Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model

• Published in: Scientific reports Vol. 12; no. 1; pp. 20260 - 11
• Main Authors: Roberts, Victoria H. J., Schabel, Matthias C., Boniface, Emily R., D’Mello, Rahul J., Morgan, Terry K., Terrobias, Juanito Jose D., Graham, Jason A., Borgelt, Laura M., Grant, Kathleen A., Sullivan, Elinor L., Lo, Jamie O.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 24.11.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 692/308/1426; 692/308/2778; 692/308/575; Amniotic fluid; Angiogenesis; Animals; Cannabinoid Receptor Agonists - metabolism; Cannabis; Cesarean section; Dronabinol - pharmacology; Female; Fetus - metabolism; Fetuses; Hallucinogens - metabolism; Humanities and Social Sciences; Ischemia; Macaca mulatta; Marijuana; multidisciplinary; Offspring; Placenta; Pregnancy; Prenatal experience; Science; Science (multidisciplinary); Tetrahydrocannabinol; THC; Transcriptomes; Vasoactive agents
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-24401-4

Cannabis use in pregnancy is associated with adverse perinatal outcomes, which are likely mediated by the placenta. However, the underlying mechanisms and specific vasoactive effects of cannabis on the placenta are unknown. Our objective was to determine the impact of chronic prenatal delta-tetrahydrocannabinol (THC, main psychoactive component of cannabis) exposure on placental function and development in a rhesus macaque model using advanced imaging. Animals were divided into two groups, control (CON, n = 5) and THC-exposed (THC, n = 5). THC-exposed animals received a THC edible daily pre-conception and throughout pregnancy. Animals underwent serial ultrasound and MRI at gestational days 85 (G85), G110, G135 and G155 (full term is ~ G168). Animals underwent cesarean delivery and placental collection at G155 for histologic and RNA-Seq analysis. THC-exposed pregnancies had significantly decreased amniotic fluid volume (p < 0.001), placental perfusion (p < 0.05), and fetal oxygen availability (p < 0.05), all indicators of placental insufficiency. Placental histological analysis demonstrated evidence of ischemic injury with microinfarctions present in THC-exposed animals only. Bulk RNA-seq demonstrated that THC alters the placental transcriptome and pathway analysis suggests dysregulated vasculature development and angiogenesis pathways. The longer-term consequences of these adverse placental findings are unknown, but they suggest that use of THC during pregnancy may deleteriously impact offspring development.