Evidence map›Paper›PMID 41489728›Full record

ArticlePharmacological reports : PR2026

Docosahexaenoic acid modulates myo-inositol and myo-inositol biosynthetic genes expression: implications for bipolar disorder.

Marlene Murray, Haley Kang, Taejun Ok, Kimberly Park, Joanne Jee Yeon Lee, Bomi Kim, Hyukje Sung, Talisa Tait, Daniel Colon Hidalgo, Yudy Guzman

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Article in Pharmacological reports : PR, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Marlene MurrayDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA. mmurray@andrews.edu.ORCID http://orcid.org/0000-0002-9621-5860
Haley KangDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0009-0005-4398-7946
Taejun OkDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.
Kimberly ParkDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0009-0003-3001-5764
Joanne Jee Yeon LeeDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0009-0004-7109-0346
Bomi KimDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0009-0003-3814-4026
Hyukje SungDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0009-0009-8364-9668
Talisa TaitDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0009-0005-1021-9115
Daniel Colon HidalgoDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0000-0002-2385-125X
Yudy GuzmanDepartment of Biology, Andrews University, Berrien Springs, Michigan, 49104, USA.ORCID http://orcid.org/0009-0009-4306-9060

Funding

Andrews University Faculty Grant N/A/
6 · The paper itself

Abstract

backgroundBipolar disorder (BD) is a mood disorder affecting approximately 1–2% of the population. It is treated primarily with mood stabilizers, which have variable efficacy and tolerability. Omega-3 polyunsaturated fatty acids, particularly docosahexaenoic acid (DHA), have emerged as potential adjunctive treatments, though clinical findings and underlying mechanisms remain inconsistent. Given that myo-inositol depletion is proposed as a common mechanism for conventional mood stabilizers, we hypothesized that DHA, which modulates components of the phosphatidylinositol pathway, would alter intracellular myo-inositol and thus modulate myo-inositol homeostasis. The aim of this study was to determine the effect of DHA on intracellular myo-inositol and the expression of key genes involved in its biosynthesis.

methodsUsing an enzymatic assay, intracellular myo-inositol levels were measured in the extracts of cells grown in the presence of DHA. The effect of DHA on the expression of the myo-inositol biosynthetic genes INO1 (inositol-1-phosphate synthase) and INM1 (inositol monophosphatase) was assessed by RT-qPCR.

resultsDHA altered intracellular myo-inositol in a concentration-dependent manner, with low concentrations decreasing levels and higher concentrations producing increases relative to untreated controls. RT-qPCR analysis showed corresponding modulation of INO1 and INM1 expression, consistent with changes in myo-inositol homeostasis. While some group differences reached statistical significance, particularly in comparisons with valproate (VPA)-treated controls, most contrasts among DHA-treated groups were not significant.

conclusionThese findings provide preliminary evidence that DHA modulates intracellular myo-inositol levels and the expression of key biosynthetic genes in yeast. The biphasic response observed suggests a dose-sensitive effect that may help explain inconsistencies in clinical outcomes. While the results support the idea that omega-3 fatty acids influence inositol homeostasis, they should be considered hypothesis-generating and warrant confirmation in mammalian models and clinical settings. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Bipolar DisorderDocosahexaenoic AcidsInositolHumansMyo-Inositol-1-Phosphate SynthasePhosphoric Monoester HydrolasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsDocosahexaenoic AcidsINO1 protein, S cerevisiaeInositolmyo-inositol-1 (or 4)-monophosphataseMyo-Inositol-1-Phosphate SynthasePhosphoric Monoester HydrolasesSaccharomyces cerevisiae ProteinsBipolar disorderDocosahexaenoic acidINM1INO1myo-inositolOmega-3 fatty acids

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.