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阿司匹林增强甲氨蝶呤对大鼠胚胎的致死性。

Potentiation of methotrexate embryolethality by aspirin in rats.

作者信息

Woo D C, McClain R M, Hoar R M

出版信息

Teratology. 1978 Feb;17(1):37-41. doi: 10.1002/tera.1420170110.

Abstract

The augmentation of methotrexate-induced embryotoxicity by aspirin was studied. Pregnant Charles River CD rats were given methotrexate or aspirin alone or in combination on gestation day 9 or 12. The frequency of fetal abnormalities was not affected and fetal body weight loss was not additive in the combined treatment. However, pretreatment with aspirin (200 mg/kg) significantly enhanced the embryolethality of methotrexate given at soes of 0.2 mg/kg on day 9 and 1.5 mg/kg on day 12. Studies with tritiated methotrexate in pregnant rats demonstrated that aspirin delayed the renal excretion of methotrexate and increased the concentrations of methotrexate in maternal plasma and the embryos. It is suggested that these effects are responsible for the observed potentiation of embryolethality.

摘要

研究了阿司匹林对甲氨蝶呤诱导的胚胎毒性的增强作用。在妊娠第9天或第12天,给怀孕的查尔斯河CD大鼠单独或联合给予甲氨蝶呤或阿司匹林。联合治疗时,胎儿异常的频率未受影响,且胎儿体重减轻也无累加效应。然而,用阿司匹林(200mg/kg)预处理可显著增强在第9天给予0.2mg/kg、第12天给予1.5mg/kg剂量的甲氨蝶呤的胚胎致死率。对怀孕大鼠使用氚标记的甲氨蝶呤进行的研究表明,阿司匹林延迟了甲氨蝶呤的肾脏排泄,并增加了母体血浆和胚胎中甲氨蝶呤的浓度。提示这些效应是观察到的胚胎致死率增强的原因。

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