Thujaplicin–copper chelates inhibit replication of human influenza viruses
Identifieur interne : 001A44 ( Main/Exploration ); précédent : 001A43; suivant : 001A45Thujaplicin–copper chelates inhibit replication of human influenza viruses
Auteurs : Daisei Miyamoto [Japon] ; Yuki Kusagaya [Japon] ; Naoko Endo [Japon] ; Ayako Sometani [Japon] ; Seiji Takeo [Japon] ; Takashi Suzuki [Japon] ; Yaeno Arima [Japon] ; Katsuyuki Nakajima [États-Unis] ; Yasuo Suzuki [Japon]Source :
- Antiviral Research [ 0166-3542 ] ; 1998.
Descripteurs français
- KwdFr :
- Animaux, Antiviraux (), Antiviraux (pharmacologie), Apoptose (), Chiens, Chélateurs (), Cuivre (), Humains, Lignée cellulaire, Monoterpènes, Méthode des plages virales, Réplication virale (), Survie cellulaire (), Tropolone (), Tropolone (analogues et dérivés), Tropolone (pharmacologie), Virus de la grippe A (), Virus de la grippe A (physiologie).
- MESH :
- analogues et dérivés : Tropolone.
- pharmacologie : Antiviraux, Tropolone.
- physiologie : Virus de la grippe A.
- Pascal (Inist)
- Activité biologique, Animaux, Antiviral, Antiviraux, Apoptose, Chien, Chiens, Chélateur, Chélateurs, Cuivre, Cuivre Métal, Humains, In vitro, Infection, Influenzavirus, Lignée MDCK, Lignée cellulaire, Lignée cellulaire établie, Monoterpènes, Mort cellulaire, Méthode des plages virales, Origine végétale, Pharmacognosie, Plante médicinale, Réplication, Réplication virale, Survie cellulaire, Thuja, Thujaplicine, Tropolone, Virus de la grippe A.
- Wicri :
- topic : Plante médicinale.
English descriptors
- KwdEn :
- Animals, Antiviral, Antiviral Agents (chemistry), Antiviral Agents (pharmacology), Apoptosis, Apoptosis (drug effects), Biological activity, Cell Line, Cell Survival (drug effects), Cell death, Chelating Agents (chemistry), Chelating agent, Copper (chemistry), Copper Metal, Dog, Dogs, Established cell line, Humans, In vitro, Infection, Influenza A virus (drug effects), Influenza A virus (physiology), Influenzavirus, Medicinal plant, Monoterpenes, Pharmacognosy, Plant origin, Replication, Thuja, Tropolone (analogs & derivatives), Tropolone (chemistry), Tropolone (pharmacology), Viral Plaque Assay, Virus Replication (drug effects).
- MESH :
- chemical , analogs & derivatives : Tropolone.
- chemical , chemistry : Antiviral Agents, Chelating Agents, Copper, Tropolone.
- chemical , pharmacology : Antiviral Agents, Tropolone.
- drug effects : Apoptosis, Cell Survival, Influenza A virus, Virus Replication.
- physiology : Influenza A virus.
- Animals, Cell Line, Dogs, Humans, Monoterpenes, Viral Plaque Assay.
- Teeft :
- Anti6iral, Anti6iral research, Apoptosis, Apoptotic, Assay, Canine kidney, Cell death, Cell growth, Cell viability, Chelate, Chem, Copper chelate, Copper chelates, Copper ions, Copper sulfate, Culture medium, Cytometric, Cytometric analysis, Cytotoxic, Cytotoxic effects, Early phase, Early stage, Hela cells, Host cells, Human apoptosis, Inhibitory effects, Lactate dehydrogenase, Mdck, Mdck cells, Metal chelates, Miyamoto, Morphological changes, Postinfection, Supernatant, Suzuki, Takizawa, Test samples, Thuja plicata, Thujaplicin, Thujaplicin copper chelates, Thujaplicins, Total cells, Viral, Viral infection, Virus, Virus infection, Zinc ions.
Abstract
Abstract: The effects of α-, β- and γ-thujaplicins and six of their metal chelates on human influenza virus-induced apoptosis in Madin–Darby canine kidney (MDCK) cells were examined by DNA fragmentation and flow cytometry. Among the compounds tested, thujaplicin–copper chelates inhibited apoptosis induced in the infected MDCK cells with influenza A/PR/8/34(H1N1), A/Shingapol/1/57(H2N2), A/Aichi/2/68(H3N2) and B/Lee/40 viruses, at concentrations of more than 5 μM. These results indicate that the copper chelates inhibit influenza virus-induced apoptosis and that the inhibitory effects may be independent of influenza virus subtype or types. Furthermore, the copper chelates also inhibited the release of the viruses from the infected MDCK cells during apoptosis. The anti-apoptotic effects of the copper chelates may occur 2–4 h postinfection, suggesting that the copper chelates affect MDCK cells directly in the early stage of influenza virus-induced apoptosis. In this study, we demonstrated that thujaplicin–copper chelates inhibit influenza virus-induced apoptosis of MDCK cells and also inhibit virus replication and release from the infected cells.
Url:
DOI: 10.1016/S0166-3542(98)00034-5
Affiliations:
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Le document en format XML
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<term>Antiviral</term>
<term>Antiviral Agents (chemistry)</term>
<term>Antiviral Agents (pharmacology)</term>
<term>Apoptosis</term>
<term>Apoptosis (drug effects)</term>
<term>Biological activity</term>
<term>Cell Line</term>
<term>Cell Survival (drug effects)</term>
<term>Cell death</term>
<term>Chelating Agents (chemistry)</term>
<term>Chelating agent</term>
<term>Copper (chemistry)</term>
<term>Copper Metal</term>
<term>Dog</term>
<term>Dogs</term>
<term>Established cell line</term>
<term>Humans</term>
<term>In vitro</term>
<term>Infection</term>
<term>Influenza A virus (drug effects)</term>
<term>Influenza A virus (physiology)</term>
<term>Influenzavirus</term>
<term>Medicinal plant</term>
<term>Monoterpenes</term>
<term>Pharmacognosy</term>
<term>Plant origin</term>
<term>Replication</term>
<term>Thuja</term>
<term>Tropolone (analogs & derivatives)</term>
<term>Tropolone (chemistry)</term>
<term>Tropolone (pharmacology)</term>
<term>Viral Plaque Assay</term>
<term>Virus Replication (drug effects)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Antiviraux ()</term>
<term>Antiviraux (pharmacologie)</term>
<term>Apoptose ()</term>
<term>Chiens</term>
<term>Chélateurs ()</term>
<term>Cuivre ()</term>
<term>Humains</term>
<term>Lignée cellulaire</term>
<term>Monoterpènes</term>
<term>Méthode des plages virales</term>
<term>Réplication virale ()</term>
<term>Survie cellulaire ()</term>
<term>Tropolone ()</term>
<term>Tropolone (analogues et dérivés)</term>
<term>Tropolone (pharmacologie)</term>
<term>Virus de la grippe A ()</term>
<term>Virus de la grippe A (physiologie)</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Antiviral Agents</term>
<term>Chelating Agents</term>
<term>Copper</term>
<term>Tropolone</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Antiviral Agents</term>
<term>Tropolone</term>
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<keywords scheme="MESH" qualifier="analogues et dérivés" xml:lang="fr"><term>Tropolone</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Apoptosis</term>
<term>Cell Survival</term>
<term>Influenza A virus</term>
<term>Virus Replication</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Antiviraux</term>
<term>Tropolone</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Virus de la grippe A</term>
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<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Influenza A virus</term>
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<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Cell Line</term>
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<term>Humans</term>
<term>Monoterpenes</term>
<term>Viral Plaque Assay</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Activité biologique</term>
<term>Animaux</term>
<term>Antiviral</term>
<term>Antiviraux</term>
<term>Apoptose</term>
<term>Chien</term>
<term>Chiens</term>
<term>Chélateur</term>
<term>Chélateurs</term>
<term>Cuivre</term>
<term>Cuivre Métal</term>
<term>Humains</term>
<term>In vitro</term>
<term>Infection</term>
<term>Influenzavirus</term>
<term>Lignée MDCK</term>
<term>Lignée cellulaire</term>
<term>Lignée cellulaire établie</term>
<term>Monoterpènes</term>
<term>Mort cellulaire</term>
<term>Méthode des plages virales</term>
<term>Origine végétale</term>
<term>Pharmacognosie</term>
<term>Plante médicinale</term>
<term>Réplication</term>
<term>Réplication virale</term>
<term>Survie cellulaire</term>
<term>Thuja</term>
<term>Thujaplicine</term>
<term>Tropolone</term>
<term>Virus de la grippe A</term>
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<keywords scheme="Teeft" xml:lang="en"><term>Anti6iral</term>
<term>Anti6iral research</term>
<term>Apoptosis</term>
<term>Apoptotic</term>
<term>Assay</term>
<term>Canine kidney</term>
<term>Cell death</term>
<term>Cell growth</term>
<term>Cell viability</term>
<term>Chelate</term>
<term>Chem</term>
<term>Copper chelate</term>
<term>Copper chelates</term>
<term>Copper ions</term>
<term>Copper sulfate</term>
<term>Culture medium</term>
<term>Cytometric</term>
<term>Cytometric analysis</term>
<term>Cytotoxic</term>
<term>Cytotoxic effects</term>
<term>Early phase</term>
<term>Early stage</term>
<term>Hela cells</term>
<term>Host cells</term>
<term>Human apoptosis</term>
<term>Inhibitory effects</term>
<term>Lactate dehydrogenase</term>
<term>Mdck</term>
<term>Mdck cells</term>
<term>Metal chelates</term>
<term>Miyamoto</term>
<term>Morphological changes</term>
<term>Postinfection</term>
<term>Supernatant</term>
<term>Suzuki</term>
<term>Takizawa</term>
<term>Test samples</term>
<term>Thuja plicata</term>
<term>Thujaplicin</term>
<term>Thujaplicin copper chelates</term>
<term>Thujaplicins</term>
<term>Total cells</term>
<term>Viral</term>
<term>Viral infection</term>
<term>Virus</term>
<term>Virus infection</term>
<term>Zinc ions</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Plante médicinale</term>
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<front><div type="abstract" xml:lang="en">Abstract: The effects of α-, β- and γ-thujaplicins and six of their metal chelates on human influenza virus-induced apoptosis in Madin–Darby canine kidney (MDCK) cells were examined by DNA fragmentation and flow cytometry. Among the compounds tested, thujaplicin–copper chelates inhibited apoptosis induced in the infected MDCK cells with influenza A/PR/8/34(H1N1), A/Shingapol/1/57(H2N2), A/Aichi/2/68(H3N2) and B/Lee/40 viruses, at concentrations of more than 5 μM. These results indicate that the copper chelates inhibit influenza virus-induced apoptosis and that the inhibitory effects may be independent of influenza virus subtype or types. Furthermore, the copper chelates also inhibited the release of the viruses from the infected MDCK cells during apoptosis. The anti-apoptotic effects of the copper chelates may occur 2–4 h postinfection, suggesting that the copper chelates affect MDCK cells directly in the early stage of influenza virus-induced apoptosis. In this study, we demonstrated that thujaplicin–copper chelates inhibit influenza virus-induced apoptosis of MDCK cells and also inhibit virus replication and release from the infected cells.</div>
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<tree><country name="Japon"><noRegion><name sortKey="Miyamoto, Daisei" sort="Miyamoto, Daisei" uniqKey="Miyamoto D" first="Daisei" last="Miyamoto">Daisei Miyamoto</name>
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<name sortKey="Seiji Takeo" sort="Seiji Takeo" uniqKey="Seiji Takeo" first="" last="Seiji Takeo">Seiji Takeo</name>
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<name sortKey="Suzuki, Takashi" sort="Suzuki, Takashi" uniqKey="Suzuki T" first="Takashi" last="Suzuki">Takashi Suzuki</name>
<name sortKey="Yasuo Suzuki" sort="Yasuo Suzuki" uniqKey="Yasuo Suzuki" first="" last="Yasuo Suzuki">Yasuo Suzuki</name>
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