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dc.contributor.author
Egorov, Alexei V.  
dc.contributor.author
Schumacher, Dagmar  
dc.contributor.author
Medert, Rebekka  
dc.contributor.author
Birnbaumer, Lutz  
dc.contributor.author
Freichel, Marc  
dc.contributor.author
Draguhn, Andreas  
dc.date.available
2020-12-16T14:01:17Z  
dc.date.issued
2019-11  
dc.identifier.citation
Egorov, Alexei V.; Schumacher, Dagmar; Medert, Rebekka; Birnbaumer, Lutz; Freichel, Marc; et al.; TRPC channels are not required for graded persistent activity in entorhinal cortex neurons; Veterinary and Human Toxicology; Hippocampus; 29; 11; 11-2019; 1038-1048  
dc.identifier.issn
1050-9631  
dc.identifier.uri
http://hdl.handle.net/11336/120563  
dc.description.abstract
Adaptive behavior requires the transient storage of information beyond the physical presence of external stimuli. This short-lasting form of memory involves sustained (“persistent”) neuronal firing which may be generated by cell-autonomous biophysical properties of neurons or/and neural circuit dynamics. A number of studies from brain slices reports intrinsically generated persistent firing in cortical excitatory neurons following suprathreshold depolarization by intracellular current injection. In layer V (LV) neurons of the medial entorhinal cortex (mEC) persistent firing depends on the activation of cholinergic muscarinic receptors and is mediated by a calcium-activated nonselective cation current (ICAN). The molecular identity of this conductance remains, however, unknown. Recently, it has been suggested that the underlying ion channels belong to the canonical transient receptor potential (TRPC) channel family and include heterotetramers of TRPC1/5, TRPC1/4, and/or TRPC1/4/5 channels. While this suggestion was based on pharmacological experiments and on effects of TRP-interacting peptides, an unambiguous proof based on TRPC channel-depleted animals is pending. Here, we used two different lines of TRPC channel knockout mice, either lacking TRPC1-, TRPC4-, and TRPC5-containing channels or lacking all seven members of the TRPC family. We report unchanged persistent activity in mEC LV neurons in these animals, ruling out that muscarinic-dependent persistent activity depends on TRPC channels.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Veterinary and Human Toxicology  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
HEPTA-TRPC KO MICE  
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MUSCARINIC  
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PERSISTENT FIRING  
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TRPC1/4/5 KO MICE  
dc.subject.classification
Biología Celular, Microbiología  
dc.subject.classification
Ciencias Biológicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
TRPC channels are not required for graded persistent activity in entorhinal cortex neurons  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2020-11-25T16:38:09Z  
dc.journal.volume
29  
dc.journal.number
11  
dc.journal.pagination
1038-1048  
dc.journal.pais
Estados Unidos  
dc.description.fil
Fil: Egorov, Alexei V.. Universität Heidelberg; Alemania  
dc.description.fil
Fil: Schumacher, Dagmar. Universität Heidelberg; Alemania  
dc.description.fil
Fil: Medert, Rebekka. Universität Heidelberg; Alemania  
dc.description.fil
Fil: Birnbaumer, Lutz. Pontificia Universidad Católica Argentina "Santa María de los Buenos Aires". Instituto de Investigaciones Biomédicas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Biomédicas; Argentina  
dc.description.fil
Fil: Freichel, Marc. Universität Heidelberg; Alemania  
dc.description.fil
Fil: Draguhn, Andreas. Universität Heidelberg; Alemania  
dc.journal.title
Hippocampus  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/hipo.23094  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/epdf/10.1002/hipo.23094  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791731/