JN AJP: Cell Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 88: 1288-1301, 2002; doi:10.1152/jn.00994.2001
0022-3077/02 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (18)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hickmott, P. W.
Right arrow Articles by Merzenich, M. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hickmott, P. W.
Right arrow Articles by Merzenich, M. M.

The Journal of Neurophysiology Vol. 88 No. 3 September 2002, pp. 1288-1301
Copyright ©2002 by the American Physiological Society

Local Circuit Properties Underlying Cortical Reorganization

Peter W. Hickmott1 and Michael M. Merzenich2

 1Department of Psychology, University of California, Riverside, 92521; and  2Departments of Otolaryngology and Physiology and Keck Center for Integrative Neuroscience, San Francisco, California 94143

Hickmott, Peter W. and Michael M. Merzenich. Local Circuit Properties Underlying Cortical Reorganization. J. Neurophysiol. 88: 1288-1301, 2002. Peripheral denervation has been shown to cause reorganization of the deafferented somatotopic region in primary somatosensory cortex (S1). However, the basic mechanisms that underlie reorganization are not well understood. In the experiments described in this paper, a novel in vivo/in vitro preparation of adult rat S1 was used to determine changes in local circuit properties associated with the denervation-induced plasticity of the cortical representation in rat S1. In the present studies, deafferentation of rat S1 was induced by cutting the radial and median nerves in the forelimb of adult rats, resulting in a rapid shift of the location of the forepaw/lower jaw border; the amount of the shift increased over the times assayed, through 28 days after denervation. The locations of both borders (i.e., original and reorganized) were marked with vital dyes, and slices from the marked region were used for whole-cell recording. Responses were evoked using electrical stimulation of supragranular S1 and recorded in supragranular neurons close to either the original or reorganized border. For each neuron, postsynaptic potentials (PSPs) were evoked by stimulation of fibers that crossed the border site (CB stim) and by equivalent stimulation that did not cross (NCB stim). Monosynaptic inhibitory postsynaptic potentials (IPSPs) were also examined after blocking excitatory transmission with 15 µM CNQX plus 100 µM DL-APV. The amplitudes of PSPs and IPSPs were compared between CB and NCB stimulation to quantify effects of the border sites on excitation and inhibition. Previous results using this preparation in the normal (i.e., without induced plasticity) rat S1 demonstrated that at a normal border both PSPs and IPSPs were smaller when evoked with CB stimulation than with NCB stimulation. For most durations of denervation, a similar bias (i.e., smaller responses with CB stimulation) for PSPs and IPSPs was observed at the site of the novel reorganized border, while no such bias was observed at the suppressed original border site. Thus changes in local circuit properties (excitation and inhibition) can reflect larger-scale changes in cortical organization. However, specific dissociations between these local circuit properties and the presence of the novel border at certain durations of denervation were also observed, suggesting that there are several intracortical processes contributing to cortical reorganization over time and that excitation and inhibition may contribute differentially to them.




This article has been cited by other articles:


Home page
Neurorehabil Neural RepairHome page
L. G. Richards, C. R. Senesac, S. B. Davis, M. L. Woodbury, and S. E. Nadeau
Bilateral Arm Training With Rhythmic Auditory Cueing in Chronic Stroke: Not Always Efficacious
Neurorehabil Neural Repair, April 1, 2008; 22(2): 180 - 184.
[Abstract] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
S. B. Moldakarimov, J. L. McClelland, and G. B. Ermentrout
A homeostatic rule for inhibitory synapses promotes temporal sharpening and cortical reorganization
PNAS, October 31, 2006; 103(44): 16526 - 16531.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
P. W. Hickmott
Changes in Intrinsic Properties of Pyramidal Neurons in Adult Rat S1 During Cortical Reorganization
J Neurophysiol, July 1, 2005; 94(1): 501 - 511.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
M. Henkemeyer, O. S. Itkis, M. Ngo, P. W. Hickmott, and I. M. Ethell
Multiple EphB receptor tyrosine kinases shape dendritic spines in the hippocampus
J. Cell Biol., December 22, 2003; 163(6): 1313 - 1326.
[Abstract] [Full Text] [PDF]


Home page
StrokeHome page
P. Cicinelli, P. Pasqualetti, M. Zaccagnini, R. Traversa, M. Oliveri, and P. M. Rossini
Interhemispheric Asymmetries of Motor Cortex Excitability in the Postacute Stroke Stage: A Paired-Pulse Transcranial Magnetic Stimulation Study
Stroke, November 1, 2003; 34(11): 2653 - 2658.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online