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Differential release of dopamine in the nucleus accumbens evoked by low-versus high-frequency medial prefrontal cortex stimulation
Authors:Daniel F. Hill  Kate L. Parent  Christopher W. Atcherley  Stephen L. Cowen  Michael L. Heien
Affiliation:1. Department of Physiology, University of Arizona, Tucson, AZ, USA;2. Department of Chemistry and Biochemistry, University of Arizona, Tucson, AZ, USA;3. Department of Research, Mayo Clinic, Scottsdale, AZ, Tucson, AZ, USA;4. Department of Psychology, University of Arizona, Tucson, AZ, USA;5. Evelyn F. McKnight Brian Institute, University of Arizona, Tucson, AZ, USA
Abstract:
The medial prefrontal cortex (mPFC) coordinates goal-directed behaviors, which may be mediated through mPFC regulation of dopamine release in the nucleus accumbens (NAc). Furthermore, frequency-specific oscillatory activity between the frontal cortex and downstream structures may facilitate inter-region communication. Although high-frequency (e.g., 60 Hz) mPFC stimulation is known to increase basal dopamine levels in the NAc, little is known about how phasic dopamine release is affected by mPFC stimulation. Understanding the frequency-specific control of phasic dopamine release by mPFC stimulation could elucidate mechanisms by which the mPFC modulates other regions. It could also inform optimization of deep brain stimulation for treatment of neurological disorders.

Objective

The goal of this work was to characterize the frequency response of NAc dopamine release resultant from mPFC stimulation. We hypothesized that the magnitude of dopamine release in the NAc would increase with increasing stimulation frequency.

Methods

Electrical stimulation of the mPFC of anesthetized rats was delivered at 4–60 Hz and at varying durations while measuring NAc dopamine release with fast-scan cyclic voltammetry.

Results

mPFC stimulation resulted in phasic dopamine release in the NAc. Furthermore, 20 Hz stimulation evoked the largest peak response for stimulation intervals >5 s when compared to higher or lower frequencies.

Conclusions

Activation of the mPFC drives dopamine release in the NAc in a complex frequency- and duration-dependent manner. This has implications for the use of deep brain stimulation treatment of disorders marked by dopaminergic dysregulation, and suggest that mPFC may exert more specialized control over neuromodulator release than previously understood.
Keywords:Medial prefrontal cortex  Nucleus accumbens  Electrical stimulation  Beta  Fast-scan cyclic voltammetry  Dopamine  Deep brain stimulation  NAc  nucleus accumbens  mPFC  medial prefrontal cortex  DBS  deep brain stimulation  LFP  local-field potential  VTA  ventral tegmental area  FSCV  fast-scan cyclic voltammetry  DA  dopamine  CV  cyclic voltammogram  CFME  carbon-fiber microelectrode
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