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@ARTICLE{Brahimi:257339,
author = {Brahimi, Yacine and Knauer, Beate and Price, Alan Tobias
and Valero-Aracama, Maria Jesus and Reboreda, Antonio and
Sauvage, Magdalena and Yoshida, Motoharu},
title = {{P}ersistent {F}iring in {H}ippocampal {CA}1 {P}yramidal
{C}ells in {Y}oung and {A}ged {R}ats.},
journal = {eNeuro},
volume = {10},
number = {3},
issn = {2373-2822},
address = {Washington, DC},
publisher = {Soc.},
reportid = {DZNE-2023-00408},
pages = {ENEURO.0479-22.2023},
year = {2023},
note = {CC BY},
abstract = {Persistent neuronal firing is often observed in working
memory and temporal association tasks both in humans and
animals, and is believed to retain necessary information in
these tasks. We have reported that hippocampal CA1 pyramidal
cells are able to support persistent firing through
intrinsic mechanisms in the presence of cholinergic
agonists. However, it still remains largely unknown how
persistent firing is affected by the development of animals
and aging. Using in vitro patch-clamp recordings from CA1
pyramidal cells in rat brain slices, we first show that the
cellular excitability of these aged rats was significantly
lower than that of the young rats, responding with fewer
spikes to current injection. In addition, we found
age-dependent modulations of input resistance, membrane
capacitance, and spike width. However, persistent firing in
aged (approximately two-year-old) rats was as strong as that
in young animals, and the properties of persistent firing
were very similar among different age groups. In addition,
medium spike afterhyperpolarization potential (mAHP), was
not increased by aging and did not correlate with the
strength of persistent firing. Lastly, we estimated the
depolarization current induced by the cholinergic
activation. This current was proportional to the increased
membrane capacitance of the aged group and was inversely
correlated with their intrinsic excitability. These
observations indicate that robust persistent firing can be
maintained in aged rats despite reduced excitability,
because of the increased amount of cholinergically induced
positive current.},
keywords = {Humans / Rats / Animals / Child, Preschool / Pyramidal
Cells: physiology / Hippocampus: physiology / Action
Potentials: physiology / Neurons / Cholinergic Agents /
afterhyperpolarization (Other) / aged rats (Other) /
cholinergic agonist (Other) / depolarization current (Other)
/ hippocampus (Other) / persistent firing (Other) /
Cholinergic Agents (NLM Chemicals)},
cin = {AG Yoshida},
ddc = {610},
cid = {I:(DE-2719)1310011},
pnm = {351 - Brain Function (POF4-351)},
pid = {G:(DE-HGF)POF4-351},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36894320},
pmc = {pmc:PMC10062487},
doi = {10.1523/ENEURO.0479-22.2023},
url = {https://pub.dzne.de/record/257339},
}