5.22μM,respectively.Especially,8(xanthohumol)and 13(kurarinol)were typical lavandulyl flavonoids in S.flavescens,which were worth further exploration.Furthermore,UPLC-Q-Exactive and GNPS molecular networking technique were used for rapid analysis of lavandulyl flavonoids from S.flavescens.A total of 15 components were identified.[Conclusions]This work lays a theoretical foundation for further separation and analysis of lavandulyl flavonoids with anti-inflammatory activity from S.flavescens.展开更多
Objective:This study used comprehensive bioinformatics analysis and network pharmacology analysis to investigate the potentially relevant mechanisms of Sophora flavescens against cervical squamous cell carcinoma.Metho...Objective:This study used comprehensive bioinformatics analysis and network pharmacology analysis to investigate the potentially relevant mechanisms of Sophora flavescens against cervical squamous cell carcinoma.Methods:Consistently altered genes involved in cervical squamous cell cancerization were analyzed in the GEO database.The chemical ingredients and target genes of Sophora flavescens were explored using the TCMSP database.We obtained the potential therapeutic targets of Sophora flavescens by intersecting the above genesets and validated them in the GEPIA database.The interaction between Sophora flavescens and target genes was predicted by molecular docking.RT-qPCR was used to verify the changes of target genes in HeLa cells treated with Sophora flavescens.Single-gene GSEA functional analysis were performed to determine the molecular mechanisms.Results:Fifteen genes related to the transformation of cervical squamous cell carcinoma were identified,among which AR and ESR1 were confirmed as targets for kaempferol,wighteone,formononetin,and phaseolinon.These compounds are the active ingredients in Sophora flavescens.Low expressions of AR and ESR1 correlate with a poor prognosis,while Sophora flavescens treatment increases the expression of AR and ESR1 in HeLa.GSEA analysis showed that AR and ESR1 mainly participate in the epithelial-mesenchymal transition in cervical squamous cell carcinoma.Conclusion:Sophora flavescens exert anti-tumor effects by targeting AR and ESR1,which may regulate cancer metastasis.展开更多
A lectin protein(SFL) with molecular weight about 32 kD which markedly agglutinated rabbit and human red blood cells was purified from the roots of Sophora flavescens Ait. This protein, and apparently inhibited the gr...A lectin protein(SFL) with molecular weight about 32 kD which markedly agglutinated rabbit and human red blood cells was purified from the roots of Sophora flavescens Ait. This protein, and apparently inhibited the growth of Fusarium vasinfectum Atk., Gibberella saubinetii (Mont.) Sacc., and Piricularia oryzae Cav. A set of degenerate PCR primer was synthesized according to the N-terminal sequence of the purified protein. The full-length cDNA coding the lectin was cloned by RT-PCR and 5'-RACE and sequenced (GenBank AF285121). The deduced amino acid sequence indicates that a preprotein with 284 amino acid residues is firstly translated and then processed to a mature protein with 254 amino acids. A N-Glycosylation site is the Asn 182 residue.展开更多
Two new lavandulylated flavanones,(2R, 3R)-8-1avandulyl-2'-methoxy-5, 7, 4'-trihydroxyflavanonol (1) and 8-1avandulyl-5,7, 4'-trihydroxyflavonol (2),were isolated from the dry roots of S opharaflavescens.Thei...Two new lavandulylated flavanones,(2R, 3R)-8-1avandulyl-2'-methoxy-5, 7, 4'-trihydroxyflavanonol (1) and 8-1avandulyl-5,7, 4'-trihydroxyflavonol (2),were isolated from the dry roots of S opharaflavescens.Their structures were eiucidated on the basis of spectroscopic data. Compounds 1 and 2 exhibited significant antibacterial activities.展开更多
Sophora flavescens Alt.,a perennial herb of Sophora in Leguminosae family,was widely distributed in the north and south of China.Its root is utilized as a traditional Chinese medicine to clear heat,drain dampness,kill...Sophora flavescens Alt.,a perennial herb of Sophora in Leguminosae family,was widely distributed in the north and south of China.Its root is utilized as a traditional Chinese medicine to clear heat,drain dampness,kill insect and promote urination by virtue of bitter and cold.Its chemical components are complex and diverse,mainly including alkaloids and flavonoids.Modern pharmacological studies have found that prenylflavonoids and quinolicidine alkaloids are the characteristic chemical constituents and the main active ingredients,with anti-inflammatory,anti-tumor,anti-oxidation,and other various biological activities.This study reviewed the chemical constituents of S.flavescens and the pharmacological effects of flavonoids in it in order to provide reference for further development.展开更多
Background:Sophora flavescens,a traditional Chinese herb medicine,has been used to prevent and cure type 2 diabetes mellitus(T2DM)both in folk medicine and medical institutions.Modern pharmacological studies have also...Background:Sophora flavescens,a traditional Chinese herb medicine,has been used to prevent and cure type 2 diabetes mellitus(T2DM)both in folk medicine and medical institutions.Modern pharmacological studies have also demonstrated that the flavonoids obtained from Sophora flavescens ethyl acetate extract(SFE)exhibited potential anti-diabetic activity.Our previous study elucidated that SFE exerts anti-T2DM effects by regulating the host-microbial metabolic axis.In the present study,we further explored the pharmacodynamic effect and the potential targets of the anti-T2DM activity of SFE by integrating network pharmacology and pharmacological evaluations.Methods:The diabetic rat model was created by streptozotocin and oral administration with SFE for 8 weeks.Then,the T2DM-related index was estimated to assess the interventional effect of SFE.Network pharmacology was applied to identify the likely targets and the pathways modulated by SFE components.Furthermore,Western blotting was applied to verify the prediction.Results:Pharmacological evaluation in vivo revealed that SFE could markedly improve the blood glucose,serum insulin secretion,insulin resistance,liver glycogen synthesis,and the liver tissue structure in T2DM rats.Through network pharmacology analysis,101 active compounds of SFE and 114 targets belonging to 128 pathways were identified.The insulin,TNF,IL-6,and PI3K/Akt pathway may be the key targets and pathway.Based on the results of network pharmacology analysis,IRS/PI3K/Akt and IKK/NF-κB/TNF pathways were selected for further validation.Subsequently,experimental results of Western blotting confirmed that SFE may exert anti-T2DM effects by modulating the IRS/PI3K/Akt and IKK/NF-κB/TNF pathways.Conclusion:SFE may protect the T2DM rats by relieving the insulin resistance and inflammation through regulating the IRS/PI3K/Akt and IKK/NF-κB/TNF pathways.The results of the present study would improve the comprehension of the pharmacological basis of SFE against T2DM and provide a theoretical basis for the clinical use of Sophora flavescens.展开更多
Glioma is a common primary intracranial tumor with high mortality and postoperative recurrence.Developing efficient therapies with lower toxicity is urgently needed.Sophora flavescens(SF)is a common Chinese medicine u...Glioma is a common primary intracranial tumor with high mortality and postoperative recurrence.Developing efficient therapies with lower toxicity is urgently needed.Sophora flavescens(SF)is a common Chinese medicine used to treat eczema,wet ulcers and itchy skin.Modern pharmacological studies have showed that SF has anti-glioma effects,but the mechanism of action remains unclear.This study aims to reveal the pharmacological mechanism of SF in treating glioma.The active components and related targets of SF were obtained from TCMSP.Genecard and Online Mendelian Inheritance in Man(OMIM)databases were used to explore the therapeutic targets for glioma.By making Venn diagram,we obtained 132 common targets of compounds and diseases.STRING databases and Cytoscape were used to construct diagrams of Protein-Protein Interaction(PPI)networks.Through the construction of PPI network,potential targets with degree value greater than the median were taken as core targets for further analysis.A total of 66 core targets were screened out.The degree values of TP53,HSP90AA1,MAPK1,and AKT1 were higher,indicating that these genes played important roles in this network.Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)pathway enrichment analyses were used to further discover the mechanism of active components in SF.Through enrichment analysis,it was found that the core targets were mainly enriched in PI3K/AKT signaling pathway,cell senescence related signaling pathway and IL-17 signaling pathway.In order to further explore the binding between active components and selected target,molecular docking was carried out.Finally,SwissADME was used to determine whether the compound could cross the blood-brain barrier.Based on network pharmacology,we speculated that matrine and formononetin in SF might inhibit PI3K/AKT signaling pathway and cellular senescence related signaling pathway by targeting AKT1,TP53,MAPK1 and other key targets.In summary,this study preliminarily explored the target and mode of action of SF in the treatment of glioma,laying the foundation for further research on its mechanism.展开更多
Objective:In order to explore the systematical regulatory mechanism of Kushen(Sophora flavescens,SF)on inflammation and cancer,we analyzed inter-molecular interactions between herbal ingredients of SF and human inflam...Objective:In order to explore the systematical regulatory mechanism of Kushen(Sophora flavescens,SF)on inflammation and cancer,we analyzed inter-molecular interactions between herbal ingredients of SF and human inflammation and cancer through network-pharmacology and molecular docking-based approaches.Methods:Firstly,ingredients and potential targets were obtained from Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform,GeneCards database,Therapeutic Targets Database and Online Mendelian Inheritance in Man database.Then,protein-protein interaction network and medicine-ingredient-target-disease network were established and analyzed via STRING and Cytoscape.Surflex-dock was performed by SybylX-2.0.Finally,functional enrichment and pathway enrichment were achieved by Gene Ontology database and Kyoto Encyclopedia of Genes and Genomes database.Results:The results showed that 113 components of SF and 53 potential targets were related in the study.SF exerts anti-inflammatory and anti-cancer mechanism through key targets located in nucleus,such as JUN,MYC,RELA,NCOA,PPARG which may trigger the NF-κB pathway,the Bcl-2/Bax pathway and other pathways to effect DNA transcriptional activity.Conclusions:The study predicted the mechanism of SF on cancer and inflammation.According to the results,we suggest that the ingredients of SF effect on DNA bingding and transcription in nuclear receptors-like JUN,MYC,RELA,NCOA,PPARG.the receptors trigger several pathways including NF-κB pathway,the Bcl-2/Bax pathway and others.Eventually,it regulats inflammatory factors and cell proliferation,senescence and apoptosis.展开更多
基金Supported by Anhui University of Chinese Medicine(2023LCTH18,2021LCTH04)Fuyang Health Commission(FY2023-007)。
文摘Sophora flavescens , which was first recorded in Shen Nong s Herbal Classic , has the functions of clearing away heat, drying dampness, killing parasites and promoting urination. In its long-term application, traditional Chinese medicine has gradually deepened its understanding of the origin and efficacy of S. flavescens . In order to explore changes in the origin and efficacy of traditional Chinese herb S. flavescens in the history of China and Japan, in this paper, the origin and development of S. flavescens in China and Japan were compared from three aspects: the origin, medicinal efficacy, and processing methods of S. flavescens in China and Japan, hoping to provide clear understanding of the medicinal plant S. flavescens .
基金Supported by Guizhou Provincial Science and Technology(ZK(2022)-362,ZK(2024)-047,[2023]ZK01)The Innovation and Entrepreneurship Training Program for Undergraduates from China[202210660131,202310660082]+2 种基金Science Foundation of Guizhou Education Technology(2022-064)University Engineering Research Center for the Prevention and Treatment of Chronic Diseases by Authentic Medicinal Materials in Guizhou Province([2023]035)Science and Technology Research Project of Guizhou Administration of Traditional Chinese Medicine(QZYY-2024-134).
文摘[Objectives]This study was conducted to screen lavandulyl flavonoids with anti-inflammatory activity from Sophora flavescens.[Methods]35 compounds were screened from traditional Chinese medicine S.flavescens using the nitric oxide(NO)anti-inflammatory activity model.[Results]Five components,8(xanthohumol),13(kurarinol),27(4-methoxysalicylic acid),28(b-resorcic acid)and 30(b-resorcic acid),exhibited significant anti-inflammatory activity,with IC 50 values of 5.99,4.76,6.96,3.41 and 5.22μM,respectively.Especially,8(xanthohumol)and 13(kurarinol)were typical lavandulyl flavonoids in S.flavescens,which were worth further exploration.Furthermore,UPLC-Q-Exactive and GNPS molecular networking technique were used for rapid analysis of lavandulyl flavonoids from S.flavescens.A total of 15 components were identified.[Conclusions]This work lays a theoretical foundation for further separation and analysis of lavandulyl flavonoids with anti-inflammatory activity from S.flavescens.
基金In 2021,Wuxi Medical Innovation Team CXTD2021023,Jiangsu Province maternal and Child Health research key funding project F201915.
文摘Objective:This study used comprehensive bioinformatics analysis and network pharmacology analysis to investigate the potentially relevant mechanisms of Sophora flavescens against cervical squamous cell carcinoma.Methods:Consistently altered genes involved in cervical squamous cell cancerization were analyzed in the GEO database.The chemical ingredients and target genes of Sophora flavescens were explored using the TCMSP database.We obtained the potential therapeutic targets of Sophora flavescens by intersecting the above genesets and validated them in the GEPIA database.The interaction between Sophora flavescens and target genes was predicted by molecular docking.RT-qPCR was used to verify the changes of target genes in HeLa cells treated with Sophora flavescens.Single-gene GSEA functional analysis were performed to determine the molecular mechanisms.Results:Fifteen genes related to the transformation of cervical squamous cell carcinoma were identified,among which AR and ESR1 were confirmed as targets for kaempferol,wighteone,formononetin,and phaseolinon.These compounds are the active ingredients in Sophora flavescens.Low expressions of AR and ESR1 correlate with a poor prognosis,while Sophora flavescens treatment increases the expression of AR and ESR1 in HeLa.GSEA analysis showed that AR and ESR1 mainly participate in the epithelial-mesenchymal transition in cervical squamous cell carcinoma.Conclusion:Sophora flavescens exert anti-tumor effects by targeting AR and ESR1,which may regulate cancer metastasis.
文摘A lectin protein(SFL) with molecular weight about 32 kD which markedly agglutinated rabbit and human red blood cells was purified from the roots of Sophora flavescens Ait. This protein, and apparently inhibited the growth of Fusarium vasinfectum Atk., Gibberella saubinetii (Mont.) Sacc., and Piricularia oryzae Cav. A set of degenerate PCR primer was synthesized according to the N-terminal sequence of the purified protein. The full-length cDNA coding the lectin was cloned by RT-PCR and 5'-RACE and sequenced (GenBank AF285121). The deduced amino acid sequence indicates that a preprotein with 284 amino acid residues is firstly translated and then processed to a mature protein with 254 amino acids. A N-Glycosylation site is the Asn 182 residue.
文摘Two new lavandulylated flavanones,(2R, 3R)-8-1avandulyl-2'-methoxy-5, 7, 4'-trihydroxyflavanonol (1) and 8-1avandulyl-5,7, 4'-trihydroxyflavonol (2),were isolated from the dry roots of S opharaflavescens.Their structures were eiucidated on the basis of spectroscopic data. Compounds 1 and 2 exhibited significant antibacterial activities.
基金supported by the National Key Research and Development Program of China(2017YFC1701200)Leading talents of science and technology innovation in Liaoning Province(XLYC1902101)Liaoning Provincial Doctoral Research Start-up Fund(2019-BS-224).
文摘Sophora flavescens Alt.,a perennial herb of Sophora in Leguminosae family,was widely distributed in the north and south of China.Its root is utilized as a traditional Chinese medicine to clear heat,drain dampness,kill insect and promote urination by virtue of bitter and cold.Its chemical components are complex and diverse,mainly including alkaloids and flavonoids.Modern pharmacological studies have found that prenylflavonoids and quinolicidine alkaloids are the characteristic chemical constituents and the main active ingredients,with anti-inflammatory,anti-tumor,anti-oxidation,and other various biological activities.This study reviewed the chemical constituents of S.flavescens and the pharmacological effects of flavonoids in it in order to provide reference for further development.
基金supported by the National Natural Science Foundation of China(No.NSFC 81872980,NSFC 81673556,NSFC 82073982)the Guangdong Basic and Applied Basic Research Special Fund,Guangdong Natural Science Fund(No.2017A030313753).
文摘Background:Sophora flavescens,a traditional Chinese herb medicine,has been used to prevent and cure type 2 diabetes mellitus(T2DM)both in folk medicine and medical institutions.Modern pharmacological studies have also demonstrated that the flavonoids obtained from Sophora flavescens ethyl acetate extract(SFE)exhibited potential anti-diabetic activity.Our previous study elucidated that SFE exerts anti-T2DM effects by regulating the host-microbial metabolic axis.In the present study,we further explored the pharmacodynamic effect and the potential targets of the anti-T2DM activity of SFE by integrating network pharmacology and pharmacological evaluations.Methods:The diabetic rat model was created by streptozotocin and oral administration with SFE for 8 weeks.Then,the T2DM-related index was estimated to assess the interventional effect of SFE.Network pharmacology was applied to identify the likely targets and the pathways modulated by SFE components.Furthermore,Western blotting was applied to verify the prediction.Results:Pharmacological evaluation in vivo revealed that SFE could markedly improve the blood glucose,serum insulin secretion,insulin resistance,liver glycogen synthesis,and the liver tissue structure in T2DM rats.Through network pharmacology analysis,101 active compounds of SFE and 114 targets belonging to 128 pathways were identified.The insulin,TNF,IL-6,and PI3K/Akt pathway may be the key targets and pathway.Based on the results of network pharmacology analysis,IRS/PI3K/Akt and IKK/NF-κB/TNF pathways were selected for further validation.Subsequently,experimental results of Western blotting confirmed that SFE may exert anti-T2DM effects by modulating the IRS/PI3K/Akt and IKK/NF-κB/TNF pathways.Conclusion:SFE may protect the T2DM rats by relieving the insulin resistance and inflammation through regulating the IRS/PI3K/Akt and IKK/NF-κB/TNF pathways.The results of the present study would improve the comprehension of the pharmacological basis of SFE against T2DM and provide a theoretical basis for the clinical use of Sophora flavescens.
基金National College Student Innovation and Entrepreneurship Training Program(202110163030).
文摘Glioma is a common primary intracranial tumor with high mortality and postoperative recurrence.Developing efficient therapies with lower toxicity is urgently needed.Sophora flavescens(SF)is a common Chinese medicine used to treat eczema,wet ulcers and itchy skin.Modern pharmacological studies have showed that SF has anti-glioma effects,but the mechanism of action remains unclear.This study aims to reveal the pharmacological mechanism of SF in treating glioma.The active components and related targets of SF were obtained from TCMSP.Genecard and Online Mendelian Inheritance in Man(OMIM)databases were used to explore the therapeutic targets for glioma.By making Venn diagram,we obtained 132 common targets of compounds and diseases.STRING databases and Cytoscape were used to construct diagrams of Protein-Protein Interaction(PPI)networks.Through the construction of PPI network,potential targets with degree value greater than the median were taken as core targets for further analysis.A total of 66 core targets were screened out.The degree values of TP53,HSP90AA1,MAPK1,and AKT1 were higher,indicating that these genes played important roles in this network.Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)pathway enrichment analyses were used to further discover the mechanism of active components in SF.Through enrichment analysis,it was found that the core targets were mainly enriched in PI3K/AKT signaling pathway,cell senescence related signaling pathway and IL-17 signaling pathway.In order to further explore the binding between active components and selected target,molecular docking was carried out.Finally,SwissADME was used to determine whether the compound could cross the blood-brain barrier.Based on network pharmacology,we speculated that matrine and formononetin in SF might inhibit PI3K/AKT signaling pathway and cellular senescence related signaling pathway by targeting AKT1,TP53,MAPK1 and other key targets.In summary,this study preliminarily explored the target and mode of action of SF in the treatment of glioma,laying the foundation for further research on its mechanism.
基金This work was supported by the National Natural Science Foundation of China(81402801,81973544,81803790)the Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme(GDHVPS2018)the Young Elite Scientists Sponsorship Program by CACM(2019-QNRC2-C14).
文摘Objective:In order to explore the systematical regulatory mechanism of Kushen(Sophora flavescens,SF)on inflammation and cancer,we analyzed inter-molecular interactions between herbal ingredients of SF and human inflammation and cancer through network-pharmacology and molecular docking-based approaches.Methods:Firstly,ingredients and potential targets were obtained from Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform,GeneCards database,Therapeutic Targets Database and Online Mendelian Inheritance in Man database.Then,protein-protein interaction network and medicine-ingredient-target-disease network were established and analyzed via STRING and Cytoscape.Surflex-dock was performed by SybylX-2.0.Finally,functional enrichment and pathway enrichment were achieved by Gene Ontology database and Kyoto Encyclopedia of Genes and Genomes database.Results:The results showed that 113 components of SF and 53 potential targets were related in the study.SF exerts anti-inflammatory and anti-cancer mechanism through key targets located in nucleus,such as JUN,MYC,RELA,NCOA,PPARG which may trigger the NF-κB pathway,the Bcl-2/Bax pathway and other pathways to effect DNA transcriptional activity.Conclusions:The study predicted the mechanism of SF on cancer and inflammation.According to the results,we suggest that the ingredients of SF effect on DNA bingding and transcription in nuclear receptors-like JUN,MYC,RELA,NCOA,PPARG.the receptors trigger several pathways including NF-κB pathway,the Bcl-2/Bax pathway and others.Eventually,it regulats inflammatory factors and cell proliferation,senescence and apoptosis.