Intermodal Competition and Compensation in Development

A large literature has attempted to verify experimentally the considerable anecdotal evidence that deprivation of input in one sensory modality leads to compensatory increases in the functioning of remaining modalities. Convincing evidence on this issue from convergent behavioral, physiological, and anatomical descriptions would provide information central to an understanding of how different brain systems become specialized to process different and specific types of information. Are there intrinsic properties of different brain regions that render them a suitable substrate to process certain and not other types of information? What is thc role of specific types of sensory input in the functional differentiation of specialized brain systems? The pertinent human literature on the effects of sensory deprivation consists almost entirely of behavioral studies, and these present a confusing array of results. Some studies report increases, some decreases, and others no differences in abilities of remaining modalities compared with those abilities in intact control subjects. This variability is no doubt due in large part to differences in the age of onset and completeness of blindness or deafness of the population under study. Additionally the etiology of the deafness or blindness is a key variable: For example, deafness secondary to encephalitis is likely to be associated with compromised functioning in several domains and thus make it difficult to separately assess the effects of the sensory deprivation per se. In the small number of studies that have controlled for these factors, there appears to be evidence for the hypothesis that elementary functions, like sensory thresholds and acuity within remaining modalities, may not display compensatory enhancement. In contrast, attentional processing and the spatial localization of information may show such enhancement (Burnstine, Greenough & Tees, 1984; Neville, 1988). Such behavioral data, if upheld, would raise specific hypotheses about the brain regions involved in intermodal compensation. For example, if major effects occur in attentional processing this would implicate nonprimary “association” areas

[1]  R. Efron TEMPORAL PERCEPTION, APHASIA AND D'EJ'A VU. , 1963, Brain : a journal of neurology.

[2]  M. Albert,et al.  Auditory sequencing and left cerebral dominance for language. , 1972, Neuropsychologia.

[3]  FRANK MORRELL,et al.  Visual System's View of Acoustic Space , 1972, Nature.

[4]  E. Carlier,et al.  Enhancement of visual responses on the primary auditory cortex of the cat after an early destruction of cochlear receptors , 1977, Brain Research.

[5]  P. Tueting,et al.  Event-related brain potentials in man , 1978 .

[6]  D. Robinson,et al.  Parietal association cortex in the primate: sensory mechanisms and behavioral modulations. , 1978, Journal of neurophysiology.

[7]  Trichur Raman Vidyasagar,et al.  Possible plasticity in the rat superior colliculus , 1978, Nature.

[8]  M. Petrides,et al.  The effect of selective anterior and posterior association cortex lesions in the monkey on performance of a visual-auditory compound discrimination test , 1978, Neuropsychologia.

[9]  T. Allison,et al.  THE FUNCTIONAL NEUROANATOMY OF EVENT RELATED POTENTIALS , 1978 .

[10]  Factors affecting the recording of visual-evoked potentials from the deaf cat primary auditory cortex (AI) , 1980, Brain Research.

[11]  B. C. Motter,et al.  The influence of attentive fixation upon the excitability of the light- sensitive neurons of the posterior parietal cortex , 1981, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[12]  M. Kutas,et al.  Event-related potential studies of cerebral specialization during reading II. Studies of congenitally deaf adults , 1982, Brain and Language.

[13]  M. Kutas,et al.  Event-related potential studies of cerebral specialization during reading I. Studies of normal adults , 1982, Brain and Language.

[14]  Marta Kutas,et al.  Altered visual-evoked potentials in congenitally deaf adults , 1983, Brain Research.

[15]  W. Greenough,et al.  1 – Intermodal Compensation following Damage or Deprivation: A Review of Behavioral and Neural Evidence , 1984 .

[16]  D. Frost Axonal growth and target selection during development: retinal projections to the ventrobasal complex and other “nonvisual” structures in neonatal Syrian hamsters , 1984, The Journal of comparative neurology.

[17]  Helen J. Neville,et al.  Attention to central and peripheral visual space in a movement detection task: an event-related potential and behavioral study. I. Normal hearing adults , 1987, Brain Research.

[18]  H. Neville,et al.  Attention to central and peripheral visual space in a movement detection task. III. Separate effects of auditory deprivation and acquisition of a visual language , 1987, Brain Research.

[19]  Helen J. Neville,et al.  Attention to central and peripheral visual space in a movement detection task: an event-related potential and behavioral study. II. Congenitally deaf adults , 1987, Brain Research.

[20]  Keiji Tanaka,et al.  Polysensory properties of neurons in the anterior bank of the caudal superior temporal sulcus of the macaque monkey. , 1988, Journal of neurophysiology.

[21]  D. Frost Transitory Neuronal Connections in Normal Development and Disease , 1989 .

[22]  D. Regan Human brain electrophysiology: Evoked potentials and evoked magnetic fields in science and medicine , 1989 .

[23]  D O Frost,et al.  Sensory Processing by Novel, Experimentally Induced Cross‐Modal Circuits a , 1990, Annals of the New York Academy of Sciences.