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Vol. 281, Issue 1, 115-122, 1997
-Aminobutyric AcidB Receptor-Mediated
Hyperpolarization in Area CA1, but not Area CA3, Hippocampal Pyramidal
Cells1
Departments of
Pharmacology (S.G.B., S.B., K.C.C.) and
Cell
Biology, Neurobiology and Anatomy (W.A.P.), Loyola University Chicago
Stritch School of Medicine, Maywood, Illinois
Fluoxetine is a 5-hydroxytryptamine (5-HT, serotonin)-selective
reuptake inhibitor (SSRI) and is one of the main drugs used for the
treatment of depression. Because it takes 2 to 3 weeks of treatment
before clinical efficacy is manifest, the acute actions of fluoxetine
cannot account for the clinical actions of the drug. The chronic
effects of fluoxetine have not been completely delineated. The
experiments detailed here investigate the chronic effects of fluoxetine
on 5-HT and
-aminobutyric acid (GABA) receptor-mediated actions
using intracellular recording techniques in hippocampal brain slices.
Rats were treated with fluoxetine for 3 weeks via osmotic
minipumps implanted s.c. Fluoxetine and norfluoxetine plasma levels
were determined. The hippocampal pyramidal cell characteristics and the
5-HT1A and GABAB receptor-mediated
hyperpolarization were measured in the CA1 and the CA3 subfields. The
5-HT4 receptor-mediated decrease in the slow
afterhyperpolarization amplitude was also recorded in area CA1. The
time constant, magnitude of the change in resistance during 300-ms
hyperpolarizing current pulses and half-decay time of the sAHP were
altered by chronic fluoxetine treatment in area CA1 pyramidal cells. No
changes were seen in any of the active or passive membrane properties
of the CA3 hippocampal pyramidal cells. Fluoxetine treatment increased
the potency of 5-HT for the 5-HT1A receptor-mediated
hyperpolarization in area CA1, but not area CA3, and decreased the
potency of baclofen for the GABAB receptor-mediated
hyperpolarization in area CA1, but not area CA3. The characteristics of
the concentration-response curve for the 5-HT-mediated decrease in sAHP
amplitude in area CA1 were not altered by fluoxetine treatment. Chronic
fluoxetine selectively and differentially altered the cell
characteristics and the 5-HT1A and GABAB
receptor-mediated responses in area CA1 of the hippocampus, which forms
the final common output of the hippocampus.