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Biophys J, March 1998, p. 1305-1319, Vol. 74, No. 3
Institute of General Pathology and Pathophysiology, 125315 Moscow, Russia
Using whole-cell patch-clamp techniques, we studied the
blockade of open N-methyl-D-aspartate (NMDA)
channels by amino-adamantane derivatives (AADs) in rat hippocampal
neurons acutely isolated by the vibrodissociation method. The rapid
concentration-jump technique was used to replace superfusion solutions.
A kinetic analysis of the interaction of AAD with open NMDA channels
revealed fast and slow components of their blockade and recovery.
Mathematical modeling showed that these kinetic components are evidence
for two distinct blocking sites of AADs in open NMDA channels. A
comparative analysis of different simplest models led us to conclude
that these AAD blocking sites can be simultaneously occupied by two blocker molecules. The voltage dependence of the AAD block suggested that both sites were located deep in the channel pore.
Biophys J, March 1998, p. 1305-1319, Vol. 74, No. 3
© 1998 by the Biophysical Society 0006-3495/98/03/1305/15 $2.00
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