Valentovic M, Bachmann K
Pharmacology. 1980;21(3):167-74. doi: 10.1159/000137429.
Hexobarbital sleep times, antipyrine-induced temperature depression, in vitro hexobarbital metabolism, and antipyrine half-life were measured in rats receiving either saline or urea pretreatments. Urea pretreatment slows hexobarbital metabolsim and prolongs hexobarbital sleep times. Urea pretreatment als shortens the duration of antipyrine-induced temperature depression as well as the half-life of antipyrine. Urea appears to contribute to the changes in drug metabolism which have been reported for nephrectomized rats, and may also contribute to aberrations of drug metabolism accompanying uremia in man.
在接受生理盐水或尿素预处理的大鼠中,测量了己巴比妥睡眠时间、安替比林诱导的体温降低、体外己巴比妥代谢以及安替比林半衰期。尿素预处理减缓了己巴比妥的代谢并延长了己巴比妥睡眠时间。尿素预处理还缩短了安替比林诱导的体温降低持续时间以及安替比林的半衰期。尿素似乎促成了已报道的肾切除大鼠的药物代谢变化,并且也可能促成人类尿毒症时伴随的药物代谢异常。