dendritic spines and pre-synaptic boutons are stable despite local deep hypothermic challenge and re-warming in vivo树突棘和pre-synaptic剑头是稳定的,尽管当地深低温挑战和re-warming体内.pdfVIP

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dendritic spines and pre-synaptic boutons are stable despite local deep hypothermic challenge and re-warming in vivo树突棘和pre-synaptic剑头是稳定的,尽管当地深低温挑战和re-warming体内.pdf

dendritic spines and pre-synaptic boutons are stable despite local deep hypothermic challenge and re-warming in vivo树突棘和pre-synaptic剑头是稳定的,尽管当地深低温挑战和re-warming体内

Dendritic Spines and Pre-Synaptic Boutons Are Stable Despite Local Deep Hypothermic Challenge and Re- Warming In Vivo Yicheng Xie1,2, Shangbin Chen1,2, Timothy Murphy1,2* 1 Kinsmen Laboratory of Neurological Research, Department of Psychiatry, University of British Columbia, Vancouver, British Columbia, Canada, 2 Brain Research Centre, University of British Columbia, Vancouver, British Columbia, Canada Abstract Background and Purpose: Deep hypothermia to 20uC is used clinically for major pediatric and adult surgical procedures. In particular, it is used in the ‘‘standstill operation’’ where blood flow is stopped for up to 30 min. Patients recovering from these procedures can exhibit neurological deficits. Such deficits could arise from changes to dendritic spines and plasticity- induced changes in network function as a result of cooling and/or re-warming. In the brain, each dendritic spine represents a single excitatory synapse and their number can be reflective of injury or plasticity-induced changes in network function. This research sought to determine whether deep hypothermia and re-warming have detrimental effects on synaptic stability and network function. Methods: In vivo 2-photon (2-P) imaging in green/yellow fluorescent protein (GFP/YFP)-expressing transgenic mice was performed to determine whether 4 hours of deep hypothermia and 2 hours of re-warming can have relatively covert effects on dendritic spine and presynaptic bouton stability. At the same time, electroencephalographic (EEG) activity was recorded to evaluate network function during deep hypothermia and re-warming. Results: We report that deep hypothermia and subsequent re-warming did not change the stability of dendritic spines or presynaptic boutons in mouse somatosensory cortex measured over 8 hours. As expected, deep hypothermia attenuated ongoing EEG activity over 0.1–80 H

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