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@ARTICLE{Knauer:140884,
author = {Knauer, Beate and Yoshida, Motoharu},
title = {{S}witching between persistent firing and depolarization
block in individual rat {CA}1 pyramidal neurons.},
journal = {Hippocampus},
volume = {29},
number = {9},
issn = {1050-9631},
address = {New York, NY [u.a.]},
publisher = {Wiley},
reportid = {DZNE-2020-07206},
pages = {817-835},
year = {2019},
abstract = {The hippocampal formation plays a role in mnemonic tasks
and epileptic discharges in vivo. In vitro, these functions
and malfunctions may relate to persistent firing (PF) and
depolarization block (DB), respectively. Pyramidal neurons
of the CA1 field have previously been reported to engage in
either PF or DB during cholinergic stimulation. However, it
is unknown whether these cells constitute disparate
populations of neurons. Furthermore, it is unclear which
cell-specific peculiarities may mediate their diverse
response properties. However, it has not been shown whether
individual CA1 pyramidal neurons can switch between PF and
DB states. Here, we used whole cell patch clamp in the
current clamp mode on in vitro CA1 pyramidal neurons from
acutely sliced rat tissue to test various intrinsic
properties which may provoke individual cells to switch
between PF and DB. We found that individual cells could
switch from PF to DB, in a cholinergic agonist concentration
dependent manner and depending on the parameters of
stimulation. We also demonstrate involvement of TRPC and
potassium channels in this switching. Finally, we report
that the probability for DB was more pronounced in the
proximal than in the distal half of CA1. These findings
offer a potential mechanism for the stronger spatial
modulation in proximal, compared to distal CA1, as place
field formation was shown to be affected by DB. Taken
together, our results suggest that PF and DB are not
mutually exclusive response properties of individual
neurons. Rather, a cell's response mode depends on a variety
of intrinsic properties, and modulation of these properties
enables switching between PF and DB.},
keywords = {Animals / CA1 Region, Hippocampal: cytology / CA1 Region,
Hippocampal: drug effects / CA1 Region, Hippocampal:
physiology / Carbachol: pharmacology / Dose-Response
Relationship, Drug / Electrophysiological Phenomena: drug
effects / Electrophysiological Phenomena: physiology /
Female / In Vitro Techniques / Male / Membrane Potentials:
drug effects / Muscarinic Agonists: pharmacology /
Patch-Clamp Techniques / Potassium Channels: metabolism /
Pyramidal Cells: drug effects / Pyramidal Cells: physiology
/ Rats / Rats, Long-Evans / TRPC Cation Channels:
antagonists $\&$ inhibitors / TRPC Cation Channels:
metabolism},
cin = {AG Yoshida},
ddc = {610},
cid = {I:(DE-2719)1310011},
pnm = {342 - Disease Mechanisms and Model Systems (POF3-342)},
pid = {G:(DE-HGF)POF3-342},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30794330},
doi = {10.1002/hipo.23078},
url = {https://pub.dzne.de/record/140884},
}