» Articles » PMID: 26799851

Stress-induced Neuroinflammatory Priming is Time of Day Dependent

Overview
Date 2016 Jan 23
PMID 26799851
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Circadian rhythms are endogenous cycles of physiology and behavior that align with the daily rotation of the planet and resulting light-dark cycle. The circadian system ensures homeostatic balance and regulates many aspects of physiology, including the stress response and susceptibility to and/or severity of stress-related sequelae. Both acute and chronic stressors amplify neuroinflammatory responses to a subsequent immune challenge, however it is not known whether circadian timing of the stressor regulates the priming response. Here, we test whether stress-induced neuroinflammatory priming is regulated by the circadian system. As has been previously shown, exposure to 100 inescapable tails shocks (IS) increased hippocampal cytokines following a subsequent inflammatory challenge. However, this effect was limited to animals that experienced the stressor during the light phase. Rats exposed to stress during the dark phase did not alter inflammatory potential following lipopolysaccharide (LPS) challenge. To determine whether microglia might be involved in diurnal differences in neuroinflammatory priming, microglia were isolated 24h after stress that occurred either during the middle of the light or dark phase. Only microglia isolated from animals stressed during the light phase demonstrated an exaggerated inflammatory response when treated ex vivo with LPS. To determine possible circadian dependency of microglia responsiveness to glucocorticoids - the likely proximal mediator for stress associated neuroinflammatory priming - microglia were isolated during the middle of the light or dark phase and treated ex vivo with corticosterone. Glucocorticoids treatment downregulated CX3CR1 and CD200R, two genes involved in microglial inflammatory "off" signaling; however, there was no effect of time of day on expression of either gene. Importantly, while absolute concentrations of corticosterone were comparable following IS during the light and dark phase, the magnitude of change in corticosterone was greater during the light phase. This work highlights the importance of studying circadian rhythms to elucidate biological mechanisms of stress.

Citing Articles

Single-Nucleus RNA Sequencing Reveals Enduring Signatures of Acute Stress and Chronic Exercise in Striatal Microglia.

Connolly M, Johnson Z, Chu L, Johnson N, Buhr T, McNeill E Genes Brain Behav. 2025; 24(2):e70019.

PMID: 40045485 PMC: 11882474. DOI: 10.1111/gbb.70019.


Diabetic Neuropathic Pain and Circadian Rhythm: A Future Direction Worthy of Study.

Yang B, Wei W, Fang J, Xue Y, Wei J J Pain Res. 2024; 17:3005-3020.

PMID: 39308994 PMC: 11414757. DOI: 10.2147/JPR.S467249.


Chronically stressed male and female mice show a similar peripheral and central pro-inflammatory profile after an immune challenge.

Bodemeier Loayza Careaga M, Wu T PLoS One. 2024; 19(2):e0297776.

PMID: 38381770 PMC: 10880960. DOI: 10.1371/journal.pone.0297776.


Effects of dim light at night in C57BL/6 J mice on recovery after spinal cord injury.

Aldrich J, Scheinfeld A, Lee S, Dusenbery K, Mahach K, Van de Veire B Exp Neurol. 2024; 375:114725.

PMID: 38365132 PMC: 10981559. DOI: 10.1016/j.expneurol.2024.114725.


The effects of chronic high-dose morphine on microgliosis and the microglial transcriptome in rat spinal cord.

Ahlstrom F, Viisanen H, Karhinen L, Matlik K, Blomqvist K, Lilius T Mol Pain. 2023; 19:17448069231183902.

PMID: 37285551 PMC: 10331785. DOI: 10.1177/17448069231183902.


References
1.
Frank M, Miguel Z, Watkins L, Maier S . Prior exposure to glucocorticoids sensitizes the neuroinflammatory and peripheral inflammatory responses to E. coli lipopolysaccharide. Brain Behav Immun. 2009; 24(1):19-30. DOI: 10.1016/j.bbi.2009.07.008. View

2.
Dunn J, Scheving L, Millet P . Circadian variation in stress-evoked increases in plasma corticosterone. Am J Physiol. 1972; 223(2):402-6. DOI: 10.1152/ajplegacy.1972.223.2.402. View

3.
Retana-Marquez S, Bonilla-Jaime H, Vazquez-Palacios G, Dominguez-Salazar E, Martinez-Garcia R, Velazquez-Moctezuma J . Body weight gain and diurnal differences of corticosterone changes in response to acute and chronic stress in rats. Psychoneuroendocrinology. 2003; 28(2):207-27. DOI: 10.1016/s0306-4530(02)00017-3. View

4.
Cohen S, Vainer E, Matar M, Kozlovsky N, Kaplan Z, Zohar J . Diurnal fluctuations in HPA and neuropeptide Y-ergic systems underlie differences in vulnerability to traumatic stress responses at different zeitgeber times. Neuropsychopharmacology. 2014; 40(3):774-90. PMC: 4289967. DOI: 10.1038/npp.2014.257. View

5.
Biber K, Neumann H, Inoue K, Boddeke H . Neuronal 'On' and 'Off' signals control microglia. Trends Neurosci. 2007; 30(11):596-602. DOI: 10.1016/j.tins.2007.08.007. View