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  1. Article ; Online: Application of omics technology to investigate the mechanism underlying the role of San Hua Tang in regulating microglia polarization and blood-brain barrier protection following ischemic stroke

    Luo, Shan / Chen, Yuanchun / Zhao, Ruoxi / Ma, Donglai / Zhao, Yanmeng / Zhang, Ying / Jiang, Jianming / Yu, Wentao

    Journal of Ethnopharmacology. 2023 Oct., v. 314 p.116640-

    2023  

    Abstract: San Hua Tang (SHT) was first mentioned in the book "The Collection of Plain Questions about Pathogenesis, Qi, and Life." SHT has the effect of dispelling wind and dredging collaterals, dredging viscera, and guiding stagnation, and is used in the ... ...

    Abstract San Hua Tang (SHT) was first mentioned in the book "The Collection of Plain Questions about Pathogenesis, Qi, and Life." SHT has the effect of dispelling wind and dredging collaterals, dredging viscera, and guiding stagnation, and is used in the treatment of ischemic stroke (IS). SHT is composed of Rheum palmatum L., Magnolia officinalis Rehder & E.H.Wilson, Citrus assamensis S.Dutta & S.C.Bhattacharya, and Notopterygium tenuifolium M.L.Sheh & F.T.Pu, which is the traditional prescription of the Tongxia method for the treatment of stroke. Tongxia is one of the "eight methods" used in traditional Chinese medicine, which plays a role in treating diseases by promoting gastrointestinal peristalsis and defecation. Studies have demonstrated a close relationship between gut microbiota metabolism and cerebral stroke; however, the role of SHT in IS treatment through gut microbiota or intestinal metabolites is unclear. Aim of the study: To explore the connotation of the Xuanfu theory and clarify the mechanism underlying SHT-mediated opening Xuanfu methods. Through metabolomics, 16S rRNA gene sequencing, and molecular biology techniques, research on the changes in the gut microbiota and blood-brain barrier (BBB) will highlight greater strategies for the treatment of stroke. We used pseudo-germ-free (PGF) rats combined with an ischemia/reperfusion (I/R) rat model for the follow-up experimental research. PGF rats were prepared by the intragastric administration of an antibiotic cocktail for 6 days, following which SHT was administered for 5 consecutive days. The I/R model was performed 1 day following the concluding administration of SHT. We detected the neurological deficit score, cerebral infarct volume, serum inflammatory factor levels (interleukin IL-6, IL-10, IL-17, and tumor necrosis factor alpha), tight junction-related proteins (Zonula occludens-1, Occludin, and Claudin-5), and small glue plasma cell-associated proteins (Cluster of Differentiation 16/Cluster of Differentiation 206, Matrix metalloproteinase, ionized calcium-binding adapter molecule 1, and C-X3-C Motif Chemokine Ligand 1) 24 h following I/R. Using 16S rRNA gene sequencing and non-targeted metabolomics analysis, we explored the relationship between fecal microecology and serum metabolites. Eventually, we analyzed the correlation between the gut microbiota and plasma metabolic profile as well as the mechanism underlying the SHT-mediated regulation of gut microbiota to protect the BBB following stroke. In IS treatment, SHT is principally involved in reducing neurological injury and the volume of cerebral infarction; protecting the intestinal mucosal barrier; increasing the levels of acetic acid, butyric acid, and propionic acid; promoting the transformation of microglia to the M2 state; reducing inflammatory reactions; and enhancing tight junctions. These therapeutic effects were not observed in the group treated with antibiotics alone or that treated with SHT in combination with antibiotics, thereby indicating SHT plays a therapeutic role through the gut microbiota. SHT regulates the gut microbiota, inhibits pro-inflammatory factors in rats with IS, alleviates an inflammatory injury of the BBB, and plays a protective role in the brain.
    Keywords Citrus ; Hansenia ; Magnolia officinalis ; Oriental traditional medicine ; Rheum palmatum ; acetic acid ; animal models ; antibiotics ; blood serum ; blood-brain barrier ; brain ; butyric acid ; chemokines ; defecation ; genes ; infarction ; interleukin-10 ; interleukin-17 ; interleukin-6 ; intestinal microorganisms ; intestines ; intragastric administration ; ischemia ; ligands ; metabolism ; metabolites ; metabolomics ; metalloproteinases ; molecular biology ; neuroglia ; occludins ; pathogenesis ; peristalsis ; propionic acid ; protective effect ; stroke ; therapeutics ; tumor necrosis factor-alpha ; wind ; Ischemic stroke ; Microglia ; Inflammatory injury ; 16S rRNA ; LCMS ; San Hua Tang
    Language English
    Dates of publication 2023-10
    Publishing place Elsevier B.V.
    Document type Article ; Online
    Note Use and reproduction
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2023.116640
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Corrigendum to "Application of omics technology to investigate the mechanism underlying the role of San Hua Tang in regulating microglia polarization and blood-brain barrier protection following ischemic stroke" [J. Ethnopharmacol. 314 (2023) 116640].

    Luo, Shan / Chen, Yuanchun / Zhao, Ruoxi / Ma, Donglai / Zhao, Yanmeng / Zhang, Ying / Jiang, Jianming / Yu, Wentao

    Journal of ethnopharmacology

    2023  Volume 319, Issue Pt 1, Page(s) 117155

    Language English
    Publishing date 2023-09-11
    Publishing country Ireland
    Document type Published Erratum
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2023.117155
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Application of omics technology to investigate the mechanism underlying the role of San Hua Tang in regulating microglia polarization and blood-brain barrier protection following ischemic stroke.

    Luo, Shan / Chen, Yuanchun / Zhao, Ruoxi / Ma, Donglai / Zhao, Yanmeng / Zhang, Ying / Jiang, Jianming / Yu, Wentao

    Journal of ethnopharmacology

    2023  Volume 314, Page(s) 116640

    Abstract: Ethnopharmacology relevance: San Hua Tang (SHT) was first mentioned in the book "The Collection of Plain Questions about Pathogenesis, Qi, and Life." SHT has the effect of dispelling wind and dredging collaterals, dredging viscera, and guiding ... ...

    Abstract Ethnopharmacology relevance: San Hua Tang (SHT) was first mentioned in the book "The Collection of Plain Questions about Pathogenesis, Qi, and Life." SHT has the effect of dispelling wind and dredging collaterals, dredging viscera, and guiding stagnation, and is used in the treatment of ischemic stroke (IS). SHT is composed of Rheum palmatum L., Magnolia officinalis Rehder & E.H.Wilson, Citrus assamensis S.Dutta & S.C.Bhattacharya, and Notopterygium tenuifolium M.L.Sheh & F.T.Pu, which is the traditional prescription of the Tongxia method for the treatment of stroke. Tongxia is one of the "eight methods" used in traditional Chinese medicine, which plays a role in treating diseases by promoting gastrointestinal peristalsis and defecation. Studies have demonstrated a close relationship between gut microbiota metabolism and cerebral stroke; however, the role of SHT in IS treatment through gut microbiota or intestinal metabolites is unclear.
    Aim of the study: To explore the connotation of the Xuanfu theory and clarify the mechanism underlying SHT-mediated opening Xuanfu methods. Through metabolomics, 16S rRNA gene sequencing, and molecular biology techniques, research on the changes in the gut microbiota and blood-brain barrier (BBB) will highlight greater strategies for the treatment of stroke.
    Materials and methods: We used pseudo-germ-free (PGF) rats combined with an ischemia/reperfusion (I/R) rat model for the follow-up experimental research. PGF rats were prepared by the intragastric administration of an antibiotic cocktail for 6 days, following which SHT was administered for 5 consecutive days. The I/R model was performed 1 day following the concluding administration of SHT. We detected the neurological deficit score, cerebral infarct volume, serum inflammatory factor levels (interleukin IL-6, IL-10, IL-17, and tumor necrosis factor alpha), tight junction-related proteins (Zonula occludens-1, Occludin, and Claudin-5), and small glue plasma cell-associated proteins (Cluster of Differentiation 16/Cluster of Differentiation 206, Matrix metalloproteinase, ionized calcium-binding adapter molecule 1, and C-X3-C Motif Chemokine Ligand 1) 24 h following I/R. Using 16S rRNA gene sequencing and non-targeted metabolomics analysis, we explored the relationship between fecal microecology and serum metabolites. Eventually, we analyzed the correlation between the gut microbiota and plasma metabolic profile as well as the mechanism underlying the SHT-mediated regulation of gut microbiota to protect the BBB following stroke.
    Results: In IS treatment, SHT is principally involved in reducing neurological injury and the volume of cerebral infarction; protecting the intestinal mucosal barrier; increasing the levels of acetic acid, butyric acid, and propionic acid; promoting the transformation of microglia to the M2 state; reducing inflammatory reactions; and enhancing tight junctions. These therapeutic effects were not observed in the group treated with antibiotics alone or that treated with SHT in combination with antibiotics, thereby indicating SHT plays a therapeutic role through the gut microbiota.
    Conclusion: SHT regulates the gut microbiota, inhibits pro-inflammatory factors in rats with IS, alleviates an inflammatory injury of the BBB, and plays a protective role in the brain.
    MeSH term(s) Rats ; Animals ; Blood-Brain Barrier ; Ischemic Stroke/drug therapy ; Ischemic Stroke/metabolism ; Microglia ; Rats, Sprague-Dawley ; RNA, Ribosomal, 16S/metabolism ; Stroke/drug therapy ; Stroke/metabolism ; Tight Junction Proteins/metabolism ; Anti-Bacterial Agents/pharmacology
    Chemical Substances RNA, Ribosomal, 16S ; Tight Junction Proteins ; Anti-Bacterial Agents
    Language English
    Publishing date 2023-05-16
    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.2023.116640
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Dihydroartemisinin broke the tumor immunosuppressive microenvironment by inhibiting YAP1 expression to enhance anti‐PD‐1 efficacy

    Peng, Qing / Li, Shenghao / Shi, Xinli / Guo, Yinglin / Hao, Liyuan / Zhang, Zhiqin / Ji, Jingmin / Zhao, Yanmeng / Li, Caige / Xue, Yu / Liu, Yiwei

    Phytotherapy Research. 2023 May, v. 37, no. 5 p.1740-1753

    2023  

    Abstract: The efficacy of anti‐PD‐1 therapy is not as expected in hepatocellular carcinoma (HCC). YAP1 was overexpressed and activated in HCC. The mechanism of YAP1 in HCC immune escape is unclear. Anti‐PD‐1 treatment increased YAP1 expression in liver tumor cells, ...

    Abstract The efficacy of anti‐PD‐1 therapy is not as expected in hepatocellular carcinoma (HCC). YAP1 was overexpressed and activated in HCC. The mechanism of YAP1 in HCC immune escape is unclear. Anti‐PD‐1 treatment increased YAP1 expression in liver tumor cells, and exhausted CD4⁺ and CD8⁺ T cells in the blood and spleen of liver tumor mice. YAP1 knockdown suppressed PD‐L1 expression, which was involved in JAK1/STAT1, 3 pathways. Moreover, Yap1 knockout elevated CD4⁺ and CD8⁺ T cells in liver tumor niche. Consistently, verteporfin, YAP1 inhibitor, decreased TGF‐β and IFN‐γ in liver tumor niche and exhausted CD8⁺ T cell in the spleen. DHA suppressed YAP1 expression and break immune evasion in liver tumor niche, characterized by decreased PD‐L1 in liver tumor cells and increased CD8⁺ T cell infiltration. Furthermore, DHA combined with anti‐PD‐1 treatment promoted CD4⁺ T cell infiltration in the spleen and CD8⁺ T cell in tumor tissues of mice. In summary, YAP1 knockdown in liver tumor cells suppressed PD‐L1 expression and recruited cytotoxic T lymphocytes (CTLs), leading to break immune evasion in tumor niche. Mechanistically, YAP1 knockdown suppressed PD‐L1 expression, which was involved in JAK1/STAT1, 3 pathways. Finally, DHA inhibited YAP1 expression, which not only inhibited liver tumor proliferation but also break the immunosuppressive niche in liver tumor tissues and improve the effect of anti‐PD‐1 therapy.
    Keywords T-lymphocytes ; cytotoxicity ; hepatoma ; immune evasion ; immunosuppression ; phytotherapy ; research ; spleen
    Language English
    Dates of publication 2023-05
    Size p. 1740-1753.
    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.7695
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  5. Article: Protective Effect of Buyang Huanwu Decoction on Cerebral Ischemia Reperfusion Injury by Alleviating Autophagy in the Ischemic Penumbra.

    Zhao, Yanmeng / Ma, Xiujuan / Yu, Wentao / Zhang, Ziwei / Wang, Wenliang / Zhou, Xiaohong / Gao, Weijuan

    Evidence-based complementary and alternative medicine : eCAM

    2021  Volume 2021, Page(s) 9937264

    Abstract: Objectives: To evaluate the protective effect of Buyang Huanwu Decoction (BHD) against cerebral ischemia reperfusion and investigate whether autophagy is involved in its mechanism of action.: Methods: Adult male Sprague Dawley rats were randomly ... ...

    Abstract Objectives: To evaluate the protective effect of Buyang Huanwu Decoction (BHD) against cerebral ischemia reperfusion and investigate whether autophagy is involved in its mechanism of action.
    Methods: Adult male Sprague Dawley rats were randomly divided into three groups: the sham, cerebral ischemia reperfusion (I/R), and I/R + BHD groups. A rat model of cerebral I/R injury was established via middle cerebral artery occlusion (MCAO) for 2 h, followed by 1, 3, and 7 d of reperfusion. Neurological scores and regional cerebral blood flow were assessed to determine whether the model was successfully established. Brain infarct volume was determined by 2,3,5-triphenyl tetrazolium chloride (TTC) staining. The apoptosis rate was detected using TdT-mediated dUTP Nick-End Labeling (TUNEL) staining, and neuronal damage was evaluated by Nissl staining. The Beclin-1 and LC3 protein levels in the ischemic core, penumbra, and contralateral area were analysed by Western blotting. The occurrence of autophagy in the penumbra was observed by transmission electron microscopy (TEM).
    Results: BHD treatment alleviated the cerebral infarct volume, neuronal apoptosis rate, and neuronal damage 3 and 7 d after cerebral I/R injury. Furthermore, 3 d after reperfusion, we observed that the Beclin-1 levels were significantly decreased in the core in the I/R group, whereas transformation of LC3 I to LC3 II exhibited no obvious differences between the sham and I/R groups. In the penumbra, the Beclin-1 levels and transformation of LC3 I to LC3 II in the I/R group were significantly increased compared with that in the sham group. However, no significant difference in the contralateral area was noted between the two groups. BHD significantly inhibited the expression of Beclin-1 and the transformation of LC3 I to LC3 II in the penumbra after cerebral I/R injury but yielded no significant changes in the core and contralateral area.
    Conclusions: BHD exerts a neuroprotective effect by inhibiting autophagy in neurons in the penumbra after cerebral I/R injury.
    Language English
    Publishing date 2021-12-07
    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 10.1155/2021/9937264
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Differentiation between bipolar disorder and major depressive disorder in adolescents: from clinical to biological biomarkers.

    Yang, Ruilan / Zhao, Yanmeng / Tan, Zewen / Lai, Juan / Chen, Jianshan / Zhang, Xiaofei / Sun, Jiaqi / Chen, Lei / Lu, Kangrong / Cao, Liping / Liu, Xuemei

    Frontiers in human neuroscience

    2023  Volume 17, Page(s) 1192544

    Abstract: Background: Mood disorders are very common among adolescents and include mainly bipolar disorder (BD) and major depressive disorder (MDD), with overlapping depressive symptoms that pose a significant challenge to realizing a rapid and accurate ... ...

    Abstract Background: Mood disorders are very common among adolescents and include mainly bipolar disorder (BD) and major depressive disorder (MDD), with overlapping depressive symptoms that pose a significant challenge to realizing a rapid and accurate differential diagnosis in clinical practice. Misdiagnosis of BD as MDD can lead to inappropriate treatment and detrimental outcomes, including a poorer ultimate clinical and functional prognosis and even an increased risk of suicide. Therefore, it is of great significance for clinical management to identify clinical symptoms or features and biological markers that can accurately distinguish BD from MDD. With the aid of bibliometric analysis, we explore, visualize, and conclude the important directions of differential diagnostic studies of BD and MDD in adolescents.
    Materials and methods: A literature search was performed for studies on differential diagnostic studies of BD and MDD among adolescents in the Web of Science Core Collection database. All studies considered for this article were published between 2004 and 2023. Bibliometric analysis and visualization were performed using the VOSviewer and CiteSpace software.
    Results: In total, 148 publications were retrieved. The number of publications on differential diagnostic studies of BD and MDD among adolescents has been generally increasing since 2012, with the United States being an emerging hub with a growing influence in the field. Boris Birmaher is the top author in terms of the number of publications, and the
    Conclusion: This is the first-ever study of bibliometric and visual analyses of differential diagnostic studies of BD and MDD in adolescents to reveal the current research status and important directions in the field. Our research and analysis results might provide some practical sources for academic scholars and clinical practice.
    Language English
    Publishing date 2023-09-15
    Publishing country Switzerland
    Document type Systematic Review
    ZDB-ID 2425477-0
    ISSN 1662-5161
    ISSN 1662-5161
    DOI 10.3389/fnhum.2023.1192544
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: 1,8-Cineole Alleviates OGD/R-Induced Oxidative Damage and Restores Mitochondrial Function by Promoting the Nrf2 Pathway.

    Liu, Zhenyi / Wang, Jing / Jin, Xiaofei / Gao, Ping / Zhao, Yanmeng / Yin, Meijuan / Ma, Xian / Xin, Ziyuan / Zhao, Yuemou / Zhou, Xiaohong / Gao, Weijuan

    Biological & pharmaceutical bulletin

    2023  Volume 46, Issue 10, Page(s) 1371–1384

    Abstract: This study examined the effects of 1,8-cineole on reducing oxidative stress injury and restoring mitochondrial function in oxygen-glucose deprivation and reoxygenation (OGD/R) HT22 cells via the nuclear factor erythrocyte 2 related factor 2 (Nrf2) ... ...

    Abstract This study examined the effects of 1,8-cineole on reducing oxidative stress injury and restoring mitochondrial function in oxygen-glucose deprivation and reoxygenation (OGD/R) HT22 cells via the nuclear factor erythrocyte 2 related factor 2 (Nrf2) pathway. The optimal concentration of 1,8-cineole to reduce OGD/R injury was screened via cell morphology, cell survival rate, and lactate dehydrogenase (LDH) leakage rate. Oxidative damage was observed by measuring superoxide dismutase (SOD), glutathione peroxidase (GSH-PX), catalase (CAT) activities, and reactive oxygen species (ROS), glutathione (GSH), protein carbonyl, malondialdehyde (MDA), lipid peroxidation (LPO) content, and 8-hydroxy-2 deoxyguanosine (8-OHDG) expression. Mitochondrial function was observed by mitochondrial membrane potential (MMP) and ATPase activity. Nrf2 pathways were observed by the expression levels of total Nrf2, nucleus Nrf2, reduced nicotinamide adenine dinucleotide phosphate (NAD(P)H): quinone oxidoreductase 1 (NQO1) and heme oxygenase-1 (HO-1), the mRNA levels of HO-1 and NQO1. Among different concentrations of 1,8-cineole for promoting HT22 cell proliferation and attenuated OGD/R injury, 10 µmol/L 1,8-cineole was the best. After 1,8-cineole treatment, SOD, GSH-PX, and CAT activities and GSH content increased, while ROS, MDA, LPO, protein carbonyl, and 8-OHDG levels decreased. 1,8-Cineole could restore MMP and increase mitochondrial enzyme activity. It could also increase the total Nrf2, nucleus Nrf2, NQO1, and HO-1, and Nrf2 inhibitor brusatol reduced the effect of 1,8-cineole. Immunofluorescence assay showed that 1,8-cineole could facilitate the transfer of Nrf2 into the nucleus. 1,8-cineole increased the mRNA levels of NQO1 and HO-1. The above results showed that 1,8-cineole could alleviate OGD/R-induced oxidative damage and restores mitochondrial function by activating the Nrf2 signal pathway.
    MeSH term(s) Oxygen/metabolism ; Reactive Oxygen Species/metabolism ; NF-E2-Related Factor 2/metabolism ; Eucalyptol/pharmacology ; Eucalyptol/metabolism ; Glucose/metabolism ; Signal Transduction ; Oxidative Stress ; Antioxidants/pharmacology ; Glutathione/metabolism ; Superoxide Dismutase/metabolism ; Mitochondria/metabolism ; Heme Oxygenase-1/metabolism
    Chemical Substances Oxygen (S88TT14065) ; Reactive Oxygen Species ; NF-E2-Related Factor 2 ; Eucalyptol (RV6J6604TK) ; Glucose (IY9XDZ35W2) ; Antioxidants ; Glutathione (GAN16C9B8O) ; Superoxide Dismutase (EC 1.15.1.1) ; Heme Oxygenase-1 (EC 1.14.14.18)
    Language English
    Publishing date 2023-08-03
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 1150271-x
    ISSN 1347-5215 ; 0918-6158
    ISSN (online) 1347-5215
    ISSN 0918-6158
    DOI 10.1248/bpb.b23-00154
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Dihydroartemisinin broke the tumor immunosuppressive microenvironment by inhibiting YAP1 expression to enhance anti-PD-1 efficacy.

    Peng, Qing / Li, Shenghao / Shi, Xinli / Guo, Yinglin / Hao, Liyuan / Zhang, Zhiqin / Ji, Jingmin / Zhao, Yanmeng / Li, Caige / Xue, Yu / Liu, Yiwei

    Phytotherapy research : PTR

    2022  Volume 37, Issue 5, Page(s) 1740–1753

    Abstract: The efficacy of anti-PD-1 therapy is not as expected in hepatocellular carcinoma (HCC). YAP1 was overexpressed and activated in HCC. The mechanism of YAP1 in HCC immune escape is unclear. Anti-PD-1 treatment increased YAP1 expression in liver tumor cells, ...

    Abstract The efficacy of anti-PD-1 therapy is not as expected in hepatocellular carcinoma (HCC). YAP1 was overexpressed and activated in HCC. The mechanism of YAP1 in HCC immune escape is unclear. Anti-PD-1 treatment increased YAP1 expression in liver tumor cells, and exhausted CD4
    MeSH term(s) Animals ; Mice ; B7-H1 Antigen/antagonists & inhibitors ; Carcinoma, Hepatocellular/drug therapy ; Carcinoma, Hepatocellular/metabolism ; CD8-Positive T-Lymphocytes ; Immunosuppressive Agents ; Liver Neoplasms/drug therapy ; Liver Neoplasms/metabolism ; Tumor Microenvironment ; YAP-Signaling Proteins/drug effects ; YAP-Signaling Proteins/genetics
    Chemical Substances artenimol (6A9O50735X) ; B7-H1 Antigen ; Immunosuppressive Agents ; YAP-Signaling Proteins
    Language English
    Publishing date 2022-12-28
    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.7695
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  9. Article ; Online: Astragaloside IV attenuates cerebral ischemia‑reperfusion injury in rats through the inhibition of calcium‑sensing receptor‑mediated apoptosis.

    Du, Shu-Jin / Zhang, Ying / Zhao, Yan-Meng / Dong, Ya-Jie / Tang, Jing-Long / Zhou, Xiao-Hong / Gao, Wei-Juan

    International journal of molecular medicine

    2020  Volume 47, Issue 1, Page(s) 302–314

    Abstract: Cerebral ischemia‑reperfusion injury (CIRI), caused by the reperfusion of blocked vessels following ischemic stroke, can lead to secondary brain injury. Throughout CIRI, apoptosis serves an important role. Astragaloside IV is a potential neuroprotectant ... ...

    Abstract Cerebral ischemia‑reperfusion injury (CIRI), caused by the reperfusion of blocked vessels following ischemic stroke, can lead to secondary brain injury. Throughout CIRI, apoptosis serves an important role. Astragaloside IV is a potential neuroprotectant that alleviates CIRI by inhibiting apoptosis. The calcium‑sensing receptor (CaSR) is a G‑protein‑coupled receptor, the activation of which aggravates ischemia‑reperfusion injury. The aim of the present study was to investigate whether the protective effect of Astragaloside IV on CIRI may be associated with the regulation of CaSR. A rat middle cerebral artery occlusion/reperfusion (MCAO/R) model and an oxygen and glucose deprivation/reoxygenation (OGD/R) model of pheochromocytoma (PC12) cells were used to study the neuronal injury induced by CIRI. Neurological function scores (NFS), 2,3,5‑triphe‑nylterazolium chloride and hematoxylin and eosin staining were used to determine brain damage in rats. Cell viability was measured to evaluate the injury of OGD/R PC12 cells. Western blotting was used to examine the expression of proteins associated with apoptosis and CaSR. The CaSR antagonist NPS‑2143 and agonist GdCl3 were used to further confirm the effects of CaSR during the process of apoptosis. The results demonstrated that Astragaloside IV alleviated CIRI by decreasing the NFS of rats, reducing the infarction volume of the brain and promoting the viability of PC12 cells, as well as inhibiting the expression of cleaved caspase‑3 and CaSR, which was induced by CIRI. The results of the present study suggested that the activation of CaSR may be involved in CIRI‑induced brain damage in rats, and that Astragaloside IV may alleviate CIRI by inhibiting CaSR activation‑induced apoptosis.
    MeSH term(s) Animals ; Apoptosis/drug effects ; Cerebrovascular Disorders/drug therapy ; Cerebrovascular Disorders/metabolism ; Cerebrovascular Disorders/pathology ; Disease Models, Animal ; Male ; Rats ; Rats, Sprague-Dawley ; Receptors, Calcium-Sensing/antagonists & inhibitors ; Receptors, Calcium-Sensing/metabolism ; Reperfusion Injury/drug therapy ; Reperfusion Injury/metabolism ; Reperfusion Injury/pathology ; Saponins/pharmacology ; Triterpenes/pharmacology
    Chemical Substances Receptors, Calcium-Sensing ; Saponins ; Triterpenes ; extracellular calcium cation-sensing receptor, rat ; astragaloside A (3A592W8XKE)
    Language English
    Publishing date 2020-11-02
    Publishing country Greece
    Document type Journal Article
    ZDB-ID 1444428-8
    ISSN 1791-244X ; 1107-3756
    ISSN (online) 1791-244X
    ISSN 1107-3756
    DOI 10.3892/ijmm.2020.4777
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: The effects of vitamin C on DDP-induced anemia in rats.

    Gao, Li-Ping / Li, Zen / Guo, Zhuo-Yu / Zhao, Yan-Meng

    Toxicology mechanisms and methods

    2013  Volume 23, Issue 6, Page(s) 383–388

    Abstract: The aim of this study was to investigate the effects of vitamin C on cisplatin (DDP)-induced anemia and explore its possible mechanisms in rats. Adult male Sprague-Dawley rats were randomly divided into six groups: control, vitamin C 50, vitamin C 100, ... ...

    Abstract The aim of this study was to investigate the effects of vitamin C on cisplatin (DDP)-induced anemia and explore its possible mechanisms in rats. Adult male Sprague-Dawley rats were randomly divided into six groups: control, vitamin C 50, vitamin C 100, DDP, DDP plus vitamin C 50 and DDP plus vitamin C 100-treated groups. DDP was intravenous injected as a single dose and vitamin C was administered by gavage. Serum erythropoietin (Epo), hemoglobin (Hb) and blood urea nitrogen (BUN) concentration were measured 4 and 14 days after DDP treatment. The changes of renal tissue were examined by light microscope. Administration of DDP to rats induced anemia and nephrotoxicity, characterized with a significant decrease in serum Epo and Hb and increase in BUN concentrations. Pathological examination revealed that DDP caused significant renal damage in rats. Vitamin C administration produced amelioration in biochemical indices of anemia and nephrotoxicity and in histological change when compared to group DDP alone; concurrent administration of vitamin C at doses of 100 mg/kg being more effective. Results from this study indicate that the novel natural antioxidant vitamin C might have protective effect against DDP-induced anemia in rats.
    MeSH term(s) Anemia/blood ; Anemia/chemically induced ; Anemia/prevention & control ; Animals ; Antineoplastic Agents/adverse effects ; Antioxidants/administration & dosage ; Antioxidants/therapeutic use ; Ascorbic Acid/administration & dosage ; Ascorbic Acid/therapeutic use ; Cisplatin/adverse effects ; Dose-Response Relationship, Drug ; Kidney/drug effects ; Kidney/pathology ; Male ; Rats ; Rats, Sprague-Dawley
    Chemical Substances Antineoplastic Agents ; Antioxidants ; Ascorbic Acid (PQ6CK8PD0R) ; Cisplatin (Q20Q21Q62J)
    Language English
    Publishing date 2013-07
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2081252-8
    ISSN 1537-6524 ; 1537-6516 ; 1051-7235
    ISSN (online) 1537-6524
    ISSN 1537-6516 ; 1051-7235
    DOI 10.3109/15376516.2013.769656
    Database MEDical Literature Analysis and Retrieval System OnLINE

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