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Reduced sensory-evoked structural plasticity in the aging barrel cortex.


ABSTRACT: Impairments in synaptic connectivity have been linked to cognitive deficits in age-related neurodegenerative disorders and healthy aging. However, the anatomical and structural bases of these impairments have not been identified yet. A hallmark of neural plasticity in young adults is short-term synaptic rearrangement, yet aged animals already display higher synaptic turnover rates at the baseline. Using two-photon excitation (2PE) microscopy, we explored if this elevated turnover alters the aged brain's response to plasticity. Following a sensory-evoked plasticity protocol involving whisker stimulation, aged mice display reduced spine dynamics (gain, loss, and turnover), decreased spine clustering, and lower spine stability when compared to young adult mice. These results suggest a deficiency of the cortical neurons of aged mice to structurally incorporate new sensory experiences, in the form of clustered, long-lasting synapses, into already existing cortical circuits. This research provides the first evidence linking experience-dependent plasticity with in vivo spine dynamics in the aged brain and supports a model of both reduced synaptic plasticity and reduced synaptic tenacity in the aged somatosensory system.

SUBMITTER: Voglewede RL 

PROVIDER: S-EPMC6732242 | biostudies-literature | 2019 Sep

REPOSITORIES: biostudies-literature

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Reduced sensory-evoked structural plasticity in the aging barrel cortex.

Voglewede Rebecca L RL   Vandemark Kaeli M KM   Davidson Andrew M AM   DeWitt Annie R AR   Heffler Marissa D MD   Trimmer Emma H EH   Mostany Ricardo R  

Neurobiology of aging 20190626


Impairments in synaptic connectivity have been linked to cognitive deficits in age-related neurodegenerative disorders and healthy aging. However, the anatomical and structural bases of these impairments have not been identified yet. A hallmark of neural plasticity in young adults is short-term synaptic rearrangement, yet aged animals already display higher synaptic turnover rates at the baseline. Using two-photon excitation (2PE) microscopy, we explored if this elevated turnover alters the aged  ...[more]

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