V1-Cal hydrogelation enhances its effects on ventricular remodeling reduction and cardiac function improvement post myocardial infarction

Myocardial infarction (MI) is a major cause of disability and mortality worldwide. A cell permeable peptide V1-Cal has shown remarkable therapeutic effects on ML However, using V1-Cal to improve long-term cardiac function after MI is presently limited by its short half-life. Herein, we co-assembled...

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Publié dans:Chemical engineering journal (Lausanne, Switzerland : 1996). - 1999. - 433(2022), Pt 1 vom: 01. Apr.
Auteur principal: Wang, Bin (Auteur)
Autres auteurs: Wu, Chengfan, He, Shufang, Wang, Yaguang, Wang, Di, Tao, Hui, Wang, Chenchen, Pang, Xiaoxi, Li, Fei, Yuan, Yue, Gross, Eric R, Liang, Gaolin, Zhang, Ye
Format: Article en ligne
Langue:English
Publié: 2022
Accès à la collection:Chemical engineering journal (Lausanne, Switzerland : 1996)
Sujets:Journal Article Myocardial infarction Supramolecular hydrogel Sustained release TRPV1 V1-Cal
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520 |a Myocardial infarction (MI) is a major cause of disability and mortality worldwide. A cell permeable peptide V1-Cal has shown remarkable therapeutic effects on ML However, using V1-Cal to improve long-term cardiac function after MI is presently limited by its short half-life. Herein, we co-assembled V1-Cal with a well-known hydrogelator Nap-Phe-Phe-Tyr (NapFFY) to obtain a new supramolecular hydrogel V1-Cal/NapFFY. We found that the hydrogel could significantly enhance the therapeutic effects of V1-Cal on ventricular remodeling reduction and cardiac function improvement in a myocardial infarction rat model. In vitro experiments indicated that co-assembly of V1-Cal with NapFFY significantly increased mechanic strength of the hydrogel, enabling a sustained release of V1-Cal for more than two weeks. In vivo experiments supported that sustained release of V1-Cal from V1-Cal/NapFFY hydrogel could effectively decrease the expression and activation of TRPV1, reduce apoptosis and the release of inflammatory factors in a MI rat model. In particular, V1-Cal/NapFFY hydrogel significantly decreased infarct size and fibrosis, while improved cardiac function 28 days post MI. We anticipate that V1-Cal/NapFFY hydrogel could be used clinically to treat MI in the near future 
650 4 |a Journal Article 
650 4 |a Myocardial infarction 
650 4 |a Supramolecular hydrogel 
650 4 |a Sustained release 
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650 4 |a V1-Cal 
700 1 |a Wu, Chengfan  |e verfasserin  |4 aut 
700 1 |a He, Shufang  |e verfasserin  |4 aut 
700 1 |a Wang, Yaguang  |e verfasserin  |4 aut 
700 1 |a Wang, Di  |e verfasserin  |4 aut 
700 1 |a Tao, Hui  |e verfasserin  |4 aut 
700 1 |a Wang, Chenchen  |e verfasserin  |4 aut 
700 1 |a Pang, Xiaoxi  |e verfasserin  |4 aut 
700 1 |a Li, Fei  |e verfasserin  |4 aut 
700 1 |a Yuan, Yue  |e verfasserin  |4 aut 
700 1 |a Gross, Eric R  |e verfasserin  |4 aut 
700 1 |a Liang, Gaolin  |e verfasserin  |4 aut 
700 1 |a Zhang, Ye  |e verfasserin  |4 aut 
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