The mammalian brain grows substantially in postnatal life. Despite wide recognition of this phenomenon, little attention has been paid to the cellular basis of ongoing brain growth. To what extent does this growth reflect the addition of new circuitry, and what role might such addition play in some of the major unexplained questions in developmental neurobiology? These enigmas include the basis of critical periods, the age-dependent response of the nervous system to injury, and the remarkable ability of the juvenile brain to store large amounts of new information. In order to successfully address these issues, the formation of novel circuitry in the developing brain must be observed and quantified by evaluating both individual neural elements (axonal branches, dendrites, synapses) and the development of entire circuits. Fortunately, the brains of many mammals comprise complex iterated circuits that can be studied by both morphological and electrophysiological methods. Examples are columns and """"""""blobs"""""""" in the visual system, columns and """"""""barrels"""""""" in the somatosensory system, glomeruli in the olfactory system, and cell islands and """"""""striasomes"""""""" in the neostriatum. Using the developing brain of several different mammalian species --including man-- we will examine systematically the development of two such circuits, olfactory glomeruli and blobs in the primary visual cortex. Part of this work will be carried out using vital imaging, confocal microscopy and magnetic resonance microscopy to examine changes in the arrangement and number of these circuits over time in living animals. In other segments of the project we will use more conventional electrophysiological and morphological approaches to examine the differentiation of neuronal elements and synaptic connections within circuits. As argued in the body of the application, the information that we hope to gain about the postnatal construction of circuitry in the mammalian brain is likely to be of central importance to both basic neurobiology and to understanding human neural development.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS029187-04
Application #
2267435
Study Section
Neurology B Subcommittee 2 (NEUB)
Project Start
1991-01-01
Project End
1997-12-31
Budget Start
1994-01-01
Budget End
1994-12-31
Support Year
4
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Duke University
Department
Biology
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Lotto, R Beau; Purves, Dale (2002) A rationale for the structure of color space. Trends Neurosci 25:84-8
Lotto, R B; Purves, D (2001) An empirical explanation of the Chubb illusion. J Cogn Neurosci 13:547-55
Yang, Z; Shimpi, A; Purves, D (2001) A wholly empirical explanation of perceived motion. Proc Natl Acad Sci U S A 98:5252-7
Nundy, S; Lotto, B; Coppola, D et al. (2000) Why are angles misperceived? Proc Natl Acad Sci U S A 97:5592-7
Purves, D; Williams, S M; Lotto, R B (2000) The relevance of visual perception to cortical evolution and development. Novartis Found Symp 228:240-54; discussion 254-8
Lotto, R B; Purves, D (2000) An empirical explanation of color contrast. Proc Natl Acad Sci U S A 97:12834-9
Purves, D; Lotto, B; Polger, T (2000) Color vision and the four-color-map problem. J Cogn Neurosci 12:233-7
Andrews, T J; Coppola, D M (1999) Idiosyncratic characteristics of saccadic eye movements when viewing different visual environments. Vision Res 39:2947-53
White, L E; Bosking, W H; Williams, S M et al. (1999) Maps of central visual space in ferret V1 and V2 lack matching inputs from the two eyes. J Neurosci 19:7089-99
Halpern, S D; Andrews, T J; Purves, D (1999) Interindividual variation in human visual performance. J Cogn Neurosci 11:521-34

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