Department of Psychiatry, University of California, San Diego, 9500 Gilman Drive MC 0804, La Jolla, CA 92093-0804, USA.
Psychopharmacology (Berl). 2010 Feb;208(3):443-54. doi: 10.1007/s00213-009-1744-8. Epub 2009 Dec 18.
Mania is a core feature of bipolar disorder (BD) that traditionally is assessed using rating scales. Studies using a new human behavioral pattern monitor (BPM) recently demonstrated that manic BD patients exhibit a specific profile of behavior that differs from schizophrenia and is characterized by increased motor activity, increased specific exploration, and perseverative locomotor patterns as assessed by spatial d.
It was hypothesized that disrupting dopaminergic homeostasis by inhibiting dopamine transporter (DAT) function would produce a BD mania-like phenotype in mice as assessed by the mouse BPM.
We compared the spontaneous locomotor and exploratory behavior of C57BL/6J mice treated with the catecholamine transporter inhibitor amphetamine or the selective DAT inhibitor GBR 12909 in the mouse BPM. We also assessed the duration of the effect of GBR 12909 by testing mice in the BPM for 3 h and its potential strain dependency by testing 129/SvJ mice.
Amphetamine produced hyperactivity and increased perseverative patterns of locomotion as reflected in reduced spatial d values but reduced exploratory activity in contrast to the increased exploration observed in BD patients. GBR 12909 increased activity and reduced spatial d in combination with increased exploratory behavior, irrespective of inbred strain. These effects persisted for at least 3 h.
Thus, selectively inhibiting the DAT produced a long-lasting cross-strain behavioral profile in mice that was consistent with that observed in manic BD patients. These findings support the use of selective DAT inhibition in animal models of the impaired dopaminergic homeostasis putatively involved in the pathophysiology of BD mania.
躁狂是双相情感障碍(BD)的核心特征,传统上使用评分量表进行评估。最近使用新型人类行为模式监测器(BPM)的研究表明,躁狂 BD 患者表现出与精神分裂症不同的特定行为模式,其特征为运动活动增加、特定探索增加以及空间 d 评估的持续运动模式。
据假设,通过抑制多巴胺转运蛋白(DAT)功能破坏多巴胺能稳态,将在小鼠中产生类似于 BD 躁狂的表型,如小鼠 BPM 评估所示。
我们比较了用儿茶酚胺转运蛋白抑制剂安非他命或选择性 DAT 抑制剂 GBR 12909 处理的 C57BL/6J 小鼠在小鼠 BPM 中的自发运动和探索行为。我们还通过在 BPM 中测试小鼠 3 小时来评估 GBR 12909 作用的持续时间,并通过测试 129/SvJ 小鼠来评估其潜在的品系依赖性。
安非他命产生了多动和增加的持续运动模式,这反映在空间 d 值降低,但与 BD 患者观察到的增加探索相比,探索性活动减少。GBR 12909 增加了活动并降低了空间 d,同时增加了探索性行为,无论近交系如何。这些影响至少持续 3 小时。
因此,选择性抑制 DAT 在小鼠中产生了一种持久的跨品系行为模式,与躁狂 BD 患者观察到的模式一致。这些发现支持在多巴胺能稳态受损的动物模型中使用选择性 DAT 抑制,这些模型可能与 BD 躁狂的病理生理学有关。