4.7 Article

Optogenetic Inhibition of Ventral Pallidum Neurons Impairs Context-Driven Salt Seeking

Journal

JOURNAL OF NEUROSCIENCE
Volume 37, Issue 23, Pages 5670-5680

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2968-16.2017

Keywords

salt appetite; ventral pallidum

Categories

Funding

  1. National Institutes of Health [F32MH106178]
  2. National Institute on Drug Abuse [T32 NIDA037202]
  3. Whitehall Foundation [2014-05-77]

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Salt appetite, in which animals can immediately seek out salt when under a novel state of sodium deprivation, is a classic example of how homeostatic systems interface with learned associations to produce an on-the-fly updating of motivated behavior. Neural activity in the ventral pallidum (VP) has been shown to encode changes in the value of salt under such conditions, both the value of salt itself (Tindell et al., 2006) and the motivational value of its predictive cues (Tindell et al., 2009; Robinson and Berridge, 2013). However, it is not known whether the VP is necessary for salt appetite in terms of seeking out salt or consuming salt following sodium depletion. Here, we used a conditioned place-preference procedure to investigate the effects of optogenetically inhibiting the VP on context-driven salt seeking and the consumption of salt following deprivation. Male rats learned to associate one context with sucrose and another context with less-desirable salt. Following sodium depletion, and in the absence of either sucrose or salt, we found that inhibiting the VP selectively reduced the elevation in time spent in the salt-paired context. VP inhibition had minimal effects on the consumption of salt once it was made available. To our knowledge, this is the first evidence that the VP or any brain region is necessary for the ability to use contextual cues to guide salt seeking. These results highlight a dissociation between deficit-driven reward seeking and reward consumption to replenish those deficits, with the former process being particularly sensitive to on-line VP activity.

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