Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Pauwelsstrasse 30, 52074 Aachen, Germany.
Psychopharmacology (Berl). 2011 Dec;218(4):733-48. doi: 10.1007/s00213-011-2368-3. Epub 2011 Jun 4.
There is increased interest in elucidating the range of symptoms of schizophrenia and their response to treatment with medications. Particularly negative and cognitive symptoms are often resistant to the therapy with currently available antipsychotics. There are even similarities between negative symptoms in psychosis and the side effects of antidopaminergic antipsychotic drugs.
The aim of this randomized, single-blinded, placebo-controlled study was to investigate the influence of a subchronic, prolonged neuroleptic-induced dopamine deficit on psychopathology and subjective well-being in healthy subjects.
Seventy-two healthy volunteers without history of psychiatric diseases were included. A 7-day antidopaminergic intervention was provided with aripiprazole, haloperidol, and reserpine. For the clinical assessment, structured interviews and psychopathology and extrapyramidal symptom scales were used.
Seven out of 18 participants (38.9%) randomized to the haloperidol group terminated the study ahead of schedule. In the reserpine and the haloperidol group, significantly higher levels of negative and positive symptoms (PANSS scale) were documented. Depressive symptoms predominantly occurred in the reserpine group. Among all participants experiencing the antidopaminergic intervention, the subgroup with positive family history among first and second-generation relatives developed more pronounced depressive symptoms. Concerning extrapyramidal motor symptoms, the haloperidol group had significantly more severe manifestations than all three other groups.
Antidopaminergic modulation in healthy subjects induced substantial impairments in several domains of subjective well-being. In particular an association between hypodopaminergic states and depressive symptoms was observed which may be amplified by a genetic predisposition.
本随机、单盲、安慰剂对照研究旨在探讨亚慢性、长期抗精神病药物诱导的多巴胺缺乏对健康受试者的精神病理学和主观幸福感的影响。
纳入 72 名无精神病史的健康志愿者。使用阿立哌唑、氟哌啶醇和利血平进行为期 7 天的抗多巴胺干预。临床评估采用结构访谈和精神病理学及锥体外系症状量表。
随机分配至氟哌啶醇组的 18 名参与者中有 7 名(38.9%)提前终止研究。在利血平和氟哌啶醇组中,记录到明显更高的阴性和阳性症状(PANSS 量表)水平。抑郁症状主要发生在利血平组。在经历抗多巴胺干预的所有参与者中,第一代和第二代亲属中有阳性家族史的亚组出现了更明显的抑郁症状。关于锥体外系运动症状,氟哌啶醇组的表现明显比其他三组都严重。
在健康受试者中进行的抗多巴胺调节会导致主观幸福感的多个领域出现明显损伤。特别是观察到低多巴胺状态与抑郁症状之间存在关联,这种关联可能会因遗传易感性而放大。