Cargando…
Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model
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-tetrahyd...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691736/ https://www.ncbi.nlm.nih.gov/pubmed/36424495 http://dx.doi.org/10.1038/s41598-022-24401-4 |
_version_ | 1784837093674975232 |
---|---|
author | 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. |
author_facet | 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. |
author_sort | Roberts, Victoria H. J. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9691736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96917362022-11-26 Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model 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. Sci Rep Article 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. Nature Publishing Group UK 2022-11-24 /pmc/articles/PMC9691736/ /pubmed/36424495 http://dx.doi.org/10.1038/s41598-022-24401-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article 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. Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model |
title | Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model |
title_full | Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model |
title_fullStr | Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model |
title_full_unstemmed | Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model |
title_short | Chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model |
title_sort | chronic prenatal delta-9-tetrahydrocannabinol exposure adversely impacts placental function and development in a rhesus macaque model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691736/ https://www.ncbi.nlm.nih.gov/pubmed/36424495 http://dx.doi.org/10.1038/s41598-022-24401-4 |
work_keys_str_mv | AT robertsvictoriahj chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT schabelmatthiasc chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT bonifaceemilyr chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT dmellorahulj chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT morganterryk chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT terrobiasjuanitojosed chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT grahamjasona chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT borgeltlauram chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT grantkathleena chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT sullivanelinorl chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel AT lojamieo chronicprenataldelta9tetrahydrocannabinolexposureadverselyimpactsplacentalfunctionanddevelopmentinarhesusmacaquemodel |