Effect of 1-beta-D-arabinofuranosyl-E-5-(2-bromovinyl)uracil against herpes simplex virus type 1 infection in immunosuppressed mice

Author:

Ijichi K1,Ashida N1,Machida H1

Affiliation:

1. Research and Development Division, Yamasa Shoyu Co., Ltd., Choshi, Japan.

Abstract

1-beta-D-Arabinofuranosyl-E-5-(2-bromovinyl)uracil (BV-araU) reduced the mortality rates of (i) 7-week-old, cyclophosphamide-treated, immunosuppressed mice (CYP mice) intraperitoneally infected with a moderately virulent strain of herpes simplex virus type 1 and (ii) 4-week-old CYP mice infected with a less virulent strain at doses of 20 and 50 mg/kg of body weight twice daily and 5 mg/kg, respectively. The degree of efficacy of BV-araU was equivalent to that of acyclovir in 4-week-old CYP mice infected with the less virulent strain. BV-araU (20 mg/kg) suppressed viral growth in various organs of CYP mice.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference11 articles.

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4. Comparison of susceptibilities of varicellazoster virus and herpes simplex viruses to nucleoside analogs;Machida H.;Antimicrob. Agents Chemother.,1986

5. Machida H. T. Abiru and T. Ikeda. 1985. Selective antiherpesvirus activity of BV-araU p. 1959-1960. In J. Ishigami (ed.) Recent advances in chemotherapy. University of Tokyo Press Tokyo.

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