Elizabeth C. Plunk, Katherine E. Manz, Andre Gomes, Kurt D. Pennell, Marissa E. Sobolewski, Ania K. Majewska
{"title":"Gestational and Lactational Exposure to Perfluorohexanoic Acid Affects Behavior in Adult Male Mice: A Preliminary Study","authors":"Elizabeth C. Plunk, Katherine E. Manz, Andre Gomes, Kurt D. Pennell, Marissa E. Sobolewski, Ania K. Majewska","doi":"10.1111/ejn.70174","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Legacy per- and polyfluoroalkyl substances (PFAS) have been associated with increased risk for male-biased neurobehavioral disorders. Industries have effectively replaced them with next-generation PFAS, including perfluorohexanoic acid (PFHxA). Zebrafish studies indicate developmental effects of PFHxA exposure on activity levels; however, the developmental neurotoxicology (DNT) of PFHxA has not been characterized in mammals. Human data reflect the need for mammalian DNT evaluations because PFHxA is found in the serum of pregnant women and in breast milk. Furthermore, postmortem studies show that PFHxA enters the brain, with the cerebellum having particularly elevated concentrations. Given this targeted brain region, we predicted that behavioral effects of PFHxA may target motor domains. To evaluate the effects of developmental PFHxA exposure, we exposed pregnant C57BL/6J mice daily from gestational day 0 through postnatal day (P)21 to vehicle (ddH2O), a lower (0.32 mg/kg of body weight [bw]) or a higher (50 mg/kg of bw) dose of PFHxA. Although this resulted in increases in the brain at P1 in the higher exposure group and in P21 in both exposure groups, by P90, PFHxA levels returned to those in control mice. We observed male-specific effects in the open-field test, the elevated plus maze, and the novel object recognition test in adulthood, with no overt effects in the hang test, inverted screen test, and gait scan. These preliminary findings indicate that PFHxA exposure may cause long-lasting changes in many behavioral domains in a mammalian model, and more research is needed to expand these evaluations to other cognitive domains.</p>\n </div>","PeriodicalId":11993,"journal":{"name":"European Journal of Neuroscience","volume":"62 1","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ejn.70174","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Legacy per- and polyfluoroalkyl substances (PFAS) have been associated with increased risk for male-biased neurobehavioral disorders. Industries have effectively replaced them with next-generation PFAS, including perfluorohexanoic acid (PFHxA). Zebrafish studies indicate developmental effects of PFHxA exposure on activity levels; however, the developmental neurotoxicology (DNT) of PFHxA has not been characterized in mammals. Human data reflect the need for mammalian DNT evaluations because PFHxA is found in the serum of pregnant women and in breast milk. Furthermore, postmortem studies show that PFHxA enters the brain, with the cerebellum having particularly elevated concentrations. Given this targeted brain region, we predicted that behavioral effects of PFHxA may target motor domains. To evaluate the effects of developmental PFHxA exposure, we exposed pregnant C57BL/6J mice daily from gestational day 0 through postnatal day (P)21 to vehicle (ddH2O), a lower (0.32 mg/kg of body weight [bw]) or a higher (50 mg/kg of bw) dose of PFHxA. Although this resulted in increases in the brain at P1 in the higher exposure group and in P21 in both exposure groups, by P90, PFHxA levels returned to those in control mice. We observed male-specific effects in the open-field test, the elevated plus maze, and the novel object recognition test in adulthood, with no overt effects in the hang test, inverted screen test, and gait scan. These preliminary findings indicate that PFHxA exposure may cause long-lasting changes in many behavioral domains in a mammalian model, and more research is needed to expand these evaluations to other cognitive domains.
期刊介绍:
EJN is the journal of FENS and supports the international neuroscientific community by publishing original high quality research articles and reviews in all fields of neuroscience. In addition, to engage with issues that are of interest to the science community, we also publish Editorials, Meetings Reports and Neuro-Opinions on topics that are of current interest in the fields of neuroscience research and training in science. We have recently established a series of ‘Profiles of Women in Neuroscience’. Our goal is to provide a vehicle for publications that further the understanding of the structure and function of the nervous system in both health and disease and to provide a vehicle to engage the neuroscience community. As the official journal of FENS, profits from the journal are re-invested in the neuroscientific community through the activities of FENS.