Huang Wen, Niu Hai, Gu Yinchun
Institute for Nanobiomedical Technology and Membrane Biology, State Key Lab of Biotherapy of Human Diseases, Cancer Center, West China Hospital, West China Medical School, Sichuan University, Gaoxing Qu, Chengdu, 610041, China.
Lipids. 2008 Aug;43(8):757-63. doi: 10.1007/s11745-008-3196-z. Epub 2008 Jun 13.
Liquid chromatography-ion trap mass spectrometry (LC/ITMS) was employed for a metabolic kinetics study of tert-butylhydroquinone (TBHQ) and its metabolites in rat serum after oral administration. The mean serum concentration-time data of TBHQ and its four metabolites (M1-M4) in both male and female rats after oral administration of TBHQ at dosages of 7, 350 and 700 mg/kg were all best-fitted by a two-compartment model with first-order absorption. TBHQ was rapidly absorbed, distributed and metabolized. The metabolites were also distributed rapidly except M2, but eliminated more slowly than TBHQ. At the doses of 350 and 700 mg/kg, the total concentrations of TBHQ and its metabolites in serum were much higher for male than female rats during the metabolic process (P < 0.01). In addition, the serum concentrations of M1, M3 and M4 were all much higher for males than for females (P < 0.01) during the metabolic process, while no significant differences between male and female rats were found (P > 0.05) for TBHQ and M2, at the doses of 350 and 700 mg/kg. The exploratory assessment of dose proportionality for TBHQ and its metabolites by the power model indicated that the TBHQ exposure increased in a more-than-dose-proportional manner, but the exposures of the metabolites M1-M4 increased in a less-than-dose-proportional manner, across the dose of 7-700 mg/kg.
采用液相色谱 - 离子阱质谱法(LC/ITMS)对叔丁基对苯二酚(TBHQ)及其在大鼠口服给药后血清中的代谢产物进行代谢动力学研究。雄性和雌性大鼠口服剂量为7、350和700 mg/kg的TBHQ后,TBHQ及其四种代谢产物(M1 - M4)的平均血清浓度 - 时间数据均最适合用具有一级吸收的二室模型来拟合。TBHQ吸收、分布和代谢迅速。除M2外,代谢产物分布也迅速,但消除比TBHQ慢。在350和700 mg/kg剂量下,代谢过程中雄性大鼠血清中TBHQ及其代谢产物的总浓度远高于雌性大鼠(P < 0.01)。此外,在350和700 mg/kg剂量下,代谢过程中雄性大鼠M1、M3和M4的血清浓度均显著高于雌性大鼠(P < 0.01),而TBHQ和M2在雄性和雌性大鼠之间未发现显著差异(P > 0.05)。通过幂模型对TBHQ及其代谢产物的剂量比例性进行探索性评估表明,在7 - 700 mg/kg剂量范围内,TBHQ的暴露量呈超剂量比例增加,而代谢产物M1 - M4的暴露量呈低于剂量比例增加。