Selective destruction of medial septal cholinergic neurons attenuates pyramidal cell suppression, but not excitation in dorsal hippocampus field CA1 induced by subcutaneous injection of formalin
F. Zheng et S. Khanna, Selective destruction of medial septal cholinergic neurons attenuates pyramidal cell suppression, but not excitation in dorsal hippocampus field CA1 induced by subcutaneous injection of formalin, NEUROSCIENC, 103(4), 2001, pp. 985-998
Using extracellular recording techniques in urethane- (1 g/kg, i.p.) anaest
hetized rats, we investigated the influence exercised by medial septal chol
inergic neurons on dorsal hippocampus field CA1 neural responses to a kind
paw injection of formalin (5%, 0.05 ml, s.c.). Cholinergic neurons of the m
edial septal region were destroyed by local microinjection of the immunotox
in 192 IgG-saporin. Compared to control vehicle microinjected animals, immu
notoxin-treatment attenuated the amplitude, but not frequency, of CA1 theta
induced by intraseptal injection of carbachol. This suggested a selective
destruction of medial septal cholinergic neurons by the immunotoxin. Such d
estruction also abolished; (i) intraseptal carbachol-induced suppression of
CA1 population spike, and (ii) stimulation-intensity dependent increase in
amplitude, but not frequency, of theta evoked on electrical stimulation in
the region of oral part of pontine reticular nucleus. Further, in comparis
on to vehicle-treated animals, selective cholinergic destruction attenuated
formalin-induced; (i) theta activation, (ii) suppression of CA1 pyramidal
cell population spike and dendritic field excitatory post synaptic potentia
l, (iii) inhibition of complex spike cell extracellular activity, and (iv)
excitation and theta-rhythmicity of local putative GABAergic interneurons.
However, pretreatment with the immunotoxin did not alter the strength and p
roportion of complex spike cells excited following injection of formalin
From these findings we suggest that medial septal cholinergic neurons media
te, at least partly, the amplitude of theta and pyramidal cell suppression
via an inhibitory network involving CA1 interneurons. The data also indicat
es that during formalin theta, the cholinergic-mediated inhibitory processi
ng does not modulate the strength and selectivity of complex spike cell exc
itation. This points to formalin-induced, non-overlapping inhibitory and ex
citatory processes that might have different functional relevance. (C) 2001
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