The long-term goal of the proposed research is to understand the mechanisms which underlie the behavioral sparing and loss of functions that follow early damage of the cerebral cortex. In the proposed studies, the morphological changes associated with spared and impaired neural functions in cats, following removal of areas 17 and 18 at different stages of development, will be examined. Experiments will focus on survival and degeneration of neurons in the retina and in area PMLS of the cerebral cortex. For the retina, the spatial distribution of morphologically identified surviving ganglion cells will be determined, and the survival related to the pattern of their axon projections in the brain and to the cat's age at the time the damage is incurred. Corollary data on ganglion cell axon projections in the brain will also be obtained. For area PMLS, counts of surviving neurons will be made in each cortical layer, and related to the age of the cat at the time the lesion is incurred. In order to relate the degenerations to the pattern of axon projections, the origin of the pathway, in PMLS to areas 17 & 18, and termination of the reciprocal pathway, will be assessed at the same developmental stages areas 17 & 18 are removed. Additional studies will examine the organization of modified brain pathways from the thalamus and from cortical areas spared by the lesion to area PMLS. Conventional anterogradely and retrogradely transported axoplasmic tracer substances will be employed to identify neurons and brain pathways, and the distribution of surviving neurons and modified pathways will be related to spared functions. The data obtained form these studies may prove fundamental to understanding the neural and psychological disorders that follow damage of the immature cerebral cortex.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH044647-03
Application #
3384025
Study Section
Neurosciences Research Review Committee (BPN)
Project Start
1989-02-01
Project End
1993-01-31
Budget Start
1991-02-01
Budget End
1992-01-31
Support Year
3
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Boston University
Department
Type
Schools of Medicine
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
Lomber, S G; Payne, B R (2001) Perinatal-lesion-induced reorganization of cerebral functions revealed using reversible cooling deactivation and attentional tasks. Cereb Cortex 11:194-209
MacNeil, M A; Lomber, S G; Payne, B R (1997) Thalamic and cortical projections to middle suprasylvian cortex of cats: constancy and variation. Exp Brain Res 114:24-32
Sun, J S; Lomber, S G; Payne, B R (1994) Expansion of suprasylvian cortex projection in the superficial layers of the superior colliculus following damage of areas 17 and 18 in developing cats. Vis Neurosci 11:13-22
Lomber, S G; Payne, B R; Cornwell, P et al. (1993) Capacity of the retinogeniculate pathway to reorganize following ablation of visual cortical areas in developing and mature cats. J Comp Neurol 338:432-57
Peters, A; Payne, B R (1993) Numerical relationships between geniculocortical afferents and pyramidal cell modules in cat primary visual cortex. Cereb Cortex 3:69-78
Shupert, C; Cornwell, P; Payne, B (1993) Differential sparing of depth perception, orienting, and optokinetic nystagmus after neonatal versus adult lesions of cortical areas 17, 18, and 19 in the cat. Behav Neurosci 107:633-50
Payne, B R (1993) Evidence for visual cortical area homologs in cat and macaque monkey. Cereb Cortex 3:1-25
Pearson, H E; Payne, B R; Cunningham, T J (1993) Microglial invasion and activation in response to naturally occurring neuronal degeneration in the ganglion cell layer of the postnatal cat retina. Brain Res Dev Brain Res 76:249-55
Mendola, J D; Payne, B R (1993) Direction selectivity and physiological compensation in the superior colliculus following removal of areas 17 and 18. Vis Neurosci 10:1019-26
Payne, B R; Siwek, D F (1991) The visual map in the corpus callosum of the cat. Cereb Cortex 1:173-88

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