Chemical properties, mode of action, and in vivo anti-herpes activities of a lignin-carbohydrate complex from Prunella vulgaris

Yongwen Zhang, Paul Pui Hay But, Vincent Eng Choon Ooi, Hong Xi Xu, Gillian D. Delaney, Spencer H.S. Lee, Song F. Lee

Résultat de recherche: Articleexamen par les pairs

94 Citations (Scopus)

Résumé

The chemical nature, the mode of action, and the in vitro and in vivo anti-HSV activities of the polysaccharide from Prunella vulgaris were characterized. The polysaccharide was isolated by ethanol precipitation, dialysis, CTAB precipitation, and gel exclusion chromatography. The isolated compound (PPS-2b) was a lignin-carbohydrate complex with a molecular weight of 8500. The carbohydrate moiety was composed of glucose, galactose, mannose, galacturonic acid, rhamnose, xylose, and arabinose with glucose as the major sugar. In plaque reduction assay, PPS-2b showed activities against HSV-1 and HSV-2. The anti-HSV activity could be abolished by periodate oxidation. Mechanism studies showed that PPS-2b inactivated HSV-1 directly, blocked HSV-1 binding to Vero cells, and inhibited HSV-1 penetration into Vero cells. A similar inhibition was observed with a gC-deficient strain of HSV-1. The in vivo activities of a Prunella cream formulated with a semi-purified fraction was assessed in a HSV-1 skin lesion model in guinea pigs and a HSV-2 genital infection model in BALB/c mice. Guinea pigs that received the Prunella cream treatment showed a significant reduction (P < 0.01) in skin lesions. Mice that received the Prunella cream treatment showed a significant reduction (P < 0.01) in mortality. In conclusion, the anti-HSV compound from P. vulgaris is a lignin-polysaccharide complex with potent activity against HSV-1 and HSV-2. Its mode of action appears to be inhibiting viral binding and penetration into host cells.

Langue d'origineEnglish
Pages (de-à)242-249
Nombre de pages8
JournalAntiviral Research
Volume75
Numéro de publication3
DOI
Statut de publicationPublished - sept. 2007

Note bibliographique

Funding Information:
This study is supported by grants from the Hong Kong Research Grants Council (CUHK 4171/99M), Innovation and Technology Fund of Hong Kong (AF/104/99), and the Faculty of Dentistry, Dalhousie University. The technical assistance of Ms. Hua Wang at the Department of Biology, the Chinese University of Hong Kong and Prof. Shumin Duan at the Institute of Virology, Chinese Academy of Preventative Medicine (Beijing) was deeply appreciated. We thank C. Brandt for providing the gC-deficient HSV-1. We also thank Profs. H. Yamada and H. Kiyohara for the gift of the pulullan standards.

ASJC Scopus Subject Areas

  • Pharmacology
  • Virology

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