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  1. Article ; Online: 16S rRNA sequencing-based evaluation of the protective effects of Hua-Zhuo-Jie-Du on rats with chronic atrophic gastritis

    Zhou, Pingping / Yang, Tianxiao / Xu, Miaochan / Zhao, Yuejia / Shen, Pengpeng / Wang, Yangang

    BMC Complement Med Ther. 2022 Dec., v. 22, no. 1 p.71-71

    2022  

    Abstract: BACKGROUND: Disturbance of the intestinal flora is a pathogenic factor for chronic atrophic gastritis (CAG). Hua-Zhuo-Jie-Du (HZJD) has been shown to be an effective Chinese herbal preparation for treating CAG. However, the effects of HZJD on the ... ...

    Abstract BACKGROUND: Disturbance of the intestinal flora is a pathogenic factor for chronic atrophic gastritis (CAG). Hua-Zhuo-Jie-Du (HZJD) has been shown to be an effective Chinese herbal preparation for treating CAG. However, the effects of HZJD on the intestinal flora of CAG is unclear. In this study, we probed the regulating effects of HZJD on intestinal microbes in CAG rats using 16S rRNA gene sequencing. METHODS: High-performance liquid chromatography (HPLC) analysis was used to perform quality control of HZJD preparations. We then administered 1-methyl-3-nitro-1-nitrosoguanidine (200 μg/ml) to Sprague–Dawley rats to establish a CAG model. HZJD and vitacoenzyme were administered orally to these rats over a 10 week period. Hematoxylin and eosin (H&E) staining was performed to observe the histopathology of CAG rats. A rarefaction curve, species accumulation curve, Chao1 index, and ACE index were calculated to assess the alpha diversity. Principal component analysis (PCA), non-metric multi-dimensional scaling (NMDS), and unweighted pair group method with arithmetic mean (UPGMA) were conducted to examine the beta diversity. The LEfSe method was used to identify differential bacteria. Differential function analysis used PCA based on KEGG function prediction. RESULTS: HPLC showed that our HZJD preparation method was feasible. H&E staining showed that HZJD significantly improved the pathological state of the gastric mucosa in CAG rats. The rarefaction curve and species accumulation curve showed that the sequencing data were reasonable. The Chao1 and ACE indices were significantly increased in CAG rats compared to the N group. Following HZJD and vitacoenzyme treatment, the Chao1 and ACE indices were decreased. PCA, NMDS, and UPGMA results showed that the M group was separated from the N, HZJD, and V groups, and LEfSe results showed that the relative abundance of Akkermansia, Oscillospira, Prevotella, and CF231 were significantly higher in the N group. Proteobacteria and Escherichia were significantly enriched in the M group, Allobaculum, Bacteroides, Jeotgalicoccus, Corynebacterium, and Sporosarcina were significantly enriched in the V group, and Firmicutes, Lactobacillus, and Turicibacter were significantly enriched in the HZJD group. CONCLUSION: HZJD exhibited a therapeutic effect on the intestinal flora of CAG rats.
    Keywords Bacteroides ; Corynebacterium ; Escherichia ; Jeotgalicoccus ; Lactobacillus ; Oscillospira ; Prevotella ; Sporosarcina ; complement ; eosin ; gastric mucosa ; gastritis ; genes ; high performance liquid chromatography ; histopathology ; intestinal microorganisms ; intestines ; models ; pathological processes and conditions ; prediction ; principal component analysis ; quality control ; species diversity ; therapeutics
    Language English
    Dates of publication 2022-12
    Size p. 71.
    Publishing place BioMed Central
    Document type Article ; Online
    ISSN 2662-7671
    DOI 10.1186/s12906-022-03542-z
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: 16S rRNA sequencing-based evaluation of the protective effects of Hua-Zhuo-Jie-Du on rats with chronic atrophic gastritis.

    Zhou, Pingping / Yang, Tianxiao / Xu, Miaochan / Zhao, Yuejia / Shen, Pengpeng / Wang, Yangang

    BMC complementary medicine and therapies

    2022  Volume 22, Issue 1, Page(s) 71

    Abstract: Background: Disturbance of the intestinal flora is a pathogenic factor for chronic atrophic gastritis (CAG). Hua-Zhuo-Jie-Du (HZJD) has been shown to be an effective Chinese herbal preparation for treating CAG. However, the effects of HZJD on the ... ...

    Abstract Background: Disturbance of the intestinal flora is a pathogenic factor for chronic atrophic gastritis (CAG). Hua-Zhuo-Jie-Du (HZJD) has been shown to be an effective Chinese herbal preparation for treating CAG. However, the effects of HZJD on the intestinal flora of CAG is unclear. In this study, we probed the regulating effects of HZJD on intestinal microbes in CAG rats using 16S rRNA gene sequencing.
    Methods: High-performance liquid chromatography (HPLC) analysis was used to perform quality control of HZJD preparations. We then administered 1-methyl-3-nitro-1-nitrosoguanidine (200 μg/ml) to Sprague-Dawley rats to establish a CAG model. HZJD and vitacoenzyme were administered orally to these rats over a 10 week period. Hematoxylin and eosin (H&E) staining was performed to observe the histopathology of CAG rats. A rarefaction curve, species accumulation curve, Chao1 index, and ACE index were calculated to assess the alpha diversity. Principal component analysis (PCA), non-metric multi-dimensional scaling (NMDS), and unweighted pair group method with arithmetic mean (UPGMA) were conducted to examine the beta diversity. The LEfSe method was used to identify differential bacteria. Differential function analysis used PCA based on KEGG function prediction.
    Results: HPLC showed that our HZJD preparation method was feasible. H&E staining showed that HZJD significantly improved the pathological state of the gastric mucosa in CAG rats. The rarefaction curve and species accumulation curve showed that the sequencing data were reasonable. The Chao1 and ACE indices were significantly increased in CAG rats compared to the N group. Following HZJD and vitacoenzyme treatment, the Chao1 and ACE indices were decreased. PCA, NMDS, and UPGMA results showed that the M group was separated from the N, HZJD, and V groups, and LEfSe results showed that the relative abundance of Akkermansia, Oscillospira, Prevotella, and CF231 were significantly higher in the N group. Proteobacteria and Escherichia were significantly enriched in the M group, Allobaculum, Bacteroides, Jeotgalicoccus, Corynebacterium, and Sporosarcina were significantly enriched in the V group, and Firmicutes, Lactobacillus, and Turicibacter were significantly enriched in the HZJD group.
    Conclusion: HZJD exhibited a therapeutic effect on the intestinal flora of CAG rats.
    MeSH term(s) Animals ; Gastric Mucosa ; Gastritis, Atrophic/drug therapy ; Gastritis, Atrophic/pathology ; Gastrointestinal Microbiome ; RNA, Ribosomal, 16S/genetics ; Rats ; Rats, Sprague-Dawley
    Chemical Substances RNA, Ribosomal, 16S
    Language English
    Publishing date 2022-03-16
    Publishing country England
    Document type Journal Article
    ISSN 2662-7671
    ISSN (online) 2662-7671
    DOI 10.1186/s12906-022-03542-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: [Inhibition of infectious bursal disease virus replication in chicken embryos by miRNAs delivered by recombinant avian adeno-associated viral vector].

    Shen, Pengpeng / Wang, Yongjuan / Sun, Huaichang / Zhang, Xinyu / Xia, Xiaoli

    Wei sheng wu xue bao = Acta microbiologica Sinica

    2011  Volume 51, Issue 2, Page(s) 256–261

    Abstract: Objective: We studied the inhibition of infectious bursal disease virus (IBDV) replication in chicken embryos by recombinant avian adeno-associated virus (AAAV)-delivered VP1- and VP2-specific microRNAs (miRNAs).: Methods and results: We co- ... ...

    Abstract Objective: We studied the inhibition of infectious bursal disease virus (IBDV) replication in chicken embryos by recombinant avian adeno-associated virus (AAAV)-delivered VP1- and VP2-specific microRNAs (miRNAs).
    Methods and results: We co-transfected AAV-293 cells with the VP1- or VP2 gene-specific miRNA expression vector pAITR-RFPmiVP1 or AITR-RFPmiVP2E, AAAV packaging vector pcDNA-ARC and adenovirus helper vector pHelper, resulting in recombinant virus rAAAV-RFPmiVP1 or rAAAV-RFPmiVP2E. We also generated the recombinant viruses rAAAV-RFP (without miRNA expression cassette) and rAAAV-RFPmiVP2con (expressing control miRNA) using the same method as the control purpose. Electron microscopy showed that the recombinant viruses had a typical morphology of AAV. We confirmed the presence of miRNA expression cassette in the recombinant viral genomes by using PCR. Our poly (A)-tailed RT-PCR showed correct expression of the miRNAs in the rAAAV-transduced DF-1 cells. We inoculated the recombinant viruses individually into 8-day-old SPF chicken embryos and then challenged them using Lukert strain IBDV on day 2 after inoculation. Our IBDV titration assay showed that the 50% tissue culture infectious dose (TCID50) of rAAAV-RFP- or rAAAV-RFPmiVP2con-inoculated group was 8.0 log10, whereas the TCID50 of rAAAV-RFPmiVP1-inoculated group decreased to 1.0 and 0.8 log10 on day 3 and 6 after challenge, respectively. Similarly, the TCID50 of rAAAV-RFPmiVP2E-inoculated group decreased to 1.5 and 2.0 log10, respectively.
    Conclusion: These data suggest that rAAAV can transduce efficiently chicken embryos and the expressed VP1- and VP2-specific miRNAs can inhibit the replication of IBDV efficiently.
    MeSH term(s) Animals ; Birnaviridae Infections/genetics ; Birnaviridae Infections/veterinary ; Birnaviridae Infections/virology ; Chick Embryo ; Chickens ; Dependovirus/genetics ; Dependovirus/metabolism ; Down-Regulation ; Genetic Vectors/genetics ; Genetic Vectors/metabolism ; Infectious bursal disease virus/genetics ; Infectious bursal disease virus/physiology ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Poultry Diseases/genetics ; Poultry Diseases/virology ; Viral Envelope Proteins/genetics ; Viral Envelope Proteins/metabolism ; Virus Replication
    Chemical Substances MicroRNAs ; Viral Envelope Proteins
    Language Chinese
    Publishing date 2011-02
    Publishing country China
    Document type English Abstract ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 412683-x
    ISSN 0001-6209 ; 0098-9150
    ISSN 0001-6209 ; 0098-9150
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Effective inhibition of infectious bursal disease virus replication by recombinant avian adeno-associated virus-delivered microRNAs.

    Wang, Yongjuan / Sun, Huaichang / Shen, Pengpeng / Zhang, Xinyu / Xia, Xiaoli

    The Journal of general virology

    2009  Volume 90, Issue Pt 6, Page(s) 1417–1422

    Abstract: RNA interference (RNAi) is a novel antiviral strategy against a variety of virus infections. Infectious bursal disease virus (IBDV) causes an economically important disease in young chickens. This study demonstrated efficient inhibition of IBDV ... ...

    Abstract RNA interference (RNAi) is a novel antiviral strategy against a variety of virus infections. Infectious bursal disease virus (IBDV) causes an economically important disease in young chickens. This study demonstrated efficient inhibition of IBDV replication by recombinant avian adeno-associated virus (rAAAV)-delivered anti-VP1 and anti-VP2 microRNAs (miRNAs). In the viral vector-transduced cells, sequence-specific miRNA expression was detected by poly(A)-tailed RT-PCR. Reporter assays using a pVP2-EGFP vector showed significant and long-lasting inhibition of VP2-EGFP expression in cells transduced with anti-VP2 miRNA-expressing rAAAV-RFPmiVP2E, but not with the control miRNA-expressing rAAAV-RFPmiVP2con or anti-VP1 miRNA-expressing rAAAV-RFPmiVP1. Semi-quantitative RT-PCR and/or virus titration assays showed a significant inhibitory effect on homologous IBDV replication in cells transduced with rAAAV-RFPmiVP1 or rAAAV-RFPmiVP2E. For two heterologous IBDV isolates, transduction with rAAAV-RFPmiVP1 led to slightly weaker but similar inhibitory effects, whereas transduction with rAAAV-RFPmiVP2E resulted in significantly weaker and different inhibitory effects. These results suggest that rAAAV could act as an efficient vector for miRNA delivery into avian cells and that VP1 is the more suitable target for interfering with IBDV replication using RNAi technology.
    MeSH term(s) Animals ; Antiviral Agents/pharmacology ; Cell Line ; Chickens ; Dependovirus/genetics ; Fibroblasts/virology ; Genetic Vectors ; Infectious bursal disease virus/drug effects ; Infectious bursal disease virus/physiology ; MicroRNAs/genetics ; MicroRNAs/pharmacology ; RNA Interference ; RNA, Viral/biosynthesis ; Transduction, Genetic ; Virus Replication/drug effects
    Chemical Substances Antiviral Agents ; MicroRNAs ; RNA, Viral
    Language English
    Publishing date 2009-03-04
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 219316-4
    ISSN 1465-2099 ; 0022-1317
    ISSN (online) 1465-2099
    ISSN 0022-1317
    DOI 10.1099/vir.0.010520-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: In vivo inhibitory activity of andrographolide derivative ADN-9 against liver cancer and its mechanisms involved in inhibition of tumor angiogenesis.

    Yang, Wei / Zhao, Jin / Wang, Yake / Xu, Haiwei / Wu, Zhenwei / Hu, Yangyang / Jiang, Kunkun / Shen, Pengpeng / Ma, Cuiyun / Guan, Zhenzhen / Zhang, Yan / Ma, Jiahui / Shang, Ning / Yan, Guangming / Wang, Zhenji / Dai, Guifu

    Toxicology and applied pharmacology

    2017  Volume 327, Page(s) 1–12

    Abstract: It is well known that liver cancer is a highly aggressive malignancy with poor prognosis. Andrographolide (AD), a major bioactive component of Andrographis paniculata (Burm. F.), is a potential anti-cancer pharmacophore and the synthesis of AD ... ...

    Abstract It is well known that liver cancer is a highly aggressive malignancy with poor prognosis. Andrographolide (AD), a major bioactive component of Andrographis paniculata (Burm. F.), is a potential anti-cancer pharmacophore and the synthesis of AD derivatives with better cytotoxicity to cancer cells has attracted considerable attentions. In the present study, we evaluated the in vivo inhibitory effects of ADN-9, a 15-benzylidene substituted derivative of AD, on the growth and metastasis of murine hepatoma H22 using an orthotopic xenograft model and a subcutaneous xenograft model, and we further studied the anti-angiogenic action and the related mechanisms of ADN-9 in vivo and in vitro. Importantly, ADN-9 remarkably suppressed the growth and metastasis of both orthotopic and subcutaneous xenograft tumors, and the serum AFP level in orthotopic hepatoma-bearing mice treated with 100mg/kg ADN-9 (ig.) was decreased to the normal level. We also found that ADN-9 showed stronger abilities than AD in shrinking tumors, suppressing the invasion and metastasis of H22 cells, decreasing the MVD and promoting tumor cell apoptosis in subcutaneous xenograft of mice. Additionally, ADN-9 exhibited stronger inhibitory activity than AD against the migration and VEGF-induced capillary-like tube formation in HUVECs, which was further proved to be associated with attenuating VEGF/VEGFR2/AKT signaling pathway. The present research provides the first evidence that a 15-substituted AD derivative is more promising than the parent compound in therapeutic treatment of liver cancer.
    MeSH term(s) Andrographis/chemistry ; Angiogenesis Inhibitors/pharmacology ; Animals ; Antineoplastic Agents, Phytogenic/pharmacology ; Diterpenes/pharmacology ; Human Umbilical Vein Endothelial Cells/drug effects ; Humans ; Liver Circulation/drug effects ; Liver Neoplasms/blood supply ; Liver Neoplasms/drug therapy ; Liver Neoplasms, Experimental/blood supply ; Liver Neoplasms, Experimental/drug therapy ; Mice ; Mice, Inbred BALB C ; Neoplasm Invasiveness/pathology ; Neoplasm Metastasis ; Neovascularization, Pathologic/pathology ; Neovascularization, Pathologic/prevention & control ; Signal Transduction/drug effects ; Vascular Endothelial Growth Factor A/antagonists & inhibitors ; Wound Healing/drug effects ; Xenograft Model Antitumor Assays
    Chemical Substances Angiogenesis Inhibitors ; Antineoplastic Agents, Phytogenic ; Diterpenes ; Vascular Endothelial Growth Factor A ; andrographolide (410105JHGR)
    Language English
    Publishing date 2017-07-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 204477-8
    ISSN 1096-0333 ; 0041-008X
    ISSN (online) 1096-0333
    ISSN 0041-008X
    DOI 10.1016/j.taap.2017.04.022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Effective inhibition of replication of infectious bursal disease virus by miRNAs delivered by vectors and targeting the VP2 gene.

    Wang, Yongjuan / Sun, Huaichang / Shen, Pengpeng / Zhang, Xinyu / Xia, Xiaoli / Xia, Bing

    Journal of virological methods

    2010  Volume 165, Issue 2, Page(s) 127–132

    Abstract: RNA interference (RNAi) is a potent mechanism against a variety of viral infections. Infectious bursal disease virus (IBDV) causes an important disease economically in chickens, which is difficult to control. As part of the development of viral vector- ... ...

    Abstract RNA interference (RNAi) is a potent mechanism against a variety of viral infections. Infectious bursal disease virus (IBDV) causes an important disease economically in chickens, which is difficult to control. As part of the development of viral vector-mediated RNAi strategy against the disease, five anti-VP2 small interference RNAs were selected for construction of microRNA (miRNA) expression vectors tailored for avian cells. Transfection of DF-1 cells with the five vectors resulted in significant inhibition of VP2-EGFP reporter gene expression. More effective miVP2A and miVP2E were selected for further study using single or double miRNA expression vectors. After demonstration of specific miRNA expression, the gene silencing effects were determined in the vector-transfected and IBDV-infected cells. Reverse transcriptase PCR and virus titration showed inhibition rates from 76 to 82% on VP2 expression and significant decreases in virus titer by individual and co-expressed miVP2A and miVP2E. The inhibitory effects lasted for at least 120 h after infection with IBDV. These data suggest that the miRNAs targeting the VP2 can inhibit efficiently replication of IBDV.
    MeSH term(s) Animals ; Birnaviridae Infections/veterinary ; Birnaviridae Infections/virology ; Cell Line ; Chick Embryo ; Gene Expression/genetics ; Genetic Vectors ; Infectious bursal disease virus/genetics ; Infectious bursal disease virus/physiology ; MicroRNAs/genetics ; RNA Interference ; Transfection ; Viral Structural Proteins/genetics ; Virus Replication
    Chemical Substances MicroRNAs ; VP2 protein, infectious bursal disease virus ; Viral Structural Proteins
    Language English
    Publishing date 2010-05
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 8013-5
    ISSN 1879-0984 ; 0166-0934
    ISSN (online) 1879-0984
    ISSN 0166-0934
    DOI 10.1016/j.jviromet.2008.12.022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Effective inhibition of infectious bursal disease virus replication by recombinant avian adeno-associated virus-delivered microRNAs

    Wang, Yongjuan / Sun, Huaichang / Shen, Pengpeng / Zhang, Xinyu / Xia, Xiaoli

    Journal of general virology. 2009 June, v. 90, pt. 6

    2009  

    Abstract: RNA interference (RNAi) is a novel antiviral strategy against a variety of virus infections. Infectious bursal disease virus (IBDV) causes an economically important disease in young chickens. This study demonstrated efficient inhibition of IBDV ... ...

    Abstract RNA interference (RNAi) is a novel antiviral strategy against a variety of virus infections. Infectious bursal disease virus (IBDV) causes an economically important disease in young chickens. This study demonstrated efficient inhibition of IBDV replication by recombinant avian adeno-associated virus (rAAAV)-delivered anti-VP1 and anti-VP2 microRNAs (miRNAs). In the viral vector-transduced cells, sequence-specific miRNA expression was detected by poly(A)-tailed RT-PCR. Reporter assays using a pVP2-EGFP vector showed significant and long-lasting inhibition of VP2–EGFP expression in cells transduced with anti-VP2 miRNA-expressing rAAAV-RFPmiVP2E, but not with the control miRNA-expressing rAAAV-RFPmiVP2con or anti-VP1 miRNA-expressing rAAAV-RFPmiVP1. Semi-quantitative RT-PCR and/or virus titration assays showed a significant inhibitory effect on homologous IBDV replication in cells transduced with rAAAV-RFPmiVP1 or rAAAV-RFPmiVP2E. For two heterologous IBDV isolates, transduction with rAAAV-RFPmiVP1 led to slightly weaker but similar inhibitory effects, whereas transduction with rAAAV-RFPmiVP2E resulted in significantly weaker and different inhibitory effects. These results suggest that rAAAV could act as an efficient vector for miRNA delivery into avian cells and that VP1 is the more suitable target for interfering with IBDV replication using RNAi technology.
    Keywords Infectious bursal disease virus ; virus replication ; antiviral properties ; RNA interference ; RNA ; Avian adeno-associated virus ; genetic vectors ; cell lines ; chickens
    Language English
    Dates of publication 2009-06
    Size p. 1417-1422.
    Document type Article
    ZDB-ID 219316-4
    ISSN 1465-2099 ; 0022-1317
    ISSN (online) 1465-2099
    ISSN 0022-1317
    Database NAL-Catalogue (AGRICOLA)

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