Home > Publications Database > Switching between persistent firing and depolarization block in individual rat CA1 pyramidal neurons. > print

001     140884
005     20250417095144.0
024 7 _ |a 10.1002/hipo.23078
|2 doi
024 7 _ |a pmid:30794330
|2 pmid
024 7 _ |a 1050-9631
|2 ISSN
024 7 _ |a 1098-1063
|2 ISSN
024 7 _ |a altmetric:76961221
|2 altmetric
037 _ _ |a DZNE-2020-07206
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Knauer, Beate
|0 P:(DE-HGF)0
|b 0
245 _ _ |a Switching between persistent firing and depolarization block in individual rat CA1 pyramidal neurons.
260 _ _ |a New York, NY [u.a.]
|c 2019
|b Wiley
264 _ 1 |3 online
|2 Crossref
|b Wiley
|c 2019-02-22
264 _ 1 |3 print
|2 Crossref
|b Wiley
|c 2019-09-01
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1744876262_17132
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a 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.
536 _ _ |a 342 - Disease Mechanisms and Model Systems (POF3-342)
|0 G:(DE-HGF)POF3-342
|c POF3-342
|f POF III
|x 0
542 _ _ |i 2019-02-22
|2 Crossref
|u http://doi.wiley.com/10.1002/tdm_license_1.1
542 _ _ |i 2019-02-22
|2 Crossref
|u http://onlinelibrary.wiley.com/termsAndConditions#vor
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a CA1 Region, Hippocampal: cytology
|2 MeSH
650 _ 2 |a CA1 Region, Hippocampal: drug effects
|2 MeSH
650 _ 2 |a CA1 Region, Hippocampal: physiology
|2 MeSH
650 _ 2 |a Carbachol: pharmacology
|2 MeSH
650 _ 2 |a Dose-Response Relationship, Drug
|2 MeSH
650 _ 2 |a Electrophysiological Phenomena: drug effects
|2 MeSH
650 _ 2 |a Electrophysiological Phenomena: physiology
|2 MeSH
650 _ 2 |a Female
|2 MeSH
650 _ 2 |a In Vitro Techniques
|2 MeSH
650 _ 2 |a Male
|2 MeSH
650 _ 2 |a Membrane Potentials: drug effects
|2 MeSH
650 _ 2 |a Muscarinic Agonists: pharmacology
|2 MeSH
650 _ 2 |a Patch-Clamp Techniques
|2 MeSH
650 _ 2 |a Potassium Channels: metabolism
|2 MeSH
650 _ 2 |a Pyramidal Cells: drug effects
|2 MeSH
650 _ 2 |a Pyramidal Cells: physiology
|2 MeSH
650 _ 2 |a Rats
|2 MeSH
650 _ 2 |a Rats, Long-Evans
|2 MeSH
650 _ 2 |a TRPC Cation Channels: antagonists & inhibitors
|2 MeSH
650 _ 2 |a TRPC Cation Channels: metabolism
|2 MeSH
700 1 _ |a Yoshida, Motoharu
|0 P:(DE-2719)2811873
|b 1
|e Last author
|u dzne
773 1 8 |a 10.1002/hipo.23078
|b : Wiley, 2019-02-22
|n 9
|p 817-835
|3 journal-article
|2 Crossref
|t Hippocampus
|v 29
|y 2019
|x 1050-9631
773 _ _ |a 10.1002/hipo.23078
|g Vol. 29, no. 9, p. 817 - 835
|0 PERI:(DE-600)1498049-6
|n 9
|q 29:9<817 - 835
|p 817-835
|t Hippocampus
|v 29
|y 2019
|x 1050-9631
856 4 _ |u https://pub.dzne.de/record/140884/files/DZNE-2020-07206_Restricted.pdf
856 4 _ |u https://pub.dzne.de/record/140884/files/DZNE-2020-07206_Restricted.pdf?subformat=pdfa
|x pdfa
909 C O |p VDB
|o oai:pub.dzne.de:140884
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
|b 1
|6 P:(DE-2719)2811873
913 1 _ |a DE-HGF
|b Gesundheit
|l Erkrankungen des Nervensystems
|1 G:(DE-HGF)POF3-340
|0 G:(DE-HGF)POF3-342
|3 G:(DE-HGF)POF3
|2 G:(DE-HGF)POF3-300
|4 G:(DE-HGF)POF
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914 1 _ |y 2019
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21