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Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos
BACKGROUND: Ketamine is a commonly used clinical anesthetic and a popular recreational drug. However, with the exception of studies about the nervous system, studies about the effect of early ketamine exposure on embryos are rare. Xenopus laevis is a commonly used vertebrate model for assessing tera...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836076/ https://www.ncbi.nlm.nih.gov/pubmed/27091482 http://dx.doi.org/10.1186/s12871-016-0188-z |
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author | Guo, Ran Liu, Guangjian Du, Min Shi, Yu Jiang, Pu Liu, Xiaoli Liu, Lan Liu, Jianxia Xu, Ying |
author_facet | Guo, Ran Liu, Guangjian Du, Min Shi, Yu Jiang, Pu Liu, Xiaoli Liu, Lan Liu, Jianxia Xu, Ying |
author_sort | Guo, Ran |
collection | PubMed |
description | BACKGROUND: Ketamine is a commonly used clinical anesthetic and a popular recreational drug. However, with the exception of studies about the nervous system, studies about the effect of early ketamine exposure on embryos are rare. Xenopus laevis is a commonly used vertebrate model for assessing teratogenicity. Therefore, we treated Xenopus embryos with ketamine to evaluate its teratogenicity on embryos. METHODS: Xenopus embryos were treated with ketamine from stages 8 to 21. Embryonic and cardiac morphology were analyzed using living embryo imaging and whole-mount RNA in situ hybridization (WMISH). Heart function was measured by heart rate and ventricular shortening fraction (VSF). The mRNA expression levels of several heart development-related genes were determined by reverse transcription quantitative polymerase chain reaction (RT-qPCR). The protein expression levels of XMLC2, phospho-histone H3 (pH3) and histone H3 were determined by western blot. RESULTS: Ketamine caused concentration-dependent increases in mortality and shortening of body length. At a dose of 0.5 mg/ml, ketamine exposure resulted in cardiac enlargement as the primary manifestation of several malformations: gut defects, a curved axis and shortened body length. Cardiac cells underwent increased proliferation. Moreover, the heart rate and ventricular shortening fraction were decreased, findings indicative of heart dysfunction. XMLC2 expression levels were down-regulated at stages 28, 32/33, 35/36 and 46. CONCLUSIONS: Ketamine exposure during early development has teratogenic effects on Xenopus embryos. The heart enlargement and decreased VSF may result from the down-regulation of XMLC2 mRNA and protein levels. These findings provide new insight into the potential fetal defects induced by ketamine exposure during early pregnancy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12871-016-0188-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4836076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48360762016-04-20 Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos Guo, Ran Liu, Guangjian Du, Min Shi, Yu Jiang, Pu Liu, Xiaoli Liu, Lan Liu, Jianxia Xu, Ying BMC Anesthesiol Research Article BACKGROUND: Ketamine is a commonly used clinical anesthetic and a popular recreational drug. However, with the exception of studies about the nervous system, studies about the effect of early ketamine exposure on embryos are rare. Xenopus laevis is a commonly used vertebrate model for assessing teratogenicity. Therefore, we treated Xenopus embryos with ketamine to evaluate its teratogenicity on embryos. METHODS: Xenopus embryos were treated with ketamine from stages 8 to 21. Embryonic and cardiac morphology were analyzed using living embryo imaging and whole-mount RNA in situ hybridization (WMISH). Heart function was measured by heart rate and ventricular shortening fraction (VSF). The mRNA expression levels of several heart development-related genes were determined by reverse transcription quantitative polymerase chain reaction (RT-qPCR). The protein expression levels of XMLC2, phospho-histone H3 (pH3) and histone H3 were determined by western blot. RESULTS: Ketamine caused concentration-dependent increases in mortality and shortening of body length. At a dose of 0.5 mg/ml, ketamine exposure resulted in cardiac enlargement as the primary manifestation of several malformations: gut defects, a curved axis and shortened body length. Cardiac cells underwent increased proliferation. Moreover, the heart rate and ventricular shortening fraction were decreased, findings indicative of heart dysfunction. XMLC2 expression levels were down-regulated at stages 28, 32/33, 35/36 and 46. CONCLUSIONS: Ketamine exposure during early development has teratogenic effects on Xenopus embryos. The heart enlargement and decreased VSF may result from the down-regulation of XMLC2 mRNA and protein levels. These findings provide new insight into the potential fetal defects induced by ketamine exposure during early pregnancy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12871-016-0188-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-18 /pmc/articles/PMC4836076/ /pubmed/27091482 http://dx.doi.org/10.1186/s12871-016-0188-z Text en © Guo et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Guo, Ran Liu, Guangjian Du, Min Shi, Yu Jiang, Pu Liu, Xiaoli Liu, Lan Liu, Jianxia Xu, Ying Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos |
title | Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos |
title_full | Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos |
title_fullStr | Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos |
title_full_unstemmed | Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos |
title_short | Early ketamine exposure results in cardiac enlargement and heart dysfunction in Xenopus embryos |
title_sort | early ketamine exposure results in cardiac enlargement and heart dysfunction in xenopus embryos |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836076/ https://www.ncbi.nlm.nih.gov/pubmed/27091482 http://dx.doi.org/10.1186/s12871-016-0188-z |
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