4.4 Article

Cocaine increases stimulation-evoked serotonin efflux in the nucleus accumbens

Journal

JOURNAL OF NEUROPHYSIOLOGY
Volume 127, Issue 3, Pages 714-724

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/jn.00420.2021

Keywords

addiction; cocaine; nucleus accumbens; serotonin; voltammetry

Funding

  1. National Institutes of Health (NIH) [R01NS112176]
  2. Minnesota Partnership for Biotechnology and Medical Genomics Grant [19.13]
  3. NIH [TL1TR002380-03, T32GM065841-17, F31NS115202-01A1, R25GM055252-23]
  4. NHMRC Senior Principal Research Fellowship [1156072]

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Although dopamine is the most implicated neurotransmitter in addiction, serotonin also plays a vital role. This study used N-shaped fast-scan cyclic voltammetry to investigate the acute effects of cocaine on phasic serotonin release in the nucleus accumbens core. The findings contribute to our understanding of the mechanism of action of cocaine and provide a baseline for further research in cocaine addiction.
Although dopamine is the most implicated neurotransmitter in the mediation of the pathophysiology of addiction, animal studies show serotonin also plays a vital role. Cocaine is one of the most common illicit drugs globally, but the role of serotonin in its mechanism of action is insufficiently characterized. Consequently, we investigated the acute effects of the psychomotor stimulant cocaine on electrical stimulation-evoked serotonin (phasic) release in the nucleus accumbens core (NAcc) of urethane-anesthetized (1.5 g/kg ip) male Sprague-Dawley rats using N-shaped fast-scan cyclic voltammetry (N-FSCV). A single carbon fiber microelectrode was first implanted in the NAcc. Stimulation was applied to the medial forebrain bundle using 60 Hz, 2 ms, 0.2 mA, 2-s biphasic pulses before and after cocaine (2 mg/kg iv) was administered. Stimulation-evoked serotonin release significantly increased 5 min after cocaine injection compared with baseline (153 +/- 21 nM vs. 257 +/- 12 nM; P = 0.0042; n = 5) but was unaffected by saline injection (1 mL/kg iv; n = 5). N-FSCV's selective measurement of serotonin release in vivo was confirmed pharmacologically via administration of the selective serotonin reuptake inhibitor escitalopram (10 mg/kg ip) that effectively increased the signal in a separate group of rats (n = 5). Selectivity to serotonin was further confirmed in vitro in which dopamine was minimally detected by N-FSCV with a serotonin to dopamine response ratio of 1:0.04 (200 nM of serotonin:1 mu M dopamine ratio; P = 0.0048; n = 5 electrodes). This study demonstrates a noteworthy influence of cocaine on serotonin dynamics, and confirms that N-FSCV can effectively and selectively measure phasic serotonin release in the NAcc. NEW & NOTEWORTHY Serotonin plays a vital role in drug addiction. Here, using N-shaped fast-scan cyclic voltammetry, we demonstrated the effect of cocaine on the phasic release of serotonin at the nucleus accumbens core. To the best of our knowledge, this has not previously been elucidated. Our results not only reinforce the role of serotonin in the mechanism of action of cocaine but also help to fill a gap in our knowledge and provide a baseline for future studies in cocaine addiction.

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