See D M, Tilles J G
Department of Medicine, University of California Irvine Medical Center, Orange 92668.
Antimicrob Agents Chemother. 1992 Feb;36(2):425-8. doi: 10.1128/AAC.36.2.425.
The therapeutic efficacy of an experimental antiviral agent, WIN 54954, was evaluated in murine myocardial infection with coxsackievirus A9 (CVA9). Eight-month-old male Swiss Webster mice were inoculated with 1.5 x 10(4) PFU of CVA9, Boston strain 13. WIN 54954, a broad-spectrum antipicornavirus agent, was administered orally in a dose of 0.25, 2.5, 25, 50, 100, or 200 mg/kg of body weight per day on days 1 to 3 after virus inoculation. Control animals received xanthan gum carrier only. Mice were sacrificed on day 4. Myocardial titers of virus were determined and found to be significantly lower in the four highest dose treatment groups (P less than 0.001 for all groups) compared with controls. Heart weights were also significantly lower compared with controls in these four groups (P less than 0.001 for all groups). When mice received 50 mg of WIN 54954 per kg daily beginning at either 48 or 72 h postinoculation, myocardial titers were once again significantly reduced compared with those of controls (P less than 0.001 for both groups). Neurological toxicity was observed in the 100- and 200-mg/kg/day groups but not in the lower-dose groups. Thus, WIN 54954 effectively reduced myocardial CVA9 replication in a murine model.
在柯萨奇病毒A9(CVA9)感染小鼠心肌的实验中,对一种实验性抗病毒药物WIN 54954的治疗效果进行了评估。选用8月龄雄性瑞士韦伯斯特小鼠,接种1.5×10⁴ 蚀斑形成单位(PFU)的CVA9波士顿株13。广谱抗微小核糖核酸病毒药物WIN 54954在病毒接种后第1至3天,按每日0.25、2.5、25、50、100或200毫克/千克体重的剂量口服给药。对照动物仅接受黄原胶载体。在第4天处死小鼠。测定心肌病毒滴度,发现四个最高剂量治疗组的病毒滴度显著低于对照组(所有组P均小于0.001)。这四组的心脏重量也显著低于对照组(所有组P均小于0.001)。当小鼠在接种后48或72小时开始每日接受每千克50毫克的WIN 54954时,与对照组相比,心肌病毒滴度再次显著降低(两组P均小于0.001)。在100和200毫克/千克/天剂量组观察到神经毒性,而低剂量组未观察到。因此,在小鼠模型中,WIN 54954有效地减少了心肌CVA9的复制。