Korean J Physiol Pharmacol.
1998 Jun;2(3):297-305.
Characteristic intracellular response to lidocaine and MK-801 of
hippocampal neurons: An in vivo intracellular neuron recording study
- Affiliations
-
- 1Department of Dental Pharmacology, Kyungpook National University School of Dentistry, Taegu 700-422, Korea.
Abstract
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This study used in vivo intracellular recording in rat hippocampus to
evaluate the effect of lidocaine and MK-801 on the membrane properties
and the synaptic responses of individual neurons to electrical
stimulation of the commissural pathway. Cells in control group
typically fired in a tonic discharge mode with an average firing
frequency of 2.4+/-0.9 Hz. Neuron in MK-801 treated group (0.2 mg/kg,
i.p.) had an average input resistance of 32.8 +/- 5.7 Mg and a membrane
time constant of 7.4 +/- 1. 8 ms. These neurons exhibited 2.4 +/- 0.2 ms
spike durations, which were similar to the average spike duration
recorded in the neurons of the control group. Slightly less than half
of these neurons were firing spontaneously with an average discharge
rate of 2.4 +/- 1.1 Hz. The average peak amplitude of the ABP following
the spikes in these groups was 7.4+/-0.6 mV with respect to the resting
membrane potentiaL Cells in MK-801 and lidocaine treated group (5
mg/kg, i.c.v.) had an average input resistance of 34.5+/-6.0 Mg and an
average time constant of 8.0+/-1.4 ms. The cells were firing
spontaneously at an average discharge rate of 0.6+/-0.4 Hz. Upon
depolarization of the membrane by 0.8 nA for 400 ms, all of the tested
cells exhibited accommodation of spike discharge. The most common
synaptic response contained an EPSP followed by early-IPSP and
late-IPSP. Analysis of the voltage dependence revealed that the
early-IPSP and late-IPSP were putative Cl-and K+-dependent,
respectively. Systemic injection of the NMDA receptor blocker, MK-801,
did not block synaptic responses to the stimulation of the commissural
pathway. No significant modifications of EPSP, early-IPSP, or late-IPSP
components were detected in the MK-801 and/or lidocaine treated group.
These results suggest that MK-801 and lidocaine manifest their CNS
effects through firing pattern of hippocampal pyramidal cells and
neural network pattern by changing the synaptic efficacy and cellular
membrane properties.