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Gestational exposure to a fluorotelomer alcohol causes behavioral abnormalities by disrupting the blood–brain barrier in offspring

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Abstract

Fluorotelomer alcohols are an alternative to neurotoxic perfluoroalkyl carboxylic acids, a sub-class of per- and poly-fluoroalkyl substances (PFAS). However, the effect of the fluorotelomer alcohol in offspring is poorly known. Here pregnant mice were exposed to various doses of the 6:2 fluorotelomer alcohol through intragastric administration from gestation day 8.5 until delivery. Results show that the fluorotelomer alcohol impaired the development of the blood–brain barrier and altered brain immune microenvironment, causing anxiety-like behavior and impairments in learning memory. Mechanistic studies suggest that this is due to the activation of the serine and threonine kinase AKT/nuclear factor kappa-b/matrix metalloproteinases signaling pathway, resulting in the degradation of the tight junction protein occludin, which in turn caused disruption of endothelial barrier function. Our findings represent the first evidence that gestational exposure to the 6:2 fluorotelomer alcohol causes neurotoxicity in offspring.

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Acknowledgements

We thank The Translational Medicine Core Facilities, Medical School, Nanjing University, Nanjing, China, for providing the experimental equipment.

Funding

This work was supported by the national natural science foundation of china (31971517 and 31870492) and nanjing university innovation and creative program for the doctor of philosophy candidate (KYCX22_0179).

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Yunhui Xia: conceptualization, investigation, formal analysis, writing-original draft. Yi Chen: methodology. Junhan Chen: investigation. Xiaodong Han: research guidance, funding acquisition. Xiaojian Wang: methodology, data curation. Dongmei Li: project administration, writing-review & editing, funding acquisition.

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Correspondence to Xiaojian Wang or Dongmei Li.

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Xia, Y., Chen, Y., Chen, J. et al. Gestational exposure to a fluorotelomer alcohol causes behavioral abnormalities by disrupting the blood–brain barrier in offspring. Environ Chem Lett 22, 967–973 (2024). https://doi.org/10.1007/s10311-024-01707-5

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  • DOI: https://doi.org/10.1007/s10311-024-01707-5

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