Department of Pharmacology, Institute of Pharmacology, Polish Academy of Sciences, Smętna 12 Street, 31-343, Kraków, Poland.
Department of Molecular Neuropharmacology, Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
Neurotox Res. 2018 Apr;33(3):532-548. doi: 10.1007/s12640-017-9831-9. Epub 2017 Nov 13.
MDMA (3,4-methylenedioxymethamphetamine) is a psychostimulant popular as a recreational drug because of its effect on mood and social interactions. MDMA acts at dopamine (DA) transporter (DAT) and serotonin (5-HT) transporter (SERT) and is known to induce damage of dopamine and serotonin neurons. MDMA is often ingested with caffeine. Caffeine as a non-selective adenosine A1/A2A receptor antagonist affects dopaminergic and serotonergic transmissions. The aim of the present study was to determine the changes in DA and 5-HT release in the mouse striatum induced by MDMA and caffeine after their chronic administration. To find out whether caffeine aggravates MDMA neurotoxicity, the content of DA and 5-HT, density of brain DAT and SERT, and oxidative damage of nuclear DNA were determined. Furthermore, the effect of caffeine on MDMA-induced changes in striatal dynorphin and enkephalin and on behavior was assessed. The DA and 5-HT release was determined with in vivo microdialysis, and the monoamine contents were measured by HPLC with electrochemical detection. DNA damage was assayed with the alkaline comet assay. DAT and SERT densities were determined by immunohistochemistry, while prodynorphin (PDYN) and proenkephalin were determined by quantitative PCR reactions. The behavioral changes were measured by the open-field (OF) test and novel object recognition (NOR) test. Caffeine potentiated MDMA-induced DA release while inhibiting 5-HT release in the mouse striatum. Caffeine also exacerbated the oxidative damage of nuclear DNA induced by MDMA but diminished DAT decrease in the striatum and worsened a decrease in SERT density produced by MDMA in the frontal cortex. Neither the striatal PDYN expression, increased by MDMA, nor exploratory and locomotor activities of mice, decreased by MDMA, were affected by caffeine. The exploration of novel object in the NOR test was diminished by MDMA and caffeine. Our data provide evidence that long-term caffeine administration has a powerful influence on functions of dopaminergic and serotonergic neurons in the mouse brain and on neurotoxic effects evoked by MDMA.
3,4-亚甲二氧基甲基苯丙胺(MDMA)是一种苯丙胺类兴奋剂,因其对情绪和社交互动的影响而被广泛用作娱乐性药物。MDMA 作用于多巴胺(DA)转运体(DAT)和 5-羟色胺(5-HT)转运体(SERT),已知其可诱导多巴胺和 5-羟色胺神经元损伤。MDMA 常与咖啡因一起摄入。咖啡因作为非选择性腺苷 A1/A2A 受体拮抗剂,影响多巴胺能和 5-羟色胺能的传递。本研究旨在确定慢性给予 MDMA 和咖啡因后,其对小鼠纹状体中 DA 和 5-HT 释放的影响。为了确定咖啡因是否加重 MDMA 的神经毒性,测定了 DA 和 5-HT 的含量、脑 DAT 和 SERT 的密度以及核 DNA 的氧化损伤。此外,还评估了咖啡因对 MDMA 诱导的纹状体强啡肽和脑啡肽变化以及行为的影响。通过活体微透析测定 DA 和 5-HT 的释放,通过 HPLC-电化学检测测定单胺含量。通过碱性彗星试验测定 DNA 损伤。通过免疫组织化学测定 DAT 和 SERT 的密度,通过定量 PCR 反应测定 prodynorphin (PDYN) 和 proenkephalin。通过旷场(OF)试验和新物体识别(NOR)试验测定行为变化。结果显示,咖啡因增强了 MDMA 诱导的小鼠纹状体中 DA 的释放,同时抑制 5-HT 的释放。咖啡因还加剧了 MDMA 诱导的核 DNA 氧化损伤,但减轻了 MDMA 引起的纹状体 DAT 减少,并加重了 MDMA 引起的额皮质 SERT 密度降低。MDMA 引起的纹状体 PDYN 表达增加以及 MDMA 引起的小鼠探索和运动活动减少均不受咖啡因影响。在 NOR 试验中,对新物体的探索因 MDMA 和咖啡因而减少。我们的数据提供了证据,表明长期给予咖啡因对小鼠大脑中多巴胺能和 5-羟色胺能神经元的功能以及 MDMA 引起的神经毒性有强大的影响。