Light affects behavioral despair involving the clock gene Period 1.

Light at night has strong effects on physiology and behavior of mammals. It affects mood in humans, which is exploited as light therapy, and has been shown to reset the circadian clock in the suprachiasmatic nuclei (SCN). This resetting is paramount to align physiological and biochemical timing to t...

Full description

Saved in:
Bibliographic Details
Main Authors: Iwona Olejniczak, Jürgen A Ripperger, Federica Sandrelli, Anna Schnell, Laureen Mansencal-Strittmatter, Katrin Wendrich, Ka Yi Hui, Andrea Brenna, Naila Ben Fredj, Urs Albrecht
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-07-01
Series:PLoS Genetics
Online Access:https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009625&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850239951175680000
author Iwona Olejniczak
Jürgen A Ripperger
Federica Sandrelli
Anna Schnell
Anna Schnell
Laureen Mansencal-Strittmatter
Katrin Wendrich
Ka Yi Hui
Andrea Brenna
Naila Ben Fredj
Urs Albrecht
author_facet Iwona Olejniczak
Jürgen A Ripperger
Federica Sandrelli
Anna Schnell
Anna Schnell
Laureen Mansencal-Strittmatter
Katrin Wendrich
Ka Yi Hui
Andrea Brenna
Naila Ben Fredj
Urs Albrecht
author_sort Iwona Olejniczak
collection DOAJ
description Light at night has strong effects on physiology and behavior of mammals. It affects mood in humans, which is exploited as light therapy, and has been shown to reset the circadian clock in the suprachiasmatic nuclei (SCN). This resetting is paramount to align physiological and biochemical timing to the environmental light-dark cycle. Here we provide evidence that light at zeitgeber time (ZT) 22 affects mood-related behaviors also in mice by activating the clock gene Period1 (Per1) in the lateral habenula (LHb), a brain region known to modulate mood-related behaviors. We show that complete deletion of Per1 in mice led to depressive-like behavior and loss of the beneficial effects of light on this behavior. In contrast, specific deletion of Per1 in the region of the LHb did not affect mood-related behavior, but suppressed the beneficial effects of light. RNA sequence analysis in the mesolimbic dopaminergic system revealed profound changes of gene expression after a light pulse at ZT22. In the nucleus accumbens (NAc), sensory perception of smell and G-protein coupled receptor signaling were affected the most. Interestingly, most of these genes were not affected in Per1 knock-out animals, indicating that induction of Per1 by light serves as a filter for light-mediated gene expression in the brain. Taken together we show that light affects mood-related behavior in mice at least in part via induction of Per1 in the LHb with consequences on mood-related behavior and signaling mechanisms in the mesolimbic dopaminergic system.
format Article
id doaj-art-af993f5867a140e5a89dcda2166da460
institution OA Journals
issn 1553-7390
1553-7404
language English
publishDate 2021-07-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Genetics
spelling doaj-art-af993f5867a140e5a89dcda2166da4602025-08-20T02:01:00ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042021-07-01177e100962510.1371/journal.pgen.1009625Light affects behavioral despair involving the clock gene Period 1.Iwona OlejniczakJürgen A RippergerFederica SandrelliAnna SchnellAnna SchnellLaureen Mansencal-StrittmatterKatrin WendrichKa Yi HuiAndrea BrennaNaila Ben FredjUrs AlbrechtLight at night has strong effects on physiology and behavior of mammals. It affects mood in humans, which is exploited as light therapy, and has been shown to reset the circadian clock in the suprachiasmatic nuclei (SCN). This resetting is paramount to align physiological and biochemical timing to the environmental light-dark cycle. Here we provide evidence that light at zeitgeber time (ZT) 22 affects mood-related behaviors also in mice by activating the clock gene Period1 (Per1) in the lateral habenula (LHb), a brain region known to modulate mood-related behaviors. We show that complete deletion of Per1 in mice led to depressive-like behavior and loss of the beneficial effects of light on this behavior. In contrast, specific deletion of Per1 in the region of the LHb did not affect mood-related behavior, but suppressed the beneficial effects of light. RNA sequence analysis in the mesolimbic dopaminergic system revealed profound changes of gene expression after a light pulse at ZT22. In the nucleus accumbens (NAc), sensory perception of smell and G-protein coupled receptor signaling were affected the most. Interestingly, most of these genes were not affected in Per1 knock-out animals, indicating that induction of Per1 by light serves as a filter for light-mediated gene expression in the brain. Taken together we show that light affects mood-related behavior in mice at least in part via induction of Per1 in the LHb with consequences on mood-related behavior and signaling mechanisms in the mesolimbic dopaminergic system.https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009625&type=printable
spellingShingle Iwona Olejniczak
Jürgen A Ripperger
Federica Sandrelli
Anna Schnell
Anna Schnell
Laureen Mansencal-Strittmatter
Katrin Wendrich
Ka Yi Hui
Andrea Brenna
Naila Ben Fredj
Urs Albrecht
Light affects behavioral despair involving the clock gene Period 1.
PLoS Genetics
title Light affects behavioral despair involving the clock gene Period 1.
title_full Light affects behavioral despair involving the clock gene Period 1.
title_fullStr Light affects behavioral despair involving the clock gene Period 1.
title_full_unstemmed Light affects behavioral despair involving the clock gene Period 1.
title_short Light affects behavioral despair involving the clock gene Period 1.
title_sort light affects behavioral despair involving the clock gene period 1
url https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009625&type=printable
work_keys_str_mv AT iwonaolejniczak lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT jurgenaripperger lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT federicasandrelli lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT annaschnell lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT annaschnell lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT laureenmansencalstrittmatter lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT katrinwendrich lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT kayihui lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT andreabrenna lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT nailabenfredj lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1
AT ursalbrecht lightaffectsbehavioraldespairinvolvingtheclockgeneperiod1