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Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway
Geniposide (GEN), a medical herb, is known for its therapeutic applications in cardiovascular diseases, though its efficacy in treating myocardial ischemia/reperfusion injury (MI/RI) is yet to be fully elucidated. This study is an endeavor to explore the potential protective mechanism of GEN against...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518652/ https://www.ncbi.nlm.nih.gov/pubmed/37682077 http://dx.doi.org/10.4081/ejh.2023.3742 |
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author | Yao, Yanmei Lin, Leqing Tang, Wenxue Shen, Yueliang Chen, Fayu Li, Ning Wang, Baiyong |
author_facet | Yao, Yanmei Lin, Leqing Tang, Wenxue Shen, Yueliang Chen, Fayu Li, Ning Wang, Baiyong |
author_sort | Yao, Yanmei |
collection | PubMed |
description | Geniposide (GEN), a medical herb, is known for its therapeutic applications in cardiovascular diseases, though its efficacy in treating myocardial ischemia/reperfusion injury (MI/RI) is yet to be fully elucidated. This study is an endeavor to explore the potential protective mechanism of GEN against MI/RI. To simulate the MI/RI condition, the left anterior descending artery was occluded for 30 min, followed by a reperfusion period of 120 min in a rat model. Three dosages (50, 100, or 150 mg/kg) of GEN were intraperitoneally injected to the Sprague-Dawley rats once a day, for seven days before the ligation of the artery. The rats were categorized into sham group, MI/RI group, and three different dosages GEN-treated groups. As the results showed, the pretreatment with GEN mitigated myocardial injury, reduced infarct volume, inhibited apoptosis, enhanced superoxide dismutase activity, and decreased malondialdehyde and myeloperoxidase activity, as well as serum creatine kinase-MB and lactate dehydrogenase levels. Moreover, GEN ameliorated MI/RI by downregulating protein expression of toll-like receptor 4, myeloid differentiation primary response 88, and p-nuclear factor-κB. In conclusion, the pretreatment of GEN may be considered as a potential therapeutic option for MI/RI. |
format | Online Article Text |
id | pubmed-10518652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-105186522023-09-26 Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway Yao, Yanmei Lin, Leqing Tang, Wenxue Shen, Yueliang Chen, Fayu Li, Ning Wang, Baiyong Eur J Histochem Article Geniposide (GEN), a medical herb, is known for its therapeutic applications in cardiovascular diseases, though its efficacy in treating myocardial ischemia/reperfusion injury (MI/RI) is yet to be fully elucidated. This study is an endeavor to explore the potential protective mechanism of GEN against MI/RI. To simulate the MI/RI condition, the left anterior descending artery was occluded for 30 min, followed by a reperfusion period of 120 min in a rat model. Three dosages (50, 100, or 150 mg/kg) of GEN were intraperitoneally injected to the Sprague-Dawley rats once a day, for seven days before the ligation of the artery. The rats were categorized into sham group, MI/RI group, and three different dosages GEN-treated groups. As the results showed, the pretreatment with GEN mitigated myocardial injury, reduced infarct volume, inhibited apoptosis, enhanced superoxide dismutase activity, and decreased malondialdehyde and myeloperoxidase activity, as well as serum creatine kinase-MB and lactate dehydrogenase levels. Moreover, GEN ameliorated MI/RI by downregulating protein expression of toll-like receptor 4, myeloid differentiation primary response 88, and p-nuclear factor-κB. In conclusion, the pretreatment of GEN may be considered as a potential therapeutic option for MI/RI. PAGEPress Publications, Pavia, Italy 2023-09-08 /pmc/articles/PMC10518652/ /pubmed/37682077 http://dx.doi.org/10.4081/ejh.2023.3742 Text en Copyright © 2023, the Author(s) https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution NonCommercial 4.0 License (CC BY-NC 4.0). |
spellingShingle | Article Yao, Yanmei Lin, Leqing Tang, Wenxue Shen, Yueliang Chen, Fayu Li, Ning Wang, Baiyong Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway |
title | Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway |
title_full | Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway |
title_fullStr | Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway |
title_full_unstemmed | Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway |
title_short | Pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tLr4/NF-κb pathway |
title_sort | pretreatment with geniposide mitigates myocardial ischemia/reperfusion injury by modulating inflammatory response through tlr4/nf-κb pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518652/ https://www.ncbi.nlm.nih.gov/pubmed/37682077 http://dx.doi.org/10.4081/ejh.2023.3742 |
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