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Purification and characterization of eugeniin as an anti-herpesvirus compound from Geum japonicum and Syzygium aromaticum.
J Pharmacol Exp Ther. 1998 Feb; 284(2):728-35.JP

Abstract

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 microg/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 the Ki values of purified human DNA polymerases alpha and beta, 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.

Authors+Show Affiliations

Virology, Toyama Medical and Pharmaceutical University, Sugitani, Toyama 930-01, Japan.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

9454821

Citation

Kurokawa, M, et al. "Purification and Characterization of Eugeniin as an Anti-herpesvirus Compound From Geum Japonicum and Syzygium Aromaticum." The Journal of Pharmacology and Experimental Therapeutics, vol. 284, no. 2, 1998, pp. 728-35.
Kurokawa M, Hozumi T, Basnet P, et al. Purification and characterization of eugeniin as an anti-herpesvirus compound from Geum japonicum and Syzygium aromaticum. J Pharmacol Exp Ther. 1998;284(2):728-35.
Kurokawa, M., Hozumi, T., Basnet, P., Nakano, M., Kadota, S., Namba, T., Kawana, T., & Shiraki, K. (1998). Purification and characterization of eugeniin as an anti-herpesvirus compound from Geum japonicum and Syzygium aromaticum. The Journal of Pharmacology and Experimental Therapeutics, 284(2), 728-35.
Kurokawa M, et al. Purification and Characterization of Eugeniin as an Anti-herpesvirus Compound From Geum Japonicum and Syzygium Aromaticum. J Pharmacol Exp Ther. 1998;284(2):728-35. PubMed PMID: 9454821.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Purification and characterization of eugeniin as an anti-herpesvirus compound from Geum japonicum and Syzygium aromaticum. AU - Kurokawa,M, AU - Hozumi,T, AU - Basnet,P, AU - Nakano,M, AU - Kadota,S, AU - Namba,T, AU - Kawana,T, AU - Shiraki,K, PY - 1998/3/7/pubmed PY - 1998/3/7/medline PY - 1998/3/7/entrez SP - 728 EP - 35 JF - The Journal of pharmacology and experimental therapeutics JO - J Pharmacol Exp Ther VL - 284 IS - 2 N2 - 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 microg/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 the Ki values of purified human DNA polymerases alpha and beta, 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. SN - 0022-3565 UR - https://www.unboundmedicine.com/medline/citation/9454821/Purification_and_characterization_of_eugeniin_as_an_anti_herpesvirus_compound_from_Geum_japonicum_and_Syzygium_aromaticum_ L2 - https://jpet.aspetjournals.org/cgi/pmidlookup?view=long&pmid=9454821 DB - PRIME DP - Unbound Medicine ER -