Activity of ventral hippocampal parvalbumin interneurons during anxiety
(2024) In Cell Reports 43(6).- Abstract
- Anxiety plays a key role in guiding behavior in response to potential
threats. Anxiety is mediated by the activation of pyramidal neurons in
the ventral hippocampus (vH), whose activity is controlled by GABAergic
inhibitory interneurons. However, how different vH interneurons might
contribute to anxiety-related processes is unclear. Here, we investigate
the role of vH parvalbumin (PV)-expressing interneurons while mice
transition from safe to more anxiogenic compartments of the elevated
plus maze (EPM). We find that vH PV interneurons increase their activity
in anxiogenic EPM compartments concomitant with dynamic changes in
inhibitory interactions between PV interneurons and pyramidal neurons.... (More) - Anxiety plays a key role in guiding behavior in response to potential
threats. Anxiety is mediated by the activation of pyramidal neurons in
the ventral hippocampus (vH), whose activity is controlled by GABAergic
inhibitory interneurons. However, how different vH interneurons might
contribute to anxiety-related processes is unclear. Here, we investigate
the role of vH parvalbumin (PV)-expressing interneurons while mice
transition from safe to more anxiogenic compartments of the elevated
plus maze (EPM). We find that vH PV interneurons increase their activity
in anxiogenic EPM compartments concomitant with dynamic changes in
inhibitory interactions between PV interneurons and pyramidal neurons.
By optogenetically inhibiting PV interneurons, we induce an increase in
the activity of vH pyramidal neurons and persistent anxiety.
Collectively, our results suggest that vH inhibitory microcircuits may
act as a trigger for enduring anxiety states.
(Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/c2c00526-eaec-461d-916f-d2e6a225fdc3
- author
- Volitaki, Emmanouela
; Forro, Thomas
; Li, Kaizhen
LU
; Nevian, Thomas
and Ciocchi, Stéphane
- publishing date
- 2024
- type
- Contribution to journal
- publication status
- published
- in
- Cell Reports
- volume
- 43
- issue
- 6
- article number
- 114295
- publisher
- Cell Press
- external identifiers
-
- scopus:85194062943
- pmid:38796850
- ISSN
- 2211-1247
- DOI
- 10.1016/j.celrep.2024.114295
- language
- English
- LU publication?
- no
- additional info
- Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.
- id
- c2c00526-eaec-461d-916f-d2e6a225fdc3
- date added to LUP
- 2026-09-09 14:07:35
- date last changed
- 2026-09-10 04:00:32
@article{c2c00526-eaec-461d-916f-d2e6a225fdc3,
abstract = {{Anxiety plays a key role in guiding behavior in response to potential <br>
threats. Anxiety is mediated by the activation of pyramidal neurons in <br>
the ventral hippocampus (vH), whose activity is controlled by GABAergic <br>
inhibitory interneurons. However, how different vH interneurons might <br>
contribute to anxiety-related processes is unclear. Here, we investigate<br>
the role of vH parvalbumin (PV)-expressing interneurons while mice <br>
transition from safe to more anxiogenic compartments of the elevated <br>
plus maze (EPM). We find that vH PV interneurons increase their activity<br>
in anxiogenic EPM compartments concomitant with dynamic changes in <br>
inhibitory interactions between PV interneurons and pyramidal neurons. <br>
By optogenetically inhibiting PV interneurons, we induce an increase in <br>
the activity of vH pyramidal neurons and persistent anxiety. <br>
Collectively, our results suggest that vH inhibitory microcircuits may <br>
act as a trigger for enduring anxiety states.<br>
<p/>}},
author = {{Volitaki, Emmanouela and Forro, Thomas and Li, Kaizhen and Nevian, Thomas and Ciocchi, Stéphane}},
issn = {{2211-1247}},
language = {{eng}},
number = {{6}},
publisher = {{Cell Press}},
series = {{Cell Reports}},
title = {{Activity of ventral hippocampal parvalbumin interneurons during anxiety}},
url = {{http://dx.doi.org/10.1016/j.celrep.2024.114295}},
doi = {{10.1016/j.celrep.2024.114295}},
volume = {{43}},
year = {{2024}},
}