Ethanol inhibits dopamine uptake via organic cation transporter 3: Implications for ethanol and cocaine co-abuse

N. J. Clauss, F. P. Mayer, W. A. Owens, M. Vitela, K. M. Clarke, M. A. Bowman, R. E. Horton, D. Gründemann, D. Schmid, M. Holy, G. G. Gould, W. Koek, H. H. Sitte, L. C. Daws*

*Corresponding author af dette arbejde

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Abstract

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.
OriginalsprogEngelsk
TidsskriftMolecular Psychiatry
Vol/bind28
Sider (fra-til)2934-2945
Antal sider12
ISSN1359-4184
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
This work was supported by R21DA046044, U18DA052527 and R01 MH093320 to LCD, W81XWH-12-1-0506 to GGG, and by grant P34670-B (to HHS) from the Austrian Science Fund/FWF. FPM received support from the Austrian Academy of Sciences (DOC and MAX KADE Fellowships, respectively).

Publisher Copyright:
© 2023, The Author(s).

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