PIPages
Labs

Jocelyn Richard

University of Minnesota, MN·Neuroscience

Cues linked to drugs can trigger strong urges that drive escalating drug use and relapse, even after long periods of abstinence. Such cues can push reward seeking that is disconnected from a person's goals or from what they actually expect to gain.

Fields

Neuroscience

Psychology

Pharmacology

Topics

addiction

relapse

reward seeking

Grants
1 known grant, through Dec 2026

What they work on

  1. Test whether separate neurons in the ventral pallidum encode the incentive value of reward cues versus the expected value of outcomes, using in vivo single-unit electrophysiology to record individual neurons during cue presentations.
  2. Determine whether ventral pallidum GABA neurons projecting to the ventral tegmental area (VTA), compared with those projecting to the thalamus, encode cue-driven reward seeking, measuring their calcium activity with fiber photometry.
  3. Test the functional role of activity in ventral pallidum output pathways in driving behavioral responses to reward-associated cues.

More about the research

This may underlie compulsive drug use despite harmful consequences. Brain-stimulation (neuromodulation) treatments for addiction are held back by a gap in knowledge. It is unclear which brain circuits drive cue-triggered reward seeking and how they differ from circuits for goal-directed choices, which rely on accurate expectations about outcomes.

Why it matters

People with drug addiction often relapse after long abstinence when they encounter drug-associated cues. Identifying the brain cells and pathways through which cues drive compulsive reward seeking may help refine brain-based therapies, such as neuromodulation, that target the circuits underlying compulsive drug use.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Neural basis of incentive and expected value representations

NIH · Mar 2022 – Dec 2026

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Marina Picciotto

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Define the role of nicotinic acetylcholine receptors in a ventral tegmental area to ventral pallidum GABA circuit and a medial septum to basolateral amygdala acetylcholine circuit that boost responding for rewards and reward-paired cues in mice.

Stephan Lammel

University of California-Berkeley, CA·Neuroscience

Test whether neurotensin signaling in the pathway from the lateral nucleus accumbens to the VTA drives hedonic feeding in mice, using optogenetics, NTS receptor blockers and a new neurotensin sensor that measures release in vitro and in vivo.

The school

University of Minnesota: 88 labs on PI Pages, $1.4B a year on research, 722 research doctorates a year.

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