Aronsen Dane, Bukholt Natasha, Schenk Susan
School of Psychology, Victoria University of Wellington, PO Box 600, Wellington, New Zealand.
Psychopharmacology (Berl). 2016 Apr;233(8):1339-47. doi: 10.1007/s00213-016-4225-x. Epub 2016 Feb 9.
3,4 Methylenedioxymethamphetamine (MDMA) preferentially stimulates the release of serotonin (5-HT) that subsequently produces behavioral responses by activation of post-synaptic receptor mechanisms. The 5-HT1A and 5-HT1B receptors are both well localized to regulate dopamine (DA) release, and have been implicated in modulating the reinforcing effects of many drugs of abuse, but a role in acquisition of self-administration has not been determined.
This study was designed to determine the effect of pharmacological manipulation of 5-HT1A and 5-HT1B receptor mechanisms on the acquisition of MDMA self-administration.
The 5-HT1B/1A receptor agonist, RU 24969 (0.0 or 3.0 mg/kg, bid), was administered for 3 days in order to down-regulate both 5-HT1A and 5-HT1B receptors. Following the pretreatment phase, latency to acquisition of MDMA self-administration was measured.
Repeated administration of RU 24969 significantly decreased the latency to acquisition and increased the proportion of animals that acquired MDMA self-administration. Dose-effect curves for the 5-HT1A-mediated hyperactivity produced by the 5-HT1A agonist, 8-OH-DPAT, and the 5-HT1B-mediated adipsic response produced by RU 24969 were shifted rightward, suggesting a desensitization of 5-HT1A and 5-HT1B receptor mechanisms.
These data suggest that the initial reinforcing effects of MDMA are modulated by 5-HT1A and/or 5-HT1B receptor mechanisms. The potential impact of these changes on the DAergic response relevant to self-administration and a possible role in conditioned reinforcement pertaining to acquisition of self-administration are discussed.
3,4-亚甲基二氧甲基苯丙胺(摇头丸)优先刺激血清素(5-羟色胺,5-HT)的释放,随后通过激活突触后受体机制产生行为反应。5-HT1A和5-HT1B受体都定位于调节多巴胺(DA)的释放,并参与调节许多滥用药物的强化作用,但它们在自我给药习得过程中的作用尚未确定。
本研究旨在确定对5-HT1A和5-HT1B受体机制进行药理学操作对摇头丸自我给药习得的影响。
给予5-HT1B/1A受体激动剂RU 24969(0.0或3.0毫克/千克,每日两次),持续3天,以下调5-HT1A和5-HT1B受体。在预处理阶段之后,测量获得摇头丸自我给药的潜伏期。
重复给予RU 24969显著缩短了获得摇头丸自我给药的潜伏期,并增加了获得摇头丸自我给药的动物比例。5-HT1A激动剂8-OH-DPAT产生的5-HT1A介导的多动以及RU 249产生的确5-HT1B介导的厌食反应的剂量效应曲线向右移动,表明5-HT1A和5-HT1B受体机制脱敏。
这些数据表明,摇头丸的初始强化作用受5-HT1A和/或5-HT1B受体机制调节。讨论了这些变化对与自我给药相关的多巴胺能反应的潜在影响,以及在与自我给药习得相关的条件强化中的可能作用。