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2000
Volume 14, Issue 16
  • ISSN: 1385-2728
  • E-ISSN: 1875-5348

Abstract

Many Chinese herbs have been tested against herpes simplex virus (HSV) in search for new anti-herpetic agents. Extracts and novel molecules such as polysaccharides, tannins, terpenes, lignans, saponins, lectins and flavonoids have been found to be effective as anti-herpetic agents. Using different in vitro and in vivo models, novel compounds isolated from Chinese herbal medicines (CHM) have been tested and demonstrated with strong inhibitory effects on HSV through different mechanisms. CHM like Camellia sinensis, Mentha piperita, Myrica rubra, Pterocarya stenoptera, Smilax glabra and Terminalia arjuna are effective even at early stage of HSV infection to hinder viral attachment and penetration. Other CHM including Chamaecyparis obtuse, Glycyrrhiza glabra, Lobelia chinesis and Ocimum basilicum are capable of interfering in viral replication. Nelumbo nucifera, Pithecellobium clypearia, Polygonum cuspidatum and Schefflera heptaphylla have been reported to block host cellular machineries while Plantago major and Prunella vulgaris have shown to induce immunomodulatory effect. It is also noticeable that some CHM showed dual and even multiple roles in combating HSV infection. Structural modifications of CHM derived compounds by changing the degree of sulfation and oxygenation, transforming specific moiety, addition of chemical groups and increasing molecular weight resulted in enhanced anti-herpetic activity with high selectivity and low toxicity. It is a hopeful attempt to develop topical microbicides which possess multiple actions on the early or late stage of HSV infections from CHM. In this review, we focus on the promising results and the working mechanisms on the anti-herpetic activities of several CHM and the potential of their clinical applications.

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/content/journals/coc/10.2174/138527210792927690
2010-10-01
2025-05-18
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/content/journals/coc/10.2174/138527210792927690
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  • Article Type:
    Research Article
Keyword(s): ACV; Acyclovir (ACV); Anti-Herpetic Agents; anti-herpetic mechanism; anti-HSV chemotherapy; bioassay-guided fractionation; cellular proteins; Chamaecyparis Obtusa; Chinese herbal medicines; corneal blindness; cross-linking; cyclin-dependent kinases; drug-resistant viral strains; encephalitis; Euphorbia Jolkini; Euphorbia Thymifolia; fetuin-binding glycoprotein (SGPF2); flavonoids; galloyltricetifavan; Geraniin; guanosine nucleoside; herpes simplex virus; herpetic stromal keratitis; heteroannular diene structure; HSV inhibition; HSV-1; HSV-2; IL-1b; IL-6; lignans; lignin-carbohydrate complex; Lobelia Chinensis; lupeol; macrophage-related cytokines; Melia Azedarach; meningitis; Mentha Piperita; microbicides; mitogen-activated; Morus Alba; mucocutaneous herpes; Mutations; Myrica Rubra; Myrica rubra; neonatal infections; non-cytotoxic concentrations; Ocimum Basilicum; oxidation process; Phyllanthus Urinaria; Plantago Major; Polygonatum Cyrtonema; Polygonum Cuspidatum; polysaccharides; protein kinase cascades; Prunella Vulgaris; Pterocarya stenoptera; Pterocarya Stenoptera; saponins; Schefflera Heptaphylla; single drug; skin lesions; Smilax glabra; Sodium rutin sulfate; structural modification; Structural modification; tannins; Terminalia Arjuna; terpenes; therapeutic HSV vaccine; thymidine kinase; TNF-a; topical microbicides; transforming specific moiety; Typhonium Divaricatum; viral DNA polymerase; viral infection; virucidal effect; virus replication
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