Author
Listed:
- Danielle O. Sambo
(University of Florida)
- Min Lin
(University of Florida)
- Anthony Owens
(University of Texas Health Science Center at San Antonio)
- Joseph J. Lebowitz
(University of Florida)
- Ben Richardson
(University of Florida)
- Darin A. Jagnarine
(University of Florida)
- Madhur Shetty
(University of North Dakota)
- Meghan Rodriquez
(University of North Dakota)
- Taiwo Alonge
(University of Florida)
- Mishaal Ali
(University of Florida)
- Jonathan Katz
(Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health)
- Long Yan
(Max Plank Institute for Neuroscience Jupiter)
- Marcelo Febo
(University of Florida)
- L. Keith Henry
(University of North Dakota)
- Adriaan W. Bruijnzeel
(University of Florida)
- Lynette Daws
(University of Texas Health Science Center at San Antonio)
- Habibeh Khoshbouei
(University of Florida)
Abstract
Dopamine neurotransmission is highly dysregulated by the psychostimulant methamphetamine, a substrate for the dopamine transporter (DAT). Through interactions with DAT, methamphetamine increases extracellular dopamine levels in the brain, leading to its rewarding and addictive properties. Methamphetamine also interacts with the sigma-1 receptor (σ1R), an inter-organelle signaling modulator. Using complementary strategies, we identified a novel mechanism for σ1R regulation of dopamine neurotransmission in response to methamphetamine. We found that σ1R activation prevents methamphetamine-induced, DAT-mediated increases in firing activity of dopamine neurons. In vitro and in vivo amperometric measurements revealed that σ1R activation decreases methamphetamine-stimulated dopamine efflux without affecting basal dopamine neurotransmission. Consistent with these findings, σ1R activation decreases methamphetamine-induced locomotion, motivated behavior, and enhancement of brain reward function. Notably, we revealed that the σ1R interacts with DAT at or near the plasma membrane and decreases methamphetamine-induced Ca2+ signaling, providing potential mechanisms. Broadly, these data provide evidence for σ1R regulation of dopamine neurotransmission and support the σ1R as a putative target for the treatment of methamphetamine addiction.
Suggested Citation
Danielle O. Sambo & Min Lin & Anthony Owens & Joseph J. Lebowitz & Ben Richardson & Darin A. Jagnarine & Madhur Shetty & Meghan Rodriquez & Taiwo Alonge & Mishaal Ali & Jonathan Katz & Long Yan & Marc, 2017.
"The sigma-1 receptor modulates methamphetamine dysregulation of dopamine neurotransmission,"
Nature Communications, Nature, vol. 8(1), pages 1-18, December.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-02087-x
DOI: 10.1038/s41467-017-02087-x
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