Braus D F, Brassen S
NeuroImage Nord, Psychiatrie sowie Zentrum für Psychosoziale Medizin, Universitätsklinikum Hamburg-Eppendorf.
Radiologe. 2005 Feb;45(2):178-85. doi: 10.1007/s00117-004-1156-z.
Recently, there has been growing interest in using functional magnetic resonance imaging (fMRI) for the evaluation of psychopharmacological drugs. fMRI studies in healthy human volunteers and psychiatric patients focus on cerebral activity following acute drug administration (single challenge) and on adaptive effects on neural networks due to long-term medication. In our own fMRI studies, the effects of olanzapine or amisulpride in never treated or medication-free schizophrenic patients using robust motor, visual, and acoustic tasks was longitudinally examined. In agreement with previous reports in the literature it could be shown that, in contrast to traditional neuroleptics, atypical drugs do not decrease the activation of the sensorimotor cortex but rather normalize the reduced frontoparietal activation as well as the neuropsychological test results. This encourages the assumption that atypical antipsychotics seem to support the recovery or normalization of frontoparietal brain dysfunction in schizophrenia. However, with these new opportunities additional methodological considerations and limitations emerge.
最近,使用功能磁共振成像(fMRI)评估精神药物的兴趣日益浓厚。对健康人类志愿者和精神疾病患者的fMRI研究聚焦于急性药物给药后(单次激发)的大脑活动以及长期用药对神经网络的适应性影响。在我们自己的fMRI研究中,纵向考察了奥氮平或氨磺必利对从未接受过治疗或未服用药物的精神分裂症患者使用稳健的运动、视觉和听觉任务时的影响。与文献中先前的报道一致,可以表明,与传统抗精神病药物相比,非典型药物不会降低感觉运动皮层的激活,而是使额顶叶激活降低以及神经心理学测试结果正常化。这促使人们推测,非典型抗精神病药物似乎有助于精神分裂症患者额顶叶脑功能障碍的恢复或正常化。然而,随着这些新机遇的出现,也出现了更多的方法学考量和局限性。