Prefrontal cortical inputs to the basal amygdala undergo pruning during late adolescence in the rat
Autor: | Jordan Balaban, Peter Graham, Sara Steinfeld, Holly Moore, Victoria L. Cressman, Alexei Shemyakin, Nelly Parisot |
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Rok vydání: | 2010 |
Předmět: |
Male
Photomicrography Aging Neurite Infralimbic cortex Biotin Prefrontal Cortex Cell Count Biology Amygdala Article Random Allocation Basal (phylogenetics) Neural Pathways Neurites medicine Animals Rats Wistar Axon Prefrontal cortex Neuronal Tract-Tracers Neurons General Neuroscience Gene Expression Regulation Developmental Dextrans Axons Rats medicine.anatomical_structure Synaptic plasticity Neuroscience Nucleus |
Zdroj: | The Journal of Comparative Neurology. |
ISSN: | 1096-9861 0021-9967 |
DOI: | 10.1002/cne.22359 |
Popis: | Transformations in affective and social behaviors, many of which involve amygdalar circuits, are hallmarks of adolescence in many mammalian species. In this study, using the rat as a model, we provide the first evidence that afferents of the basal amygdala (BA) undergo significant structural remodeling during adolescence. We used quantitative tract-tracing and gene expression profiling methods to characterize changes in the medial prefrontal cortical (mPFC) inputs to the BA across ages analogous to the late juvenile period [postnatal day (P) 25], late adolescence (P45), and adulthood (P90) in the rat. As assessed after deposition of Fluorogold into the BA, the number of BA-projecting neurons in the mPFC remained stable between P25 and P45 but decreased by about 50% between P45 and P90. Anterograde tract tracing with biotin dextran amine deposits centered in the ventral prelimbic cortex revealed that, during this period, the density of mPFC-derived axon terminals in the BA also decrease significantly, an effect particularly evident in the dorsal basolateral nucleus. Within the BA, there were also highly significant changes in gene expression indicative of neurite or synaptic plasticity, most notably in the Ras/GTPase superfamily, and in pathways that regulate cytoskeletal dynamics and steroid synthesis/lipid metabolism. These data provide convergent evidence that mPFC inputs to the BA are pruned during late adolescence or early adulthood. Moreover, the structural remodeling within these afferents may be accompanied by significant changes in neurite plasticity within the BA. |
Databáze: | OpenAIRE |
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