4.7 Article

Multiphasic Temporal Dynamics in Responses of Midbrain Dopamine Neurons to Appetitive and Aversive Stimuli

Journal

JOURNAL OF NEUROSCIENCE
Volume 33, Issue 11, Pages 4710-4725

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.3883-12.2013

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Funding

  1. World Class University program through the National Research Foundation of Korea
  2. Ministry of Education, Science and Technology [R32-2008-000-10218-0]
  3. Howard Hughes Medical Institute
  4. National Research Foundation of Korea [R32-2012-000-10218-0, 2012R1A1A2006996] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The transient response of dopamine neurons has been described as reward prediction error (RPE), with activation or suppression by events that are better or worse than expected, respectively. However, at least a minority of neurons are activated by aversive or high-intensity stimuli, casting doubt on the generality of RPE in describing the dopamine signal. To overcome limitations of previous studies, we studied neuronal responses to a wider variety of high-intensity and aversive stimuli, and we quantified and controlled aversiveness through a choice task in which macaques sacrificed juice to avoid aversive stimuli. Whereas most previous work has portrayed the RPE as a single impulse or phase, here we demonstrate its multiphasic temporal dynamics. Aversive or high-intensity stimuli evoked a triphasic sequence of activation-suppression-activation extending over a period of 40-700 ms. The initial activation at short latencies (40-120 ms) reflected sensory intensity. The influence of motivational value became dominant between 150 and 250 ms, with activation in the case of appetitive stimuli, and suppression in the case of aversive and neutral stimuli. The previously unreported late activation appeared to be a modest rebound after strong suppression. Similarly, strong activation by reward was often followed by suppression. We suggest that these rebounds may result from overcompensation by homeostatic mechanisms in some cells. Our results are consistent with a realistic RPE, which evolves over time through a dynamic balance of excitation and inhibition.

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