Watanabe K, Matsunaga T, Narimatsu S, Yamamoto I, Yoshimura H
Department of Hygienic Chemistry, Faculty of Pharmaceutical Sciences, Hokuriku University, Kanazawa, Japan.
Res Commun Chem Pathol Pharmacol. 1992 Dec;78(3):373-6.
Hepatic microsomal oxidation of 11-oxo-delta 8-tetrahydrocannabinol (11-oxo-delta 8-THC) and 9-anthraldehyde (9-AA) to the corresponding carboxylic acids was investigated using six strains of male and female mice (ddN, ddY, C57BL, DBA, C3H and ICR). No significant sex difference was observed in the activity toward 11-oxo-delta 8-THC except for ICR, whereas the activity toward 9-AA was significantly higher in female than in male of ddN, C57BL, DBA and C3H mice. The present study suggests that female specific form(s) of cytochrome P450 may be responsible at least in part for the microsomal oxidation of 9-AA, but not that of 11-oxo- delta 8-THC.
使用六株雄性和雌性小鼠(ddN、ddY、C57BL、DBA、C3H和ICR)研究了11-氧代-δ8-四氢大麻酚(11-oxo-δ8-THC)和9-蒽醛(9-AA)在肝微粒体中氧化为相应羧酸的情况。除ICR外,未观察到对11-氧代-δ8-THC活性的显著性别差异,而在ddN、C57BL、DBA和C3H小鼠中,雌性对9-AA的活性显著高于雄性。本研究表明,细胞色素P450的雌性特异性形式可能至少部分负责9-AA的微粒体氧化,但不负责11-氧代-δ8-THC的微粒体氧化。