Stevens K E, Luthman J, Lindqvist E, Johnson R G, Rose G M
Department of Psychiatry, University of Colorado Health Sciences Center, Denver, USA.
Pharmacol Biochem Behav. 1996 Apr;53(4):817-23. doi: 10.1016/0091-3057(95)02083-7.
Central dopamine systems appear to play an important role in sensory information processing. In particular, the filtering (or gating) of repetitive auditory stimuli is modulated by pharmacological manipulations that affect dopaminergic neurotransmission. The present study further addressed the role of dopamine in auditory gating. Three-day-old male Sprague-Dawley rats, pretreated with desipramine, received intracisternal injections of 6-hydroxydopamine (6-OHDA; 75 micrograms in 10 microliters) or the vehicle. At 4 months of age the rats were implanted for evoked potential recording and auditory gating was assessed using a paired click paradigm. Neonatally administered 6-OHDA did not alter gating in the adult rats. However, unlike for the control group, systemic amphetamine (1.83 mg/kg, IP) failed to disrupt gating in the treated rats. Apomorphine (1.0 mg/kg, SC) disrupted gating in both groups. Neonatal 6-OHDA treatment caused significant reductions in dopamine levels in the striatum, nucleus accumbens, and substantia nigra/ventral tegmental regions. There was an inverse relationship between substantia nigra/ ventral tegmental area dopamine levels and auditory gating. Overall, the results suggest that amphetamine-induced auditory gating loss requires presynaptic dopamine release, but that the deficiency occurs through postsynaptic dopamine receptor activation.
中枢多巴胺系统似乎在感觉信息处理中发挥重要作用。特别是,重复性听觉刺激的过滤(或门控)会受到影响多巴胺能神经传递的药理学操作的调节。本研究进一步探讨了多巴胺在听觉门控中的作用。对3日龄雄性斯普拉格-道利大鼠预先给予地昔帕明处理后,向其脑池内注射6-羟基多巴胺(6-OHDA;10微升中含75微克)或溶剂。在4月龄时,将大鼠植入用于诱发电位记录的装置,并使用配对点击范式评估听觉门控。新生期给予6-OHDA并未改变成年大鼠的门控。然而,与对照组不同,全身性给予苯丙胺(1.83毫克/千克,腹腔注射)未能破坏处理组大鼠的门控。阿扑吗啡(1.0毫克/千克,皮下注射)破坏了两组的门控。新生期6-OHDA处理导致纹状体、伏隔核和黑质/腹侧被盖区的多巴胺水平显著降低。黑质/腹侧被盖区多巴胺水平与听觉门控之间存在负相关关系。总体而言,结果表明苯丙胺诱导的听觉门控丧失需要突触前多巴胺释放,但这种缺陷是通过突触后多巴胺受体激活发生的。