Gaunt S D, Baker D C, Green R A
Am J Vet Res. 1981 Nov;42(11):1982-4.
Acute acetaminophen (ACM) toxicosis was induced in cats and the therapeutic benefit of N-acetylcysteine (NAC) was demonstrated. Groups of 4 adult cats were treated as follows: group A-given ACM only; group B- given ACM and then treated with NAC, starting at 0 hour; group C-given ACM and then treated with NAC, starting at 4 hours; and group D-treated with NAC only. Acetaminophen was given as a single oral dose or 143 mg/kg, and the NAC regimen consisted of 4 oral doses (200 mg/kg, given 3 times and 100 mg/kg, given once) with 2 hours between doses. Group A cats developed increased methemoglobin concentration, depletion of erythrocyte reduced glutathione, and increased Heinz body formation. Group B cats also developed methemoglobinemia, depletion of glutathione, and increased Heinz body formation, but the magnitude of these changes was significantly less (P less than 0.05) than in group A. In group C, the findings were similar to group A through 4 hours, but thereafter, significant hematologic improvement was noted. The level of Heinz bodies in group C was intermediate between the values for groups A and B. In group D cats, no significant changes from base line were noted. Evidence of hepatotoxicity was not seen in any group as based on daily determinations of plasma alanine aminotransferase and sorbitol dehydrogenase activities.
在猫身上诱发了急性对乙酰氨基酚(ACM)中毒,并证明了N-乙酰半胱氨酸(NAC)的治疗益处。将4只成年猫分为几组,治疗如下:A组——仅给予ACM;B组——给予ACM,然后从0小时开始用NAC治疗;C组——给予ACM,然后从4小时开始用NAC治疗;D组——仅用NAC治疗。对乙酰氨基酚以143 mg/kg的单次口服剂量给药,NAC治疗方案包括4次口服剂量(200 mg/kg,给药3次,100 mg/kg,给药1次),给药间隔为2小时。A组猫出现高铁血红蛋白浓度升高、红细胞还原型谷胱甘肽耗竭以及海因茨小体形成增加。B组猫也出现了高铁血红蛋白血症、谷胱甘肽耗竭以及海因茨小体形成增加,但这些变化的程度明显小于A组(P小于0.05)。在C组中,4小时内的结果与A组相似,但此后,血液学有显著改善。C组中海因茨小体的水平介于A组和B组之间。在D组猫中,未观察到与基线相比有显著变化。根据每日测定的血浆丙氨酸氨基转移酶和山梨醇脱氢酶活性,在任何一组中均未发现肝毒性证据。