Obray J Daniel, Small Christina A, Baldwin Emily K, Jang Eun Young, Lee Jin Gyeom, Yang Chae Ha, Yorgason Jordan T, Steffensen Scott C
Department of Psychology and Neuroscience, Brigham Young University, Provo, UT, United States.
Research Center for Convergence Toxicology, Korea Institute of Toxicology, Daejeon, South Korea.
Front Cell Neurosci. 2022 Jul 12;16:944243. doi: 10.3389/fncel.2022.944243. eCollection 2022.
Dopamine (DA) is a cell-signaling molecule that does not readily cross the blood-brain barrier. Despite this, peripherally administered DA enhances DA levels in the nucleus accumbens and alters DA-related behaviors. This study was designed to investigate whether DA subtype-2 receptors are involved in the enhancement of nucleus accumbens (NAc) DA levels elicited by intravenous DA administration. This was accomplished by using microdialysis in the NAc and extracellular single unit recordings of putative DA neurons in the ventral tegmental area (VTA). Additionally, the reinforcing properties of intravenous DA were investigated using a place conditioning paradigm and the effects of intravenous DA on ultrasonic vocalizations were assessed. Following administration of intravenous dopamine, the firing rate of putative DA neurons in the VTA displayed a biphasic response and DA levels in the nucleus accumbens were enhanced. Pretreatment with domperidone, a peripheral-only DA D2 receptor (D2R) antagonist, reduced intravenous DA mediated increases in VTA DA neuron activity and NAc DA levels. Pretreatment with phentolamine, a peripheral α-adrenergic receptor antagonist, did not alter the effects of IV DA on mesolimbic DA neurotransmission. These results provide evidence for peripheral D2R mediation of the effects of intravenous DA on mesolimbic DA signaling.
多巴胺(DA)是一种不易穿过血脑屏障的细胞信号分子。尽管如此,外周给予的DA会提高伏隔核中的DA水平,并改变与DA相关的行为。本研究旨在调查DA 2型受体是否参与静脉注射DA引起的伏隔核(NAc)DA水平的升高。这是通过在NAc中使用微透析以及对腹侧被盖区(VTA)中假定的DA神经元进行细胞外单单位记录来实现的。此外,使用位置条件化范式研究了静脉注射DA的强化特性,并评估了静脉注射DA对超声波发声的影响。静脉注射多巴胺后,VTA中假定的DA神经元的放电率呈现双相反应,伏隔核中的DA水平升高。使用仅作用于外周的DA D2受体(D2R)拮抗剂多潘立酮进行预处理,可降低静脉注射DA介导的VTA中DA神经元活动和NAc中DA水平的增加。使用外周α-肾上腺素能受体拮抗剂酚妥拉明进行预处理,不会改变静脉注射DA对中脑边缘DA神经传递的影响。这些结果为外周D2R介导静脉注射DA对中脑边缘DA信号传导的作用提供了证据。