Lahti Adrienne C, Holcomb Henry H, Weiler Martin A, Medoff Deborah R, Tamminga Carol A
Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, Maryland 21228, USA.
Biol Psychiatry. 2003 Apr 1;53(7):601-8. doi: 10.1016/s0006-3223(02)01602-5.
Using positron emission tomography (PET) with (15)O water, we compared regional cerebral blood flow (rCBF) patterns induced by clozapine or haloperidol in individuals with schizophrenia. Based on the known clinical characteristics of each drug, we hypothesized that brain regions where the drugs show similar rCBF patterns are among those mediating their antipsychotic actions; whereas, regions where the drugs produce different rCBF patterns are among those mediating their different drug actions, namely, haloperidol's motor side effects or clozapine's unique therapeutic action.
Persons with schizophrenia were scanned using PET with (15)O water, first after withdrawal of all psychotropic medication (n = 6), then again after treatment with therapeutic doses of haloperidol (n = 5) or clozapine (n = 5).
Both drugs increased rCBF in the ventral striatum and decreased rCBF in hippocampus and ventrolateral frontal cortex. The rCBF increase associated with haloperidol was greater than that with clozapine in the dorsal and ventral striatum; the rCBF increase with clozapine was greater than that with haloperidol in cortical regions, including anterior cingulate and dorsolateral frontal cortex.
These data suggest that the rCBF increase in ventral striatum and/or the decrease in hippocampus and/or ventrolateral frontal cortex mediate a common component of antipsychotic action of these drugs. The increased rCBF in dorsal striatum by haloperidol could well be associated with its prominent motor side effects, whereas the increased rCBF in the anterior cingulate or dorsolateral frontal cortex may mediate the superior antipsychotic action of clozapine. The proposals based on these preliminary observations require further study.
我们使用正电子发射断层扫描(PET)结合(15)O水,比较了氯氮平和氟哌啶醇在精神分裂症患者中诱导的局部脑血流量(rCBF)模式。基于每种药物已知的临床特征,我们假设药物显示相似rCBF模式的脑区是介导其抗精神病作用的脑区;而药物产生不同rCBF模式的脑区是介导其不同药物作用的脑区,即氟哌啶醇的运动副作用或氯氮平独特的治疗作用。
对精神分裂症患者使用PET结合(15)O水进行扫描,首先在停用所有精神药物后(n = 6),然后在使用治疗剂量的氟哌啶醇(n = 5)或氯氮平(n = 5)治疗后再次扫描。
两种药物均使腹侧纹状体的rCBF增加,海马体和腹外侧前额叶皮质的rCBF减少。在背侧和腹侧纹状体中,与氟哌啶醇相关的rCBF增加大于氯氮平;在包括前扣带回和背外侧前额叶皮质在内的皮质区域,氯氮平引起的rCBF增加大于氟哌啶醇。
这些数据表明,腹侧纹状体rCBF的增加和/或海马体和/或腹外侧前额叶皮质的减少介导了这些药物抗精神病作用的共同成分。氟哌啶醇使背侧纹状体rCBF增加很可能与其明显的运动副作用有关,而前扣带回或背外侧前额叶皮质rCBF的增加可能介导了氯氮平优越的抗精神病作用。基于这些初步观察提出的建议需要进一步研究。