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In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1
Herpes simplex virus type 1 (HSV-1) is a commonly occurring human pathogen worldwide. There is an urgent need to discover and develop new alternative agents for the management of HSV-1 infection. Tripterygium hypoglaucum (level) Hutch (Celastraceae) is a traditional Chinese medicine plant with many...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SP Wuhan Institute of Virology, CAS
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090710/ https://www.ncbi.nlm.nih.gov/pubmed/20960307 http://dx.doi.org/10.1007/s12250-010-3092-6 |
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author | Ren, Zhe Zhang, Chuan-hai Wang, Lian-jun Cui, Yun-xia Qi, Ren-bin Yang, Chong-ren Zhang, Ying-jun Wei, Xiao-yi Lu, Da-xiang Wang, Yi-fei |
author_facet | Ren, Zhe Zhang, Chuan-hai Wang, Lian-jun Cui, Yun-xia Qi, Ren-bin Yang, Chong-ren Zhang, Ying-jun Wei, Xiao-yi Lu, Da-xiang Wang, Yi-fei |
author_sort | Ren, Zhe |
collection | PubMed |
description | Herpes simplex virus type 1 (HSV-1) is a commonly occurring human pathogen worldwide. There is an urgent need to discover and develop new alternative agents for the management of HSV-1 infection. Tripterygium hypoglaucum (level) Hutch (Celastraceae) is a traditional Chinese medicine plant with many pharmacological activities such as anti-inflammation, anti-tumor and antifertility. The usual medicinal part is the roots which contain about a 1% yield of alkaloids. A crude total alkaloids extract was prepared from the roots of T. hypoglaucum amd its antiviral activity against HSV-1 in Vero cells was evaluated by cytopathic effect (CPE) assay, plaque reduction assay and by RT-PCR analysis. The alkaloids extract presented low cytotoxicity (CC(50) = 46.6 μg/mL) and potent CPE inhibition activity, the 50% inhibitory concentration (IC(50)) was 6.5 μg/mL, noticeably lower than that of Acyclovir (15.4 μg /mL). Plaque formation was significantly reduced by the alkaloids extract at concentrations of 6.25 μg/mL to 12.5 μg/mL, the plaque reduction ratio reached 55% to 75 which was 35% higher than that of Acyclovir at the same concentration. RT-PCR analysis showed that, the transcription of two important delayed early genes UL30 and UL39, and a late gene US6 of HSV-1 genome all were suppressed by the alkaloids extract, the expression inhibiting efficacy compared to the control was 74.6% (UL30), 70.9% (UL39) and 62.6% (US6) respectively at the working concentration of 12.5μg/mL. The above results suggest a potent anti-HSV-1 activity of the alkaloids extract in vitro. |
format | Online Article Text |
id | pubmed-7090710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | SP Wuhan Institute of Virology, CAS |
record_format | MEDLINE/PubMed |
spelling | pubmed-70907102020-03-24 In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1 Ren, Zhe Zhang, Chuan-hai Wang, Lian-jun Cui, Yun-xia Qi, Ren-bin Yang, Chong-ren Zhang, Ying-jun Wei, Xiao-yi Lu, Da-xiang Wang, Yi-fei Virol Sin Article Herpes simplex virus type 1 (HSV-1) is a commonly occurring human pathogen worldwide. There is an urgent need to discover and develop new alternative agents for the management of HSV-1 infection. Tripterygium hypoglaucum (level) Hutch (Celastraceae) is a traditional Chinese medicine plant with many pharmacological activities such as anti-inflammation, anti-tumor and antifertility. The usual medicinal part is the roots which contain about a 1% yield of alkaloids. A crude total alkaloids extract was prepared from the roots of T. hypoglaucum amd its antiviral activity against HSV-1 in Vero cells was evaluated by cytopathic effect (CPE) assay, plaque reduction assay and by RT-PCR analysis. The alkaloids extract presented low cytotoxicity (CC(50) = 46.6 μg/mL) and potent CPE inhibition activity, the 50% inhibitory concentration (IC(50)) was 6.5 μg/mL, noticeably lower than that of Acyclovir (15.4 μg /mL). Plaque formation was significantly reduced by the alkaloids extract at concentrations of 6.25 μg/mL to 12.5 μg/mL, the plaque reduction ratio reached 55% to 75 which was 35% higher than that of Acyclovir at the same concentration. RT-PCR analysis showed that, the transcription of two important delayed early genes UL30 and UL39, and a late gene US6 of HSV-1 genome all were suppressed by the alkaloids extract, the expression inhibiting efficacy compared to the control was 74.6% (UL30), 70.9% (UL39) and 62.6% (US6) respectively at the working concentration of 12.5μg/mL. The above results suggest a potent anti-HSV-1 activity of the alkaloids extract in vitro. SP Wuhan Institute of Virology, CAS 2010-04-09 /pmc/articles/PMC7090710/ /pubmed/20960307 http://dx.doi.org/10.1007/s12250-010-3092-6 Text en © Wuhan Institute of Virology, CAS and Springer-Verlag Berlin Heidelberg 2010 |
spellingShingle | Article Ren, Zhe Zhang, Chuan-hai Wang, Lian-jun Cui, Yun-xia Qi, Ren-bin Yang, Chong-ren Zhang, Ying-jun Wei, Xiao-yi Lu, Da-xiang Wang, Yi-fei In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1 |
title | In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1 |
title_full | In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1 |
title_fullStr | In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1 |
title_full_unstemmed | In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1 |
title_short | In vitro anti-viral activity of the total alkaloids from Tripterygium hypoglaucum against herpes simplex virus type 1 |
title_sort | in vitro anti-viral activity of the total alkaloids from tripterygium hypoglaucum against herpes simplex virus type 1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090710/ https://www.ncbi.nlm.nih.gov/pubmed/20960307 http://dx.doi.org/10.1007/s12250-010-3092-6 |
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