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Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals

The traditional Chinese herb Lonicerae Japonicae Flos has shown significant clinical benefits in the treatment of heart failure, but the mechanism remains unclear. As the main active ingredient found in the plasma after oral administration of Lonicerae Japonicae Flos, chlorogenic acid (CGA) has been...

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Autores principales: Tian, Lei, Su, Cong‐Ping, Wang, Qing, Wu, Fu‐Jian, Bai, Rui, Zhang, Hui‐Min, Liu, Jin‐Ying, Lu, Wen‐Jing, Wang, Wei, Lan, Feng, Guo, Shu‐Zhen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584503/
https://www.ncbi.nlm.nih.gov/pubmed/31033175
http://dx.doi.org/10.1111/jcmm.14351
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author Tian, Lei
Su, Cong‐Ping
Wang, Qing
Wu, Fu‐Jian
Bai, Rui
Zhang, Hui‐Min
Liu, Jin‐Ying
Lu, Wen‐Jing
Wang, Wei
Lan, Feng
Guo, Shu‐Zhen
author_facet Tian, Lei
Su, Cong‐Ping
Wang, Qing
Wu, Fu‐Jian
Bai, Rui
Zhang, Hui‐Min
Liu, Jin‐Ying
Lu, Wen‐Jing
Wang, Wei
Lan, Feng
Guo, Shu‐Zhen
author_sort Tian, Lei
collection PubMed
description The traditional Chinese herb Lonicerae Japonicae Flos has shown significant clinical benefits in the treatment of heart failure, but the mechanism remains unclear. As the main active ingredient found in the plasma after oral administration of Lonicerae Japonicae Flos, chlorogenic acid (CGA) has been reported to possess anti‐inflammatory, anti‐oxidant and anti‐apoptosis function. We firstly confirmed the cardioprotective effects of CGA in transverse aortic constriction (TAC)‐induced heart failure mouse model, through mitigating the TNF‐α–induced toxicity. We further used TNF‐α‐induced cardiac injury in human induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs) to elucidate the underlying mechanisms. CGA pre‐treatment could reverse TNF‐α–induced cellular injuries, including improved cell viability, increased mitochondrial membrane potential and inhibited cardiomyocytes apoptosis. We then examined the NF‐κB/p65 and major mitogen‐activated protein kinases (MAPKs) signalling pathways involved in TNF‐α–induced apoptosis of hiPSC‐CMs. Importantly, CGA can directly inhibit NF‐κB signal by suppressing the phosphorylation of NF‐κB/p65. As for the MAPKs, CGA suppressed the activity of only c‐Jun N‐terminal kinase (JNK), but enhanced extracellular signal‐regulated kinase1/2 (ERK1/2) and had no effect on p38. In summary, our study revealed that CGA has profound cardioprotective effects through inhibiting the activation of NF‐κB and JNK pathway, providing a novel therapeutic alternative for prevention and treatment of heart failure.
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spelling pubmed-65845032019-07-01 Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals Tian, Lei Su, Cong‐Ping Wang, Qing Wu, Fu‐Jian Bai, Rui Zhang, Hui‐Min Liu, Jin‐Ying Lu, Wen‐Jing Wang, Wei Lan, Feng Guo, Shu‐Zhen J Cell Mol Med Original Articles The traditional Chinese herb Lonicerae Japonicae Flos has shown significant clinical benefits in the treatment of heart failure, but the mechanism remains unclear. As the main active ingredient found in the plasma after oral administration of Lonicerae Japonicae Flos, chlorogenic acid (CGA) has been reported to possess anti‐inflammatory, anti‐oxidant and anti‐apoptosis function. We firstly confirmed the cardioprotective effects of CGA in transverse aortic constriction (TAC)‐induced heart failure mouse model, through mitigating the TNF‐α–induced toxicity. We further used TNF‐α‐induced cardiac injury in human induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs) to elucidate the underlying mechanisms. CGA pre‐treatment could reverse TNF‐α–induced cellular injuries, including improved cell viability, increased mitochondrial membrane potential and inhibited cardiomyocytes apoptosis. We then examined the NF‐κB/p65 and major mitogen‐activated protein kinases (MAPKs) signalling pathways involved in TNF‐α–induced apoptosis of hiPSC‐CMs. Importantly, CGA can directly inhibit NF‐κB signal by suppressing the phosphorylation of NF‐κB/p65. As for the MAPKs, CGA suppressed the activity of only c‐Jun N‐terminal kinase (JNK), but enhanced extracellular signal‐regulated kinase1/2 (ERK1/2) and had no effect on p38. In summary, our study revealed that CGA has profound cardioprotective effects through inhibiting the activation of NF‐κB and JNK pathway, providing a novel therapeutic alternative for prevention and treatment of heart failure. John Wiley and Sons Inc. 2019-04-29 2019-07 /pmc/articles/PMC6584503/ /pubmed/31033175 http://dx.doi.org/10.1111/jcmm.14351 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Tian, Lei
Su, Cong‐Ping
Wang, Qing
Wu, Fu‐Jian
Bai, Rui
Zhang, Hui‐Min
Liu, Jin‐Ying
Lu, Wen‐Jing
Wang, Wei
Lan, Feng
Guo, Shu‐Zhen
Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals
title Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals
title_full Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals
title_fullStr Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals
title_full_unstemmed Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals
title_short Chlorogenic acid: A potent molecule that protects cardiomyocytes from TNF‐α–induced injury via inhibiting NF‐κB and JNK signals
title_sort chlorogenic acid: a potent molecule that protects cardiomyocytes from tnf‐α–induced injury via inhibiting nf‐κb and jnk signals
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6584503/
https://www.ncbi.nlm.nih.gov/pubmed/31033175
http://dx.doi.org/10.1111/jcmm.14351
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