{"title":"Sex-dependent protective effects of a ketogenic diet following prenatal stress exposure: Evidence from adolescent rats","authors":"Veronica Begni , Alessia Marchesin , Rodrigo Orso , Kerstin Camile Creutzberg , Federica Precetti , Annamaria Cattaneo , Marco Andrea Riva","doi":"10.1016/j.bbi.2026.106301","DOIUrl":null,"url":null,"abstract":"<div><div>Exposure to stress during gestation (prenatal stress, PNS) disrupts neurodevelopmental trajectories and increases vulnerability to neuropsychiatric disorders, through dysregulation of different molecular pathways. PNS-induced alterations frequently emerge during adolescence, a highly dynamic maturational period, highlighting a critical window in which therapeutic interventions may modify pathological outcomes. Here, we investigated whether a post-weaning ketogenic diet (KD) could modulate PNS-induced behavioral and molecular alterations in adolescent Sprague–Dawley rats. At weaning offspring from dams exposed to repeated restraint stress during gestation were assigned to a control diet (CD) or KD. Behavioral testing was conducted during adolescence, and prefrontal cortex (PFC) was analyzed for excitatory/inhibitory markers, redox regulators, and inflammatory mediators. PNS induced sociability deficits that were ameliorated by KD. A two-step cluster analysis identified ∼50–55 % of PNS offspring as “vulnerable,” whereas KD reduced this proportion to 22 % in males and 12 % in females. At the molecular level, KD exerted sex-dependent effects in the PFC: in males, it enhanced inhibitory interneuron markers and reduced pro-inflammatory transcripts while altering NRF2/KEAP1 redox signaling; in females, it increased NRF2 and partially restored GCLC1, while PNS selectively disrupted inhibitory and excitatory markers. Together, these findings demonstrate that post-weaning KD rescues PNS-induced social deficits and reshapes PFC molecular profiles, engaging sex-specific mechanisms of resilience. In summary, diet-based interventions during adolescence may represent a promising strategy to counteract developmental stress-related vulnerability.</div></div>","PeriodicalId":9199,"journal":{"name":"Brain, Behavior, and Immunity","volume":"134 ","pages":"Article 106301"},"PeriodicalIF":7.5000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain, Behavior, and Immunity","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0889159126000498","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Exposure to stress during gestation (prenatal stress, PNS) disrupts neurodevelopmental trajectories and increases vulnerability to neuropsychiatric disorders, through dysregulation of different molecular pathways. PNS-induced alterations frequently emerge during adolescence, a highly dynamic maturational period, highlighting a critical window in which therapeutic interventions may modify pathological outcomes. Here, we investigated whether a post-weaning ketogenic diet (KD) could modulate PNS-induced behavioral and molecular alterations in adolescent Sprague–Dawley rats. At weaning offspring from dams exposed to repeated restraint stress during gestation were assigned to a control diet (CD) or KD. Behavioral testing was conducted during adolescence, and prefrontal cortex (PFC) was analyzed for excitatory/inhibitory markers, redox regulators, and inflammatory mediators. PNS induced sociability deficits that were ameliorated by KD. A two-step cluster analysis identified ∼50–55 % of PNS offspring as “vulnerable,” whereas KD reduced this proportion to 22 % in males and 12 % in females. At the molecular level, KD exerted sex-dependent effects in the PFC: in males, it enhanced inhibitory interneuron markers and reduced pro-inflammatory transcripts while altering NRF2/KEAP1 redox signaling; in females, it increased NRF2 and partially restored GCLC1, while PNS selectively disrupted inhibitory and excitatory markers. Together, these findings demonstrate that post-weaning KD rescues PNS-induced social deficits and reshapes PFC molecular profiles, engaging sex-specific mechanisms of resilience. In summary, diet-based interventions during adolescence may represent a promising strategy to counteract developmental stress-related vulnerability.
期刊介绍:
Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals.
As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.