Prenatal omega-3 fatty acids supplementation mitigates some schizophrenia-like deficits in offspring: A PET and MRI study in a rat model

Omega-3 fatty acids (OM) have been employed as adjunctive therapy in patients with schizophrenia, but their potential as a preventive strategy remains unclear. This study aims to evaluate whether dietary OM supplementation during pregnancy may prevent schizophrenia-like deficits in a maternal immune stimulation (MIS) model. Pregnant Wistar rats were injected with PolyI:C (i.e. MIS) or Saline on gestational day 15. They were fed with OM-enriched chow, either from MIS until delivery (OM7) or throughout gestation (OM21). Two control groups (Saline-naïve & MIS-naïve) were maintained on standard chow. In adulthood, offspring were assessed through tests for locomotion, anxiety and short- and long-term memory (STM, LTM). Brain glucose metabolism and structural in vivo neuroimaging studies were performed using PET and MRI techniques. OM7/OM21 treatments prevented the hyperlocomotion in MIS-offspring while STM deficits were only improved by OM7. Both OM7/OM21 treatments prevented certain metabolic and volumetric changes in the cortex, as well as the enlargement of the ventricles. Additionally, OM21 protected WM integrity in MIS-offspring. Altogether, our study highlights the potential of prenatal OM dietary supplementation to ameliorate some of the SCZ-like deficits observed in the MIS model.

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Publication Details

Journal
Translational Psychiatry
Published
2025-10-24
DOI
https://doi.org/10.1038/s41398-025-03612-z
Citations
1
Primary Topic
Fatty Acid Research and Health
Type
article
Field-Weighted Citation Impact
1.12
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article

Prenatal omega-3 fatty acids supplementation mitigates some schizophrenia-like deficits in offspring: A PET and MRI study in a rat model

Diego Romero‐Miguel, María Luisa Soto‐Montenegro, Marta Casquero‐Veiga, Nicolás Lamanna‐Rama et al.
1 citations
Translational Psychiatry
Fatty Acid Research and Health
1.12
article

Prenatal omega-3 fatty acids supplementation mitigates some schizophrenia-like deficits in offspring: A PET and MRI study in a rat model

Diego Romero‐Miguel, María Luisa Soto‐Montenegro, Marta Casquero‐Veiga, Nicolás Lamanna‐Rama, Vanessa Gómez‐Rangel, Ravit Hadar, Christine Winter, Manuel Desco, Raquel Chávez-Valencia
article en
1 citations

Abstract

Omega-3 fatty acids (OM) have been employed as adjunctive therapy in patients with schizophrenia, but their potential as a preventive strategy remains unclear. This study aims to evaluate whether dietary OM supplementation during pregnancy may prevent schizophrenia-like deficits in a maternal immune stimulation (MIS) model. Pregnant Wistar rats were injected with PolyI:C (i.e. MIS) or Saline on gestational day 15. They were fed with OM-enriched chow, either from MIS until delivery (OM7) or throughout gestation (OM21). Two control groups (Saline-naïve & MIS-naïve) were maintained on standard chow. In adulthood, offspring were assessed through tests for locomotion, anxiety and short- and long-term memory (STM, LTM). Brain glucose metabolism and structural in vivo neuroimaging studies were performed using PET and MRI techniques. OM7/OM21 treatments prevented the hyperlocomotion in MIS-offspring while STM deficits were only improved by OM7. Both OM7/OM21 treatments prevented certain metabolic and volumetric changes in the cortex, as well as the enlargement of the ventricles. Additionally, OM21 protected WM integrity in MIS-offspring. Altogether, our study highlights the potential of prenatal OM dietary supplementation to ameliorate some of the SCZ-like deficits observed in the MIS model.

Translational PsychiatryVol. 15(1)
Universidad Rey Juan Carlos (ES), Hospital General Universitario Gregorio Marañón (ES), Instituto de Neurociencias (ES), Centro de Investigación Biomédica en Red de Salud Mental (ES), Hospital Universitario Fundación Jiménez Díaz (ES), Spanish National Centre for Cardiovascular Research (ES), Universidad Carlos III de Madrid (ES), Charité - Universitätsmedizin Berlin (DE)
Openalex Percentile: Top 18%
Fatty Acid Research and Health
1.12
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