4.7 Article

Dopamine Release in Nucleus Accumbens Is under Tonic Inhibition by Adenosine A1 Receptors Regulated by Astrocytic ENT1 and Dysregulated by Ethanol

期刊

JOURNAL OF NEUROSCIENCE
卷 42, 期 9, 页码 1738-1751

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1548-21.2021

关键词

adenosine; astrocytes; dopamine; equilibrative nucleoside transporter 1; ethanol; tonic inhibition

资金

  1. UK Medical Research Council [MR/V013599/1]
  2. University of Oxford John Fell Fund [0008310]
  3. Biotechnology and Biological Sciences Research Council Doctoral Training grant
  4. St John's College, Oxford University

向作者/读者索取更多资源

Activation of Y striatal adenosine A1 receptors can inhibit dopamine release, with this inhibition modulated by astrocytic ENT1 and ethanol. The release of dopamine in the nucleus accumbens core is under tonic inhibition by A1Rs and this process is regulated by adenosine tone in the striatum, suggesting a complex interplay between neurotransmitters and astrocytic transporters in the regulation of dopamine dynamics.
Y Striatal adenosine A1 receptor (A1R) activation can inhibit dopamine release. A1Rs on other striatal neurons are activated by an adenosine tone that is limited by equilibrative nucleoside transporter 1 (ENT1) that is enriched on astrocytes and is ethanol sensitive. We explored whether dopamine release in nucleus accumbens core is under tonic inhibition by A1Rs, and is regulated by astrocytic ENT1 and ethanol. In ex vivo striatal slices from male and female mice, A1R agonists inhibited dopamine release evoked electrically or optogenetically and detected using fast-scan cyclic voltammetry, most strongly for lower stimulation frequencies and pulse numbers, thereby enhancing the activity-dependent contrast of dopamine release. Conversely, A1R antagonists reduced activity-dependent contrast but enhanced evoked dopamine release levels, even for single optogenetic pulses indicating an underlying tonic inhibition. The ENT1 inhibitor nitrobenzylthioinosine reduced dopamine release and promoted A1R-mediated inhibition, and, conversely, virally mediated astrocytic overexpression of ENT1 enhanced dopamine release and relieved A1R-mediated inhibition. By imaging the genetically encoded fluorescent adenosine sensor [GPCR-activation based (GRAB)-Ado], we identified a striatal extracellular adenosine tone that was elevated by the ENT1 inhibitor and sensitive to gliotoxin fluorocitrate. Finally, we identified that ethanol (50 min) promoted A1R-mediated inhibition of dopamine release, through diminishing adenosine uptake via ENT1. Together, these data reveal that dopamine output dynamics are gated by a striatal adenosine tone, limiting amplitude but promoting contrast, regulated by ENT1, and promoted by ethanol. These data add to the diverse mechanisms through which ethanol modulates striatal dopamine, and to emerging datasets supporting astrocytic transporters as important regulators of striatal function.

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