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


     


J Neurophysiol 82: 248-254, 1999;
0022-3077/99 $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 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 Google Scholar
Google Scholar
Right arrow Articles by Bekar, L. K.
Right arrow Articles by Walz, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bekar, L. K.
Right arrow Articles by Walz, W.

The Journal of Neurophysiology Vol. 82 No. 1 July 1999, pp. 248-254
Copyright ©1999 by the American Physiological Society

Evidence for Chloride Ions as Intracellular Messenger Substances in Astrocytes

Lane K. Bekar and Wolfgang Walz

Department of Physiology, University of Saskatchewan, Saskatoon, Saskatchewan, S7N 5E5 Canada

Bekar, Lane K. and Wolfgang Walz. Evidence for Chloride Ions as Intracellular Messenger Substances in Astrocytes. J. Neurophysiol. 82: 248-254, 1999.Cultured rat hippocampal astrocytes were used to investigate the mechanism underlying the suppression of Ba2+-sensitive K+ currents by GABAA receptor activation. Muscimol application had two effects on whole cell currents: opening of the well-known Cl- channel of the GABAA receptor and a secondary longer-lasting blockade of outward K+ currents displaying both peak and plateau phases. This blockade was independent of both Na+ (inside and outside) and ATP in the pipette. It also seemed to be independent of muscimol binding to the receptor because picrotoxin application showed no effect on the K+ conductance. The effect is blocked when anion efflux is prevented by replacing Cl- with gluconate (both inside and out) and is enhanced with more permeant anions such as Br- and I-. Moreover, the effect is reproduced in the absence of muscimol by promoting Cl- efflux via lowering of extracellular Cl- levels. These results, along with the requirement for Cl- efflux in muscimol experiments, show a strong dependency of the secondary blockade on Cl- efflux through the Cl- channel of the GABAA receptor. We therefore conclude that changes in the intracellular Cl- concentration alter the outward K+ conductances of astrocytes. Such a Cl--mediated modulation of an astrocytic K+ conductance will have important consequences for the progression of spreading depression through brain tissue and for astrocytic swelling in pathological situations.




This article has been cited by other articles:


Home page
J. Physiol.Home page
W. R. Proctor, L. Diao, R. K. Freund, M. D. Browning, and P. H. Wu
Synaptic GABAergic and glutamatergic mechanisms underlying alcohol sensitivity in mouse hippocampal neurons
J. Physiol., August 15, 2006; 575(1): 145 - 159.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
Y.-P. Fan, E. M. Horn, and T. G. Waldrop
Biophysical Characterization of Rat Caudal Hypothalamic Neurons: Calcium Channel Contribution to Excitability
J Neurophysiol, December 1, 2000; 84(6): 2896 - 2903.
[Abstract] [Full Text] [PDF]




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