Study of the protective effects of Chlorella
碩士 === 國立臺灣海洋大學 === 食品科學系 === 99 === This study investigated the hot water extration of Chlorella pyrenoidosa (Chlorella pyrenoidosa extract, CpE) for inhibiting influenza A virus infection on in vitro and in vivo model. In vitro cell aaay, the sequence of CpE treatment is according to the adsorptio...
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ndltd-TW-099NTOU52530522015-10-16T04:03:28Z http://ndltd.ncl.edu.tw/handle/28414569885065437711 Study of the protective effects of Chlorella 探討小球藻萃取物抗A 型流行性感冒病毒 林睫侖 碩士 國立臺灣海洋大學 食品科學系 99 This study investigated the hot water extration of Chlorella pyrenoidosa (Chlorella pyrenoidosa extract, CpE) for inhibiting influenza A virus infection on in vitro and in vivo model. In vitro cell aaay, the sequence of CpE treatment is according to the adsorption step of virus infection; then divide into before virus adsorption (pre-treatment) and after virus adsorption (post-treatment). We use cell viability assay (MTS assay), cytopathic effect (CPE) assay, plaque assay, and viral RNA expression (real-time PCR) to study the protective effects of CpE. The beeter inhibition effect of CpE on influenza virus infection is during pre-treatment stage, and CpE-2 has the best protective effect. The concentration of CpE-1 and CpE-2 at more than 125 g/ml, the anti-hemagglutination ability of CpE has 2 HAU (hemagglutinating unit). CpE directly reacted the virus particles (virucidal) can effectively inhibit the plaque formation, but CpE directly reacted cell (cell-treatment) has no significant inhibitory effect. In virucidal treatment, 5 and 10 mg/ml of CpE-2 show more than 95% of inhibition effect. Above all, the inhibition mechanism of influenza virus infection of CpE is directly affecting on the adsorption of influenza virus to host cell. In BALB/c mice animal model, the 4 weeks-old mice infecte with lethal doses influenza virus and the mortality rate is 100%. The mice feeded CpE-2 for a week and CpE-2 direct treated with virus (virucide) before infection, the mortality rate of these mice are effectively reduced. RNA expression of mouse lung were detected by real-time PCR, influenza virus H1N1-NP, and inflammational cytokine: TNF-a, IL-1b, 2 IL-6, and antiviral cytokine: IFN-g, IL-12 in CpE-2 treated group were lower than virus alone group, histological also showed less infiltration of nertuophils, indicating CpE-2 treated can reduced virus infection and inflammation of lung. In summary, the Chlorella pyrenoidosa extract show a protective effect against influenza virus infection on both in vitro cell and animal experiment. Chang-Jer Wu 吳彰哲 2011 學位論文 ; thesis 86 zh-TW |
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碩士 === 國立臺灣海洋大學 === 食品科學系 === 99 === This study investigated the hot water extration of Chlorella
pyrenoidosa (Chlorella pyrenoidosa extract, CpE) for inhibiting influenza
A virus infection on in vitro and in vivo model. In vitro cell aaay, the
sequence of CpE treatment is according to the adsorption step of virus
infection; then divide into before virus adsorption (pre-treatment) and
after virus adsorption (post-treatment). We use cell viability assay (MTS
assay), cytopathic effect (CPE) assay, plaque assay, and viral RNA
expression (real-time PCR) to study the protective effects of CpE. The
beeter inhibition effect of CpE on influenza virus infection is during
pre-treatment stage, and CpE-2 has the best protective effect. The
concentration of CpE-1 and CpE-2 at more than 125 g/ml, the
anti-hemagglutination ability of CpE has 2 HAU (hemagglutinating unit).
CpE directly reacted the virus particles (virucidal) can effectively inhibit
the plaque formation, but CpE directly reacted cell (cell-treatment) has no
significant inhibitory effect. In virucidal treatment, 5 and 10 mg/ml of
CpE-2 show more than 95% of inhibition effect. Above all, the inhibition
mechanism of influenza virus infection of CpE is directly affecting on the
adsorption of influenza virus to host cell. In BALB/c mice animal model,
the 4 weeks-old mice infecte with lethal doses influenza virus and the
mortality rate is 100%. The mice feeded CpE-2 for a week and CpE-2
direct treated with virus (virucide) before infection, the mortality rate of
these mice are effectively reduced.
RNA expression of mouse lung were detected by real-time PCR,
influenza virus H1N1-NP, and inflammational cytokine: TNF-a, IL-1b,
2
IL-6, and antiviral cytokine: IFN-g, IL-12 in CpE-2 treated group were
lower than virus alone group, histological also showed less infiltration of
nertuophils, indicating CpE-2 treated can reduced virus infection and
inflammation of lung.
In summary, the Chlorella pyrenoidosa extract show a protective
effect against influenza virus infection on both in vitro cell and animal
experiment.
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author2 |
Chang-Jer Wu |
author_facet |
Chang-Jer Wu 林睫侖 |
author |
林睫侖 |
spellingShingle |
林睫侖 Study of the protective effects of Chlorella |
author_sort |
林睫侖 |
title |
Study of the protective effects of Chlorella |
title_short |
Study of the protective effects of Chlorella |
title_full |
Study of the protective effects of Chlorella |
title_fullStr |
Study of the protective effects of Chlorella |
title_full_unstemmed |
Study of the protective effects of Chlorella |
title_sort |
study of the protective effects of chlorella |
publishDate |
2011 |
url |
http://ndltd.ncl.edu.tw/handle/28414569885065437711 |
work_keys_str_mv |
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