J Physiol Society Meetings
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 580, Number 1, 171-179, April 1, 2007 DOI: 10.1113/jphysiol.2006.126888
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
580/1/171    most recent
jphysiol.2006.126888v1
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 Beato, M.
Right arrow Articles by Sivilotti, L. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Beato, M.
Right arrow Articles by Sivilotti, L. G.
Related Collections
Right arrow Neuroscience

NEUROSCIENCE

The kinetics of inhibition of rat recombinant heteromeric {alpha}1beta glycine receptors by the low-affinity antagonist SR-95531

Marco Beato1, Valeria Burzomato1 and Lucia G. Sivilotti1

1 Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK

The GABAA antagonist SR-95531 (gabazine) is known to block glycine receptors, albeit with low affinity. We have studied the effect of SR-95531 on rat recombinant {alpha}1beta glycine receptors expressed in human embryonic kidney (HEK293) cells by recording macroscopic currents elicited by rapid glycine application to outside-out patches. SR-95531 has a fast unbinding rate (koffSR, about 3000 s–1) and this means that the time course of its unbinding is comparable to the expected time course of the transmitter in the cleft. We also found that equilibrium applications of SR-95531 reduced the response to brief glycine applications by an amount inversely proportional to the duration of glycine application. The fast unbinding rate of SR-95531 from the glycine receptor will make it useful for establishing the time course of glycine concentration at glycinergic synapses.

(Received 18 December 2006; accepted after revision 8 January 2007; first published online 11 January 2007)
Corresponding author M. Beato: Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK. Email: m.beato{at}ucl.ac.uk




This article has been cited by other articles:


Home page
J. Neurosci.Home page
M. Beato
The Time Course of Transmitter at Glycinergic Synapses onto Motoneurons
J. Neurosci., July 16, 2008; 28(29): 7412 - 7425.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2007 The Physiological Society.