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  1. Article: Du Huo Ji Sheng Tang inhibits Notch1 signaling and subsequent NLRP3 activation to alleviate cartilage degradation in KOA mice.

    Chen, Wen-Jin / Zhuang, Yin / Peng, Wei / Cui, Wei / Zhang, Shu-Jun / Wang, Jian-Wei

    Chinese medicine

    2023  Volume 18, Issue 1, Page(s) 80

    Abstract: ... to cure. The traditional medicine Du Huo Ji Sheng Tang (DHJST) has been used for the treatment of KOA ...

    Abstract Background: Knee osteoarthritis (KOA) has a complex pathological mechanism and is difficult to cure. The traditional medicine Du Huo Ji Sheng Tang (DHJST) has been used for the treatment of KOA for more than one thousand years, but its mechanism for treating KOA has not been revealed. In our previous study, we confirmed that DHJST inhibited the activation of NLRP3 signaling in rats and humans. In the current study, we aimed to determine how DHJST inhibits NLRP3 to alleviate knee cartilage damage.
    Methods: Mice were injected with NLRP3 shRNA or Notch1-overexpressing adenovirus into the tail vein to construct systemic NLRP3 low-expressing or Notch1 high-expressing mice. Mice were injected with papain into the knee joint to replicate the KOA model. DHJST was used to treat KOA model mice with different backgrounds. The thickness of the right paw was measured to evaluate toe swelling. The pathohistological changes and the levels of IL-1β, MMP2, NLRP3, Notch1, collagen 2, collagen 4, HES1, HEY1, and Caspase3 were detected by HE staining, ELISA, immunohistochemical staining, western blotting, or real-time qPCR.
    Results: DHJST reduced tissue swelling and serum and knee cartilage IL-1β levels, inhibited cartilage MMP2 expression, increased collagen 2 and collagen 4 levels, decreased Notch1 and NLRP3 positive expression rates in cartilage, and decreased HES1 and HEY1 mRNA levels in KOA model mice. In addition, NLRP3 interference decreased cartilage MMP2 expression and increased collagen 2 and collagen 4 levels without affecting the expression levels of notch1, HES1 and HEY1 mRNA levels in the synovium of KOA mice. In KOA mice with NLRP interference, DHJST further reduced tissue swelling and knee cartilage damage in mice. Finally, Notch1-overexpressing mice not only showed more severe tissue swelling and knee cartilage degradation but also abolished the therapeutic effect of DHJST on KOA mice. Importantly, the inhibitory effects of DHJST on the mRNA expression of NLRP3, Caspase3 and IL-1β in the knee joint of KOA mice were completely limited after Notch1 overexpression.
    Conclusion: DHJST significantly reduced inflammation and cartilage degradation in KOA mice by inhibiting Ntoch1 signaling and its subsequent NLRP3 activation in the knee joint.
    Language English
    Publishing date 2023-06-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 2260322-0
    ISSN 1749-8546
    ISSN 1749-8546
    DOI 10.1186/s13020-023-00784-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: The Protective Effect of Sheng Mai Yin on Diabetic Cardiomyopathy via NLRP3/Caspase-1 Pathway.

    Li, Jing-Ya / Zhao, Chun-Chun / Peng, Jian-Fei / Zhang, Meng / Wang, Liang / Yin, Gang / Zhou, Peng

    Evidence-based complementary and alternative medicine : eCAM

    2022  Volume 2022, Page(s) 1234434

    Abstract: Sheng Mai Yin (SMY) has therapeutic effects on myocardial infarction (MI), heart failure (HF ...

    Abstract Sheng Mai Yin (SMY) has therapeutic effects on myocardial infarction (MI), heart failure (HF), diabetic cardiomyopathy (DCM), and myocarditis. To study whether SMY can relieve pyroptosis and play a protective role in diabetic cardiomyopathy, a molecular docking technique was used to predict the possible mechanism of SMY against DCM. Then, a DCM rat model was induced by intraperitoneal injection of streptozotocin (STZ), divided into 5 groups: the DM group (model), SMY-L group (2.7 mL/kg SMY), SMY-M group (5.4 mL/kg SMY), SMY-H group (10.8 mL/kg SMY), and Met group (120 mg/kg metformin). Rats in the CTL group (control) and DM group were given normal saline. After 8 weeks, the levels of blood glucose, lipids, and myocardial enzymes were detected according to the kit instructions. Cardiac function was detected by echocardiography. HE and Masson were used to observing the pathological changes, collagen deposition, and collagen volume fraction (CVF). The apoptosis rate of cardiomyocytes was determined by Tunel. The IL-1
    Language English
    Publishing date 2022-12-01
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2171158-6
    ISSN 1741-4288 ; 1741-427X
    ISSN (online) 1741-4288
    ISSN 1741-427X
    DOI 10.1155/2022/1234434
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The Identification of the Biomarkers of Sheng-Ji Hua-Yu Formula Treated Diabetic Wound Healing Using Modular Pharmacology.

    Jiang, Jing-Si / Zhang, Ying / Luo, Ying / Ru, Yi / Luo, Yue / Fei, Xiao-Ya / Song, Jian-Kun / Ding, Xiao-Jie / Zhang, Zhan / Yang, Dan / Yin, Shuang-Yi / Zhang, Hui-Ping / Liu, Tai-Yi / Li, Bin / Kuai, Le

    Frontiers in pharmacology

    2021  Volume 12, Page(s) 726158

    Abstract: Sheng-Ji Hua-Yu (SJHY) formula has been proved to reduce the severity of diabetic wound healing ...

    Abstract Sheng-Ji Hua-Yu (SJHY) formula has been proved to reduce the severity of diabetic wound healing without significant adverse events in our previous clinical trials. However, based on multi-target characteristics, the regulatory network among herbs, ingredients, and hub genes remains to be elucidated. The current study aims to identify the biomarkers of the SJHY formula for the treatment of diabetic wound healing. First, a network of components and targets for the SJHY formula was constructed using network pharmacology. Second, the ClusterONE algorithm was used to build a modular network and identify hub genes along with kernel pathways. Third, we verified the kernel targets by molecular docking to select hub genes. In addition, the biomarkers of the SJHY formula were validated by animal experiments in a diabetic wound healing mice model. The results revealed that the SJHY formula downregulated the mRNA expression of
    Language English
    Publishing date 2021-11-16
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587355-6
    ISSN 1663-9812
    ISSN 1663-9812
    DOI 10.3389/fphar.2021.726158
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Du Huo Ji Sheng Tang inhibits Notch1 signaling and subsequent NLRP3 activation to alleviate cartilage degradation in KOA mice

    Wen-jin Chen / Yin Zhuang / Wei Peng / Wei Cui / Shu-jun Zhang / Jian-wei Wang

    Chinese Medicine, Vol 18, Iss 1, Pp 1-

    2023  Volume 15

    Abstract: ... to cure. The traditional medicine Du Huo Ji Sheng Tang (DHJST) has been used for the treatment of KOA ...

    Abstract Abstract Background Knee osteoarthritis (KOA) has a complex pathological mechanism and is difficult to cure. The traditional medicine Du Huo Ji Sheng Tang (DHJST) has been used for the treatment of KOA for more than one thousand years, but its mechanism for treating KOA has not been revealed. In our previous study, we confirmed that DHJST inhibited the activation of NLRP3 signaling in rats and humans. In the current study, we aimed to determine how DHJST inhibits NLRP3 to alleviate knee cartilage damage. Methods Mice were injected with NLRP3 shRNA or Notch1-overexpressing adenovirus into the tail vein to construct systemic NLRP3 low-expressing or Notch1 high-expressing mice. Mice were injected with papain into the knee joint to replicate the KOA model. DHJST was used to treat KOA model mice with different backgrounds. The thickness of the right paw was measured to evaluate toe swelling. The pathohistological changes and the levels of IL-1β, MMP2, NLRP3, Notch1, collagen 2, collagen 4, HES1, HEY1, and Caspase3 were detected by HE staining, ELISA, immunohistochemical staining, western blotting, or real-time qPCR. Results DHJST reduced tissue swelling and serum and knee cartilage IL-1β levels, inhibited cartilage MMP2 expression, increased collagen 2 and collagen 4 levels, decreased Notch1 and NLRP3 positive expression rates in cartilage, and decreased HES1 and HEY1 mRNA levels in KOA model mice. In addition, NLRP3 interference decreased cartilage MMP2 expression and increased collagen 2 and collagen 4 levels without affecting the expression levels of notch1, HES1 and HEY1 mRNA levels in the synovium of KOA mice. In KOA mice with NLRP interference, DHJST further reduced tissue swelling and knee cartilage damage in mice. Finally, Notch1-overexpressing mice not only showed more severe tissue swelling and knee cartilage degradation but also abolished the therapeutic effect of DHJST on KOA mice. Importantly, the inhibitory effects of DHJST on the mRNA expression of NLRP3, Caspase3 and IL-1β in the knee joint of KOA ...
    Keywords Osteoarthritis ; DHJST ; NLRP3 ; Notch1 ; Mice ; Inflammation ; Other systems of medicine ; RZ201-999
    Subject code 616
    Language English
    Publishing date 2023-06-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: The Protective Effect of Sheng Mai Yin on Diabetic Cardiomyopathy via NLRP3/Caspase-1 Pathway

    Jing-Ya Li / Chun-Chun Zhao / Jian-Fei Peng / Meng Zhang / Liang Wang / Gang Yin / Peng Zhou

    Evidence-Based Complementary and Alternative Medicine, Vol

    2022  Volume 2022

    Abstract: Sheng Mai Yin (SMY) has therapeutic effects on myocardial infarction (MI), heart failure (HF ...

    Abstract Sheng Mai Yin (SMY) has therapeutic effects on myocardial infarction (MI), heart failure (HF), diabetic cardiomyopathy (DCM), and myocarditis. To study whether SMY can relieve pyroptosis and play a protective role in diabetic cardiomyopathy, a molecular docking technique was used to predict the possible mechanism of SMY against DCM. Then, a DCM rat model was induced by intraperitoneal injection of streptozotocin (STZ), divided into 5 groups: the DM group (model), SMY-L group (2.7 mL/kg SMY), SMY-M group (5.4 mL/kg SMY), SMY-H group (10.8 mL/kg SMY), and Met group (120 mg/kg metformin). Rats in the CTL group (control) and DM group were given normal saline. After 8 weeks, the levels of blood glucose, lipids, and myocardial enzymes were detected according to the kit instructions. Cardiac function was detected by echocardiography. HE and Masson were used to observing the pathological changes, collagen deposition, and collagen volume fraction (CVF). The apoptosis rate of cardiomyocytes was determined by Tunel. The IL-1β level was determined by ELISA and RT-PCR. The expressions of NLRP3, caspase-1, and GSDMD were measured using RT-PCR and Western blotting. The docking results suggested that SMY may act on NLRP3 and its downstream signal pathway. The in vivo results showed that SMY could reduce blood glucose and lipid levels, improve heart function, improve histopathological changes and myocardial enzymes, and alleviate cardiomyocyte apoptosis and myocardial fibrosis. SMY inhibited the mRNA and protein expressions of NLRP3, ASC, Caspase-1, and GSDMD and IL-1β production. SMY can reduce DCM by regulating the NLRP3/caspase-1 signaling pathway, providing a new research direction for the treatment of DCM.
    Keywords Other systems of medicine ; RZ201-999
    Subject code 630
    Language English
    Publishing date 2022-01-01T00:00:00Z
    Publisher Hindawi Limited
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Gene set enrichment analysis and ingenuity pathway analysis to identify biomarkers in Sheng-ji Hua-yu formula treated diabetic ulcers.

    Ru, Yi / Zhang, Ying / Xiang, Yan-Wei / Luo, Ying / Luo, Yue / Jiang, Jing-Si / Song, Jian-Kun / Fei, Xiao-Ya / Yang, Dan / Zhang, Zhan / Zhang, Hui-Ping / Liu, Tai-Yi / Yin, Shuang-Yi / Li, Bin / Kuai, Le

    Journal of ethnopharmacology

    2021  Volume 285, Page(s) 114845

    Abstract: Ethnopharmacological relevance: Sheng-ji Hua-yu (SJHY) formula is a Chinese herbal prescription ...

    Abstract Ethnopharmacological relevance: Sheng-ji Hua-yu (SJHY) formula is a Chinese herbal prescription for diabetic ulcers (DUs) treatment, which can accelerate wound reconstruction and shorten the healing time. However, its mechanism role maintains unclear.
    Aim of the study: To elucidate the molecular mechanisms of SJHY application on DUs.
    Materials and methods: To begin with, transcriptome sequencing was adopted to identified differentially expression mRNAs among normal ulcers, DUs, and DUs + SJHY treatment in vivo. Liquid chromatography-tandem mass spectrometry was applied for the quality control of SJHY formula. GO and KEGG enrichment analysis were used to identify the mechanisms underlying the therapeutic effect of SJHY formula, and then gene set enrichment analysis and ingenuity pathway analysis were conducted for functional analysis. Further, qPCR detection was performed in vivo for validation.
    Results: SJHY administration could regulate the glucose metabolic process, AMPK and HIF-1 pathway to accelerate healing processes of DUs. Besides, CRHR1, SHH, and GAL were identified as the critical targets, and SLC6A3, GRP, FGF23, and CYP27B1 were considered as the upstream genes of SJHY treatment. Combined with animal experiments, the prediction results were validated in DUs mice model.
    Conclusions: This study used modular pharmacology analysis to identify the biomarkers of SJHY formula and provide the potential therapeutic targets for DUs treatment as well.
    MeSH term(s) Animals ; Humans ; Mice ; Diabetes Complications ; Diabetes Mellitus, Experimental ; Drugs, Chinese Herbal/therapeutic use ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Skin Ulcer/drug therapy ; Skin Ulcer/etiology ; Wound Healing/drug effects
    Chemical Substances Drugs, Chinese Herbal ; RNA, Messenger ; Sheng-ji Hua-yu
    Language English
    Publishing date 2021-11-17
    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.2021.114845
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Gene set enrichment analysis and ingenuity pathway analysis to identify biomarkers in Sheng-ji Hua-yu formula treated diabetic ulcers

    Ru, Yi / Zhang, Ying / Xiang, Yan-wei / Luo, Ying / Luo, Yue / Jiang, Jing-si / Song, Jian-kun / Fei, Xiao-ya / Yang, Dan / Zhang, Zhan / Zhang, Hui-ping / Liu, Tai-yi / Yin, Shuang-yi / Li, Bin / Kuai, Le

    Journal of ethnopharmacology. 2022 Mar. 01, v. 285

    2022  

    Abstract: Sheng-ji Hua-yu (SJHY) formula is a Chinese herbal prescription for diabetic ulcers (DUs) treatment ...

    Abstract Sheng-ji Hua-yu (SJHY) formula is a Chinese herbal prescription for diabetic ulcers (DUs) treatment, which can accelerate wound reconstruction and shorten the healing time. However, its mechanism role maintains unclear.To elucidate the molecular mechanisms of SJHY application on DUs.To begin with, transcriptome sequencing was adopted to identified differentially expression mRNAs among normal ulcers, DUs, and DUs + SJHY treatment in vivo. Liquid chromatography-tandem mass spectrometry was applied for the quality control of SJHY formula. GO and KEGG enrichment analysis were used to identify the mechanisms underlying the therapeutic effect of SJHY formula, and then gene set enrichment analysis and ingenuity pathway analysis were conducted for functional analysis. Further, qPCR detection was performed in vivo for validation.SJHY administration could regulate the glucose metabolic process, AMPK and HIF-1 pathway to accelerate healing processes of DUs. Besides, CRHR1, SHH, and GAL were identified as the critical targets, and SLC6A3, GRP, FGF23, and CYP27B1 were considered as the upstream genes of SJHY treatment. Combined with animal experiments, the prediction results were validated in DUs mice model.This study used modular pharmacology analysis to identify the biomarkers of SJHY formula and provide the potential therapeutic targets for DUs treatment as well.
    Keywords biomarkers ; genes ; glucose ; liquid chromatography ; pharmacology ; prediction ; quality control ; tandem mass spectrometry ; therapeutics ; traditional medicine ; transcriptome
    Language English
    Dates of publication 2022-0301
    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.2021.114845
    Database NAL-Catalogue (AGRICOLA)

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  8. Article ; Online: Developing an activity and absorption-based quality control platform for Chinese traditional medicine: Application to Zeng-Sheng-Ping(Antitumor B).

    Yin, Taijun / Yang, Guanyi / Ma, Yong / Xu, Beibei / Hu, Ming / You, Ming / Gao, Song

    Journal of ethnopharmacology

    2015  Volume 172, Page(s) 195–201

    Abstract: Ethnopharmacological relevance: Zeng-Sheng-Ping (ZSP), also called antitumor B, is a marketed ...

    Abstract Ethnopharmacological relevance: Zeng-Sheng-Ping (ZSP), also called antitumor B, is a marketed Chinese traditional medicine used for cancer prevention.
    Aim of the study: Currently, for the quality control of Chinese traditional medicines, marker compounds are not selected based on bioactivities and pharmaceutical behaviors in most of the cases. Therefore, even if the "quality" of the medicine is controlled, the pharmacological effect could still be inconsistent. The aim of this study is to establish an activity and absorption-based platform to select marker compound(s) for the quality control of Chinese traditional medicines.
    Materials and methods: We used ZSP as a reference Chinese traditional medicine to establish the platform. Activity guided fractionation approach was used to purify the major components from ZSP. NMR and MS spectra were used to elucidate the structure of the isolated compounds. MTT assay against oral carcinoma cell line (SCC2095) was performed to evaluate the activities. UPLC-MS/MS was used to quantify the pure compounds in ZSP and the active fraction. The permeabilities of the identified compounds were evaluated in the Caco-2 cell culture model. The intracellular accumulation of the isolated compounds was evaluated in the SCC2095 cells.
    Results: The major compounds were identified from ZSP. The contents, anti-proliferation activities, permeabilities, and intracellular accumulations of these compounds were also evaluated. The structure of these purified compounds were identified by comparing the NMR and MS data with those of references as rutaevine (1), limonin (2), evodol (3), obacunone (4), fraxinellone (5), dictamnine (6), maackiain (7), trifolirhizin (8), and matrine (9). The IC50 of compounds 5, 6, and 7 against SCC2095 cells were significantly lower than that of ZSP. The uptake permeability of compounds 5, 6, and 7 were 2.58 ± 0.3 × 10(-5), 4.33 ± 0.5 × 10(-5), and 4.27 ± 0.8 × 10(-5) respectively in the Caco-2 cell culture model. The intracellular concentrations of these compounds showed that compounds 5, 6, and 7 were significantly accumulated inside the cells.
    Conclusion: Based on the activity against oral carcinoma cell line as well as the absorption permeability, compound 5, 6, and 7 are selected as quality control markers for ZSP. An activity and absorption-based platform was established and successfully used for the quality control of ZSP.
    MeSH term(s) Alkaloids/analysis ; Alkaloids/isolation & purification ; Benzofurans/analysis ; Benzofurans/isolation & purification ; Benzoxepins/analysis ; Benzoxepins/isolation & purification ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Drugs, Chinese Herbal/chemistry ; Drugs, Chinese Herbal/pharmacology ; Glucosides/analysis ; Glucosides/isolation & purification ; Glucosides/pharmacokinetics ; Heterocyclic Compounds, 4 or More Rings/analysis ; Heterocyclic Compounds, 4 or More Rings/isolation & purification ; Heterocyclic Compounds, 4 or More Rings/pharmacokinetics ; Humans ; Limonins/analysis ; Limonins/isolation & purification ; Medicine, Chinese Traditional/standards ; Permeability ; Pterocarpans/analysis ; Pterocarpans/isolation & purification ; Pterocarpans/pharmacokinetics ; Quality Control ; Quinolines/analysis ; Quinolines/isolation & purification ; Quinolines/pharmacokinetics ; Quinolizines/analysis ; Quinolizines/isolation & purification ; Triterpenes/analysis ; Triterpenes/isolation & purification
    Chemical Substances Alkaloids ; Antitumor B ; Benzofurans ; Benzoxepins ; Drugs, Chinese Herbal ; Glucosides ; Heterocyclic Compounds, 4 or More Rings ; Limonins ; Pterocarpans ; Quinolines ; Quinolizines ; Triterpenes ; trifolirhizin ; fraxinellone (28808-62-0) ; rutaevin (33237-37-5) ; obacunone (751-03-1) ; dictamnine (HQZ3798D0A) ; limonin (L0F260866S) ; matrine (N390W430AC) ; inermin (TF360D25IJ)
    Language English
    Publishing date 2015-08-22
    Publishing country Ireland
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2015.06.019
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Book: Wo guo gong li yi yuan yi sheng zhi ye xin li yan jiu

    Yin, Wenqiang

    gong zuo juan dai de guan li xue shi jiao = Physicans' occupational psychology in China public hospitas : a management perspective on burnout

    2014  

    Title variant Physicans' occupational psychology in China public hospitas :
    Author's details Yin Wenqiang, Huang Dongmei zhu
    MeSH term(s) Burnout, Professional/psychology ; Physicians/psychology ; Hospitals, Public/organization & administration
    Keywords China
    Language Chinese
    Size 2, 2, 133 pages.
    Edition Di 1 ban.
    Document type Book
    ISBN 9787516141274 ; 7516141275
    Database Catalogue of the US National Library of Medicine (NLM)

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  10. Book: "Fo shuo sheng jing" can juan

    Huang, Zheng / Jiang, Yin

    (Dun huang shu fa jing pin xuan ; / Huang Zheng, Jiang Yin bianzhu[...])

    2002  

    Series title Dun huang shu fa jing pin xuan
    / Huang Zheng, Jiang Yin bianzhu[...]
    Language Chinese
    Size 53 S, Ill
    Publisher Xiling yinshe
    Publishing place Hangzhou
    Document type Book
    ISBN 7805175446 ; 9787805175447
    Database Former special subject collection: coastal and deep sea fishing

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