Viel Henri, Rocques Hélène, Martin Jennifer, Chartier Christophe
AFSSA site de NIORT, Laboratoire d'Etudes et de Recherches Caprines, 60 rue de Pied de Fond, B.P. 3081, 79012, Niort Cedex, France.
Parasitol Res. 2007 Dec;102(1):163-6. doi: 10.1007/s00436-007-0744-z. Epub 2007 Sep 15.
Preliminary results obtained in mice, rats and piglets experimentally infected with Cryptosporidium sp have indicated a partial prophylactic or curative efficacy of nitazoxanide when administered between 50 and 250 mg/kg BW. In this study, the efficacy of nitazoxanide was evaluated in goat neonates experimentally infected with Cryptosporidium sp oocysts. Forty-seven 2- to 4-day-old kids were experimentally infected once on day 0 with 10(6) Cryptosporidium oocysts isolated from a dead kid, and allocated to three groups. Group 1 acted as control untreated group, group 2 received nitazoxanide for 8 days from day -1 to day 6 at a daily dose rate of 200 mg/kg BW, group 3 received nitazoxanide for 7 days from day 2 to day 8 at 100 mg/kg BW. Individual oocyst shedding was monitored by daily examination of faecal smears stained by carbol fuchsin and scored semi-quantitatively (zero to four). The other criteria included for nitazoxanide evaluation were weight gain and mortality. In the control group, oocyst shedding that started 3 days post-inoculation (PI) was maximal 6-7 days PI (mean scores ranging from 1.69 to 1.94) and became undetectable from day 16 PI. In group 2, oocyst shedding started 1 day later, peaked 9-11 days PI (1.33 to 1.5) and vanished day 18 PI. In group 3, results were similar to those of group 1 except for the mean scores ranging from 1.0 to 1.58. No significant difference was seen for weight gains between groups. Five kids died in group 1 as well as in group 3, whereas seven kids died in group 2. An acute toxicity of nitazoxanide was suspected as soon as the first 2 days of treatment.
在小鼠、大鼠和仔猪上进行的实验性感染隐孢子虫的初步结果表明,硝唑尼特以50至250mg/kg体重给药时具有部分预防或治疗效果。在本研究中,评估了硝唑尼特对实验性感染隐孢子虫卵囊的新生山羊的疗效。47只2至4日龄的羔羊在第0天用从一只死亡羔羊分离的10(6)个隐孢子虫卵囊进行一次实验性感染,并分为三组。第1组作为未治疗的对照组,第2组从第-1天至第6天以200mg/kg体重的日剂量率接受硝唑尼特治疗8天,第3组从第2天至第8天以100mg/kg体重接受硝唑尼特治疗7天。通过每天检查用石炭酸品红染色的粪便涂片来监测个体卵囊排出情况,并进行半定量评分(0至4分)。评估硝唑尼特的其他标准包括体重增加和死亡率。在对照组中,接种后3天开始的卵囊排出在接种后6至7天达到最大值(平均评分范围为1.69至1.94),从接种后第16天开始无法检测到。在第2组中,卵囊排出1天后开始,在接种后9至第11天达到峰值(1.33至1.5),并在接种后第18天消失。在第3组中,结果与第1组相似,只是平均评分范围为1.0至1.58。各组之间的体重增加没有显著差异。第1组和第3组各有5只羔羊死亡,而第2组有7只羔羊死亡。在治疗的头2天就怀疑硝唑尼特存在急性毒性。