Selected article for: "clinical application and present study"

Author: Fukuchi, Kunihiko; Sakagami, Hiroshi; Sugita, Yoshiaki; Takao, Koichi; Asai, Daisuke; Terakubo, Shigemi; Takemura, Hiromu; Ohno, Hirokazu; Horiuchi, Misaki; Suguro, Madoka; Fujisawa, Tomohiro; Toeda, Kazuki; Oizumi, Hiroshi; Yasui, Toshikazu; Oizumi, Takaaki
Title: Quantification of the Ability of Natural Products to Prevent Herpes Virus Infection
  • Cord-id: hs79la0x
  • Document date: 2020_10_6
  • ID: hs79la0x
    Snippet: Background: Herpes simplex virus (HSV) is usually dormant and becomes apparent when body conditions decline. We investigated the anti-HSV activity of various natural and synthetic compounds for future clinical application. Methods: Mock- and HSV-infected Vero cells were treated for three days with various concentrations of samples. For short exposure, 100-fold concentrated virus were preincubated for 3 min with samples, diluted to normal multiplicity of infection (MOI), before the addition to th
    Document: Background: Herpes simplex virus (HSV) is usually dormant and becomes apparent when body conditions decline. We investigated the anti-HSV activity of various natural and synthetic compounds for future clinical application. Methods: Mock- and HSV-infected Vero cells were treated for three days with various concentrations of samples. For short exposure, 100-fold concentrated virus were preincubated for 3 min with samples, diluted to normal multiplicity of infection (MOI), before the addition to the cells. Anti-HSV activity was evaluated by the chemotherapy index. Results: Alkaline extracts of the leaves of Sasa sp. (SE) and pine cone (PCE) showed higher anti-HSV activity than 20 Japanese traditional herb medicines (Kampo formulas), four popular polyphenols, and 119 chromone-related compounds. Exposure of HSV to SE or PCE for 3 min almost completely eliminated the infectivity of HSV, whereas much longer exposure time was required for Kakkonto, the most active Kampo formulae. Anti-HSV activity of PCE and Kakkonto could be detected only when they were dissolved by alkaline solution (pH 8.0), but not by neutral buffer (pH 7.4). Anti-HSV activity of SE and povidone iodine was stable if they were diluted with neutral buffer. Conclusions: The present study suggests the applicability of SE and PCE for treatment of oral HSV and possibly other viruses.

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