Campbell A, Baldessarini R J, Teicher M H
Department of Psychiatry, Harvard Medical School, Belmont, MA.
Psychopharmacology (Berl). 1988;94(1):46-51. doi: 10.1007/BF00735879.
Developing rats are far more sensitive than adults to the behavioral effects of haloperidol. The present results support the hypothesis that this change may reflect age-related changes in brain responses such as alterations in drug-receptor or drug-effector mechanisms. Dose-response studies of catalepsy and ptosis were conducted in male Sprague-Dawley rats aged 30, 56, or 100 days. Resulting dose-effect curves were approximately parallel and showed rightward shifts with highly significant progressive increases of ED50. Similar developmental decreases in drug sensitivity (3-6x) were found following systemic (PO or IP) administration of haloperidol or the phenothiazine neuroleptic perphenazine, which differ markedly in structure, potency, distribution, and metabolism. Age-related decreases in drug sensitivity (3-4x) were also found using intracerebroventricular (ICV) administration of both agents in an attempt to bypass potential "pharmacokinetic" influences. Since the age-dependent decrease in sensitivity to both neuroleptics was found during the rising phase of drug action (1st hour) and ranked: PO greater than IP greater than ICV, some change in absorption and distribution of both drugs may occur in addition to the apparently important maturational decrease in target-organ sensitivity indicated by the responses to direct ICV injection and by the similarity of results obtained with dissimilar agents.
发育中的大鼠对氟哌啶醇的行为影响比成年大鼠敏感得多。目前的结果支持这样一种假说,即这种变化可能反映了与年龄相关的大脑反应变化,如药物受体或药物效应机制的改变。对30日龄、56日龄或100日龄的雄性斯普拉格-道利大鼠进行了僵住症和眼睑下垂的剂量反应研究。所得的剂量效应曲线大致平行,并显示出向右移动,ED50有极显著的逐渐增加。在口服(PO)或腹腔注射(IP)给予氟哌啶醇或吩噻嗪类抗精神病药奋乃静后,发现了类似的药物敏感性发育性降低(3 - 6倍),这两种药物在结构、效力、分布和代谢方面有显著差异。在脑室内(ICV)给予这两种药物时,也发现了与年龄相关的药物敏感性降低(3 - 4倍),以试图绕过潜在的“药代动力学 ”影响。由于在药物作用的上升阶段(第1小时)发现了对两种抗精神病药的敏感性随年龄下降,且排序为:PO大于IP大于ICV,除了对直接脑室内注射的反应以及不同药物获得的结果相似所表明的靶器官敏感性明显的成熟性降低外,这两种药物在吸收和分布方面可能还会发生一些变化。