Antiviral activities and pharmacokinetics of penciclovir and famciclovir in Pekin ducks chronically infected with duck hepatitis B virus

被引:18
作者
Tsiquaye, KN
Sutton, D
Maung, M
Boyd, MR
机构
[1] SMITHKLINE BEECHAM PHARMACEUT,BETCHWORTH RH3 7AJ,SURREY,ENGLAND
[2] SMITHKLINE BEECHAM PHARMACEUT,EPSOM KT18 5XQ,SURREY,ENGLAND
关键词
antiviral; famciclovir; hepatitis; penciclovir;
D O I
10.1177/095632029600700305
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Famciclovir (FCV) is the oral form of the potent and selective antiherpesvirus agent penciclovir (PCV). In order to provide more information on the spectrum of activity of PCV, the activities of FCV and PCV against duck hepatitis B virus (DHBV) in chronically infected ducks were examined. As part of this investigation, the oral pharmacokinetics of FCV and PCV were determined in ducks. Oral treatment of DHBV-infected ducks (twice daily for 21 days) with either PCV (20 mg kg(-1) or 100 mg kg(-1)) or FCV (5 mg kg(-1) or 25 mg kg(-1)) suppressed virus replication, as measured by both plasma viral DNA and DNA polymerase levels. Both markers were reduced to undetectable levels within 4 days of the start of treatment, and after the cessation of treatment there was a delay of 2 to 8 days before plasma DHBV DNA and DNA polymerase levels began to increase, indicating that virus replication had resumed. The demonstration of efficacy of PCV and its oral form FCV against DHBV suggested that the two compounds may have clinical benefits. against human hepatitis B virus. Clinical trials are currently ongoing.
引用
收藏
页码:153 / 159
页数:7
相关论文
共 34 条
  • [1] CONTROLLED CLINICAL-TRIAL OF ACYCLOVIR IN CHRONIC HEPATITIS-B VIRUS-INFECTION
    ALEXANDER, GJM
    FAGAN, EA
    HEGARTY, JE
    YEO, J
    EDDLESTON, ALWF
    WILLIAMS, R
    [J]. JOURNAL OF MEDICAL VIROLOGY, 1987, 21 (01) : 81 - 87
  • [2] AN OVERVIEW OF THE FURTHER EVALUATION OF PENCICLOVIR AGAINST HERPES-SIMPLEX VIRUS AND VARICELLA-ZOSTER VIRUS IN CELL-CULTURE HIGHLIGHTING CONTRASTS WITH ACYCLOVIR
    BACON, TH
    SCHINAZI, RF
    [J]. ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1993, 4 : 25 - 36
  • [3] Beasley R.P., 1984, VIRAL HEPATITIS LIVE, P209
  • [4] PENCICLOVIR - A REVIEW OF ITS SPECTRUM OF ACTIVITY, SELECTIVITY, AND CROSS-RESISTANCE PATTERN
    BOYD, MR
    SAFRIN, S
    KERN, ER
    [J]. ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1993, 4 : 3 - 11
  • [5] ANTIHERPESVIRUS ACTIVITY OF 9-(4-HYDROXY-3-HYDROXYMETHYLBUT-1-YL)GUANINE (BRL-39123) IN CELL-CULTURE
    BOYD, MR
    BACON, TH
    SUTTON, D
    COLE, M
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (08) : 1238 - 1242
  • [6] ANTIVIRAL STRATEGIES IN CHRONIC HEPATITIS-B VIRUS-INFECTION .2. INHIBITION OF DUCK HEPATITIS-B VIRUS INVITRO USING CONVENTIONAL ANTIVIRAL AGENTS AND SUPERCOILED-DNA ACTIVE COMPOUNDS
    CIVITICO, G
    WANG, YY
    LUSCOMBE, C
    BISHOP, N
    TACHEDJIAN, G
    GUST, I
    LOCARNINI, S
    [J]. JOURNAL OF MEDICAL VIROLOGY, 1990, 31 (02) : 90 - 97
  • [7] MODE OF ANTIVIRAL ACTION OF PENCICLOVIR IN MRC-5 CELLS INFECTED WITH HERPES-SIMPLEX VIRUS TYPE-1 (HSV-1), HSV-2, AND VARICELLA-ZOSTER VIRUS
    EARNSHAW, DL
    BACON, TH
    DARLISON, SJ
    EDMONDS, K
    PERKINS, RM
    HODGE, RAV
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (12) : 2747 - 2757
  • [8] THE EFFECTS OF DELAYED-ONSET CHEMOTHERAPY USING FAMCICLOVIR OR VALACICLOVIR IN A MURINE IMMUNOSUPPRESSION MODEL FOR HSV-1
    FIELD, HJ
    THACKRAY, AM
    [J]. ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1995, 6 (04) : 210 - 216
  • [9] COMPARISON OF EFFICACIES OF FAMCICLOVIR AND VALACICLOVIR AGAINST HERPES-SIMPLEX VIRUS TYPE-1 IN A MURINE IMMUNOSUPPRESSION MODEL
    FIELD, HJ
    TEWARI, D
    SUTTON, D
    THACKRAY, AM
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (05) : 1114 - 1119
  • [10] COMPARISON OF PROPERTIES OF WOODCHUCK HEPATITIS-VIRUS AND HUMAN HEPATITIS-B VIRUS ENDOGENOUS DNA-POLYMERASES
    HANTZ, O
    OOKA, T
    VITVITSKI, L
    PICHOUD, C
    TREPO, C
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1984, 25 (02) : 242 - 246