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脑心通/PPAR信号通路通过激活自噬抑制心肌肥大。

Naoxintong/PPAR Signaling Inhibits Cardiac Hypertrophy via Activation of Autophagy.

作者信息

Yuan Shuping, Jin Jianhua, Chen Lu, Hou Yongzhong, Wang Hong

机构信息

Institute of Life Sciences, Jiangsu University, Zhenjiang, Jiangsu 212013, China.

Department of Oncology, Affiliated Wujin People's Hospital, Jiangsu University, Changzhou 212017, China.

出版信息

Evid Based Complement Alternat Med. 2017;2017:3801976. doi: 10.1155/2017/3801976. Epub 2017 Feb 15.

DOI:10.1155/2017/3801976
PMID:28293264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5331281/
Abstract

As a traditional Chinese medicine, Naoxintong capsule (NXT) has been approved by China Food and Drug Administration (CFDA), which is used for cardiocerebrovascular disease treatment. Here we found that NXT extract significantly promoted H9c2 cardiomyocyte cell autophagy involved in increased autophagy-associated gene expression leading to inhibition of mTOR signaling. Moreover, NXT extract increased PPAR protein expression and transcription activity of H9c2 cell. Consistent with this, in PPAR gene silenced H9c2 cells, NXT had no effect on autophagy and mTOR signaling. Furthermore, NXT/PPAR-mediated H9c2 autophagy led to inhibition of cardiomyocyte cell hypertrophy. These findings suggest that the extract of NXT inhibited H9c2 cardiomyocyte cell hypertrophy via PPAR-mediated cell autophagy.

摘要

作为一种传统中药,脑心通胶囊(NXT)已获中国食品药品监督管理总局(CFDA)批准,用于治疗心脑血管疾病。在此我们发现,NXT提取物显著促进H9c2心肌细胞自噬,这涉及自噬相关基因表达增加,进而导致mTOR信号传导受到抑制。此外,NXT提取物增加了H9c2细胞的PPAR蛋白表达和转录活性。与此一致的是,在PPAR基因沉默的H9c2细胞中,NXT对自噬和mTOR信号传导没有影响。此外,NXT/PPAR介导的H9c2自噬导致心肌细胞肥大受到抑制。这些发现表明,NXT提取物通过PPAR介导的细胞自噬抑制H9c2心肌细胞肥大。

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本文引用的文献

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Naoxintong/PPARα Signaling Inhibits H9c2 Cell Apoptosis and Autophagy in Response to Oxidative Stress.脑心通/PPARα信号通路抑制H9c2细胞在氧化应激反应中的凋亡和自噬。
Evid Based Complement Alternat Med. 2016;2016:4370381. doi: 10.1155/2016/4370381. Epub 2016 Sep 7.
2
Identification of "Multiple Components-Multiple Targets-Multiple Pathways" Associated with Naoxintong Capsule in the Treatment of Heart Diseases Using UPLC/Q-TOF-MS and Network Pharmacology.基于超高效液相色谱/四极杆飞行时间质谱联用技术和网络药理学的脑心通胶囊治疗心脏病“多成分-多靶点-多通路”机制研究
Evid Based Complement Alternat Med. 2016;2016:9468087. doi: 10.1155/2016/9468087. Epub 2016 Mar 31.
3
Front Pharmacol. 2024 Jun 27;15:1402763. doi: 10.3389/fphar.2024.1402763. eCollection 2024.
4
polysaccharides attenuates pressure-overload-induced pathological cardiac hypertrophy.多糖可减轻压力超负荷诱导的病理性心脏肥大。
Front Pharmacol. 2023 Mar 23;14:1127123. doi: 10.3389/fphar.2023.1127123. eCollection 2023.
5
Evaluation of the anti-inflammatory and antioxidant pharmcodynamic compoents of naoxintong capsules as a basis of broad spectrum effects.脑心通胶囊抗炎、抗氧化药效物质基础及多效作用评价。
Pharm Biol. 2021 Dec;59(1):242-251. doi: 10.1080/13880209.2020.1870506.
6
attenuates Ang II-induced pathological cardiac hypertrophy via upregulating peroxisome proliferator-activated receptors gamma.通过上调过氧化物酶体增殖物激活受体γ减轻血管紧张素II诱导的病理性心脏肥大。
Ann Transl Med. 2020 Sep;8(17):1064. doi: 10.21037/atm-20-2118.
7
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