Research Pilot Projects Program, 2025–2027 “GABAergic Pallidal-Hypothalamic Circuit Control of Approach-Avoidance Conflict”

Research Areas

  • Neural circuits of approach-avoidance behavior
  • Optogenetics and fiber photometry in mice
  • Immunohistochemistry and microscopy
  • Behavioral neuroscience

Scientific Achievements

  • Dr. Maria-Rios has contributed to high-impact neuroscience research, including peer-reviewed publications that define functional subregional differences in neuronal excitability, findings that deepen understanding of how reward and motivational circuits operate at the cellular level.
  • Her work helps bridge cellular neurophysiology and behavioral neuroscience, contributing mechanistic insight into neuropsychiatric conditions involving maladaptive reward learning and motivation.

Funding

RCMI Funding:

  • NIH/NIMHD U54MD007600

Other funding as PI:

  • NSF-GRFP (2017–2020): Epigenetic regulation of individual variations in associative learning phenotypes
  • F99 NS120544 (2020–2022): Elucidating the role of nucleus accumbens activity in the propensity to attribute incentive salience to reward cues
  • K00 MH136687, NIMH: Ventral Pallidal Circuits Governing Approach/Avoidance Conflict

Scientific Advance

Individual Variation in Intrinsic Neuronal Properties of Nucleus Accumbens Core and Shell Medium Spiny Neurons in Animals Prone to Sign- or Goal-Track
Published in bioRxiv, Volume 12, 2025, PMCID: PMCID: PMC11996421
This study investigates how natural individual differences in brain cell physiology relate to behavioral traits associated with addiction-like behaviors. Dr. Maria-Rios and collaborators used a well-established animal model that classifies rats as sign-trackers (STs) or goal-trackers (GTs) based on how they attribute motivational value to cues paired with a reward. They recorded electrical activity from medium spiny neurons (MSNs), the primary neuron type in the nucleus accumbens, a brain region essential for reward and motivation. The researchers found that ST rats, which are more prone to assigning incentive value to cues and are more susceptible to addiction-like relapse, exhibited lower intrinsic excitability in neurons from the nucleus accumbens core compared to GT rats. These findings suggest that innate differences in how individual neurons respond to inputs may underlie behavioral differences in incentive learning and vulnerability to addiction. This mechanistic insight helps explain why some individuals may be more prone to addictive behaviors than others and could inform more targeted strategies for prevention and treatment.
NIH/NINDS (F99 NS120544) / NIH/NIDA awards, including K08 DA037912, R01 DA044960, and T32 DA007281.
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