Spear L P, Shalaby I A, Brick J
Psychopharmacology (Berl). 1980;70(1):47-58. doi: 10.1007/BF00432369.
Chronic haloperidol treatment during prenatal and postnatal development was found to induce long-term behavioral and psychopharmacological effects. Rats tested shortly after termination of the chronic treatment at weaning or as young adults were hyperactive in the open field and exhibited an attenuated behavioral response to amphetamine and an accentuated cataleptic response to later doses of haloperidol, when compared with control offspring of the same age. Tests at an intermediate interval (adolescence period) showed no significant difference from control offspring on any of these behavioral measures. Adult rats administered haloperidol chronically for the same duration were also hyperactive after termination of treatment. In contrast to the effects of haloperidol during development, these adults exhibited an accentuated behavioral response to amphetamine and an attenuated cataleptic response to a later dose of haloperidol. Compensatory mechanisms in response to chronic haloperidol treatment during development thus appear to be different from those in adulthood.
研究发现,在产前和产后发育期间进行慢性氟哌啶醇治疗会产生长期的行为和精神药理学影响。与同龄对照后代相比,断奶时或成年早期慢性治疗结束后不久接受测试的大鼠在旷场中表现出多动,对苯丙胺的行为反应减弱,对后期剂量氟哌啶醇的僵住反应增强。在中间间隔期(青春期)进行的测试显示,在任何这些行为指标上与对照后代均无显著差异。成年大鼠长期接受相同疗程的氟哌啶醇治疗后,在治疗结束后也表现出多动。与发育期间氟哌啶醇的作用相反,这些成年大鼠对苯丙胺的行为反应增强,对后期剂量氟哌啶醇的僵住反应减弱。因此,发育期间对慢性氟哌啶醇治疗的代偿机制似乎与成年期不同。