VOLATILE ANESTHETIC ACTIONS ON SYNAPTIC GABAA RECEPTORS
VOLATILE ANESTHETIC ACTIONS ON SYNAPTIC GABAA RECEPTORS
批准号:
6386686
负责人:
ROBERT A PEARCE
金额:
$20.89万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-05-01 至 2002-07-31
关键词:
GABA receptor anesthetics chemical kinetics electrophysiology halothane hippocampus laboratory rat membrane channels neural transmission neuropharmacology neurotransmitter metabolism pharmacokinetics pyramidal cells receptor expression single cell analysis synapses tissue /cell culture voltage /patch clamp
中文摘要
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英文摘要
DESCRIPTION: (Adapted from the applicant's abstract) In preliminary
studies, the investigator has observed that two volatile anesthetics exert
agent-specific actions on two physiologically distinct and anatomically
segregated GABAA receptors in hippocampal CA1 pyramidal cells; he has
provided evidence that these currents, the cell body GABAA/fast and the
dendritic GABAA/slow, mediate suppression of bursting activity and
paired-pulse depression, respectively, and thus may have different
functional roles with respect to seizures and learning respectively.
Preliminary results in which the ability of general anesthetics to enhance
GABA function is lost under conditions in which the milieu of the
intracellular side of the channel is changed have led to the suggestion that
this unique effect of anesthetics on the GABA channel is due to an
intracellular action. In the present study Dr. Pearce proposes to test the
hypothesis that agent-specific effects on the two GABA currents may account
for some clinical differences among agents, and to extend the results to the
molecular level. In 3 specific aims, he will (1) test the hypothesis that
the separate amnestic and convulsant properties of volatile anesthetics and
related agents result from their agent-specific actions on these two
currents by extending the series to additional agents including two
experimental compounds; (2) examine the mechanisms by which anesthetics
alter channel kinetic parameters; and (3) identify the intracellular factors
necessary for anesthetic-induced alterations and define their roles.
Methods include extracellular and whole cell ruptured patch recording in
hippocampal slice, and single channel recordings from excised patches from
the slice and from HEK293 cells in which GABAA receptors have been
expressed.
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海外基金