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Photoperiod Regulates Corticosterone Rhythms by Altered Adrenal Sensitivity via Melatonin-Independent Mechanisms in Fischer 344 Rats and C57BL/6J Mice
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mcne.1993.1022openalex-snapshot
Diurnal Regulation of Glucocorticoid Receptor and Mineralocorticoid Receptor mRNAs in Rat Hippocampus
inferredcites →https://doi.org/10.1007/s00441-002-0581-4openalex-snapshot
Mammalian melatonin receptors: molecular biology and signal transduction
inferredcites →https://doi.org/10.1016/0006-8993(72)90054-6openalex-snapshot
Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat
inferredcites →https://doi.org/10.1016/0300-9629(93)90004-nopenalex-snapshot
Seasonal changes in in vivo cortisol response to acth and in plasma and pituitary concentrations of ACTH in a desert rodent, the sand rat (Psammomys obesus)
inferredcites →https://doi.org/10.1016/j.cmet.2005.09.009openalex-snapshot
Light activates the adrenal gland: Timing of gene expression and glucocorticoid release
inferredcites →https://doi.org/10.1016/j.cmet.2006.07.002openalex-snapshot
The circadian rhythm of glucocorticoids is regulated by a gating mechanism residing in the adrenal cortical clock
inferredcites →https://doi.org/10.1016/j.cub.2008.06.076openalex-snapshot
Ancestral TSH Mechanism Signals Summer in a Photoperiodic Mammal
inferredcites →https://doi.org/10.1016/j.cub.2010.10.048openalex-snapshot
A Molecular Switch for Photoperiod Responsiveness in Mammals
inferredcites →https://doi.org/10.1016/j.cub.2010.11.038openalex-snapshot
Acute Induction of Eya3 by Late-Night Light Stimulation Triggers TSHβ Expression in Photoperiodism
inferredcites →https://doi.org/10.1016/j.mce.2011.06.042openalex-snapshot
Circadian rhythms in the hypothalamo–pituitary–adrenal (HPA) axis
inferredcites →https://doi.org/10.1016/j.neuroscience.2011.09.036openalex-snapshot
Interactions of the serotonin and circadian systems: nature and nurture in rhythms and blues
inferredcites →https://doi.org/10.1016/s0006-8993(97)01302-4openalex-snapshot
Photoperiod regulation of mineralocorticoid receptor mRNA expression in hamster hippocampus
inferredcites →https://doi.org/10.1016/s0006-8993(97)01303-6openalex-snapshot
Effects of photoperiod on brain corticosteroid receptors and the stress response in the golden hamster (Mesocricetus auratus)
inferredcites →https://doi.org/10.1016/s0169-328x(98)00273-3openalex-snapshot
Natural melatonin `knockdown' in C57BL/6J mice: rare mechanism truncates serotonin N-acetyltransferase
inferredcites →https://doi.org/10.1038/nature02117openalex-snapshot
Light-induced hormone conversion of T4 to T3 regulates photoperiodic response of gonads in birds
inferredcites →https://doi.org/10.1038/nature06738openalex-snapshot
Thyrotrophin in the pars tuberalis triggers photoperiodic response
inferredcites →https://doi.org/10.1046/j.0007-1331.2001.00736.xopenalex-snapshot
Sympathoadrenal System Differentially Affects Photoperiodic Changes in Humoral Immunity of Siberian Hamsters (Phodopus sungorus)
inferredcites →https://doi.org/10.1073/pnas.0806962106openalex-snapshot
Adrenal peripheral clock controls the autonomous circadian rhythm of glucocorticoid by causing rhythmic steroid production
inferredcites →https://doi.org/10.1073/pnas.0808952105openalex-snapshot
Involvement of thyrotropin in photoperiodic signal transduction in mice
inferredcites →https://doi.org/10.1093/jn/128.9.1415openalex-snapshot
Adrenocortical Responsiveness to Adrenocorticotropic Hormone Is Enhanced in Chronically Food-Restricted Rats
inferredcites →https://doi.org/10.1095/biolreprod57.1.134openalex-snapshot
Reproductive Photoresponsiveness in Unmanipulated Male Fischer 344 Laboratory Rats1
inferredcites →https://doi.org/10.1111/j.1460-9568.2010.07586.xopenalex-snapshot
Glucocorticoid-mediated nycthemeral and photoperiodic regulation of tph2 expression
inferredcites →https://doi.org/10.1126/science.3941912openalex-snapshot
Genetic Control of Melatonin Synthesis in the Pineal Gland of the Mouse
inferredcites →https://doi.org/10.1152/ajpendo.00287.2001openalex-snapshot
Corticosterone-dependent driving influence of the suprachiasmatic nucleus on adrenal sensitivity to ACTH
inferredcites →https://doi.org/10.1152/ajpregu.00042.2003openalex-snapshot
Adrenal splanchnic innervation contributes to the diurnal rhythm of plasma corticosterone in rats by modulating adrenal sensitivity to ACTH
inferredcites →https://doi.org/10.1152/ajpregu.00396.2006openalex-snapshot
Differential response of type 2 deiodinase gene expression to photoperiod between photoperiodic Fischer 344 and nonphotoperiodic Wistar rats
inferredcites →https://doi.org/10.1152/ajpregu.1978.235.5.r210openalex-snapshot
Nycthemeral rhythm in adrenal responsiveness to ACTH
inferredcites →https://doi.org/10.1152/ajpregu.1987.253.2.r321openalex-snapshot
Adrenal, thyroid, and testicular hormone rhythms in male golden hamsters on long and short days
inferredcites →https://doi.org/10.1152/ajpregu.1998.275.5.r1399openalex-snapshot
Innervation of mammalian white adipose tissue: implications for the regulation of total body fat
inferredcites →https://doi.org/10.1177/0748730406293053openalex-snapshot
Transcriptional Profiling in the Adrenal Gland Reveals Circadian Regulation of Hormone Biosynthesis Genes and Nucleosome Assembly Genes
inferredcites →https://doi.org/10.1210/edrv-1-2-109openalex-snapshot
The Pineal and Its Hormones in the Control of Reproduction in Mammals*
inferredcites →https://doi.org/10.1210/en.2005-0057openalex-snapshot
The Reciprocal Switching of Two Thyroid Hormone-Activating and -Inactivating Enzyme Genes Is Involved in the Photoperiodic Gonadal Response of Japanese Quail
inferredcites →https://doi.org/10.1210/en.2006-1432openalex-snapshot
Short Days Increase Hypothalamic-Pituitary-Adrenal Axis Responsiveness
inferredcites →https://doi.org/10.1210/en.2007-1009openalex-snapshot
Rhythmic Expression of Functional MT1 Melatonin Receptors in the Rat Adrenal Gland
inferredcites →https://doi.org/10.1210/endo-100-1-138openalex-snapshot
Circadian Patterns of Stress-Induced ACTH Secretion Are Modified by Corticosterone Responses
inferredcites →https://doi.org/10.1210/endo-109-1-70openalex-snapshot
Adrenal Sensitivity to Adrenocorticotropin Varies Diurnally*
inferredcites →https://doi.org/10.1210/endo-98-6-1475openalex-snapshot
Daily Variation in Concentration of Plasma Corticosteroid in Hypophysectomized Rats
inferredcites →https://doi.org/10.1371/journal.pone.0005650openalex-snapshot
Effects of Nocturnal Light on (Clock) Gene Expression in Peripheral Organs: A Role for the Autonomic Innervation of the Liver
inferredcites →https://doi.org/10.1385/endo:28:3:325openalex-snapshot
Neural Circuitry in the Regulation of Adrenal Corticosterone Rhythmicity
inferredcites →https://doi.org/10.1523/jneurosci.0145-09.2009openalex-snapshot
Melatonin Transmits Photoperiodic Signals through the MT1 Melatonin Receptor
inferredcites →https://doi.org/10.1677/joe.1.06206openalex-snapshot
Responses induced by arginine-vasopressin injection in the plasma concentrations of adrenocorticotropic hormone, cortisol, growth hormone and metabolites around weaning time in goats
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Deficiency of the Circadian Clock Gene Rev-Erbα Induces Mood Disorders and Dysregulation of the Serotonergic System in Mice
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Short photoperiod restores ventral subicular lesion‐induced deficits in affective and socio‐cognitive behavior in male Wistar rats
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Juvenile social isolation affects maternal care in rats: involvement of allopregnanolone
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Long-term artificial/natural daytime light affects mood, melatonin, corticosterone, and gut microbiota in rats
inferred← citeshttps://doi.org/10.1007/s13105-025-01075-wopenalex-snapshot
Sex impact on daily activity and physiological, metabolic and hormonal responses to different photoperiod regimens in diet-induced obese fischer 344 rats
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Photoperiodic changes in hippocampal neurogenesis and plasma metabolomic profiles in relation to depression-like behavior in mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.02.023openalex-snapshot
Changes in photoperiod alter Glut4 expression in skeletal muscle of C57BL/6J mice
inferred← citeshttps://doi.org/10.1016/j.brainres.2020.146725openalex-snapshot
Effect of postnatal photoperiod on DNA methylation dynamics in the mouse brain
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In vivo synaptic potency, short-term and long-term plasticity at the hippocampal Schaffer collateral-CA1 synapses: Role of different light–dark cycles in male rats
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2015.08.010openalex-snapshot
Antidepressant-like effect of bright light is potentiated by l-serine administration in a mouse model of seasonal affective disorder
inferred← citeshttps://doi.org/10.1016/j.cbpa.2025.111961openalex-snapshot
The influence of light wavelength on HPA axis function in non-human animals: A meta-analysis
inferred← citeshttps://doi.org/10.1016/j.domaniend.2013.01.001openalex-snapshot
Cloacal gland, endocrine testicular, and adrenocortical photoresponsiveness in male Japanese quail exposed to short days
inferred← citeshttps://doi.org/10.1016/j.mce.2013.05.012openalex-snapshot
The circadian clock and glucocorticoids – Interactions across many time scales
inferred← citeshttps://doi.org/10.1016/j.mehy.2019.109447openalex-snapshot
Does photoperiodism involve a seasonal and non-pathological Warburg effect?
inferred← citeshttps://doi.org/10.1016/j.metabol.2023.155770openalex-snapshot
Photoperiod and metabolic health: evidence, mechanism, and implications
inferred← citeshttps://doi.org/10.1016/j.molmet.2021.101179openalex-snapshot
A physiological glucocorticoid rhythm is an important regulator of brown adipose tissue function
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Caloric restriction and neuropsychiatric phenotypes: A critical review of preclinical data
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Early-life Photoperiod Influences Depression-like Behavior, Prepulse Inhibition of the Acoustic Startle Response, and Hippocampal Astrogenesis in Mice
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Deficiency of the circadian clock gene Rev-erbα induces mood disorder-like behaviours and dysregulation of the serotonergic system in mice
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2013.10.013openalex-snapshot
Photoperiodic responses of depression-like behavior, the brain serotonergic system, and peripheral metabolism in laboratory mice
inferred← citeshttps://doi.org/10.1017/s0007114515003396openalex-snapshot
Dietary protein ingested before and during short photoperiods makes an impact on affect-related behaviours and plasma composition of amino acids in mice
inferred← citeshttps://doi.org/10.1038/npp.2013.329openalex-snapshot
Exercise-Associated Changes in the Corticosterone Response to Acute Restraint Stress: Evidence for Increased Adrenal Sensitivity and Reduced Corticosterone Response Duration
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Photoperiod effects on corticosterone and seasonal clocks in cafeteria-induced obese fischer 344 rats are influenced by gut microbiota
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Metabolism disturbance by light/dark cycle switching depends on the rat health status: the role of grape seed flavanols
inferred← citeshttps://doi.org/10.1096/fba.2024-00115openalex-snapshot
Photoperiod influences visceral adiposity and the adipose molecular clock independent of temperature in wild‐derived Peromyscus leucopus
inferred← citeshttps://doi.org/10.1111/jne.12241openalex-snapshot
Photoperiodic Effects on Seasonal Physiology, Reproductive Status and Hypothalamic Gene Expression in Young Male F 344 Rats
inferred← citeshttps://doi.org/10.1152/ajpendo.00209.2012openalex-snapshot
Photoperiod regulates dietary preferences and energy metabolism in young developing Fischer 344 rats but not in same-age Wistar rats
inferred← citeshttps://doi.org/10.1152/japplphysiol.00972.2018openalex-snapshot
Seasonal differences in rhythmicity of salivary cortisol in healthy adults
inferred← citeshttps://doi.org/10.1152/physiolgenomics.00026.2014openalex-snapshot
Mathematical modeling of light-mediated HPA axis activity and downstream implications on the entrainment of peripheral clock genes
inferred← citeshttps://doi.org/10.1155/2018/8217345openalex-snapshot
Photoperiodic Programming of the SCN and Its Role in Photoperiodic Output
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The Hepato-Hypothalamic-Pituitary-Adrenal-Renal Axis: Mathematical Modeling of Cortisol’s Production, Metabolism, and Seasonal Variation
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The SCN-HPA-Periphery Circadian Timing System: Mathematical Modeling of Clock Synchronization and the Effects of Photoperiod on Jetlag Adaptation
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The impact of sleep disorders on glucose metabolism: endocrine and molecular mechanisms
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Modeling the Influence of Seasonal Differences in the HPA Axis on Synchronization of the Circadian Clock and Cell Cycle
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Comparative diurnal and seasonal variations of ACTH, cortisol and aldosterone in Ouled Djellal and D’Man sheep breeds reared in arid lands
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Exposure of C57BL/6J mice to long photoperiod during early life stages increases body weight and alters plasma metabolomic profiles in adulthood
inferred← citeshttps://doi.org/10.17816/morph.633001openalex-snapshot
Seasonal changes in absolute and relative organ weight in 3-month male Wistar rats
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Seasonal Adaptation of Mammalian Development: Effect of Early-Life Photoperiod on Reproduction, Somatic Growth, and Neurobehavioral Systems
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The Influence of Light Wavelength on HPA Axis Function in Non-human Animals: A Meta-analysis
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Feeding and adrenal entrainment stimuli are both necessary for normal circadian oscillation of peripheral clocks in mice housed under different photoperiods
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Melatonin adjusts the expression pattern of clock genes in the suprachiasmatic nucleus and induces antidepressant-like effect in a mouse model of seasonal affective disorder
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