|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Department of Otolaryngology - HNS, University of California, San Francisco, CA, USA; W.M. Keck Center for Integrative Neuroscience, University of California, San Francisco, CA, USA
2 Department of Otolaryngology - HNS, University of California, San Francisco, CA, USA
3 Laboratoire IDM, UPRES-EA 3192, Universite de Rennes I, Rennes, France
* To whom correspondence should be addressed. E-mail: ben{at}phy.ucsf.edu.
The current study was conducted to extend our understanding of changes in spatial organization and response properties of cortical neurons in the developing mammalian forebrain. Extracellular multi-unit responses to tones were recorded from a dense array of penetrations covering entire isofrequency contours in the primary auditory cortex (AI) of pentobarbital anesthetized kittens. Ages ranged from postnatal day 14 (P14), shortly after acquisition of normal auditory response thresholds, through postnatal day 111 (P111), when the kittens were largely mature. Spatial organization of the AI was tonotopically ordered by P14. The tonotopic gradient decreased with chronological maturation. At P14 the gradient was approximately 3.5 kHz/mm. By P111 it had declined to approximately 2.5 kHz/mm, so that the cortical region encompassing a fixed 3 to 15 kHz frequency range enlarged along its posterior-anterior dimension. Response properties of developing AI neurons changed in both frequency selectivity and intensity selectivity. The mean frequency tuning bandwidth increased with age. Initially, tuning bandwidths were narrow throughout the entire AI. With progressive maturation, broader bandwidths were observed in areas dorsal and ventral to a central region in which neurons remained narrowly tuned. The resulting spatial organization of tuning bandwidth was similar to that reported in adult cats. The majority of recording sites manifested non-monotonic rate/level functions at all ages. However, the proportion of sites with monotonic rate/level functions increased with age. No spatial organization of rate/level functions (monotonic and non-monotonic) was observed through P111. The relatively late development of bandwidth tuning in the AI compared with the early presence of tonotopic organization suggests that different developmental processes are responsible for structuring these two dimensions of acoustic selectivity.
This article has been cited by other articles:
![]() |
A. J. Norena, B. Gourevitch, M. Pienkowski, G. Shaw, and J. J. Eggermont Increasing Spectrotemporal Sound Density Reveals an Octave-Based Organization in Cat Primary Auditory Cortex J. Neurosci., September 3, 2008; 28(36): 8885 - 8896. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Razak and Z. M. Fuzessery Development of Inhibitory Mechanisms Underlying Selectivity for the Rate and Direction of Frequency-Modulated Sweeps in the Auditory Cortex J. Neurosci., February 14, 2007; 27(7): 1769 - 1781. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. de Villers-Sidani, E. F. Chang, S. Bao, and M. M. Merzenich Critical Period Window for Spectral Tuning Defined in the Primary Auditory Cortex (A1) in the Rat J. Neurosci., January 3, 2007; 27(1): 180 - 189. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. F. Chang, S. Bao, K. Imaizumi, C. E. Schreiner, and M. M. Merzenich Development of spectral and temporal response selectivity in the auditory cortex PNAS, November 8, 2005; 102(45): 16460 - 16465. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. J. Norena and J. J. Eggermont Enriched Acoustic Environment after Noise Trauma Reduces Hearing Loss and Prevents Cortical Map Reorganization J. Neurosci., January 19, 2005; 25(3): 699 - 705. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pienkowski and R. V. Harrison Tone Frequency Maps and Receptive Fields in the Developing Chinchilla Auditory Cortex J Neurophysiol, January 1, 2005; 93(1): 454 - 466. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Visit Other APS Journals Online |