Unilateral infarction of the visual cortex (VC) induced an increase in dendritic spine turnover in contralateral VC

After brain stroke, appropriate functional recovery is most important for improvement of quality of life. Cortical hemisphere contralateral to the infarction site plays an important role in functional recovery process. However, the underlying processes occurring in contralateral hemisphere during recovery has not yet been elucidated. We have previously reported that the turnover of synaptic spine of somatosensory cortex (SSC) is increased at 1st week after stroke in contralateral SSC infarction. After this period, neuronal circuit is remodeled, and functional compensation is achieved by processing bilateral information to remaining SSC [18]. In the present study, to examine whether similar changes are observed in different brain regions, we have induced an infarction in the visual cortex (VC). We found that the spinal remodeling in contralateral VC was also increased at 1st week after VC stroke. However, the magnitude of changes was not as great as those seen in SSC infraction. These results indicate that the regional difference may exist in the ability to induce functional recovery after ischemic brain damage.

[1]  Hideo Tsukada,et al.  Neuronal Circuit Remodeling in the Contralateral Cortical Hemisphere during Functional Recovery from Cerebral Infarction , 2009, The Journal of Neuroscience.

[2]  T. Murphy,et al.  Extensive Turnover of Dendritic Spines and Vascular Remodeling in Cortical Tissues Recovering from Stroke , 2007, The Journal of Neuroscience.

[3]  W. Gan,et al.  Choice of cranial window type for in vivo imaging affects dendritic spine turnover in the cortex , 2007, Nature Neuroscience.

[4]  K. Svoboda,et al.  Rapid dendritic morphogenesis in CA1 hippocampal dendrites induced by synaptic activity. , 1999, Science.

[5]  N. Kasthuri,et al.  Long-term dendritic spine stability in the adult cortex , 2002, Nature.

[6]  KM Harris,et al.  Three-dimensional structure of dendritic spines and synapses in rat hippocampus (CA1) at postnatal day 15 and adult ages: implications for the maturation of synaptic physiology and long-term potentiation [published erratum appears in J Neurosci 1992 Aug;12(8):following table of contents] , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  B. Johansson,et al.  Neuronal Plasticity and Dendritic Spines: Effect of Environmental Enrichment on Intact and Postischemic Rat Brain , 2002, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[8]  Yue Cao,et al.  Pilot study of functional MRI to assess cerebral activation of motor function after poststroke hemiparesis. , 1998, Stroke.

[9]  Keith D. White,et al.  Functional MRI of Language in Aphasia: A Review of the Literature and the Methodological Challenges , 2007, Neuropsychology Review.

[10]  C. Calautti,et al.  Functional Neuroimaging Studies of Motor Recovery After Stroke in Adults: A Review , 2003, Stroke.

[11]  O W Witte,et al.  Induction of bilateral plasticity in sensory cortical maps by small unilateral cortical infarcts in rats , 2003, The European journal of neuroscience.

[12]  M. Viergever,et al.  Recovery of Sensorimotor Function after Experimental Stroke Correlates with Restoration of Resting-State Interhemispheric Functional Connectivity , 2010, The Journal of Neuroscience.

[13]  T. Nemoto,et al.  Maternal separation decreases the stability of mushroom spines in adult mice somatosensory cortex , 2009, Brain Research.

[14]  N. Ward,et al.  Future perspectives in functional neuroimaging in stroke recovery. , 2007, Europa medicophysica.

[15]  G. Ellis‐Davies,et al.  Structural basis of long-term potentiation in single dendritic spines , 2004, Nature.

[16]  Richard S. J. Frackowiak,et al.  The functional anatomy of motor recovery after stroke in humans: A study with positron emission tomography , 1991, Annals of neurology.

[17]  Lorraine O. Ramig,et al.  Translating principles of neural plasticity into research on speech motor control recovery and rehabilitation. , 2008, Journal of speech, language, and hearing research : JSLHR.

[18]  Kristen M. Harris,et al.  Erratum: Three-dimensional structure of dendritic spines and synapses in rat hippocampus (CA1) at postnatal day 15 and adult ages: Implications for the maturation of synaptic physiology and long-term potentiation (J Neurosci (July 1992) 12 (2685-2705)) , 1992 .

[19]  B. Johansson Brain plasticity and stroke rehabilitation. The Willis lecture. , 2000, Stroke.

[20]  F. Engert,et al.  Dendritic spine changes associated with hippocampal long-term synaptic plasticity , 1999, Nature.

[21]  K. Svoboda,et al.  Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex , 2002, Nature.

[22]  J. Nabekura,et al.  Resting Microglia Directly Monitor the Functional State of Synapses In Vivo and Determine the Fate of Ischemic Terminals , 2009, The Journal of Neuroscience.

[23]  G. Feng,et al.  Imaging Neuronal Subsets in Transgenic Mice Expressing Multiple Spectral Variants of GFP , 2000, Neuron.

[24]  T. Murphy,et al.  Imaging the Impact of Cortical Microcirculation on Synaptic Structure and Sensory-Evoked Hemodynamic Responses In Vivo , 2007, PLoS biology.

[25]  D. Corbett,et al.  Efficacy of Rehabilitative Experience Declines with Time after Focal Ischemic Brain Injury , 2004, The Journal of Neuroscience.