Adams J D, Lavoie E J, O'Mara-Adams K J, Hoffmann D, Carey K D, Marshall M V
Cancer Lett. 1985 Sep 15;28(2):195-201. doi: 10.1016/0304-3835(85)90075-8.
The pharmacokinetics of N'-nitrosonornicotine (NNN) and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) in the Syrian golden hamster, the CD-1 mouse, and the baboon were compared to the pharmacokinetics in the Fischer rat. The formation and biological half-life of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), the major metabolite of NNK, was also studied in these animal species. The biological half-life of NNN in these 4 animal species ranged from 0.24 h to 3.06 h, that of NNK from 0.21 h to 0.43 h and NNAL from 0.48 h to 2.9 h. The pharmacokinetic data obtained in the baboon suggest that treatment with NNN and NNK causes an enzyme induction which accelerates the rate of elimination of these compounds.
将叙利亚金黄地鼠、CD-1小鼠和狒狒体内N'-亚硝基降烟碱(NNN)和4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)的药代动力学与Fischer大鼠体内的药代动力学进行了比较。还研究了NNK的主要代谢产物4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁醇(NNAL)的形成和生物半衰期。在这4种动物物种中,NNN的生物半衰期为0.24小时至3.06小时,NNK为0.21小时至0.43小时,NNAL为0.48小时至2.9小时。在狒狒身上获得的药代动力学数据表明,用NNN和NNK治疗会引起酶诱导,从而加速这些化合物的消除速率。