Bouyer J J, Joseph J P, Rougeul A
Psychopharmacology (Berl). 1979 Sep;65(1):55-8. doi: 10.1007/BF00491978.
In freely moving cats, systemic administration of Chlorpromazine (CPZ) and Haloperidol (HP), two neuroleptics which presumably block catecholamine receptors, leads to a suppression of the waking mu-type rhythms. There is a clear difference, however, in that CPZ leads to slow wave sleep while HP only induces sustained drowsiness. The difference in their action is tentatively explained by their differential effect on an enzyme that is not involved in the metabolism of biogenic amines, tryptophan pyrrolase. We suggest that it is through this pathway that CPZ might increase and HP might decrease brain tryptophan and thereby lead to opposite changes in brain 5-HT content.
在自由活动的猫身上,系统给予氯丙嗪(CPZ)和氟哌啶醇(HP)这两种可能阻断儿茶酚胺受体的神经安定药,会导致清醒时的μ型节律受到抑制。然而,两者存在明显差异,即CPZ会导致慢波睡眠,而HP仅引起持续性嗜睡。它们作用的差异初步解释为它们对一种不参与生物胺代谢的酶——色氨酸吡咯酶的不同影响。我们认为,CPZ可能通过这条途径增加、而HP可能降低脑内色氨酸,从而导致脑内5-羟色胺含量出现相反变化。