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Therapeutic Methods and Therapies TCIM
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1.
J Ethnopharmacol ; 134(2): 468-74, 2011 Mar 24.
Article in English | MEDLINE | ID: mdl-21211557

ABSTRACT

AIM OF THE STUDY: Extracts from the aerial parts of the South African resurrection plant Myrothamnus flabellifolia Welw. have been used traditionally against infections of the upper respiratory tract and skin diseases. A polyphenol-enriched extract was investigated for potential antiviral effects against herpes simplex virus type 1 (HSV-1) and adenovirus, and the underlying mode of action was to be studied. MATERIALS AND METHODS: Antiviral effects of an acetone-water extract (MF) from Myrothamnus flabellifolia on HSV-1 and adenovirus type 3 were tested in infected Vero cells by plaque reduction assay, MTT test and immunofluorescence. The influence of the extract on the HSV-1 envelope glycoprotein D was shown by Western blot. Organotypic full thickness skin models consisting of multilayer skin equivalents were used for the investigation of MF effects on HSV-1 replication. RESULTS: MF exhibited strong antiviral activity against HSV-1. The HSV-1-specific inhibitory concentration (IC(50)) was determined as 0.4 µg/mL and the cytotoxic concentration (CC(50)) against Vero cells as 50 µg/mL. A selectivity index (SI) (ratio of CC(50) to IC(50)) of approximately 120 was calculated when MF was added to the virus inoculum for 1h at 37°C prior to infection. The replication of adenovirus 3 was not affected by MF. MF abolished virus entry into the host cell by blocking viral attachment to the cell surface. When added after attachment at a concentration of >6 µg/mL, the extract also inhibited penetration of HSV-1 into the host cell. Polyphenolic compounds from MF directly interacted with viral particles, leading to the oligomerisation of envelope proteins as demonstrated for the essential viral glycoprotein D (gD). Using organotypic full thickness tissue cultures, it was shown that treatment of HSV-1 infected cultures with the MF resulted in reduced viral spread. CONCLUSIONS: A polyphenol-enriched extract from Myrothamnus flabellifolia strongly acts against HSV-1 by blocking viral entry into the cells.


Subject(s)
Antiviral Agents/therapeutic use , Herpes Simplex/drug therapy , Herpesvirus 1, Human/drug effects , Magnoliopsida/chemistry , Phytotherapy , Plant Extracts/therapeutic use , Proanthocyanidins/therapeutic use , Adenoviridae/drug effects , Adenoviridae Infections/microbiology , Animals , Antiviral Agents/pharmacology , Cell Line , Chlorocebus aethiops , Herpes Simplex/microbiology , Herpesvirus 1, Human/chemistry , Herpesvirus 1, Human/pathogenicity , Humans , Inhibitory Concentration 50 , Keratinocytes/drug effects , Keratinocytes/microbiology , Plant Components, Aerial , Plant Extracts/pharmacology , Proanthocyanidins/pharmacology , Skin/drug effects , Skin/microbiology , Vero Cells , Viral Envelope Proteins/chemistry , Virus Integration/drug effects
2.
Fitoterapia ; 82(3): 408-13, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21129454

ABSTRACT

The polyphenol-enriched aqueous extract RF from the aerial parts of Rhododendron ferrugineum exhibited strong antiviral activity against herpes simplex virus type-1 while adenovirus 3 was not affected. RF exhibited an IC(50) of 7.4 µg/mL and a selectivity index of 64 when added to the virus inoculum prior to infection. RF abolished virus entry into the host cell by blocking attachment to the cell surface. When added after attachment at a concentration of >25 µg/mL, RF inhibited also penetration of HSV-1 into the host cell. RF directly interacts with viral envelope proteins as demonstrated for the viral glycoprotein gD.


Subject(s)
Antiviral Agents/therapeutic use , Herpes Simplex/drug therapy , Herpesvirus 1, Human/drug effects , Phytotherapy , Plant Extracts/therapeutic use , Rhododendron , Virus Attachment/drug effects , Animals , Antiviral Agents/pharmacology , Chlorocebus aethiops , Glycoproteins/metabolism , Herpes Simplex/metabolism , Herpes Simplex/virology , Inhibitory Concentration 50 , Plant Components, Aerial , Plant Extracts/pharmacology , Vero Cells , Viral Envelope Proteins/metabolism
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