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Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats
BACKGROUND: This study aimed to determine the effects of Indomethacin (IMC) treatment on embryo implantation and histomorphology of uterus, ovary, and other vital organs and its effective dosage in establishing embryo implantation dysfunction model in Sprague-Dawley (SD) rats. MATERIALS AND METHODS:...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641546/ https://www.ncbi.nlm.nih.gov/pubmed/37964780 http://dx.doi.org/10.1016/j.sjbs.2023.103837 |
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author | Amir, Maria Yimer, Nurhusien Hiew, Mark Yusoff, Sabri Mohd Hussen, Bedru Quddus, Abdul |
author_facet | Amir, Maria Yimer, Nurhusien Hiew, Mark Yusoff, Sabri Mohd Hussen, Bedru Quddus, Abdul |
author_sort | Amir, Maria |
collection | PubMed |
description | BACKGROUND: This study aimed to determine the effects of Indomethacin (IMC) treatment on embryo implantation and histomorphology of uterus, ovary, and other vital organs and its effective dosage in establishing embryo implantation dysfunction model in Sprague-Dawley (SD) rats. MATERIALS AND METHODS: The experiments were performed on 24 (6 × 4 groups) adult female SD rats aged 12 weeks old. G1 was the control group and received a normal diet with normal saline. However, on pregnancy days 3 (Pd3) and 4 (Pd4), G2, G3, and G4 were given normal saline and subcutaneously administered IMC twice daily at different doses of 4.33, 4.66 and 5.00 mg/kg body weight, respectively. The rats were euthanized on day 8 of pregnancy (Pd8). The uterus was excised and examined for signs of pregnancy, followed by tissue samples from liver, kidney, and ovary (for histomorphological examination using haematoxylin and eosin stain). RESULTS: All IMC treatment doses disrupted the implantation process and caused a significant reduction in embryo development. Analysis for histopathological changes revealed that IMC doses above 4.33 mg/kg body weight caused more adverse reproductive health effects in rats. Vasoconstriction and micro vascularization were detected in the liver, while degenerative Bowman's capsules and inflammatory cells were observed in kidney sections from IMC-treated rats. CONCLUSION: IMC therapy interfered with implantation and embryo development in rats, resulting in significant uterine vasoconstriction and atrophy, 4.33 mg/kg bwt dose appeared to be optimum to establish embryo implantation dysfunction in SD rats. |
format | Online Article Text |
id | pubmed-10641546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-106415462023-11-14 Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats Amir, Maria Yimer, Nurhusien Hiew, Mark Yusoff, Sabri Mohd Hussen, Bedru Quddus, Abdul Saudi J Biol Sci Original Article BACKGROUND: This study aimed to determine the effects of Indomethacin (IMC) treatment on embryo implantation and histomorphology of uterus, ovary, and other vital organs and its effective dosage in establishing embryo implantation dysfunction model in Sprague-Dawley (SD) rats. MATERIALS AND METHODS: The experiments were performed on 24 (6 × 4 groups) adult female SD rats aged 12 weeks old. G1 was the control group and received a normal diet with normal saline. However, on pregnancy days 3 (Pd3) and 4 (Pd4), G2, G3, and G4 were given normal saline and subcutaneously administered IMC twice daily at different doses of 4.33, 4.66 and 5.00 mg/kg body weight, respectively. The rats were euthanized on day 8 of pregnancy (Pd8). The uterus was excised and examined for signs of pregnancy, followed by tissue samples from liver, kidney, and ovary (for histomorphological examination using haematoxylin and eosin stain). RESULTS: All IMC treatment doses disrupted the implantation process and caused a significant reduction in embryo development. Analysis for histopathological changes revealed that IMC doses above 4.33 mg/kg body weight caused more adverse reproductive health effects in rats. Vasoconstriction and micro vascularization were detected in the liver, while degenerative Bowman's capsules and inflammatory cells were observed in kidney sections from IMC-treated rats. CONCLUSION: IMC therapy interfered with implantation and embryo development in rats, resulting in significant uterine vasoconstriction and atrophy, 4.33 mg/kg bwt dose appeared to be optimum to establish embryo implantation dysfunction in SD rats. Elsevier 2023-12 2023-10-18 /pmc/articles/PMC10641546/ /pubmed/37964780 http://dx.doi.org/10.1016/j.sjbs.2023.103837 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Amir, Maria Yimer, Nurhusien Hiew, Mark Yusoff, Sabri Mohd Hussen, Bedru Quddus, Abdul Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats |
title | Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats |
title_full | Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats |
title_fullStr | Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats |
title_full_unstemmed | Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats |
title_short | Effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats |
title_sort | effect of indomethacin on embryo implantation and histomorphology of uterus, ovary, kidney, and liver of rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10641546/ https://www.ncbi.nlm.nih.gov/pubmed/37964780 http://dx.doi.org/10.1016/j.sjbs.2023.103837 |
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