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<p>Smoking cannabis remains the most common mode of consumption amongst pregnant people, yet the effects on placentation remain poorly understood. While prior studies have focused on exposure to single components of cannabis (i.e., Δ9-THC and CBD), this approach overlooks the complex toxicology and pharmacology of cannabis smoke exposure. In this study, we used an in vitro model of human trophoblast differentiation to investigate the impact of CaSE&#xa0;(cannabis smoke extract) compared to Δ9-THC. We show that CaSE, but not Δ9-THC induces <i>CYP1A1</i> expression, a marker of exposure to combustion by-products. CaSE reduced hCG protein levels and <i>syncytin-1</i> gene expression, suggesting impaired syncytialization. Lower concentrations of CaSE (1%, 2.5%) elevated reactive oxygen species without impacting membrane potential, whereas higher concentrations (5%, 10%) disrupted mitochondrial respiration, indicating dose-dependent bioenergetic dysfunction. Antioxidant genes, superoxide dismutase 1 and 2, were distinctly altered indicating the divergence in oxidative stress responses. Interestingly, CB1R antagonism rescued the effects of Δ9-THC exposure, but not CaSE-mediated effects on differentiation markers. Since most cannabis users consume cannabis by smoking, and smoke exposure differs from single components (Δ9-THC), it is important that preclinical models consider smoking when evaluating the impacts of cannabis use during pregnancy.</p>

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Cannabis smoke extract disrupts trophoblast differentiation and causes mitochondrial dysfunction beyond the effects of Δ9-THC alone

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月26日

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  • Cristina Monaco,
  • Mahek Minhas,
  • Tina Podinic,
  • Joshua P. Nederveen,
  • Amica-Mariae Lucas,
  • Thane Tomy,
  • Gregg T. Tomy,
  • Alison C. Holloway,
  • Sandeep Raha

摘要

Smoking cannabis remains the most common mode of consumption amongst pregnant people, yet the effects on placentation remain poorly understood. While prior studies have focused on exposure to single components of cannabis (i.e., Δ9-THC and CBD), this approach overlooks the complex toxicology and pharmacology of cannabis smoke exposure. In this study, we used an in vitro model of human trophoblast differentiation to investigate the impact of CaSE (cannabis smoke extract) compared to Δ9-THC. We show that CaSE, but not Δ9-THC induces CYP1A1 expression, a marker of exposure to combustion by-products. CaSE reduced hCG protein levels and syncytin-1 gene expression, suggesting impaired syncytialization. Lower concentrations of CaSE (1%, 2.5%) elevated reactive oxygen species without impacting membrane potential, whereas higher concentrations (5%, 10%) disrupted mitochondrial respiration, indicating dose-dependent bioenergetic dysfunction. Antioxidant genes, superoxide dismutase 1 and 2, were distinctly altered indicating the divergence in oxidative stress responses. Interestingly, CB1R antagonism rescued the effects of Δ9-THC exposure, but not CaSE-mediated effects on differentiation markers. Since most cannabis users consume cannabis by smoking, and smoke exposure differs from single components (Δ9-THC), it is important that preclinical models consider smoking when evaluating the impacts of cannabis use during pregnancy.