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The effect of diazepam in the recovery of rabbits from acute acetaminophen intoxication.

机译:地西epa对急性对乙酰氨基酚中毒恢复家兔的作用。

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We have recently shown that diazepam can reduce mortality of acute iron overdose in rats. The mechanism for that effect is not yet defined. Our objective in the present study was to assess whether diazepam can similarly reduce mortality of experimental acute acetaminophen intoxication. Survival of rabbits was compared among four groups receiving 3 g/kg (body weight) of acetaminophen (LD40) orally each, followed by: 1) nothing (group I), 2) one oral dose of 140 mg/kg N-acetylcystein (NAC) an hour later (group II), 3) intramuscular injection of 7 mg/kg diazepam (group III), 4) intramuscular injection of 7 mg/kg diazepam and one oral dose of 140 mg/kg NAC an hour later (group IV). 37.5% of rabbits in group I died after 16 hours, whereas none of the rabbits in group III died, (p = 0.04). No animal died during the 96-hour observation period in groups II and IV. Two and four hours post drug administration, acetaminophen plasma concentrations (APC) were significantly lower among rabbits in group III than in group I (p = 0.0007 and 0.01, respectively) and significantly lower among rabbits in group IV than in those in group II (p<0.0001 and p = 0.03, respectively). Acetaminophen plasma concentrations 2 hours after drug administration were also significantly lower among rabbits in group III than in those in group II (p = 0.0002). Seven and 24 hours after dosage, APC tended to be higher among rabbits in group III than in those in group I, but not significantly so. Administration of diazepam without NAC did not prevent liver and renal dysfunction. We conclude that early administration of diazepam in acute experimental acetaminophen overdose in rabbits reduced APC and mortality, probably by slowing intestinal motility, which resulted in delayed acetaminophen absorption from the gastrointestinal tract.
机译:我们最近显示,地西epa可以降低大鼠急性铁过量的死亡率。尚未确定这种作用的机制。我们在本研究中的目的是评估地西epa是否可以同样降低实验性对乙酰氨基酚中毒的死亡率。比较四组分别口服3 g / kg(体重)对乙酰氨基酚(LD40)的兔子的存活率,然后进行以下比较:1)无(I组),2)一次口服剂量为140 mg / kg N-乙酰半胱氨酸( NAC)一小时后(II组),3)肌内注射7 mg / kg地西epa(III组),4)肌内注射7 mg / kg地西and和一小时口服140 mg / kg NAC(组IV)。第一组的兔子中有37.5%在16小时后死亡,而第三组的兔子中没有一只死亡(p = 0.04)。 II和IV组在96小时的观察期内没有动物死亡。给药后两小时和四小时,对乙酰氨基酚血浆浓度(APC)在第三组的兔子中显着低于第一组(分别为p = 0.0007和0.01),在第四组的兔子中显着低于第二组( p <0.0001和p = 0.03)。给药后2小时,III组兔子的对乙酰氨基酚血浆浓度也显着低于II组(p = 0.0002)。给药后7小时和24小时,III组中的兔子的APC倾向于高于I组中的兔子,但不是显着的。不使用NAC的地西给药不能预防肝肾功能障碍。我们得出的结论是,在兔子的急性实验性对乙酰氨基酚过量中早期给予地西reduced可降低APC和死亡率,可能是通过减慢肠蠕动,从而导致对乙酰氨基酚从胃肠道吸收延迟。

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