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Lee, S. L. T.

Publications and source records attributed to Lee, S. L. T..

2 recordsLinked to original sources

Similar processing of novelty in rat dorsal and intermediate CA1 despite differences in spatial tuning

Elucidating the fundamental neural mechanisms of hippocampal information processing is necessary for understanding memory formation and related brain disorders. Differences in hippocampal genetics, anatomy, and connectivity across the longitudinal axis suggest functional heterogeneity in this structure. The dorsal pole is suggested to be primarily involved in spatial processing, whereas the ventral pole is implicated in emotional processing. Connectivity and genetic studies show this functional segregation is more prominent near their respective poles and weaker toward the intermediate region. The current study compares the firing properties of CA1 cells in the dorsal and intermediate regions of the hippocampus during spatial or social/odor novelty. We measured basic spatial properties, firing rate response, and remapping to the spatial re-configuration of a linear track or the social/odor presentation of a novel male conspecific, female bedding, or coyote urine. Behaviorally, the average rat exhibited slower maze running latencies during the novel spatial manipulation and spent more time adjacent to the chamber containing the novel social/odor stimulus. As previously shown, dorsal cells had fewer, smaller place fields, and higher spatial information content than intermediate cells in the hippocampus. Despite the differences in place field characteristics, cells in both regions responded similarly to spatial and social/odor manipulations. Taken together, these data support the differentiation of some functions, together with an overlap of other functions progressing along the longitudinal axis, which may facilitate the integration of information throughout the hippocampus.

neuroscience↗

Natural variation in the oxytocin receptor gene predicts social observation in female prairie voles

Genetic variation in the oxytocin receptor gene (Oxtr) has been linked to differences in brain OXTR expression and long-term social bonds, but whether it shapes the moment-to-moment dynamics of early social interactions is unclear. Here we examined how the intronic Oxtr single nucleotide polymorphism (SNP) NT213739 in female prairie voles (Microtus ochrogaster) shapes their dynamic social interactions with an opposite-sex conspecific. Leveraging a computational pipeline to analyze the movements of freely interacting voles, we found that C/C females, which expressed higher OXTR levels in the nucleus accumbens than T/T females, spent more time socially observing novel males from a distance, especially early in interactions. This genotype-phenotype relationship persisted in multiple contexts, including the social preference test. Thus, natural Oxtr variation biases social observation in females toward unfamiliar males before bonds form, consistent with models where accumbens OXTR enhances the salience of social cues. These findings show that SNPs can shape subtle behavioral dimensions in early social encounters, with important implications for the role of oxytocin in the study of social attachment.

neuroscience↗