Photic sensitivity for circadian response to light varies with photoperiod

The response of the circadian system to light varies markedly depending on photic history. Under short day lengths, hamsters exhibit larger maximal light-induced phase shifts as compared with those under longer photoperiods. However, effects of photoperiod length on sensitivity to subsaturating ligh...

Full description

Saved in:
Bibliographic Details
Published in:Journal of biological rhythms Vol. 27; no. 4; p. 308
Main Authors: Glickman, Gena, Webb, Ian C, Elliott, Jeffrey A, Baltazar, Ricardo M, Reale, Meghan E, Lehman, Michael N, Gorman, Michael R
Format: Journal Article
Language:English
Published: United States 01.08.2012
Subjects:
ISSN:1552-4531, 1552-4531
Online Access:Get more information
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract The response of the circadian system to light varies markedly depending on photic history. Under short day lengths, hamsters exhibit larger maximal light-induced phase shifts as compared with those under longer photoperiods. However, effects of photoperiod length on sensitivity to subsaturating light remain unknown. Here, Syrian hamsters were entrained to long or short photoperiods and subsequently exposed to a 15-min light pulse across a range of irradiances (0-68.03 µW/cm(2)) to phase shift activity rhythms. Phase advances exhibited a dose response, with increasing irradiances eliciting greater phase resetting in both conditions. Photic sensitivity, as measured by the half-saturation constant, was increased 40-fold in the short photoperiod condition. In addition, irradiances that generated similar phase advances under short and long days produced equivalent phase delays, and equal photon doses produced larger delays in the short photoperiod condition. Mechanistically, equivalent light exposure induced greater pERK, PER1, and cFOS immunoreactivity in the suprachiasmatic nuclei of animals under shorter days. Patterns of immunoreactivity in all 3 proteins were related to the size of the phase shift rather than the intensity of the photic stimulus, suggesting that photoperiod modulation of light sensitivity lies upstream of these events within the signal transduction cascade. This modulation of light sensitivity by photoperiod means that considerably less light is necessary to elicit a circadian response under the relatively shorter days of winter, extending upon the known seasonal changes in sensitivity of sensory systems. Further characterizing the mechanisms by which photoperiod alters photic response may provide a potent tool for optimizing light treatment for circadian and affective disorders in humans.
AbstractList The response of the circadian system to light varies markedly depending on photic history. Under short day lengths, hamsters exhibit larger maximal light-induced phase shifts as compared with those under longer photoperiods. However, effects of photoperiod length on sensitivity to subsaturating light remain unknown. Here, Syrian hamsters were entrained to long or short photoperiods and subsequently exposed to a 15-min light pulse across a range of irradiances (0-68.03 µW/cm(2)) to phase shift activity rhythms. Phase advances exhibited a dose response, with increasing irradiances eliciting greater phase resetting in both conditions. Photic sensitivity, as measured by the half-saturation constant, was increased 40-fold in the short photoperiod condition. In addition, irradiances that generated similar phase advances under short and long days produced equivalent phase delays, and equal photon doses produced larger delays in the short photoperiod condition. Mechanistically, equivalent light exposure induced greater pERK, PER1, and cFOS immunoreactivity in the suprachiasmatic nuclei of animals under shorter days. Patterns of immunoreactivity in all 3 proteins were related to the size of the phase shift rather than the intensity of the photic stimulus, suggesting that photoperiod modulation of light sensitivity lies upstream of these events within the signal transduction cascade. This modulation of light sensitivity by photoperiod means that considerably less light is necessary to elicit a circadian response under the relatively shorter days of winter, extending upon the known seasonal changes in sensitivity of sensory systems. Further characterizing the mechanisms by which photoperiod alters photic response may provide a potent tool for optimizing light treatment for circadian and affective disorders in humans.The response of the circadian system to light varies markedly depending on photic history. Under short day lengths, hamsters exhibit larger maximal light-induced phase shifts as compared with those under longer photoperiods. However, effects of photoperiod length on sensitivity to subsaturating light remain unknown. Here, Syrian hamsters were entrained to long or short photoperiods and subsequently exposed to a 15-min light pulse across a range of irradiances (0-68.03 µW/cm(2)) to phase shift activity rhythms. Phase advances exhibited a dose response, with increasing irradiances eliciting greater phase resetting in both conditions. Photic sensitivity, as measured by the half-saturation constant, was increased 40-fold in the short photoperiod condition. In addition, irradiances that generated similar phase advances under short and long days produced equivalent phase delays, and equal photon doses produced larger delays in the short photoperiod condition. Mechanistically, equivalent light exposure induced greater pERK, PER1, and cFOS immunoreactivity in the suprachiasmatic nuclei of animals under shorter days. Patterns of immunoreactivity in all 3 proteins were related to the size of the phase shift rather than the intensity of the photic stimulus, suggesting that photoperiod modulation of light sensitivity lies upstream of these events within the signal transduction cascade. This modulation of light sensitivity by photoperiod means that considerably less light is necessary to elicit a circadian response under the relatively shorter days of winter, extending upon the known seasonal changes in sensitivity of sensory systems. Further characterizing the mechanisms by which photoperiod alters photic response may provide a potent tool for optimizing light treatment for circadian and affective disorders in humans.
The response of the circadian system to light varies markedly depending on photic history. Under short day lengths, hamsters exhibit larger maximal light-induced phase shifts as compared with those under longer photoperiods. However, effects of photoperiod length on sensitivity to subsaturating light remain unknown. Here, Syrian hamsters were entrained to long or short photoperiods and subsequently exposed to a 15-min light pulse across a range of irradiances (0-68.03 µW/cm(2)) to phase shift activity rhythms. Phase advances exhibited a dose response, with increasing irradiances eliciting greater phase resetting in both conditions. Photic sensitivity, as measured by the half-saturation constant, was increased 40-fold in the short photoperiod condition. In addition, irradiances that generated similar phase advances under short and long days produced equivalent phase delays, and equal photon doses produced larger delays in the short photoperiod condition. Mechanistically, equivalent light exposure induced greater pERK, PER1, and cFOS immunoreactivity in the suprachiasmatic nuclei of animals under shorter days. Patterns of immunoreactivity in all 3 proteins were related to the size of the phase shift rather than the intensity of the photic stimulus, suggesting that photoperiod modulation of light sensitivity lies upstream of these events within the signal transduction cascade. This modulation of light sensitivity by photoperiod means that considerably less light is necessary to elicit a circadian response under the relatively shorter days of winter, extending upon the known seasonal changes in sensitivity of sensory systems. Further characterizing the mechanisms by which photoperiod alters photic response may provide a potent tool for optimizing light treatment for circadian and affective disorders in humans.
Author Webb, Ian C
Baltazar, Ricardo M
Glickman, Gena
Reale, Meghan E
Elliott, Jeffrey A
Gorman, Michael R
Lehman, Michael N
Author_xml – sequence: 1
  givenname: Gena
  surname: Glickman
  fullname: Glickman, Gena
  email: glickman@ucsd.edu
  organization: Center for Chronobiology and Department of Psychology, University of California, San Diego, La Jolla, CA 92093-0109, USA. glickman@ucsd.edu
– sequence: 2
  givenname: Ian C
  surname: Webb
  fullname: Webb, Ian C
– sequence: 3
  givenname: Jeffrey A
  surname: Elliott
  fullname: Elliott, Jeffrey A
– sequence: 4
  givenname: Ricardo M
  surname: Baltazar
  fullname: Baltazar, Ricardo M
– sequence: 5
  givenname: Meghan E
  surname: Reale
  fullname: Reale, Meghan E
– sequence: 6
  givenname: Michael N
  surname: Lehman
  fullname: Lehman, Michael N
– sequence: 7
  givenname: Michael R
  surname: Gorman
  fullname: Gorman, Michael R
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22855575$$D View this record in MEDLINE/PubMed
BookMark eNpNjztPwzAUhS1URB-wMyGPLAG_bpyMqKI8VAkGmCPHvqVGaRxst6j_nkoUiemc4TufdKZk1IceCbnk7IZzrW-ZVpWWTHGhgFWiPCETDiAKBZKP_vUxmab0yRgrayXPyFiICgA0TMjz6zpkb2nCPvnsdz7v6SpEan20xnnT04hpCH1CmgPt_Mc6052JHhP99nlNh8M8DBh9cOfkdGW6hBfHnJH3xf3b_LFYvjw8ze-WhZUl5MLUHLG2coVMMckdlAhGOF5LrVzLODpTllJZp2TLtGlLqBkHJaF1FqCtxIxc_3qHGL62mHKz8cli15kewzY1_GDlUIMWB_TqiG7bDbpmiH5j4r75-y9-AD2KXtQ
CitedBy_id crossref_primary_10_1371_journal_pone_0076365
crossref_primary_10_1016_j_margen_2014_04_011
crossref_primary_10_1177_07487304231180953
crossref_primary_10_1016_j_physbeh_2021_113691
crossref_primary_10_3390_clockssleep1030025
crossref_primary_10_1016_j_scitotenv_2017_07_056
crossref_primary_10_1038_srep38479
crossref_primary_10_1111_obr_12019
crossref_primary_10_1177_0748730417718347
crossref_primary_10_1016_j_physbeh_2020_112939
crossref_primary_10_1016_j_cbpa_2016_10_008
crossref_primary_10_1155_2013_153839
crossref_primary_10_1016_j_yhbeh_2014_01_002
crossref_primary_10_1177_07487304241265439
crossref_primary_10_1177_0748730418796036
crossref_primary_10_1038_s44323_024_00013_1
crossref_primary_10_1080_15502724_2021_1872383
crossref_primary_10_3390_clockssleep1030032
crossref_primary_10_1016_j_yhbeh_2013_10_008
crossref_primary_10_1007_s11033_014_3551_5
crossref_primary_10_3389_fneur_2017_00464
crossref_primary_10_1080_07420528_2017_1324471
crossref_primary_10_1016_j_isci_2022_104310
crossref_primary_10_1016_j_psychres_2013_05_023
crossref_primary_10_1038_s44323_025_00029_1
crossref_primary_10_1177_0748730415598875
crossref_primary_10_3109_07420528_2013_808652
crossref_primary_10_3389_fneur_2021_625334
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1177/0748730412450826
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Biology
EISSN 1552-4531
ExternalDocumentID 22855575
Genre Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: PHS HHS
  grantid: NICHD36460
– fundername: NINDS NIH HHS
  grantid: NS067934
– fundername: NINDS NIH HHS
  grantid: F31 NS067934
– fundername: NINDS NIH HHS
  grantid: NS30235
GroupedDBID ---
-TM
.2E
.2F
.2G
.2J
.2N
01A
0R~
1~K
29J
31R
31S
31U
31X
31Y
31Z
4.4
53G
54M
5GY
5VS
AABMB
AABOD
AACKU
AACMV
AACTG
AADUE
AAEWN
AAGGD
AAGMC
AAJIQ
AAJOX
AAJPV
AAKGS
AANSI
AAPEO
AAQDB
AAQXH
AAQXI
AARDL
AARIX
AATAA
AATBZ
AAUAS
AAXOT
AAYTG
AAZBJ
ABAWP
ABCCA
ABCJG
ABDWY
ABEIX
ABFWQ
ABHKI
ABHQH
ABIVO
ABJIS
ABJNI
ABKRH
ABLUO
ABNCE
ABPGX
ABPNF
ABQKF
ABQXT
ABRHV
ABUJY
ABVFX
ABVVC
ABYTW
ACARO
ACDSZ
ACDXX
ACFEJ
ACFMA
ACFYK
ACGBL
ACGFS
ACGOD
ACGZU
ACJER
ACJTF
ACLFY
ACLHI
ACLZU
ACNXM
ACOFE
ACOXC
ACPRK
ACROE
ACRPL
ACSIQ
ACUAV
ACUIR
ACXKE
ACXMB
ADBBV
ADDLC
ADEIA
ADMPF
ADNBR
ADNMO
ADNON
ADRRZ
ADTBJ
ADUKL
ADVBO
ADYCS
ADZZY
AECGH
AECVZ
AEDTQ
AEKYL
AENEX
AEPTA
AEQLS
AERKM
AESZF
AEUHG
AEWDL
AEWHI
AEXFG
AEXNY
AFEET
AFKBI
AFKRG
AFMOU
AFQAA
AFRAH
AFUIA
AFVCE
AFWMB
AGHKR
AGKLV
AGNHF
AGPXR
AGWFA
AGWNL
AHDMH
AHHFK
AHMBA
AI.
AIGRN
AJABX
AJEFB
AJMMQ
AJSCY
AJUZI
AJXAJ
AJXGE
ALKWR
ALMA_UNASSIGNED_HOLDINGS
ALTZF
AMCVQ
ANDLU
ARTOV
ASPBG
AUTPY
AUVAJ
AVWKF
AYAKG
AZFZN
B3H
B8M
B8O
B8R
B8Z
B93
B94
BBRGL
BDDNI
BKIIM
BKOMP
BKSCU
BPACV
BSEHC
BWJAD
BYIEH
CAG
CBRKF
CDWPY
CFDXU
CGR
COF
CORYS
CQQTX
CS3
CUTAK
CUY
CVF
DB0
DC-
DC.
DC0
DD-
DD0
DE-
DF0
DO-
DOPDO
DU5
DV7
DV9
D~Y
EBS
ECM
EIF
EJD
EMOBN
F5P
FEDTE
FHBDP
GROUPED_SAGE_PREMIER_JOURNAL_COLLECTION
H13
HF~
HVGLF
HZ~
IAG
IAO
IEA
IGS
IHR
INH
INR
IVC
J8X
K.F
K.J
M4V
N9A
NPM
O9-
P.B
P2P
PQQKQ
Q1R
Q7K
Q7L
Q7R
Q7U
Q7X
Q82
Q83
ROL
S01
SAUOL
SBI
SCNPE
SDB
SFB
SFC
SFK
SFT
SGA
SGO
SGP
SGR
SGV
SGX
SGZ
SHG
SNB
SPJ
SPP
SPQ
SPV
SQCSI
STM
VH1
WHG
ZONMY
ZPPRI
ZRKOI
ZSSAH
~KM
7X8
AAPII
ABIDT
ABJZC
ADEBD
AJGYC
AJHME
AJVBE
ID FETCH-LOGICAL-c365t-a91ee9c3fe04031d56e5a2d19374db01eda6634cd43b07ab659015435bdc55b82
IEDL.DBID 7X8
ISICitedReferencesCount 35
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000307021800005&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1552-4531
IngestDate Sun Sep 28 08:00:59 EDT 2025
Thu Apr 03 06:56:58 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 4
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c365t-a91ee9c3fe04031d56e5a2d19374db01eda6634cd43b07ab659015435bdc55b82
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 22855575
PQID 1031159572
PQPubID 23479
ParticipantIDs proquest_miscellaneous_1031159572
pubmed_primary_22855575
PublicationCentury 2000
PublicationDate 2012-Aug
20120801
PublicationDateYYYYMMDD 2012-08-01
PublicationDate_xml – month: 08
  year: 2012
  text: 2012-Aug
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Journal of biological rhythms
PublicationTitleAlternate J Biol Rhythms
PublicationYear 2012
SSID ssj0006943
Score 2.1857631
Snippet The response of the circadian system to light varies markedly depending on photic history. Under short day lengths, hamsters exhibit larger maximal...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 308
SubjectTerms Analysis of Variance
Animals
Circadian Rhythm - physiology
Cricetinae
Extracellular Signal-Regulated MAP Kinases - metabolism
Humans
Immunohistochemistry
Light
Male
Mesocricetus - metabolism
Mesocricetus - physiology
Motor Activity - physiology
Motor Activity - radiation effects
Period Circadian Proteins - metabolism
Photic Stimulation
Photoperiod
Proto-Oncogene Proteins c-fos - metabolism
Suprachiasmatic Nucleus - metabolism
Suprachiasmatic Nucleus - radiation effects
Time Factors
Title Photic sensitivity for circadian response to light varies with photoperiod
URI https://www.ncbi.nlm.nih.gov/pubmed/22855575
https://www.proquest.com/docview/1031159572
Volume 27
WOSCitedRecordID wos000307021800005&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8NAEB7UKnjx_agvVvC6tNns5HESEYsIlh4Uegv7KgqS1KYW_PfOZlN6EgQvuYSFMMzOfPPI9wHcREoLNCLnuUVLBQoqriQarl1GIZNSCpogNpEOh9l4nI_ahlvdrlUuY2ITqG1lfI-85-UIKPViKm6nn9yrRvnpaiuhsQ6dmKCM9-p0vGILT8LWnGcZ45KcbTWm7FHmzMi5vfYyQRSR_A4wm0Qz2P3vJ-7BTgsx2V3wiX1Yc-UBbAXRye9DeBq9VfSG1X51PWhHMEKuzLzPTENUwGZhb9axecU-fPHOFk1FzXzTlk3peOX5kSt7BK-Dh5f7R94qKnATJzjnKo-cy008cXR348hi4lAJSyAulVb3I2cVIRBprIx1P1U68X-mIiEqbQ2izsQxbJRV6U6BSel0YrV1IjLS89TTmYkUiqpcm6KyXbheGqkgj_VjCFW66qsuVmbqwkmwdDEN1BqFEBkiIcizP5w-h21CLyJs411AZ0L31V3CplnM3-vZVeMK9ByOnn8AsNu9dg
linkProvider ProQuest
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Photic+sensitivity+for+circadian+response+to+light+varies+with+photoperiod&rft.jtitle=Journal+of+biological+rhythms&rft.au=Glickman%2C+Gena&rft.au=Webb%2C+Ian+C&rft.au=Elliott%2C+Jeffrey+A&rft.au=Baltazar%2C+Ricardo+M&rft.date=2012-08-01&rft.issn=1552-4531&rft.eissn=1552-4531&rft.volume=27&rft.issue=4&rft.spage=308&rft_id=info:doi/10.1177%2F0748730412450826&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1552-4531&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1552-4531&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1552-4531&client=summon