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Biology subjects

Herrera, M. L.

Publications and source records attributed to Herrera, M. L..

2 recordsLinked to original sources

Understanding Brain Aging Through Behavioural and Microglial Changes: A Lifespan Approach

Aging is characterized by progressive physiological decline linked to inflammaging, a chronic low-grade inflammatory state. This study investigates age-related behavioural changes and their correlation with microglial function in female Sprague Dawley rats across their lifespan. Using a longitudinal design at 2, 6, 12, and 24 months of age, we assessed motor performance, mood-related behaviours, and spatial cognition alongside microglial morphometric analysis in key brain regions. Results showed that motor and cognitive performance began to decline significantly at 12 months, with severe impairments and depressive-like behaviours appearing by 24 months. These deficits were paralleled by progressive gliosis in the hippocampus and striatum. Microglial morphometric analysis further indicated a more reactive, region-dependent phenotype, with cells in the striatum adopting a smaller area, reduced perimeter, and fewer intersections. These findings provide compelling evidence for significant age-dependent deterioration in motor performance, mood regulation, and cognitive abilities in female rats. Our data strongly suggest an underlying progression of neurobiological changes, with microglial dysfunction and neuroinflammation being central candidates. This research contributes valuable insights into the cellular correlates of behavioural decline across the female lifespan, serving as a reference for the multifaceted changes that occur during normal aging.

neuroscience↗

Rearing conditions bidirectionally modulate cognitive abilities and AP-1 signaling in hippocampal neurons in a cell type-specific manner.

Environmental conditions profoundly influence cognitive development, particularly during early life. Transcriptional and epigenetic mechanisms may serve as molecular substrates for the lasting effects of environmental enrichment (EE) and impoverishment (IE) on cognitive abilities and hippocampal function. However, the specific gene programs driving these changes remain largely unknown. In this study, EE and IE modulated the cognitive abilities of mice in opposing directions. By combining hippocampal microdissection and genetic tagging of neuronal nuclei with genome-wide analyses of gene expression, chromatin accessibility, histone acetylation, and DNA methylation, we uncovered profound differences in the transcriptional and epigenetic profiles of CA1 pyramidal neurons and dentate gyrus (DG) granule neurons. These analyses revealed cell type-specific genomic changes induced by EE and IE, highlighting distinct patterns of neuroadaptation within each population. This multiomic screen pinpointed the activity-regulated transcription factor AP-1 as a crucial mediator of neuroadaptation to conditions during early life in both cell types, albeit through distinct downstream mechanisms. Conditional deletion of Fos, a core AP-1 subunit, in excitatory neurons hampered EE-induced cognitive enhancement, further underscoring the pivotal role of this transcription factor in neuroadaptation.

neuroscience↗