Te. Albertson et al., THE EFFECTS OF LINDANE AND LONG-TERM POTENTIATION (LTP) ON PYRAMIDAL CELL EXCITABILITY IN THE RAT HIPPOCAMPAL SLICE, Neurotoxicology, 18(2), 1997, pp. 469-477
An in vitro orthodromic stimulation technique was used to examine the
effects of lindane and long-term potentiation (LTP) inducing stimuli,
alone or in combination, on the excitatory afferent terminal of CA1 py
ramidal cells and on recurrent collateral evoked inhibition using the
rat hippocampal slice model. Hippocampal slices of 400 mu m thickness
were perfused with oxygenated artificial cerebrospinal fluid. Stimulat
ion of Schaffer collateral/commissural fibers produced extracellular e
xcitatory postsynaptic potential (EPSP) and/or population spike (PS) r
esponses recorded from electrodes in the CAI region. A paired-pulse te
chnique was used to measure gamma-aminobutyric acid (GABA(A))-mediated
recurrent inhibition before and after treatments. After both lindane
and LTP, larger PS amplitudes for a given stimulus intensity were seen
. The resulting leftward shift in the curve of the PS amplitude versus
stimulus intensity was larger after LTP than after 25 mu M lindane. B
oth lindane and LTP treatments reduced PS thresholds and reduced or el
iminated recurrent inhibition as measured by paired-pulse stimulation
at the 15 msec interval. The reduction of recurrent inhibition after b
oth treatments was more pronounced at lower stimulus intensities. When
LTP stimuli were applied after lindane exposure a further large shift
to the left was seen in the PS amplitude versus stimulus intensity cu
rve. A smaller shift to the left was seen in the PS amplitude versus s
timulus intensify curve only at the higher stimuli when lindane exposu
re occurred after LTP. Only at low stimulus intensities were further a
rgumentations seen in PS amplitudes when the ITP stimuli was followed
by a second LTP stimuli. Previous exposure to 25 mu M lindane stimuli
does not block the development of a further robust LTP in this in vitr
o model. (C) 1997 Intox Press, Inc.