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Volume 17, Number 11,
Issue of June 1, 1997
pp. 3990-4005
Copyright ©1997 Society for Neuroscience
Interneurons of the Dentate-Hilus Border of the Rat Dentate
Gyrus: Morphological and Electrophysiological Heterogeneity
Received Dec. 23, 1996; revised March 5, 1997; accepted March 10, 1997.
David D. Mott1,
Dennis
A. Turner2, 3, 6,
Maxine M. Okazaki4, and
Darrell V. Lewis3, 5
1 Department of Pharmacology, Emory University,
Atlanta, Georgia 30322, Departments of 2 Surgery
(Neurosurgery), 3 Neurobiology, 4 Pharmacology,
and 5 Pediatrics (Neurology), Duke University Medical
Center, Durham, North Carolina 27710, and 6 Department of
Neurosurgery, Veterans Administration Medical Center, Durham, North
Carolina 27705
Interneurons located near the border of the dentate granule cell
layer and the hilus were studied in hippocampal slices using whole-cell
current clamp and biocytin staining. Because these interneurons exhibit
both morphological and electrophysiological diversity, we asked whether
passive electrotonic parameters or repetitive firing behavior
correlated with axonal distribution. Each interneuron was distinguished
by a preferred axonal distribution in the molecular layer or granule
cell layer, and four groups could be discerned, the axons of which
arborized in (1) the granule cell layer, (2) the inner molecular layer,
(3) the outer molecular layer, and (4) diffusely in the molecular
layer. In our sample, interneurons with axons arborizing diffusely in
the molecular layer were most frequent, and those with axons restricted
to the granule cell layer were least frequent. Resting potential, input resistance, time constant, electrotonic length, and spike frequency adaptation (SFA) were not significantly different among the four groups, and the variability in SFA between cells with similar axonal
distributions was striking. Clear differences in action potential
morphology and afterhyperpolarizations, however, emerged when
nonadapting interneurons were compared with those exhibiting SFA.
Interneurons exhibiting SFA had characteristically broader spikes,
progressive slowing of action potential repolarization during
repetitive firing, and slow afterhyperpolarizations that distinguished
them from nonadapting interneurons. We propose that the variability in
repetitive firing behavior and morphology exhibited by each of these
interneurons makes each interneuron unique and may provide a high level
of fine tuning of inhibitory control critical to information processing
in the dentate.
Key words:
interneurons;
spike frequency adaptation;
accommodation;
dentate gyrus;
inhibition;
action potential;
electrotonic length;
basket cell
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