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Cannabinoid exposure and altered DNA methylation in rat and human sperm
Little is known about the reproductive effects of paternal cannabis exposure. We evaluated associations between cannabis or tetrahydrocannabinol (THC) exposure and altered DNA methylation in sperm from humans and rats, respectively. DNA methylation, measured by reduced representation bisulfite seque...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986792/ https://www.ncbi.nlm.nih.gov/pubmed/30521419 http://dx.doi.org/10.1080/15592294.2018.1554521 |
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author | Murphy, Susan K. Itchon-Ramos, Nilda Visco, Zachary Huang, Zhiqing Grenier, Carole Schrott, Rose Acharya, Kelly Boudreau, Marie-Helene Price, Thomas M. Raburn, Douglas J. Corcoran, David L. Lucas, Joseph E. Mitchell, John T. McClernon, F. Joseph Cauley, Marty Hall, Brandon J. Levin, Edward D. Kollins, Scott H. |
author_facet | Murphy, Susan K. Itchon-Ramos, Nilda Visco, Zachary Huang, Zhiqing Grenier, Carole Schrott, Rose Acharya, Kelly Boudreau, Marie-Helene Price, Thomas M. Raburn, Douglas J. Corcoran, David L. Lucas, Joseph E. Mitchell, John T. McClernon, F. Joseph Cauley, Marty Hall, Brandon J. Levin, Edward D. Kollins, Scott H. |
author_sort | Murphy, Susan K. |
collection | PubMed |
description | Little is known about the reproductive effects of paternal cannabis exposure. We evaluated associations between cannabis or tetrahydrocannabinol (THC) exposure and altered DNA methylation in sperm from humans and rats, respectively. DNA methylation, measured by reduced representation bisulfite sequencing, differed in the sperm of human users from non-users by at least 10% at 3,979 CpG sites. Pathway analyses indicated Hippo Signaling and Pathways in Cancer as enriched with altered genes (Bonferroni p < 0.02). These same two pathways were also enriched with genes having altered methylation in sperm from THC-exposed versus vehicle-exposed rats (p < 0.01). Data validity is supported by significant correlations between THC exposure levels in humans and methylation for 177 genes, and substantial overlap in THC target genes in rat sperm (this study) and genes previously reported as having altered methylation in the brain of rat offspring born to parents both exposed to THC during adolescence. In humans, cannabis use was also associated with significantly lower sperm concentration. Findings point to possible pre-conception paternal reproductive risks associated with cannabis use. |
format | Online Article Text |
id | pubmed-6986792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-69867922020-02-11 Cannabinoid exposure and altered DNA methylation in rat and human sperm Murphy, Susan K. Itchon-Ramos, Nilda Visco, Zachary Huang, Zhiqing Grenier, Carole Schrott, Rose Acharya, Kelly Boudreau, Marie-Helene Price, Thomas M. Raburn, Douglas J. Corcoran, David L. Lucas, Joseph E. Mitchell, John T. McClernon, F. Joseph Cauley, Marty Hall, Brandon J. Levin, Edward D. Kollins, Scott H. Epigenetics Research Paper Little is known about the reproductive effects of paternal cannabis exposure. We evaluated associations between cannabis or tetrahydrocannabinol (THC) exposure and altered DNA methylation in sperm from humans and rats, respectively. DNA methylation, measured by reduced representation bisulfite sequencing, differed in the sperm of human users from non-users by at least 10% at 3,979 CpG sites. Pathway analyses indicated Hippo Signaling and Pathways in Cancer as enriched with altered genes (Bonferroni p < 0.02). These same two pathways were also enriched with genes having altered methylation in sperm from THC-exposed versus vehicle-exposed rats (p < 0.01). Data validity is supported by significant correlations between THC exposure levels in humans and methylation for 177 genes, and substantial overlap in THC target genes in rat sperm (this study) and genes previously reported as having altered methylation in the brain of rat offspring born to parents both exposed to THC during adolescence. In humans, cannabis use was also associated with significantly lower sperm concentration. Findings point to possible pre-conception paternal reproductive risks associated with cannabis use. Taylor & Francis 2018-12-18 /pmc/articles/PMC6986792/ /pubmed/30521419 http://dx.doi.org/10.1080/15592294.2018.1554521 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Paper Murphy, Susan K. Itchon-Ramos, Nilda Visco, Zachary Huang, Zhiqing Grenier, Carole Schrott, Rose Acharya, Kelly Boudreau, Marie-Helene Price, Thomas M. Raburn, Douglas J. Corcoran, David L. Lucas, Joseph E. Mitchell, John T. McClernon, F. Joseph Cauley, Marty Hall, Brandon J. Levin, Edward D. Kollins, Scott H. Cannabinoid exposure and altered DNA methylation in rat and human sperm |
title | Cannabinoid exposure and altered DNA methylation in rat and human sperm |
title_full | Cannabinoid exposure and altered DNA methylation in rat and human sperm |
title_fullStr | Cannabinoid exposure and altered DNA methylation in rat and human sperm |
title_full_unstemmed | Cannabinoid exposure and altered DNA methylation in rat and human sperm |
title_short | Cannabinoid exposure and altered DNA methylation in rat and human sperm |
title_sort | cannabinoid exposure and altered dna methylation in rat and human sperm |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986792/ https://www.ncbi.nlm.nih.gov/pubmed/30521419 http://dx.doi.org/10.1080/15592294.2018.1554521 |
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