Sansone M, Melzacka M, Vetulani J
Pharmacol Biochem Behav. 1985 Jul;23(1):137-40. doi: 10.1016/0091-3057(85)90140-6.
To assess the role of trazodone metabolism in its depressant action on conditioned avoidance response we investigated whether in the mouse brain 3-chlorophenylpiperazine (CPP) is formed from trazodone, whether trazodone metabolism is affected by a drug metabolism inhibitor, proadifen, and how trazodone, CPP and their combinations act on avoidance responses in proadifen-pretreated mice. It was found that CPP is formed from trazodone in mice, that proadifen inhibits trazodone metabolism, and that the moderate and transient inhibitory effect of trazodone on avoidance responses is dramatically potentiated and prolonged in proadifen-pretreated mice. This effect, and inhibition of unconditioned escape response observed in mice receiving lower doses of trazodone after proadifen pretreatment, were counteracted by CPP. The results indicate that the inhibitory action of trazodone on avoidance response is caused by the parent compound, and that it is brief and moderate because of the rapid metabolism of the drug with formation of CPP which counteracts the depressant effect of the parent compound.
为评估曲唑酮代谢在其对条件性回避反应的抑制作用中的作用,我们研究了在小鼠脑中曲唑酮是否会生成3-氯苯基哌嗪(CPP),药物代谢抑制剂丙胺太林是否会影响曲唑酮的代谢,以及曲唑酮、CPP及其组合对丙胺太林预处理小鼠的回避反应有何作用。结果发现,小鼠脑中曲唑酮会生成CPP,丙胺太林会抑制曲唑酮代谢,且在丙胺太林预处理的小鼠中,曲唑酮对回避反应的中度和短暂抑制作用会显著增强并延长。这种作用,以及在丙胺太林预处理后接受较低剂量曲唑酮的小鼠中观察到的对非条件逃避反应的抑制,均被CPP抵消。结果表明,曲唑酮对回避反应的抑制作用是由母体化合物引起的,且由于药物快速代谢生成CPP抵消了母体化合物的抑制作用,所以这种抑制作用短暂且中度。