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  1. Article: Paeoniflorin-free subfraction of Paeonia lactiflora Pall. shows the potential of anti-hepatic fibrosis: an integrated analysis of network pharmacology and experimental validation

    Zhang, Qian / Wu, Yuzhuo / Ge, Maoxu / Xia, Guiyang / Xia, Huan / Wang, Lingyan / Wei, Xiaohong / He, Hongwei / Lin, Sheng

    Journal of ethnopharmacology. 2022 Dec. 05, v. 299

    2022  

    Abstract: Hepatic fibrosis is a major consequence of liver disease. Radix Paeoniae Rubra (RPR), the dry root of Paeonia lactiflora Pall., has a long history of clinical application in traditional Chinese medicine (TCM) for the treatment of liver diseases. The ... ...

    Abstract Hepatic fibrosis is a major consequence of liver disease. Radix Paeoniae Rubra (RPR), the dry root of Paeonia lactiflora Pall., has a long history of clinical application in traditional Chinese medicine (TCM) for the treatment of liver diseases. The researches of RPR active ingredients are mainly focused on paeoniflorin. However, the functional roles of other ingredients have not been clarified sufficiently in the treatment of hepatic fibrosis with RPR. This study was to figure out the anti-hepatic fibrosis potential and mechanisms of CS-4, one of the paeoniflorin-free subfraction of RPR. With the guide of bioassay, CS-4, a subfraction of RPR showed in vitro inhibition of hepatic stellate cell activation, was obtained using multiple chromatographic techniques. Its ingredients were determined by UPLC-Q-TOF-MS/MS. Then, the target profiles of ingredients were obtained from the HERB database, and the disease targets were collected from the DisGeNET database. Through the network pharmacology method, a protein-protein interaction network of CS-4 against hepatic fibrosis was established to analyze and excavate the potential therapeutic targets. Combined with the KEGG analysis, a series of signaling pathways were obtained, thereby validated by western blot analysis. The paeoniflorin-free subfraction of RPR, CS-4, was obtained and showed the most potential anti-fibrotic effect in vitro. A total of 20 main ingredients were identified from CS-4 and considered as its active ingredients. From HERB and DisGeNET databases, 1460 potential targets of CS-4 and 1180 disease targets were obtained, respectively. The overlapped 79 targets were considered to exert the potential anti-fibrosis effect of CS-4, such as JAK2, MYC, SMAD3, and IFNG. The gene enrichment analysis revealed that classical TGF-β/Smad signaling pathway and nonclassical TGF-β/PI3K-AKT signaling pathway may be two of the main mechanisms of CS-4 against hepatic fibrosis, which supported by western blot analysis. In this study, a paeoniflorin-free subfraction with potential anti-hepatic fibrosis activity in vitro, CS-4, was obtained from RPR. Its multiple ingredients, multiple targets, and multiple mechanisms against hepatic fibrosis were explained by network pharmacology and verified by western blot analysis to further support the clinical applications of RPR.
    Keywords Oriental traditional medicine ; Paeonia lactiflora ; Western blotting ; bioassays ; chromatography ; databases ; fibrosis ; genes ; liver ; liver cirrhosis ; pharmacology ; protein-protein interactions ; therapeutics
    Language English
    Dates of publication 2022-1205
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2022.115678
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Paeoniflorin-free subfraction of Paeonia lactiflora Pall. shows the potential of anti-hepatic fibrosis: an integrated analysis of network pharmacology and experimental validation.

    Zhang, Qian / Wu, Yuzhuo / Ge, Maoxu / Xia, Guiyang / Xia, Huan / Wang, Lingyan / Wei, Xiaohong / He, Hongwei / Lin, Sheng

    Journal of ethnopharmacology

    2022  Volume 299, Page(s) 115678

    Abstract: Ethnopharmacological relevance: Hepatic fibrosis is a major consequence of liver disease. Radix Paeoniae Rubra (RPR), the dry root of Paeonia lactiflora Pall., has a long history of clinical application in traditional Chinese medicine (TCM) for the ... ...

    Abstract Ethnopharmacological relevance: Hepatic fibrosis is a major consequence of liver disease. Radix Paeoniae Rubra (RPR), the dry root of Paeonia lactiflora Pall., has a long history of clinical application in traditional Chinese medicine (TCM) for the treatment of liver diseases. The researches of RPR active ingredients are mainly focused on paeoniflorin. However, the functional roles of other ingredients have not been clarified sufficiently in the treatment of hepatic fibrosis with RPR.
    Aim of the study: This study was to figure out the anti-hepatic fibrosis potential and mechanisms of CS-4, one of the paeoniflorin-free subfraction of RPR.
    Materials and methods: With the guide of bioassay, CS-4, a subfraction of RPR showed in vitro inhibition of hepatic stellate cell activation, was obtained using multiple chromatographic techniques. Its ingredients were determined by UPLC-Q-TOF-MS/MS. Then, the target profiles of ingredients were obtained from the HERB database, and the disease targets were collected from the DisGeNET database. Through the network pharmacology method, a protein-protein interaction network of CS-4 against hepatic fibrosis was established to analyze and excavate the potential therapeutic targets. Combined with the KEGG analysis, a series of signaling pathways were obtained, thereby validated by western blot analysis.
    Results: The paeoniflorin-free subfraction of RPR, CS-4, was obtained and showed the most potential anti-fibrotic effect in vitro. A total of 20 main ingredients were identified from CS-4 and considered as its active ingredients. From HERB and DisGeNET databases, 1460 potential targets of CS-4 and 1180 disease targets were obtained, respectively. The overlapped 79 targets were considered to exert the potential anti-fibrosis effect of CS-4, such as JAK2, MYC, SMAD3, and IFNG. The gene enrichment analysis revealed that classical TGF-β/Smad signaling pathway and nonclassical TGF-β/PI3K-AKT signaling pathway may be two of the main mechanisms of CS-4 against hepatic fibrosis, which supported by western blot analysis.
    Conclusion: In this study, a paeoniflorin-free subfraction with potential anti-hepatic fibrosis activity in vitro, CS-4, was obtained from RPR. Its multiple ingredients, multiple targets, and multiple mechanisms against hepatic fibrosis were explained by network pharmacology and verified by western blot analysis to further support the clinical applications of RPR.
    MeSH term(s) Drugs, Chinese Herbal/chemistry ; Drugs, Chinese Herbal/pharmacology ; Drugs, Chinese Herbal/therapeutic use ; Glucosides ; Humans ; Liver Cirrhosis/drug therapy ; Monoterpenes ; Network Pharmacology ; Paeonia/chemistry ; Phosphatidylinositol 3-Kinases ; Proto-Oncogene Proteins c-akt ; Tandem Mass Spectrometry/methods ; Transforming Growth Factor beta
    Chemical Substances Drugs, Chinese Herbal ; Glucosides ; Monoterpenes ; Transforming Growth Factor beta ; peoniflorin (21AIQ4EV64) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1)
    Language English
    Publishing date 2022-09-01
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2022.115678
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Discovery of 9 O -Substituted Palmatine Derivatives as a New Class of Anti-COL1A1 Agents Via Repressing TGF-β1/Smads and JAK1/STAT3 Pathways

    Tianyun Fan / Maoxu Ge / Zhihao Guo / Hongwei He / Na Zhang / Yinghong Li / Danqing Song

    Molecules, Vol 25, Iss 4, p

    2020  Volume 773

    Abstract: Twenty 9 O -substituted palmatine derivatives were prepared and tested for their biological effect against collagen α1 (I) (COL1A1) promotor in human hepatic stellate LX-2 cells. The structure−activity relationship (SAR) indicated that the introduction ... ...

    Abstract Twenty 9 O -substituted palmatine derivatives were prepared and tested for their biological effect against collagen α1 (I) (COL1A1) promotor in human hepatic stellate LX-2 cells. The structure−activity relationship (SAR) indicated that the introduction of a benzyl motif on the 9 O atom was favorable for activity. Among them, compound 6c provided the highest inhibitory effect against COL1A1 with an IC 50 value of 3.98 μM, and it also dose-dependently inhibited the expression of fibrogenic COL1A1, α-soomth muscle actin (α-SMA), matrix metalloprotein 2 (MMP2) in both mRNA and protein levels, indicating extensive inhibitory activity against fibrogenesis. A further primary mechanism study indicated that it might repress the hepatic fibrogenesis via inhibiting both canonical transforming growth factor-beta 1 (TGF-β1)/Smads and non-canonical janus-activated kinase 1 (JAK1)/singal transducer and activator of transcription 3 (STAT3) signaling pathways. Additionally, 6c owned a high safety profile with the LD 50 value of over 1000 mg·kg −1 in mice. These results identified palmatine derivatives as a novel class of anti-fibrogenic agents, and provided powerful information for further structure optimization.
    Keywords hepatic fibrosis ; palmatine ; structure−activity relationship ; col1a1 ; tgf-β1/smads pathway ; jak1/stat3 pathway ; Organic chemistry ; QD241-441
    Subject code 500
    Language English
    Publishing date 2020-02-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Discovery of 9O-Substituted Palmatine Derivatives as a New Class of anti-COL1A1 Agents via Repressing TGF-β1/Smads and JAK1/STAT3 Pathways.

    Fan, Tianyun / Ge, Maoxu / Guo, Zhihao / He, Hongwei / Zhang, Na / Li, Yinghong / Song, Danqing

    Molecules (Basel, Switzerland)

    2020  Volume 25, Issue 4

    Abstract: Twenty 9O-substituted palmatine derivatives were prepared and tested for their biological effect against collagen α1 (I) (COL1A1) promotor in human hepatic stellate LX-2 cells. The structure-activity relationship (SAR) indicated that the introduction of ... ...

    Abstract Twenty 9O-substituted palmatine derivatives were prepared and tested for their biological effect against collagen α1 (I) (COL1A1) promotor in human hepatic stellate LX-2 cells. The structure-activity relationship (SAR) indicated that the introduction of a benzyl motif on the 9O atom was favorable for activity. Among them, compound 6c provided the highest inhibitory effect against COL1A1 with an IC
    MeSH term(s) Berberine Alkaloids/chemistry ; Berberine Alkaloids/pharmacology ; Collagen Type I/antagonists & inhibitors ; Collagen Type I/genetics ; Collagen Type I/metabolism ; Dose-Response Relationship, Drug ; Gene Expression ; Hepatic Stellate Cells/drug effects ; Hepatic Stellate Cells/metabolism ; Humans ; Janus Kinase 1/metabolism ; Models, Biological ; Molecular Structure ; STAT3 Transcription Factor/metabolism ; Signal Transduction/drug effects ; Smad Proteins/metabolism ; Structure-Activity Relationship ; Transforming Growth Factor beta1/metabolism
    Chemical Substances Berberine Alkaloids ; Collagen Type I ; STAT3 Transcription Factor ; STAT3 protein, human ; Smad Proteins ; Transforming Growth Factor beta1 ; collagen type I, alpha 1 chain ; JAK1 protein, human (EC 2.7.10.2) ; Janus Kinase 1 (EC 2.7.10.2) ; palmatine (G50C034217)
    Language English
    Publishing date 2020-02-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules25040773
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Inflammasome Is Activated in the Liver of Cholestatic Patients and Aggravates Hepatic Injury in Bile Duct-Ligated Mouse.

    Cai, Shi-Ying / Ge, Maoxu / Mennone, Albert / Hoque, Rafaz / Ouyang, Xinshou / Boyer, James L

    Cellular and molecular gastroenterology and hepatology

    2019  Volume 9, Issue 4, Page(s) 679–688

    Abstract: Background & aims: Inflammation plays an important role in the pathogenesis of cholestatic liver injury, but it is unclear whether the inflammasome is involved and is the objective of this study.: Methods: Gene expression was analyzed in the livers ... ...

    Abstract Background & aims: Inflammation plays an important role in the pathogenesis of cholestatic liver injury, but it is unclear whether the inflammasome is involved and is the objective of this study.
    Methods: Gene expression was analyzed in the livers of patients with primary biliary cholangitis (n = 15) and primary sclerosing cholangitis (n = 15). Bile duct ligation (BDL) or sham operation was performed in wild-type (WT) and Caspase-1
    Results: Caspase-1, NLRP1, NLRP3 and IL-1β were significantly increased in the livers of cholestatic patients when compared to healthy control subjects (n = 9). Significantly higher levels of plasma IL-1β (826 vs 345 pg/ml), ALT (674 vs 482 U/L) and ALP (900 vs 622 U/L) were seen in WT BDL mice compared to Casp1
    Conclusions: The inflammasome exacerbates cholestatic liver injury, but bile acids do not directly activate the inflammasome.
    MeSH term(s) Animals ; Bile Ducts/surgery ; Caspase 1/genetics ; Cells, Cultured ; Cholangitis/complications ; Cholangitis/immunology ; Cholangitis/pathology ; Cholangitis, Sclerosing ; Cholestasis/immunology ; Cholestasis/pathology ; Disease Models, Animal ; Hepatocytes ; Humans ; Inflammasomes/genetics ; Inflammasomes/immunology ; Ligation ; Liver/immunology ; Liver/pathology ; Liver Failure, Acute/immunology ; Liver Failure, Acute/pathology ; Macrophages ; Mice ; Mice, Knockout ; Primary Cell Culture
    Chemical Substances Inflammasomes ; Casp1 protein, mouse (EC 3.4.22.36) ; Caspase 1 (EC 3.4.22.36)
    Keywords covid19
    Language English
    Publishing date 2019-12-27
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ISSN 2352-345X
    ISSN (online) 2352-345X
    DOI 10.1016/j.jcmgh.2019.12.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Tripartite motif-containing 25 facilitates immunosuppression and inhibits apoptosis of glioma via activating NF-κB.

    Ge, Mao-Xu / Shi, Yi-Kang / Liu, Dong

    Experimental biology and medicine (Maywood, N.J.)

    2022  Volume 247, Issue 17, Page(s) 1529–1541

    Abstract: As a crucial tumor type of the central nervous system, gliomas are characterized by a dismal prognosis. Tripartite motif-containing 25 (TRIM25), an essential E3 ubiquitin ligase, participates in various biological processes. This study sought to ... ...

    Abstract As a crucial tumor type of the central nervous system, gliomas are characterized by a dismal prognosis. Tripartite motif-containing 25 (TRIM25), an essential E3 ubiquitin ligase, participates in various biological processes. This study sought to demonstrate its functional role in gliomas. Data obtained from publicly available databases - including The Cancer Genome Atlas (TCGA), the Chinese Glioma Genome Atlas (CGGA), and the Repository for Molecular Brain Neoplasia Data (REMBRANDT) - were employed. TRIM25 expression pattern and its association with different clinical characteristics were analyzed. Kaplan-Meier analysis was utilized to compare different TRIM25 expressions with glioma patients' survival. Subsequently, we performed bioinformatic analyses to investigate the biological functions of TRIM25, which were further validated by
    MeSH term(s) Apoptosis ; B7-H1 Antigen ; Glioma/metabolism ; Humans ; Immunosuppression Therapy ; NF-kappa B/metabolism ; Transcription Factors/metabolism ; Tripartite Motif Proteins/metabolism ; Tumor Microenvironment ; Ubiquitin-Protein Ligases/metabolism
    Chemical Substances B7-H1 Antigen ; NF-kappa B ; Transcription Factors ; Tripartite Motif Proteins ; TRIM25 protein, human (EC 2.3.2.27) ; Ubiquitin-Protein Ligases (EC 2.3.2.27)
    Language English
    Publishing date 2022-06-20
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 4015-0
    ISSN 1535-3699 ; 1525-1373 ; 0037-9727
    ISSN (online) 1535-3699 ; 1525-1373
    ISSN 0037-9727
    DOI 10.1177/15353702221099460
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Sclareol attenuates liver fibrosis through SENP1-mediated VEGFR2 SUMOylation and inhibition of downstream STAT3 signaling.

    Ge, Mao-Xu / Niu, Wei-Xiao / Bao, Yun-Yang / Lu, Zhen-Ning / He, Hong-Wei

    Phytotherapy research : PTR

    2023  Volume 37, Issue 9, Page(s) 3898–3912

    Abstract: Liver fibrosis is a key global health care burden. Sclareol, isolated from Salvia sclarea, possesses various biological activities. Its effect on liver fibrosis remains unknown. This study was proposed to evaluate the antifibrotic activity of sclareol ( ... ...

    Abstract Liver fibrosis is a key global health care burden. Sclareol, isolated from Salvia sclarea, possesses various biological activities. Its effect on liver fibrosis remains unknown. This study was proposed to evaluate the antifibrotic activity of sclareol (SCL) and explore its underlying mechanisms. Stimulated hepatic stellate cells served as an in vitro liver fibrosis model. The expression of fibrotic markers was assessed by western blot and real-time PCR. Two classical animal models, bile duct-ligated rats and carbon tetrachloride-treated mice, were utilized for the in vivo experiments. The liver function and fibrosis degree were determined by serum biochemical and histopathological analyses. VEGFR2 SUMOylation was analyzed using coimmunoprecipitation assay. Our results indicated that SCL treatment restricted the profibrotic propensity of activated HSCs. In fibrotic rodents, SCL administration alleviated hepatic injury and reduced collagen accumulation. Mechanistic studies indicated that SCL downregulated the protein level of SENP1 and enhanced VEGFR2 SUMOylation in LX-2 cells, which affected its intracellular trafficking. Blockade of the interaction between VEGFR2 and STAT3 was observed, resulting in the suppression of downstream STAT3 phosphorylation. Our findings demonstrated that SCL has therapeutic efficacy against liver fibrosis through mediating VEGFR2 SUMOylation, suggesting that SCL may be a potential candidate compound for its treatment.
    MeSH term(s) Rats ; Mice ; Animals ; Sumoylation ; Liver Cirrhosis/drug therapy ; Liver ; Signal Transduction ; Fibrosis ; Hepatic Stellate Cells
    Chemical Substances sclareol (B607NP0Q8Y)
    Language English
    Publishing date 2023-05-02
    Publishing country England
    Document type Journal Article
    ZDB-ID 639136-9
    ISSN 1099-1573 ; 0951-418X
    ISSN (online) 1099-1573
    ISSN 0951-418X
    DOI 10.1002/ptr.7845
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Sclareol attenuates liver fibrosis through SENP1‐mediated VEGFR2 SUMOylation and inhibition of downstream STAT3 signaling

    Ge, Mao‐xu / Niu, Wei‐xiao / Bao, Yun‐yang / Lu, Zhen‐ning / He, Hong‐wei

    Phytotherapy Research. 2023 Sept., v. 37, no. 9 p.3898-3912

    2023  

    Abstract: Liver fibrosis is a key global health care burden. Sclareol, isolated from Salvia sclarea, possesses various biological activities. Its effect on liver fibrosis remains unknown. This study was proposed to evaluate the antifibrotic activity of sclareol ( ... ...

    Abstract Liver fibrosis is a key global health care burden. Sclareol, isolated from Salvia sclarea, possesses various biological activities. Its effect on liver fibrosis remains unknown. This study was proposed to evaluate the antifibrotic activity of sclareol (SCL) and explore its underlying mechanisms. Stimulated hepatic stellate cells served as an in vitro liver fibrosis model. The expression of fibrotic markers was assessed by western blot and real‐time PCR. Two classical animal models, bile duct‐ligated rats and carbon tetrachloride‐treated mice, were utilized for the in vivo experiments. The liver function and fibrosis degree were determined by serum biochemical and histopathological analyses. VEGFR2 SUMOylation was analyzed using coimmunoprecipitation assay. Our results indicated that SCL treatment restricted the profibrotic propensity of activated HSCs. In fibrotic rodents, SCL administration alleviated hepatic injury and reduced collagen accumulation. Mechanistic studies indicated that SCL downregulated the protein level of SENP1 and enhanced VEGFR2 SUMOylation in LX‐2 cells, which affected its intracellular trafficking. Blockade of the interaction between VEGFR2 and STAT3 was observed, resulting in the suppression of downstream STAT3 phosphorylation. Our findings demonstrated that SCL has therapeutic efficacy against liver fibrosis through mediating VEGFR2 SUMOylation, suggesting that SCL may be a potential candidate compound for its treatment.
    Keywords Salvia sclarea ; Western blotting ; animals ; bile ; blood serum ; carbon ; collagen ; fibrosis ; health services ; histopathology ; liver cirrhosis ; liver function ; models ; phosphorylation ; phytotherapy ; precipitin tests ; protein content ; quantitative polymerase chain reaction ; sumoylation ; vascular endothelial growth factor receptor-2
    Language English
    Dates of publication 2023-09
    Size p. 3898-3912.
    Publishing place John Wiley & Sons, Ltd.
    Document type Article ; Online
    Note JOURNAL ARTICLE
    ZDB-ID 639136-9
    ISSN 1099-1573 ; 0951-418X
    ISSN (online) 1099-1573
    ISSN 0951-418X
    DOI 10.1002/ptr.7845
    Database NAL-Catalogue (AGRICOLA)

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  9. Article ; Online: Advances in understanding the regulatory mechanism of cholesterol 7α-hydroxylase.

    Ge, Mao-Xu / Shao, Rong-Guang / He, Hong-Wei

    Biochemical pharmacology

    2019  Volume 164, Page(s) 152–164

    Abstract: The conversion of cholesterol to bile acids (BAs) contributes to the elimination of total cholesterol from the body. In addition, manipulating BA homeostasis by modulating cholesterol 7α-hydroxylase (CYP7A1) may affect the metabolic processing of ... ...

    Abstract The conversion of cholesterol to bile acids (BAs) contributes to the elimination of total cholesterol from the body. In addition, manipulating BA homeostasis by modulating cholesterol 7α-hydroxylase (CYP7A1) may affect the metabolic processing of cholesterol, exerting therapeutic effects on hypercholesterolemia and cardiovascular diseases. Multiple mechanisms (such as various nuclear receptors and regulatory factors) are involved in CYP7A1 modulation. Recently, microRNAs, protein degradation pathways, and the gut microbiota have been identified to participate in these sophisticated networks. In this review, research progress on the regulatory mechanism of CYP7A1 is summarized.
    MeSH term(s) Animals ; Cholesterol/metabolism ; Cholesterol 7-alpha-Hydroxylase/metabolism ; Enzyme Inhibitors/pharmacology ; Enzyme Inhibitors/therapeutic use ; Gastrointestinal Microbiome/drug effects ; Gastrointestinal Microbiome/physiology ; Homeostasis/physiology ; Humans ; Hypercholesterolemia/drug therapy ; Hypercholesterolemia/metabolism
    Chemical Substances Enzyme Inhibitors ; Cholesterol (97C5T2UQ7J) ; Cholesterol 7-alpha-Hydroxylase (EC 1.14.14.23)
    Language English
    Publishing date 2019-04-10
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 208787-x
    ISSN 1873-2968 ; 0006-2952
    ISSN (online) 1873-2968
    ISSN 0006-2952
    DOI 10.1016/j.bcp.2019.04.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: The anti-hepatic fibrosis effects of dihydrotanshinone I are mediated by disrupting the yes-associated protein and transcriptional enhancer factor D2 complex and stimulating autophagy.

    Ge, Maoxu / Liu, Hong / Zhang, Yixuan / Li, Naren / Zhao, Shuangshuang / Zhao, Wuli / Zhen, Yongzhan / Yu, Jianzhong / He, Hongwei / Shao, Rong-Guang

    British journal of pharmacology

    2017  Volume 174, Issue 10, Page(s) 1147–1160

    Abstract: Background and purpose: Dihydrotanshinone I (DHI), a lipophilic component of traditional Chinese medicine Salvia miltiorrhiza Bunge, has various therapeutic effects. We investigated the anti-fibrotic effect of DHI and its underlying mechanisms in vitro ... ...

    Abstract Background and purpose: Dihydrotanshinone I (DHI), a lipophilic component of traditional Chinese medicine Salvia miltiorrhiza Bunge, has various therapeutic effects. We investigated the anti-fibrotic effect of DHI and its underlying mechanisms in vitro and in vivo.
    Experimental approach: Rats subjected to bile duct ligation (BDL) were treated with DHI (25 mg·kg
    Key results: In BDL rats, DHI administration attenuated liver necrosis, bile duct proliferation and collagen accumulation and reduced the expression of genes associated with fibrogenesis, including Tgfb1, Mmp-2, Acta2 and Col1a1. DHI (1, 5, 10 μmol·L
    Conclusions and implications: DHI exerts anti-fibrotic effects in BDL rats, LX-2 cells and rat pHSCs by inhibiting the YAP and TEAD2 complex and stimulating autophagy. These findings indicate that DHI may be a potential therapeutic for the treatment of liver fibrosis.
    MeSH term(s) Animals ; Apoptosis Regulatory Proteins/antagonists & inhibitors ; Apoptosis Regulatory Proteins/genetics ; Apoptosis Regulatory Proteins/metabolism ; Autophagy/drug effects ; Bile Ducts/pathology ; Bile Ducts/surgery ; Cell Line ; Dose-Response Relationship, Drug ; Hepatic Stellate Cells/drug effects ; Humans ; Ligation ; Liver Cirrhosis/drug therapy ; Liver Cirrhosis/genetics ; Liver Cirrhosis/pathology ; Male ; Molecular Structure ; Phenanthrenes/administration & dosage ; Phenanthrenes/chemistry ; Phenanthrenes/pharmacology ; Rats ; Rats, Sprague-Dawley ; Structure-Activity Relationship ; Transcription Factors/antagonists & inhibitors ; Transcription Factors/genetics ; Transcription Factors/metabolism
    Chemical Substances Apoptosis Regulatory Proteins ; Phenanthrenes ; Transcription Factors ; Yap1 protein, rat ; dihydrotanshinone I (562G9360V6)
    Language English
    Publishing date 2017-04-06
    Publishing country England
    Document type Journal Article
    ZDB-ID 80081-8
    ISSN 1476-5381 ; 0007-1188
    ISSN (online) 1476-5381
    ISSN 0007-1188
    DOI 10.1111/bph.13766
    Database MEDical Literature Analysis and Retrieval System OnLINE

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