Biology subjects

Lichtman, D.

Publications and source records attributed to Lichtman, D..

3 recordsLinked to original sources

bioRxiv2026

The Periaqueductal Gray Selectively Supports Reversal Learning During a Flexible Discrimination Task in Mice

Flexible, goal-directed behavior depends on the ability to update value representations in response to changing contingencies. This ability depends on distributed brain networks, calling for use of whole-brain imaging. Widely used in human research, whole-brain imaging in rodents has been a major challenge that has only recently been properly addressed. Using functional MRI in behaving mice performing a go/no-go odor discrimination task, we compared neural activity during initial cue-reward learning (acquisition) and subsequent contingency reversal. To link neural activity to underlying learning processes, we modeled value updating using a model-free reinforcement-learning algorithm. Trial-by-trial estimates of state-action values allowed us to dissociate acquisition from reversal-related signals, revealing that ventral striatal responses tracked expected value during acquisition, whereas reversal learning additionally recruited the periaqueductal gray (PAG), a midbrain structure classically linked to threat processing and aversive learning. PAG activity closely followed model-derived signatures of reversal learning, implicating it in the suppression of previously rewarded actions and in updating behavior in the absence of explicit punishment. These findings reveal a previously unrecognized computational role for the PAG in value-based decision-making and cognitive flexibility, and substantiate task-fMRI as a powerful tool to study the rodent brain at a mesoscale resolution.

neuroscience↗

bioRxiv2025

Dopamine release effects on striatal blood oxygenation and whole brain plasticity underlying associative learning

Dopaminergic signaling in the nucleus accumbens (NAc) is central to reward-based learning, but its relationship to brain-wide hemodynamics remains unclear. Using concurrent fMRI and dopamine photometry in awake, behaving mice, we reveal that associative learning induces a gradual temporal shift in NAc blood oxygenation responses that mirrors dopamine release dynamics. This shift emerges with cue-reward learning and extends across a distributed network including prefrontal, insular, and hypothalamic regions. Further, dopamine transients tightly correspond with local BOLD signals, and variations in reward value modulate delayed BOLD responses in both the NAc and additional subcortical structures. Removing dopaminergic contributions abolishes this reward-related modulation, demonstrating that BOLD signals encode dopaminergic value prediction. These findings establish a mechanistic link between dopamine signaling and widespread neural plasticity during learning.

neuroscience↗

bioRxiv2020

Structural and Functional Brain-wide Alterations in A350V IQSEC2 Mutant Mice Displaying Autistic-like Behavior

IQSEC2 is an X-linked gene which is associated with autism spectrum disorder (ASD), intellectual disability and epilepsy. IQSEC2 is a postsynaptic density protein, localized on excitatory synapses as part of the NMDA receptor complex and is suggested to play a role in AMPA receptor trafficking and mediation of long-term depression. Here, we present brain-wide structural volumetric and functional connectivity characterization in a novel mouse model with a missense mutation in the IQ domain of IQSEC2 (A350V). Using high-resolution structural and functional MRI, we show that animals with the A350V mutation display increased whole-brain volume which was further found to be specific to the cortex and hippocampus. Moreover, using a data-driven approach we demonstrate that A350V mice present alterations in structure-function relations of the frontal, auditory, and visual networks. Examination of these alterations revealed an increase in functional connectivity between the anterior cingulate cortex and the dorsomedial striatum. We also show that corticostriatal functional connectivity is correlated with individual variability in social behavior only in A350V mice, as assessed using the three-chamber social preference test. Our results at the systems-level bridge the impact of previously reported changes in AMPA receptor trafficking to network-level disruption and impaired social behavior. Further, the A350V mouse model recapitulates similarly reported brain-wide changes in other ASD mouse models, with substantially different cellular-level pathologies that nonetheless result in similar brain-wide alterations, suggesting that novel therapeutic approaches in ASD that result in systems-level rescue will be relevant to IQSEC2 mutations. Significance StatementSeveral recent studies have characterized the changes in the organization of brain networks in animal models of autism spectrum disorders (ASD). Here we assessed the effect of an A350V missense mutation in the IQSEC2 gene, which is associated with ASD, on brain-wide functional connectivity and its relation to social behavior deficits in A350V mice relative to controls. We found that the A350V IQSEC2 model results in disrupted functional connectivity of the anterior cingulate cortex and the dorsomedial striatum. Critically, disrupted increased corticostriatal functional connectivity is predictive of individual variability in social interaction only in A350V mice implicating this pathway in the pathophysiology of the A350V IQSEC2 mutation.

neuroscience↗