Department of Neurochemistry, Institute of Psychiatry and Neurology, 9 Sobieskiego St., 02-957, Warsaw, Poland.
Department of Experimental Pharmacology, Mossakowski Medical Research Centre, Polish Academy of Sciences, 5 Pawińskiego St., 02-106, Warsaw, Poland.
Behav Brain Res. 2020 Sep 1;393:112745. doi: 10.1016/j.bbr.2020.112745. Epub 2020 Jun 3.
One characteristic feature of addictive drugs is their ability to induce, after a single exposure, a lasting sensitization to the next doses; the underlying neuroplastic changes supposedly involve the brain dopamine system. We aimed at identifying putative relationships between alterations in extracellular dorsal striatal dopamine, HVA and DOPAC levels and in frequency-modulated 50-kHz ultrasonic vocalizations rate response during repeated intraperitoneal amphetamine treatment. Measurements were performed before and after amphetamine doses 1, 2, 7 and 8 (Amph1, Amph2, Amph7 and Amph8; treatment days 1, 7, 12 and 23, respectively). Amphetamine was confirmed to induce sensitization of the vocalization response, but an extended recording time (180 instead of 20 min) revealed that sensitization of this response requires more time to develop than hitherto believed. Baseline extracellular dopamine level increased initially, declined after a series of daily amphetamine doses and showed some tendency for recovery after drug withdrawal. Baseline extracellular DOPAC (but not HVA) showed a continuous decline during the treatment. There was no significant change in the integrated short-term (3-h) extracellular dopamine response, whereas the respective DOPAC collection lowered significantly after repeated drug treatment. Extracellular DOPAC is believed to originate mostly from newly synthesized dopamine, hence the declines in its baseline and post-amphetamine levels suggest falling dopamine synthesis. These results indicate that sensitization of the appetitive vocalization response to amphetamine continues despite reduced dorsal striatal dopamine synthesis and involves no changes in amphetamine-induced dopamine release.
成瘾药物的一个特征是,它们仅单次暴露就能诱导对后续剂量的持久敏化;据推测,潜在的神经可塑性变化涉及大脑多巴胺系统。我们旨在确定细胞外背侧纹状体多巴胺、HVA 和 DOPAC 水平的变化与重复腹腔内安非他命治疗期间频率调制 50-kHz 超声发声率反应之间的潜在关系。在安非他命剂量 1、2、7 和 8(Amph1、Amph2、Amph7 和 Amph8;治疗天数 1、7、12 和 23)之前和之后进行了测量。安非他命被证实可诱导发声反应的敏化,但延长的记录时间(180 分钟而非 20 分钟)表明,这种反应的敏化需要比以前认为的更长的时间来发展。细胞外多巴胺水平最初升高,在一系列每日安非他命剂量后下降,并在停药后显示出恢复的趋势。细胞外 DOPAC(但不是 HVA)在治疗期间持续下降。短期(3 小时)细胞外多巴胺反应的整合没有显著变化,而重复药物治疗后相应的 DOPAC 收集显著降低。细胞外 DOPAC 主要来自新合成的多巴胺,因此其基线和安非他命后水平的下降表明多巴胺合成减少。这些结果表明,尽管背侧纹状体多巴胺合成减少,但对安非他命的奖赏性发声反应的敏化仍在继续,并且不涉及安非他命诱导的多巴胺释放变化。