Areal differences in diameter and length of corticofugal projections.

Cortical areas differ in the size and distribution of neuronal cell bodies, density, and distribution of myelinated axons, connections, and functional properties. We find that they also differ in the diameter of long corticofugal axons, with the thickest axons originating from primary motor, somatosensory, and visual areas and the thinnest ones from prefrontal and temporal areas. Since diameter is proportional to axonal conduction velocity, it can be inferred that action potentials issued from the different areas will be relayed to their targets at different speed. Conduction delays also depend on conduction distance. By computing conduction velocity and conduction distances, we found the longest conduction delays for the primary visual and temporal areas and the shortest for the premotor, primary motor, and somatosensory areas, compatible with the available electrophysiological data. These findings seem to establish a new principle in cortical organization relevant to the pathophysiology of neurological or psychiatric illnesses as well as to the speed of information processing in cortical circuits.

[1]  W. Singer,et al.  The development of neural synchrony and large-scale cortical networks during adolescence: relevance for the pathophysiology of schizophrenia and neurodevelopmental hypothesis. , 2011, Schizophrenia bulletin.

[2]  Sonja Grün,et al.  Saccade-Related Modulations of Neuronal Excitability Support Synchrony of Visually Elicited Spikes , 2011, Cerebral cortex.

[3]  Mark H. Johnson,et al.  Mapping Infant Brain Myelination with Magnetic Resonance Imaging , 2011, The Journal of Neuroscience.

[4]  S. Tobimatsu,et al.  Altered white matter fractional anisotropy and social impairment in children with autism spectrum disorder , 2010, Brain Research.

[5]  M. Behen,et al.  Alterations in frontal lobe tracts and corpus callosum in young children with autism spectrum disorder. , 2010, Cerebral cortex.

[6]  A. Toga,et al.  The Development of the Corpus Callosum in the Healthy Human Brain , 2010, The Journal of Neuroscience.

[7]  C. Westin,et al.  Corpus Callosum Abnormalities and Their Association with Psychotic Symptoms in Patients with Schizophrenia , 2010, Biological Psychiatry.

[8]  C. Caltagirone,et al.  In vivo structural neuroanatomy of corpus callosum in Alzheimer's disease and mild cognitive impairment using different MRI techniques: a review. , 2010, Journal of Alzheimer's disease : JAD.

[9]  Nicolas Brunel,et al.  Sensory neural codes using multiplexed temporal scales , 2010, Trends in Neurosciences.

[10]  Giorgio M. Innocenti,et al.  Dendritic Bundles, Minicolumns, Columns, and Cortical Output Units , 2010, International Journal of Developmental Neuroscience.

[11]  Ingo Bojak,et al.  Axonal Velocity Distributions in Neural Field Equations , 2010, PLoS Comput. Biol..

[12]  R. Caminiti,et al.  Evolution amplified processing with temporally dispersed slow neuronal connectivity in primates , 2009, Proceedings of the National Academy of Sciences.

[13]  Maria V. Sanchez-Vives,et al.  Inducing Illusory Ownership of a Virtual Body , 2009, Front. Neurosci..

[14]  J. A. Roberts,et al.  Modeling distributed axonal delays in mean-field brain dynamics. , 2008, Physical review. E, Statistical, nonlinear, and soft matter physics.

[15]  Kate L. Christison-Lagay,et al.  A mechanism for neuronal coincidence revealed in the crayfish antennule , 2008, Proceedings of the National Academy of Sciences.

[16]  Jens Frahm,et al.  Rhesus monkey and human share a similar topography of the corpus callosum as revealed by diffusion tensor MRI in vivo. , 2008, Cerebral cortex.

[17]  S. Schütz-Bosbach,et al.  On agency and body-ownership: Phenomenological and neurocognitive reflections , 2007, Consciousness and Cognition.

[18]  D. Hansel,et al.  Role of delays in shaping spatiotemporal dynamics of neuronal activity in large networks. , 2005, Physical review letters.

[19]  T. Tsumoto,et al.  Change of conduction velocity by regional myelination yields constant latency irrespective of distance between thalamus and cortex , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[20]  O. Terasaki,et al.  Transcallosal conduction time measured by visual hemifield stimulation with face images , 2002, Neuroreport.

[21]  Francisco Aboitiz,et al.  Species Differences and Similarities in the Fine Structure of the Mammalian Corpus callosum , 2001, Brain, Behavior and Evolution.

[22]  A. Reiner,et al.  Pathway tracing using biotinylated dextran amines , 2000, Journal of Neuroscience Methods.

[23]  Refractor Vision , 2000, The Lancet.

[24]  U. Meincke,et al.  Transcallosal inhibition and motor conduction studies in patients with schizophrenia using transcranial magnetic stimulation , 1999, British Journal of Psychiatry.

[25]  E. Welker,et al.  Constant and variable aspects of axonal phenotype in cerebral cortex. , 1998, Cerebral cortex.

[26]  G. Innocenti Exuberant development of connections, and its possible permissive role in cortical evolution , 1995, Trends in Neurosciences.

[27]  B. Meyer,et al.  Inhibitory and excitatory interhemispheric transfers between motor cortical areas in normal humans and patients with abnormalities of the corpus callosum. , 1995, Brain : a journal of neurology.

[28]  M. Steriade Two channels in the cerebellothalamocortical system , 1995, The Journal of comparative neurology.

[29]  Patrice Y. Simard,et al.  Time is of the essence: a conjecture that hemispheric specialization arises from interhemispheric conduction delay. , 1994, Cerebral cortex.

[30]  G. Innocenti,et al.  Computational Structure of Visual Callosal Axons , 1994, The European journal of neuroscience.

[31]  G. Innocenti,et al.  Morphology of Callosal Axons Interconnecting Areas 17 and 18 of the Cat , 1994, The European journal of neuroscience.

[32]  B. Day,et al.  Interhemispheric inhibition of the human motor cortex. , 1992, The Journal of physiology.

[33]  P. Rakić,et al.  Cytological and quantitative characteristics of four cerebral commissures in the rhesus monkey , 1990, The Journal of comparative neurology.

[34]  V E Amassian,et al.  Comparison of human transcallosal responses evoked by magnetic coil and electrical stimulation. , 1989, Electroencephalography and clinical neurophysiology.

[35]  L. R. Stanford,et al.  Conduction velocity variations minimize conduction time differences among retinal ganglion cell axons. , 1987, Science.

[36]  V. Swayze,et al.  Two Hemispheres—One Brain: Functions of the Corpus Callosum , 1987 .

[37]  S G Waxman,et al.  Small-diameter nonmyelinated axons in the primate corpus callosum. , 1980, Archives of neurology.

[38]  T. Powell,et al.  A study of the axon initial segment and proximal axon of neurons in the primate motor and somatic sensory cortices. , 1979, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[39]  H. Swadlow,et al.  Characteristics of interhemispheric impulse conduction between prelunate gyri of the rhesus monkey , 1978, Experimental Brain Research.

[40]  M. Piercy Functions of the corpus callosum: Ciba Foundation Study Group No. 20. Edited by E.G. Ettlinger. J. and A. Churchill, London. 156 pp. 20s , 1966 .

[41]  I. H. Coriat,et al.  Histological Studies on the Localization of Cerebral Function , 1906 .

[42]  G. Innocenti Development and evolution: two determinants of cortical connectivity. , 2011, Progress in brain research.

[43]  Patrick R Hof,et al.  Functional Trade-Offs in White Matter Axonal Scaling , 2008, The Journal of Neuroscience.

[44]  M. D. Rugg,et al.  The effect of stimulus intensity on visual evoked potential estimates of interhemispheric transmission time , 2004, Experimental Brain Research.

[45]  G M Innocenti,et al.  Schizophrenia, neurodevelopment and corpus callosum , 2003, Molecular Psychiatry.

[46]  D. J. Felleman,et al.  Distributed hierarchical processing in the primate cerebral cortex. , 1991, Cerebral cortex.

[47]  V. Mountcastle,et al.  An organizing principle for cerebral function : the unit module and the distributed system , 1978 .

[48]  G. Edelman,et al.  The Mindful Brain: Cortical Organization and the Group-Selective Theory of Higher Brain Function , 1978 .

[49]  S G Waxman,et al.  Integrative properties and design principles of axons. , 1975, International review of neurobiology.

[50]  W. Singer,et al.  Frontiers in Integrative Neuroscience Integrative Neuroscience Neural Synchrony in Cortical Networks: History, Concept and Current Status , 2022 .

[51]  N. Logothetis,et al.  Frontiers in Integrative Neuroscience Integrative Neuroscience Directed Interactions between Auditory and Superior Temporal Cortices and Their Role in Sensory Integration , 2022 .