Valproic Acid Phase Shifts the Rhythmic Expression of PERIOD2::LUCIFERASE
Abstract
Valproic acid (VPA) is an anticonvulsant used to treat bipolar disorder, a psychiatric disease associated with disturbances in circadian rhythmicity. Little is known about how VPA affects circadian rhythms. The authors cultured tissues containing the master brain pacemaker for circadian rhythmicity, the suprachiasmatic nuclei (SCN), and skin fibroblasts from transgenic PERIOD2::LUCIFERASE (PER2::LUC) mice and studied the effect of VPA on the circadian PER2::LUC rhythm by measuring bioluminescence. VPA (1 mM) significantly phase advanced the PER2::LUC rhythm when applied at a time point corresponding to the lowest (trough, ~ZT 0) PER2::LUC expression but phase delayed the PER2::LUC rhythm when the drug was administered at the time of highest (peak, ~ZT 12) protein expression. In addition, it significantly increased the overall amplitude of PER2::LUC oscillations at time points at or close to ZT 12 but had no effect on period. Real-time PCR analyses on mouse and human fibroblasts revealed that expressions of other clock genes were increased after 2 h treatment with VPA. Because VPA is known to inhibit histone deacetylation, the authors treated cultures with an established histone deacetylation inhibitor, trichostatin A (TSA; 20 ng/mL), to compare the effect of VPA and TSA on molecular rhythmicity. They found that TSA had similar effects on the PER2::LUC rhythm as VPA. Furthermore, VPA and TSA significantly increased acetylation on histone H3 but in comparison little on histone H4. Lithium is another commonly used treatment for bipolar disorder. Therefore, the authors also studied the impact of lithium chloride (LiCl; 10 mM) on the PER2::LUC rhythm. LiCl delayed the phase, but in contrast to VPA and TSA, LiCl lengthened the PER2::LUC period and had no effect on histone acetylation. These results demonstrate that VPA can delay or advance the phase, as well as increase the amplitude, of the PERIOD2::LUCIFERASE rhythm depending on the circadian time of application. Furthermore, the authors show that LiCl delays the phase and lengthens the period of the PER2::LUC rhythm, confirming previous reports on circadian lithium effects. These different molecular effects may underlie differential chronotherapeutic effects of VPA and lithium.
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Antidepressant and mood-stabilizing medications, such as lithium, valproic acid and SSRIs, all have dramatic effects on gene expression rhythms that may, at least in part, underlie their therapeutic efficacy.
“antidepressant and mood-stabilizing medications, such as lithium, valproic acid and selective serotonin reuptake inhibitors (SSRIs), all have dramatic effects on gene expression rhythms that may, at least in part, underlie their therapeutic efficacy215–217”
From Rhythms of life: circadian disruption and brain disorders across the lifespan (2019) · cites this paper as [216]
Several first-line pharmacological treatments for psychiatric disorders, such as lithium for bipolar disorder and SSRIs for major depressive disorders, modulate the circadian clock.
“Several first-line pharmacological treatments for psychiatric disorders, such as lithium for bipolar disorder and SSRIs for major depressive disorders, modulate the circadian clock216,217,329–331.”
From Rhythms of life: circadian disruption and brain disorders across the lifespan (2019) · cites this paper as [216]
Targeting rhythms or components of the clock using pharmacological agents might be therapeutically beneficial.
“they suggest that targeting rhythms or components of the clock using pharmacological agents might be therapeutically beneficial215,216,331”
From Rhythms of life: circadian disruption and brain disorders across the lifespan (2019) · cites this paper as [216]
Many of the most effective treatments for brain disorders and other diseases modulate clock function.
“Many of the most effective treatments for brain disorders and other diseases modulate clock function216,326,330,332,333.”
From Rhythms of life: circadian disruption and brain disorders across the lifespan (2019) · cites this paper as [216]
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References 45 · Cited by 97
- Authors
- Johansson, A.-S., Brask, J., Owe-Larsson, B., Hetta, J., & Lundkvist, G. B. S.
- Affiliations
- Karolinska Institutet (SE)
- Linköping University (SE)
- Department of Clinical Neuroscience, Karolinska Institutet at Karolinska University Hospital Huddinge, Stockholm, Sweden
- Karolinska University Hospital (SE)
- Corresponding author
- Lundkvist, Gabriella B.S.
- Venue
- Journal of Biological Rhythms
- Publisher
- SAGE Publications
- Published
- 2011-11-30
- Volume
- 26
- Issue
- 6
- Pages
- 541-551
- ISSN
- 0748-7304 (ISSN-L)
- 1552-4531
- OpenAlex
- W2073482315
- Cited by
- 97
- References
- 45
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 6 · 2023: 7 · 2022: 5 · 2021: 10 · 2020: 2 · 2019: 4 · 2018: 5 · 2017: 7 · 2016: 13 · 2015: 10 · 2014: 9 · 2013: 7 · 2012: 4
- FWCI
- 2.96
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Biological Rhythms (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Vetenskapsrådet
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- valproic acid, circadian rhythm, suprachiasmatic nucleus, clock genes, histone deacetylation, trichostatin A, histone H3 acetylation, lithium chloride, bipolar disorder, chronotherapy, phase shift, circadian period, fibroblasts, bioluminescence, histone acetylation
- MeSH terms
- Animals, Anticonvulsants, Cells, Cultured, Circadian Rhythm, Female, Fibroblasts, Humans, Hydroxamic Acids, Lithium, Luciferases, Luminescent Measurements, Mice, Transgenic, Recombinant Fusion Proteins, Suprachiasmatic Nucleus, Valproic Acid, Mice, Histone Deacetylase Inhibitors, Period Circadian Proteins
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