Ibarra Froylán, Vera Yolanda, Quiroz Héctor, Cantó Jorge, Castillo Rafael, Hernández Alicia, Ochoa Pedro
Departamento de Parasitología, Fac. de Med. Vet. y Zoot., UNAM. Cd. Universitaria, 04510 Mexico, DF, Mexico.
Vet Parasitol. 2004 Feb 26;120(1-2):65-74. doi: 10.1016/j.vetpar.2003.12.005.
The aim of the present study was to determine the effective dose of an experimental fasciolicide called compound alpha or 5-chloro-2-methylthio-6-(1-napthyloxy)1H-benzimidazole in experimentally and naturally infected cattle. In the first experiment, 24 fluke-free heifers were each infected with 800 metacercariae of Fasciola hepatica and re-infected on day 45 with other 600 cysts per animal. On day 75, when the animals had 4- and 10-week-old flukes respectively, they were divided into four groups (G) of six animals each according to fluke egg counts. Groups 1-3 received compound alpha at 10, 12 and 14 mg/kg/p.o., respectively. G4 remained as an untreated control. Twenty days after treatment, the animals were sacrificed for the recovery of flukes. Efficacy was assessed as a percentage of egg or fluke reduction relative to the untreated control. In the second experiment (naturally infected cattle), 24-year-old steers positive to F. hepatica eggs were blocked into four groups of five animals each. Groups 1-3 received compound alpha at 10, 12 and 14 mg/kg/p.o., respectively. Group 4 served as a non-treated control. All procedures to determine efficacy were carried out as mentioned in the first experiment. The results in the first study showed a percentage on egg reduction of 97.3, 100 and 100 and overall fluke reduction of 94.3, 100 and 100 for Groups 1-3, respectively. In the second study, the percentage of egg reduction was of 87.5, 99.1 and 100 and overall efficacy regarding fluke reduction was of 84.2, 99.6, and 100 for Groups 1-3, respectively. It is concluded that the effective dose selected for compound alpha was of 12 mg/kg/p.o. in cattle having an induced or natural F. hepatica infection.
本研究的目的是确定一种名为复方α或5-氯-2-甲硫基-6-(1-萘氧基)1H-苯并咪唑的实验性杀片形吸虫剂在实验性和自然感染牛中的有效剂量。在第一个实验中,24头未感染吸虫的小母牛每头感染800个肝片形吸虫囊蚴,并在第45天再次感染,每头动物再感染600个囊蚴。在第75天,当动物分别感染了4周龄和10周龄的吸虫时,根据吸虫卵计数将它们分为四组(G组),每组6只动物。第1-3组分别按10、12和14mg/kg口服给予复方α。第4组作为未治疗的对照。治疗20天后,处死动物以回收吸虫。疗效以相对于未治疗对照的虫卵或吸虫减少百分比来评估。在第二个实验(自然感染牛)中,将24头对肝片形吸虫卵呈阳性的2岁公牛分成四组,每组5头动物。第1-3组分别按10、12和14mg/kg口服给予复方α。第4组作为未治疗的对照。所有确定疗效的程序均如第一个实验所述进行。第一项研究的结果显示,第1-3组的虫卵减少百分比分别为97.3%、100%和100%,吸虫总体减少率分别为94.3%、100%和100%。在第二项研究中,第1-3组的虫卵减少百分比分别为87.5%、99.1%和100%,吸虫减少的总体疗效分别为84.2%、99.6%和100%。得出的结论是,对于诱导感染或自然感染肝片形吸虫的牛,复方α的有效剂量为12mg/kg口服。