Department of Cellular and Integrative Physiology, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.
Center for Physiology and Pharmacology, Medical University of Vienna, 1090, Vienna, Austria.
Mol Psychiatry. 2023 Jul;28(7):2934-2945. doi: 10.1038/s41380-023-02064-5. Epub 2023 Jun 13.
Concurrent cocaine and alcohol use is among the most frequent drug combination, and among the most dangerous in terms of deleterious outcomes. Cocaine increases extracellular monoamines by blocking dopamine (DA), norepinephrine (NE) and serotonin (5-HT) transporters (DAT, NET and SERT, respectively). Likewise, ethanol also increases extracellular monoamines, however evidence suggests that ethanol does so independently of DAT, NET and SERT. Organic cation transporter 3 (OCT3) is an emergent key player in the regulation of monoamine signaling. Using a battery of in vitro, in vivo electrochemical, and behavioral approaches, as well as wild-type and constitutive OCT3 knockout mice, we show that ethanol's actions to inhibit monoamine uptake are dependent on OCT3. These findings provide a novel mechanistic basis whereby ethanol enhances the neurochemical and behavioral effects of cocaine and encourage further research into OCT3 as a target for therapeutic intervention in the treatment of ethanol and ethanol/cocaine use disorders.
同时使用可卡因和酒精是最常见的药物组合之一,就有害后果而言也是最危险的组合之一。可卡因通过阻断多巴胺(DA)、去甲肾上腺素(NE)和血清素(5-HT)转运体(分别为 DAT、NET 和 SERT)来增加细胞外单胺。同样,乙醇也会增加细胞外单胺,但有证据表明,乙醇的作用独立于 DAT、NET 和 SERT。有机阳离子转运蛋白 3(OCT3)是调节单胺信号的新兴关键因素。我们使用一系列体外、体内电化学和行为方法,以及野生型和组成型 OCT3 敲除小鼠,表明乙醇抑制单胺摄取的作用依赖于 OCT3。这些发现为乙醇增强可卡因的神经化学和行为效应提供了一个新的机制基础,并鼓励进一步研究 OCT3 作为治疗乙醇和乙醇/可卡因使用障碍的治疗靶点。