Cargando…

HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice

Hyperpolarization‐activated and cyclic nucleotide‐gated (HCN) channels mediate the I (h) current in the murine hippocampus. Disruption of the I (h) current by knockout of HCN1, HCN2 or tetratricopeptide repeat‐containing Rab8b‐interacting protein has been shown to affect physiological processes such...

Descripción completa

Detalles Bibliográficos
Autores principales: Günther, Anne, Luczak, Vincent, Gruteser, Nadine, Abel, Ted, Baumann, Arnd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850037/
https://www.ncbi.nlm.nih.gov/pubmed/30585408
http://dx.doi.org/10.1111/gbb.12550
_version_ 1783469330316394496
author Günther, Anne
Luczak, Vincent
Gruteser, Nadine
Abel, Ted
Baumann, Arnd
author_facet Günther, Anne
Luczak, Vincent
Gruteser, Nadine
Abel, Ted
Baumann, Arnd
author_sort Günther, Anne
collection PubMed
description Hyperpolarization‐activated and cyclic nucleotide‐gated (HCN) channels mediate the I (h) current in the murine hippocampus. Disruption of the I (h) current by knockout of HCN1, HCN2 or tetratricopeptide repeat‐containing Rab8b‐interacting protein has been shown to affect physiological processes such as synaptic integration and maintenance of resting membrane potentials as well as several behaviors in mice, including depressive‐like and anxiety‐like behaviors. However, the potential involvement of the HCN4 isoform in these processes is unknown. Here, we assessed the contribution of the HCN4 isoform to neuronal processing and hippocampus‐based behaviors in mice. We show that HCN4 is expressed in various regions of the hippocampus, with distinct expression patterns that partially overlapped with other HCN isoforms. For behavioral analysis, we specifically modulated HCN4 expression by injecting recombinant adeno‐associated viral (rAAV) vectors mediating expression of short hairpin RNA against hcn4 (shHcn4) into the dorsal hippocampus of mice. HCN4 knockdown produced no effect on contextual fear conditioning or spatial memory. However, a pronounced anxiogenic effect was evident in mice treated with shHcn4 compared to control littermates. Our findings suggest that HCN4 specifically contributes to anxiety‐like behaviors in mice.
format Online
Article
Text
id pubmed-6850037
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Blackwell Publishing Ltd
record_format MEDLINE/PubMed
spelling pubmed-68500372019-11-15 HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice Günther, Anne Luczak, Vincent Gruteser, Nadine Abel, Ted Baumann, Arnd Genes Brain Behav Original Articles Hyperpolarization‐activated and cyclic nucleotide‐gated (HCN) channels mediate the I (h) current in the murine hippocampus. Disruption of the I (h) current by knockout of HCN1, HCN2 or tetratricopeptide repeat‐containing Rab8b‐interacting protein has been shown to affect physiological processes such as synaptic integration and maintenance of resting membrane potentials as well as several behaviors in mice, including depressive‐like and anxiety‐like behaviors. However, the potential involvement of the HCN4 isoform in these processes is unknown. Here, we assessed the contribution of the HCN4 isoform to neuronal processing and hippocampus‐based behaviors in mice. We show that HCN4 is expressed in various regions of the hippocampus, with distinct expression patterns that partially overlapped with other HCN isoforms. For behavioral analysis, we specifically modulated HCN4 expression by injecting recombinant adeno‐associated viral (rAAV) vectors mediating expression of short hairpin RNA against hcn4 (shHcn4) into the dorsal hippocampus of mice. HCN4 knockdown produced no effect on contextual fear conditioning or spatial memory. However, a pronounced anxiogenic effect was evident in mice treated with shHcn4 compared to control littermates. Our findings suggest that HCN4 specifically contributes to anxiety‐like behaviors in mice. Blackwell Publishing Ltd 2019-01-22 2019-02 /pmc/articles/PMC6850037/ /pubmed/30585408 http://dx.doi.org/10.1111/gbb.12550 Text en © 2018 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Günther, Anne
Luczak, Vincent
Gruteser, Nadine
Abel, Ted
Baumann, Arnd
HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice
title HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice
title_full HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice
title_fullStr HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice
title_full_unstemmed HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice
title_short HCN4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice
title_sort hcn4 knockdown in dorsal hippocampus promotes anxiety‐like behavior in mice
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850037/
https://www.ncbi.nlm.nih.gov/pubmed/30585408
http://dx.doi.org/10.1111/gbb.12550
work_keys_str_mv AT guntheranne hcn4knockdownindorsalhippocampuspromotesanxietylikebehaviorinmice
AT luczakvincent hcn4knockdownindorsalhippocampuspromotesanxietylikebehaviorinmice
AT grutesernadine hcn4knockdownindorsalhippocampuspromotesanxietylikebehaviorinmice
AT abelted hcn4knockdownindorsalhippocampuspromotesanxietylikebehaviorinmice
AT baumannarnd hcn4knockdownindorsalhippocampuspromotesanxietylikebehaviorinmice