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Propylthiouracil Is Teratogenic in Murine Embryos

BACKGROUND: Hyperthyroidism during pregnancy is treated with the antithyroid drugs (ATD) propylthiouracil (PTU) and methimazole (MMI). PTU currently is recommended as the drug of choice during early pregnancy. Yet, despite widespread ATD use in pregnancy, formal studies of ATD teratogenic effects ha...

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Autores principales: Benavides, Valeria C., Mallela, Murali K., Booth, Carmen J., Wendler, Christopher C., Rivkees, Scott A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329451/
https://www.ncbi.nlm.nih.gov/pubmed/22529993
http://dx.doi.org/10.1371/journal.pone.0035213
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author Benavides, Valeria C.
Mallela, Murali K.
Booth, Carmen J.
Wendler, Christopher C.
Rivkees, Scott A.
author_facet Benavides, Valeria C.
Mallela, Murali K.
Booth, Carmen J.
Wendler, Christopher C.
Rivkees, Scott A.
author_sort Benavides, Valeria C.
collection PubMed
description BACKGROUND: Hyperthyroidism during pregnancy is treated with the antithyroid drugs (ATD) propylthiouracil (PTU) and methimazole (MMI). PTU currently is recommended as the drug of choice during early pregnancy. Yet, despite widespread ATD use in pregnancy, formal studies of ATD teratogenic effects have not been performed. METHODS: We examined the teratogenic effects of PTU and MMI during embryogenesis in mice. To span different periods of embryogenesis, dams were treated with compounds or vehicle daily from embryonic day (E) 7.5 to 9.5 or from E3.5 to E7.5. Embryos were examined for gross malformations at E10.5 or E18.5 followed by histological and micro-CT analysis. Influences of PTU on gene expression levels were examined by RNA microarray analysis. RESULTS: When dams were treated from E7.5 to E9.5 with PTU, neural tube and cardiac abnormalities were observed at E10.5. Cranial neural tube defects were significantly more common among the PTU-exposed embryos than those exposed to MMI or vehicle. Blood in the pericardial sac, which is a feature indicative of abnormal cardiac function and/or abnormal vasculature, was observed more frequently in PTU-treated than MMI-treated or vehicle-treated embryos. Following PTU treatment, a total of 134 differentially expressed genes were identified. Disrupted genetic pathways were those associated with cytoskeleton remodeling and keratin filaments. At E 18.5, no gross malformations were evident in either ATD group, but the number of viable PTU embryos per dam at E18.5 was significantly lower from those at E10.5, indicating loss of malformed embryos. These data show that PTU exposure during embryogenesis is associated with delayed neural tube closure and cardiac abnormalities. In contrast, we did not observe structural or cardiac defects associated with MMI exposure except at the higher dose. We find that PTU exposure during embryogenesis is associated with fetal loss. These observations suggest that PTU has teratogenic potential.
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spelling pubmed-33294512012-04-23 Propylthiouracil Is Teratogenic in Murine Embryos Benavides, Valeria C. Mallela, Murali K. Booth, Carmen J. Wendler, Christopher C. Rivkees, Scott A. PLoS One Research Article BACKGROUND: Hyperthyroidism during pregnancy is treated with the antithyroid drugs (ATD) propylthiouracil (PTU) and methimazole (MMI). PTU currently is recommended as the drug of choice during early pregnancy. Yet, despite widespread ATD use in pregnancy, formal studies of ATD teratogenic effects have not been performed. METHODS: We examined the teratogenic effects of PTU and MMI during embryogenesis in mice. To span different periods of embryogenesis, dams were treated with compounds or vehicle daily from embryonic day (E) 7.5 to 9.5 or from E3.5 to E7.5. Embryos were examined for gross malformations at E10.5 or E18.5 followed by histological and micro-CT analysis. Influences of PTU on gene expression levels were examined by RNA microarray analysis. RESULTS: When dams were treated from E7.5 to E9.5 with PTU, neural tube and cardiac abnormalities were observed at E10.5. Cranial neural tube defects were significantly more common among the PTU-exposed embryos than those exposed to MMI or vehicle. Blood in the pericardial sac, which is a feature indicative of abnormal cardiac function and/or abnormal vasculature, was observed more frequently in PTU-treated than MMI-treated or vehicle-treated embryos. Following PTU treatment, a total of 134 differentially expressed genes were identified. Disrupted genetic pathways were those associated with cytoskeleton remodeling and keratin filaments. At E 18.5, no gross malformations were evident in either ATD group, but the number of viable PTU embryos per dam at E18.5 was significantly lower from those at E10.5, indicating loss of malformed embryos. These data show that PTU exposure during embryogenesis is associated with delayed neural tube closure and cardiac abnormalities. In contrast, we did not observe structural or cardiac defects associated with MMI exposure except at the higher dose. We find that PTU exposure during embryogenesis is associated with fetal loss. These observations suggest that PTU has teratogenic potential. Public Library of Science 2012-04-18 /pmc/articles/PMC3329451/ /pubmed/22529993 http://dx.doi.org/10.1371/journal.pone.0035213 Text en Benavides et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Benavides, Valeria C.
Mallela, Murali K.
Booth, Carmen J.
Wendler, Christopher C.
Rivkees, Scott A.
Propylthiouracil Is Teratogenic in Murine Embryos
title Propylthiouracil Is Teratogenic in Murine Embryos
title_full Propylthiouracil Is Teratogenic in Murine Embryos
title_fullStr Propylthiouracil Is Teratogenic in Murine Embryos
title_full_unstemmed Propylthiouracil Is Teratogenic in Murine Embryos
title_short Propylthiouracil Is Teratogenic in Murine Embryos
title_sort propylthiouracil is teratogenic in murine embryos
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329451/
https://www.ncbi.nlm.nih.gov/pubmed/22529993
http://dx.doi.org/10.1371/journal.pone.0035213
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