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Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain
OBJECTIVES AND AIM: This study was designed to analyze the relationship between the expression of c-Fos protein and apoptosis in the hippocampus following propofol administration in infant mice. There are reports that certain drugs, including the general anesthetics applied in pediatrics and obstetr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229778/ https://www.ncbi.nlm.nih.gov/pubmed/22144767 http://dx.doi.org/10.4103/0253-7613.89819 |
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author | Cui, Yin Ling-Shan, Gou Yi, Liu Xing-Qi, Wang Xue-Mei, Zhuang Xiao-Xing, Yin |
author_facet | Cui, Yin Ling-Shan, Gou Yi, Liu Xing-Qi, Wang Xue-Mei, Zhuang Xiao-Xing, Yin |
author_sort | Cui, Yin |
collection | PubMed |
description | OBJECTIVES AND AIM: This study was designed to analyze the relationship between the expression of c-Fos protein and apoptosis in the hippocampus following propofol administration in infant mice. There are reports that certain drugs, including the general anesthetics applied in pediatrics and obstetrics, could block N-methyl-D-aspartate glutamate receptors and activate γ-aminobutyric acid type A receptors. Furthermore, some anesthetics could trigger neuroapoptosis and the expression of c-Fos in the developing rodent brain. Propofol is a general anesthetic increasingly used in pediatrics and obstetrics, and is reported to be able to interact with both γ-aminobutyric acid type A and N-methyl-D-aspartate glutamate receptors. No adequate evaluations have been available as to whether the dosage of propofol to maintain anaesthesia could trigger the expression of c-Fos and apoptosis. MATERIALS AND METHODS: Intraperitoneal injections of propofol (50, 100 and 150 mg/kg) or vehicle were administered every 90 minutes (4 times) in infant mice (5–7 days old). 30 minutes after the final administration, the protein expressions of c-Fos and cleaved-caspase-3 in the hippocampus were determined by immunohistochemistry and Western blotting. RESULTS: It was demonstrated that the expressions of cleaved-caspase-3 and c-Fos were upregulated in the hippocampal CA3 region in this study. CONCLUSIONS: The upregulated c-Fos expression induced by repeated injections of propofol might evoke neuroapoptosis. |
format | Online Article Text |
id | pubmed-3229778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32297782011-12-05 Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain Cui, Yin Ling-Shan, Gou Yi, Liu Xing-Qi, Wang Xue-Mei, Zhuang Xiao-Xing, Yin Indian J Pharmacol Research Article OBJECTIVES AND AIM: This study was designed to analyze the relationship between the expression of c-Fos protein and apoptosis in the hippocampus following propofol administration in infant mice. There are reports that certain drugs, including the general anesthetics applied in pediatrics and obstetrics, could block N-methyl-D-aspartate glutamate receptors and activate γ-aminobutyric acid type A receptors. Furthermore, some anesthetics could trigger neuroapoptosis and the expression of c-Fos in the developing rodent brain. Propofol is a general anesthetic increasingly used in pediatrics and obstetrics, and is reported to be able to interact with both γ-aminobutyric acid type A and N-methyl-D-aspartate glutamate receptors. No adequate evaluations have been available as to whether the dosage of propofol to maintain anaesthesia could trigger the expression of c-Fos and apoptosis. MATERIALS AND METHODS: Intraperitoneal injections of propofol (50, 100 and 150 mg/kg) or vehicle were administered every 90 minutes (4 times) in infant mice (5–7 days old). 30 minutes after the final administration, the protein expressions of c-Fos and cleaved-caspase-3 in the hippocampus were determined by immunohistochemistry and Western blotting. RESULTS: It was demonstrated that the expressions of cleaved-caspase-3 and c-Fos were upregulated in the hippocampal CA3 region in this study. CONCLUSIONS: The upregulated c-Fos expression induced by repeated injections of propofol might evoke neuroapoptosis. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3229778/ /pubmed/22144767 http://dx.doi.org/10.4103/0253-7613.89819 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cui, Yin Ling-Shan, Gou Yi, Liu Xing-Qi, Wang Xue-Mei, Zhuang Xiao-Xing, Yin Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain |
title | Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain |
title_full | Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain |
title_fullStr | Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain |
title_full_unstemmed | Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain |
title_short | Repeated administration of propofol upregulated the expression of c-Fos and cleaved-caspase-3 proteins in the developing mouse brain |
title_sort | repeated administration of propofol upregulated the expression of c-fos and cleaved-caspase-3 proteins in the developing mouse brain |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3229778/ https://www.ncbi.nlm.nih.gov/pubmed/22144767 http://dx.doi.org/10.4103/0253-7613.89819 |
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