Campbell A, Herschel M, Sommer B, Madsen J R, Cohen B M, Baldessarini R J
Neuropharmacology. 1982 Jul;21(7):663-9. doi: 10.1016/0028-3908(82)90009-0.
Striking circadian changes in behavioral sensitivity to haloperidol were found by measurements of cataleptic responses in rats trained in a controlled lighting cycle (lights on, 7:00 a.m.--7:00 p.m.). Thus, catalepsy was maximal at about 4:00 p.m. and minimal at about 4:00 a.m., virtually the opposite of the circadian rhythm of spontaneous behavioral activity in drug-free rats. At a given dose of haloperidol, catalepsy scores differed 2- to 3-fold, and the ED50 shifted left nearly 10-fold from a.m. to p.m. After fixed doses of haloperidol, tissue levels of the drug, as determined by a sensitive and selective radioreceptor assay, differed by 2- to 6-fold through the 24 hr cycle and brain levels closely followed the circadian changes in behavior. These results suggest a pharmacokinetic contribution to the circadian changes in behavioral response, although additional pharmacodynamic factors are also considered.
通过在可控光照周期(上午7:00至下午7:00开灯)中训练的大鼠的僵住反应测量,发现了对氟哌啶醇行为敏感性的显著昼夜节律变化。因此,僵住反应在下午4:00左右最大,在凌晨4:00左右最小,这与未用药大鼠自发行为活动的昼夜节律几乎相反。在给定剂量的氟哌啶醇下,僵住反应评分相差2至3倍,ED50从上午到下午向左移动近10倍。给予固定剂量的氟哌啶醇后,通过灵敏且特异的放射受体测定法测定的药物组织水平在24小时周期内相差2至6倍,且脑内水平紧密跟随行为的昼夜节律变化。这些结果表明药代动力学对行为反应的昼夜节律变化有贡献,尽管也考虑了其他药效学因素。