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绿原酸:一种有效分子,通过抑制 NF-κB 和 JNK 信号通路来保护心肌细胞免受 TNF-α诱导的损伤。

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

机构信息

School of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.

Beijing Laboratory for Cardiovascular Precision Medicine, Anzhen Hospital, Capital Medical University, Beijing, China.

出版信息

J Cell Mol Med. 2019 Jul;23(7):4666-4678. doi: 10.1111/jcmm.14351. Epub 2019 Apr 29.

DOI:10.1111/jcmm.14351
PMID:31033175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6584503/
Abstract

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.

摘要

传统中药金银花在治疗心力衰竭方面显示出显著的临床益处,但作用机制尚不清楚。作为金银花口服给药后在血浆中发现的主要活性成分,绿原酸(CGA)已被报道具有抗炎、抗氧化和抗细胞凋亡的功能。我们首先通过减轻 TNF-α 诱导的毒性,证实了 CGA 在主动脉缩窄(TAC)诱导的心力衰竭小鼠模型中的心脏保护作用。我们进一步使用 TNF-α 诱导的人诱导多能干细胞衍生的心肌细胞(hiPSC-CMs)中的心脏损伤来阐明潜在的机制。CGA 预处理可以逆转 TNF-α 诱导的细胞损伤,包括提高细胞活力、增加线粒体膜电位和抑制心肌细胞凋亡。然后,我们检查了参与 TNF-α 诱导的 hiPSC-CMs 凋亡的 NF-κB/p65 和主要丝裂原活化蛋白激酶(MAPKs)信号通路。重要的是,CGA 可以通过抑制 NF-κB/p65 的磷酸化直接抑制 NF-κB 信号。对于 MAPKs,CGA 仅抑制 c-Jun N 端激酶(JNK)的活性,而增强细胞外信号调节激酶 1/2(ERK1/2),对 p38 没有影响。总之,我们的研究表明,CGA 通过抑制 NF-κB 和 JNK 通路的激活具有深刻的心脏保护作用,为心力衰竭的预防和治疗提供了一种新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/9e8302069468/JCMM-23-4666-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/ea75074289b7/JCMM-23-4666-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/db8d057ca067/JCMM-23-4666-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/035912f0b7fe/JCMM-23-4666-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/d97c632846c4/JCMM-23-4666-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/f8caf754ae80/JCMM-23-4666-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/0e7e5468f960/JCMM-23-4666-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/cea5cf032c7d/JCMM-23-4666-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/9e8302069468/JCMM-23-4666-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/ea75074289b7/JCMM-23-4666-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/db8d057ca067/JCMM-23-4666-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/035912f0b7fe/JCMM-23-4666-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/d97c632846c4/JCMM-23-4666-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/f8caf754ae80/JCMM-23-4666-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/0e7e5468f960/JCMM-23-4666-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/cea5cf032c7d/JCMM-23-4666-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dac/6584503/9e8302069468/JCMM-23-4666-g008.jpg

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