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| Natura: | Artículo científico |
| Lingua: | en |
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Free radical biology & medicine
2025
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| Accesso online: | https://pubmed.ncbi.nlm.nih.gov/40451467/ |
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| author | Li, Zhaoqing Chen, Ruolan Qin, Luning Xu, Xiaojian Wang, Xuezhe Zhang, Guoliang Liu, Zhijun Wang, Banghui Li, Bing Chu, Xian-Ming |
| author_facet | Li, Zhaoqing Chen, Ruolan Qin, Luning Xu, Xiaojian Wang, Xuezhe Zhang, Guoliang Liu, Zhijun Wang, Banghui Li, Bing Chu, Xian-Ming Li, Zhaoqing Chen, Ruolan Qin, Luning Xu, Xiaojian Wang, Xuezhe Zhang, Guoliang Liu, Zhijun Wang, Banghui Li, Bing Chu, Xian-Ming |
| collection | PubMed - marine biology |
| contents | The peptide from C- Phycocyanin alleviates myocardial ischemia-reperfusion injury by suppressing ferroptosis via upregulating UCHL3. Li, Zhaoqing Chen, Ruolan Qin, Luning Xu, Xiaojian Wang, Xuezhe Zhang, Guoliang Liu, Zhijun Wang, Banghui Li, Bing Chu, Xian-Ming Animals Myocardial Reperfusion Injury Mice Ferroptosis Male Oxidative Stress Myocytes, Cardiac Phycocyanin Mice, Inbred C57BL Reactive Oxygen Species Rats Cell Line Up-Regulation Antioxidants Myocardial Infarction Myocardial ischemia-reperfusion injury (MIRI) constitutes an essential hurdle following reperfusion therapy for acute myocardial infarction (AMI), which the mechanism involves oxidative stress, inflammatory response, calcium overload, and ferroptosis, etc. MAQAAEYYR (P2), a kind of marine-derived bioactive peptide from C-Phycocyanin (C-PC), exhibits remarkable antioxidant properties. Due to its low molecular weight, P2 exhibits superior bioavailability compared to C-PC. A previous study has confirmed that C-PC could alleviate ischemia-reperfusion (I/R)-induced cardiac dysfunction. However, whether the peptide derived from C-PC has the potential to protect the heart against ischemia-reperfusion injury deserves consideration and investigation. In this study, C57BL/6 male mice and H9C2 cardiomyocytes were used to construct myocardial ischemia-reperfusion (MI/R) and oxygen-glucose deprivation/reoxygenation (OGD/R) injury models in vivo and in vitro respectively. We demonstrated that P2 significantly improved myocardial function, myocardial enzymes, myocardial fibrosis, and mitochondrial ultrastructure, while mitigating oxidative stress damage and ferroptosis caused by MI/R. In vitro, P2 markedly enhanced cell viability, suppressed the generation of reactive oxygen species (ROS) and malondialdehyde (MDA), elevated glutathione (GSH) and superoxide dismutase (SOD) levels, and prevented the occurrence of ferroptosis. Furthermore, we revealed that ubiquitin carboxyl terminal hydrolase L3 (UCHL3) knockdown reversed the protective effect of P2 against OGD/R-induced cardiomyocyte ferroptosis. This study demonstrated that P2 protects the myocardium against ischemia-reperfusion injury and mitigates ferroptosis by upregulating UCHL3. It provides a foundation for the potential application prospects of marine-derived bioactive peptides in cardiovascular disease management. |
| format | Artículo científico |
| id | pubmed_40451467 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | Free radical biology & medicine |
| record_format | pubmed |
| spellingShingle | The peptide from C- Phycocyanin alleviates myocardial ischemia-reperfusion injury by suppressing ferroptosis via upregulating UCHL3. Li, Zhaoqing Chen, Ruolan Qin, Luning Xu, Xiaojian Wang, Xuezhe Zhang, Guoliang Liu, Zhijun Wang, Banghui Li, Bing Chu, Xian-Ming Animals Myocardial Reperfusion Injury Mice Ferroptosis Male Oxidative Stress Myocytes, Cardiac Phycocyanin Mice, Inbred C57BL Reactive Oxygen Species Rats Cell Line Up-Regulation Antioxidants Myocardial Infarction The peptide from C- Phycocyanin alleviates myocardial ischemia-reperfusion injury by suppressing ferroptosis via upregulating UCHL3. Li, Zhaoqing Chen, Ruolan Qin, Luning Xu, Xiaojian Wang, Xuezhe Zhang, Guoliang Liu, Zhijun Wang, Banghui Li, Bing Chu, Xian-Ming Animals Myocardial Reperfusion Injury Mice Ferroptosis Male Oxidative Stress Myocytes, Cardiac Phycocyanin Mice, Inbred C57BL Reactive Oxygen Species Rats Cell Line Up-Regulation Antioxidants Myocardial Infarction Myocardial ischemia-reperfusion injury (MIRI) constitutes an essential hurdle following reperfusion therapy for acute myocardial infarction (AMI), which the mechanism involves oxidative stress, inflammatory response, calcium overload, and ferroptosis, etc. MAQAAEYYR (P2), a kind of marine-derived bioactive peptide from C-Phycocyanin (C-PC), exhibits remarkable antioxidant properties. Due to its low molecular weight, P2 exhibits superior bioavailability compared to C-PC. A previous study has confirmed that C-PC could alleviate ischemia-reperfusion (I/R)-induced cardiac dysfunction. However, whether the peptide derived from C-PC has the potential to protect the heart against ischemia-reperfusion injury deserves consideration and investigation. In this study, C57BL/6 male mice and H9C2 cardiomyocytes were used to construct myocardial ischemia-reperfusion (MI/R) and oxygen-glucose deprivation/reoxygenation (OGD/R) injury models in vivo and in vitro respectively. We demonstrated that P2 significantly improved myocardial function, myocardial enzymes, myocardial fibrosis, and mitochondrial ultrastructure, while mitigating oxidative stress damage and ferroptosis caused by MI/R. In vitro, P2 markedly enhanced cell viability, suppressed the generation of reactive oxygen species (ROS) and malondialdehyde (MDA), elevated glutathione (GSH) and superoxide dismutase (SOD) levels, and prevented the occurrence of ferroptosis. Furthermore, we revealed that ubiquitin carboxyl terminal hydrolase L3 (UCHL3) knockdown reversed the protective effect of P2 against OGD/R-induced cardiomyocyte ferroptosis. This study demonstrated that P2 protects the myocardium against ischemia-reperfusion injury and mitigates ferroptosis by upregulating UCHL3. It provides a foundation for the potential application prospects of marine-derived bioactive peptides in cardiovascular disease management. |
| title | The peptide from C- Phycocyanin alleviates myocardial ischemia-reperfusion injury by suppressing ferroptosis via upregulating UCHL3. |
| topic | Animals Myocardial Reperfusion Injury Mice Ferroptosis Male Oxidative Stress Myocytes, Cardiac Phycocyanin Mice, Inbred C57BL Reactive Oxygen Species Rats Cell Line Up-Regulation Antioxidants Myocardial Infarction |
| url | https://pubmed.ncbi.nlm.nih.gov/40451467/ |