Efficacy of Acyclovir on Virus Replication in Infected Tissues and Virus Reactivation from Explanted Tissues in Mouse Encephalitis Model of Herpes Simplex Virus Type 1

Herpes Simplex Virus Type 1 마우스 뇌염모델에서의 조직내 바이러스 증식 및 재활성에 미치는 Acyclovir의 약효

  • Lee, Chong-Kyo (Pharmaceutical Screening Center, Korea Research Institute of Chemical Technology) ;
  • Kim, Jee-Hyun (Pharmaceutical Screening Center, Korea Research Institute of Chemical Technology) ;
  • Bae, Pan-Kee (Pharmaceutical Screening Center, Korea Research Institute of Chemical Technology) ;
  • Pi, Mi-Kyung (Pharmaceutical Screening Center, Korea Research Institute of Chemical Technology) ;
  • Kim, Hae-Soo (Pharmaceutical Screening Center, Korea Research Institute of Chemical Technology)
  • 이종교 (한국화학연구소 의약활성연구실) ;
  • 김지현 (한국화학연구소 의약활성연구실) ;
  • 배판기 (한국화학연구소 의약활성연구실) ;
  • 피미경 (한국화학연구소 의약활성연구실) ;
  • 김해수 (한국화학연구소 의약활성연구실)
  • Published : 1999.09.30

Abstract

To investigate viral pathogenesis and in vivo efficacy of acyclovir (ACV) in mouse HSV-1 encephalitis models, female BALB/c mice aged 5 weeks were inoculated with strain F either intranasally (IN) or intracerebrally (IC). ACV-treatment by intraperitomeal injection with 0, 5, 10 and 25 mg/kg b.i.d. for 6 days was commenced 1 h after infection. Body weight and signs of clinical disease were noted daily up to 2 weeks. $ED_{50}$ of ACV in IN infection was <5 mg/kg and 14.1 mg/kg in IC infection. Tissues of central nervous system were collected from 2 mice per group everyday up to 5 day p.i. and the virus titers were measured. In IN infection model, high titers in eyes and trigeminal nerves were observed. ACV-treatment showed significant reduction of the titers in all the isolated. In IC infection model, cerebrum, cerebellum and brain stem showed high virus titers. ACV-treatment showed less significant reduction of virus titers than that in IN infection model. Reactivation of explanted trigeminal nerves from mice 30 day p.i. was monitored. In all of ACV treated mice reactivation was observed, i.e. even the highest dose of ACV did not inhibit the establishment of viral latency.

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