RT Journal Article
SR Electronic
T1 Purification and Characterization of Eugeniin as an Anti-herpesvirus Compound from Geum japonicum andSyzygium aromaticum
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 728
OP 735
VO 284
IS 2
A1 Kurokawa, Masahiko
A1 Hozumi, Toyoharu
A1 Basnet, Purusotam
A1 Nakano, Michio
A1 Kadota, Shigetoshi
A1 Namba, Tuneo
A1 Kawana, Takashi
A1 Shiraki, Kimiyasu
YR 1998
UL http://jpet.aspetjournals.org/content/284/2/728.abstract
AB The hot-water extract of Geum japonicum has been shown to exhibit prophylactic and therapeutic anti-herpes simplex virus (HSV) activity in murine infection models. Eugeniin was purified as an anti-HSV compound from the extract and also was isolated from another herbal extract (Syzygium aromaticum) that had exhibited anti-HSV activity in mice. Thus the anti-HSV action of eugeniin was characterized. The effective concentration (5.0 μg/ml) for 50% plaque reduction of eugeniin for wild HSV type 1 (HSV-1) on Vero cells was 13.9-fold lower than its 50% cytotoxic concentration determined by a yield-reduction assay. Eugeniin also inhibited the growth of acyclovir-phosphonoacetic acid-resistant HSV-1, thymidine kinase-deficient HSV-1 and wild HSV type 2. Eugeniin as well as phosphonoacetic acid inhibited viral DNA and late viral protein syntheses in their infected Vero cells, but not cellular protein synthesis at its inhibitory concentrations. Purified HSV-1 DNA polymerase activity was inhibited by eugeniin noncompetitively with respect to dTTP. Its apparent Ki value for euginiin was 8.2- and 5.8-fold lower than theKi values of purified human DNA polymerases α and β, respectively. Thus one of the major target sites of inhibitory action of eugeniin is viral DNA synthesis; the inhibitory action for viral DNA polymerase activity was novel compared with anti-HSV nucleoside analogs. The American Society for Pharmacology and Experimental Therapeutics