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Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats

To examine the effects of human amniotic fluid stem cells (hAFSCs) transplantation on bladder function and molecular changes in diabetic rats, 60 female Sprague-Dawley rats were used for study. Three groups were assigned including sham control rats, streptozotocin (STZ, 60 mg/kg)-induced diabetic ra...

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Autores principales: Liang, Ching-Chung, Shaw, Sheng-Wen Steven, Huang, Yung-Hsin, Lin, Yi-Hao, Lee, Tsong-Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794746/
https://www.ncbi.nlm.nih.gov/pubmed/29391467
http://dx.doi.org/10.1038/s41598-018-20512-z
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author Liang, Ching-Chung
Shaw, Sheng-Wen Steven
Huang, Yung-Hsin
Lin, Yi-Hao
Lee, Tsong-Hai
author_facet Liang, Ching-Chung
Shaw, Sheng-Wen Steven
Huang, Yung-Hsin
Lin, Yi-Hao
Lee, Tsong-Hai
author_sort Liang, Ching-Chung
collection PubMed
description To examine the effects of human amniotic fluid stem cells (hAFSCs) transplantation on bladder function and molecular changes in diabetic rats, 60 female Sprague-Dawley rats were used for study. Three groups were assigned including sham control rats, streptozotocin (STZ, 60 mg/kg)-induced diabetic rats and STZ-induced diabetic rats plus bladder hAFSCs transplantation. Compared to controls, diabetic rats had decreased body weight but increased bladder weight. Cystometries showed non-voiding contraction, residual volume, voided volume and intercontraction interval increased significantly in diabetic rats at week 4 and 12 after DM induction, but improved after hAFSCs transplantation. The immunoreactivities and mRNAs of nerve growth factor (NGF) decreased significantly in diabetic bladder at week 4 and 12 after DM induction, but recovered after hAFSCs transplantation. The immunoreactivities and mRNAs of M2 and M3 muscarinic receptor increased significantly in diabetic bladder at week 4 after DM induction but recovered after hAFSCs transplantation. The immunoreactivity of 8-hydroxy-20-deoxyguanosine increased significantly in diabetic bladder at week 4 and 12 after DM induction but reduced after hAFSCs transplantation. The present study showed bladder dysfunction in STZ-induced diabetic rats could be improved by hAFSCs transplantation into bladder, which may be related to the recovery of bladder NGF and muscarinic receptors.
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spelling pubmed-57947462018-02-12 Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats Liang, Ching-Chung Shaw, Sheng-Wen Steven Huang, Yung-Hsin Lin, Yi-Hao Lee, Tsong-Hai Sci Rep Article To examine the effects of human amniotic fluid stem cells (hAFSCs) transplantation on bladder function and molecular changes in diabetic rats, 60 female Sprague-Dawley rats were used for study. Three groups were assigned including sham control rats, streptozotocin (STZ, 60 mg/kg)-induced diabetic rats and STZ-induced diabetic rats plus bladder hAFSCs transplantation. Compared to controls, diabetic rats had decreased body weight but increased bladder weight. Cystometries showed non-voiding contraction, residual volume, voided volume and intercontraction interval increased significantly in diabetic rats at week 4 and 12 after DM induction, but improved after hAFSCs transplantation. The immunoreactivities and mRNAs of nerve growth factor (NGF) decreased significantly in diabetic bladder at week 4 and 12 after DM induction, but recovered after hAFSCs transplantation. The immunoreactivities and mRNAs of M2 and M3 muscarinic receptor increased significantly in diabetic bladder at week 4 after DM induction but recovered after hAFSCs transplantation. The immunoreactivity of 8-hydroxy-20-deoxyguanosine increased significantly in diabetic bladder at week 4 and 12 after DM induction but reduced after hAFSCs transplantation. The present study showed bladder dysfunction in STZ-induced diabetic rats could be improved by hAFSCs transplantation into bladder, which may be related to the recovery of bladder NGF and muscarinic receptors. Nature Publishing Group UK 2018-02-01 /pmc/articles/PMC5794746/ /pubmed/29391467 http://dx.doi.org/10.1038/s41598-018-20512-z Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Liang, Ching-Chung
Shaw, Sheng-Wen Steven
Huang, Yung-Hsin
Lin, Yi-Hao
Lee, Tsong-Hai
Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats
title Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats
title_full Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats
title_fullStr Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats
title_full_unstemmed Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats
title_short Improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats
title_sort improvement in bladder dysfunction after bladder transplantation of amniotic fluid stem cells in diabetic rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794746/
https://www.ncbi.nlm.nih.gov/pubmed/29391467
http://dx.doi.org/10.1038/s41598-018-20512-z
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