Scientific Reports (Mar 2024)

Prenatal delta-9-tetrahydrocannabinol exposure alters fetal neurodevelopment in rhesus macaques

  • Kimberly S. Ryan,
  • Joshua A. Karpf,
  • Chi Ngai Chan,
  • Olivia L. Hagen,
  • Trevor J. McFarland,
  • J. Wes Urian,
  • Xiaojie Wang,
  • Emily R. Boniface,
  • Melanie H. Hakar,
  • Jose Juanito D. Terrobias,
  • Jason A. Graham,
  • Scarlet Passmore,
  • Kathleen A. Grant,
  • Elinor L. Sullivan,
  • Marjorie R. Grafe,
  • Julie A. Saugstad,
  • Christopher D. Kroenke,
  • Jamie O. Lo

DOI
https://doi.org/10.1038/s41598-024-56386-7
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 14

Abstract

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Abstract Prenatal cannabis use is associated with adverse offspring neurodevelopmental outcomes, however the underlying mechanisms are relatively unknown. We sought to determine the impact of chronic delta-9-tetrahydrocannabinol (THC) exposure on fetal neurodevelopment in a rhesus macaque model using advanced imaging combined with molecular and tissue studies. Animals were divided into two groups, control (n = 5) and THC-exposed (n = 5), which received a daily THC edible pre-conception and throughout pregnancy. Fetal T2-weighted MRI was performed at gestational days 85 (G85), G110, G135 and G155 to assess volumetric brain development. At G155, animals underwent cesarean delivery with collection of fetal cerebrospinal fluid (CSF) for microRNA (miRNA) studies and fetal tissue for histologic analysis. THC exposure was associated with significant age by sex interactions in brain growth, and differences in fetal brain histology suggestive of brain dysregulation. Two extracellular vesicle associated-miRNAs were identified in THC-exposed fetal CSF; pathway analysis suggests that these miRNAs are associated with dysregulated axonal guidance and netrin signaling. This data is indicative of subtle molecular changes consistent with the observed histological data, suggesting a potential role for fetal miRNA regulation by THC. Further studies are needed to determine whether these adverse findings correlate with long-term offspring neurodevelopmental health.

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