JN Miami Valley Hospital
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 70: 2117-2127, 1993;
0022-3077/93 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
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 Google Scholar
Google Scholar
Right arrow Articles by Juliano, S. L.
Right arrow Articles by Eslin, D. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Juliano, S. L.
Right arrow Articles by Eslin, D. E.

Journal of Neurophysiology, Vol 70, Issue 5 2117-2127, Copyright © 1993 by APS


ARTICLES

Development of metabolic activity patterns in the somatosensory cortex of cats

S. L. Juliano, R. A. Code, M. Tommerdahl and D. E. Eslin
Department of Anatomy and Cell Biology and Neuroscience, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814.

1. The development of cortical responses to somatic stimulation was studied in kittens 2-5 wk of age using the 2-deoxyglucose (2DG) technique. During the 2DG experiment each kitten received an innocuous intermittent vertical displacement stimulus to the forepaw. 2. The pattern of metabolic activity was substantially different in young animals compared with adults. In the individual autoradiographs of the 2-wk-old kittens stimulus-evoked 2DG uptake in primary somatosensory cortex was localized to a small spot in the upper portion of the cortex, whereas in the adult the label extended vertically through the cortical layers and appeared more column-like. Individual patches of label were substantially smaller and less dense in young animals. Over a period of several weeks the evoked activity evolved to the more extensive adult pattern. The 2DG uptake displayed a mature distribution by approximately 4-5 wk of age. During this period, the cortical architecture also evolved from an immature to a mature arrangement. 3. The evoked activity was reconstructed into two-dimensional maps; the distribution of label > or = 1.5 SD above background was considered to be stimulus related. In the adult, the pattern appeared as a strip or strips of increased metabolic activity that extended in the rostrocaudal direction for approximately 1 mm. In contrast, the activity pattern in animals 2-4 wk old was less discretely organized into "strips" and was more diffusely spread over several mms of somatosensory cortex. The two-dimensional pattern gradually coalesced into a more localized strip by approximately 4-5 wk of age. Although the pattern of label was more widespread in the young animals, the absolute distance of the spread of activity did not vary substantially, regardless of the age of the animal. 4. Other measurements regarding the distribution of activity at different ages indicate that the amount of cortex activated increases in absolute terms, although the percent of cortex activated by the stimulus decreases. The overall intensity of the 2DG uptake as measured on the two-dimensional maps increases with age, as does the variability of the 2DG uptake; a wider range of intensity values is seen in the adult. Plots created from the individual two-dimensional reconstructions allowed a measure of "patch strength" at different ages. These histograms relate the most intense region of uptake in a given map to the spatial distribution of activity spreading in the medial and lateral directions.(ABSTRACT TRUNCATED AT 400 WORDS)





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