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通关丸通过调节凋亡和纤维化通路减轻阿霉素和异丙肾上腺素诱导的心肌肥厚和纤维化。

TongGuanWan Alleviates Doxorubicin- and Isoproterenol-Induced Cardiac Hypertrophy and Fibrosis by Modulating Apoptotic and Fibrotic Pathways.

机构信息

Hanbang Cardio-Renal Syndrome Research Center, Wonkwang University, 460, Iksan-daero, Iksan 54538, Republic of Korea.

College of Oriental Medicine and Professional Graduate School of Oriental Medicine, Wonkwang University, 460, Iksan-daero, Iksan 54538, Republic of Korea.

出版信息

Int J Mol Sci. 2024 Sep 30;25(19):10573. doi: 10.3390/ijms251910573.

DOI:10.3390/ijms251910573
PMID:39408900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11476530/
Abstract

Heart failure, a major public health issue, often stems from prolonged stress or damage to the heart muscle, leading to cardiac hypertrophy. This can progress to heart failure and other cardiovascular problems. Doxorubicin (DOX), a common chemotherapy drug, and isoproterenol (ISO), a β-adrenergic agonist, both induce cardiac hypertrophy through different mechanisms. This study investigates TongGuanWan (TGW,), a traditional herbal remedy, for its effects on cardiac hypertrophy and fibrosis in DOX-induced H9c2 cells and ISO-induced mouse models. TGW was found to counteract DOX-induced increases in H9c2 cell surface area ( = 8, < 0.01) and improve biomarkers like ANP ( = 3, < 0.01)) and BNP ( = 3, < 0.01). It inhibited the MAPK pathway ( = 4, < 0.01) and GATA-4/calcineurin/NFAT-3 signaling, reduced inflammation by decreasing NF-κB p65 translocation, and enhanced apoptosis-related factors such as caspase-3 ( = 3, < 0.01), caspase-9 ( = 3, < 0.01), Bax ( = 3, < 0.01), and Bcl-2 ( = 3, < 0.01). Flow cytometry showed TGW reduced apoptotic cell populations. In vivo, TGW reduced heart ( = 810, < 0.01), and left ventricle weights ( = 67), cardiac hypertrophy markers ( = 3, < 0.01), and perivascular fibrosis in ISO-induced mice, with Western blot analysis confirming decreased levels of fibrosis-related factors like fibronectin, α-SMA ( = 3, < 0.05), and collagen type I ( = 3, < 0.05). These findings suggest TGW has potential as a therapeutic option for cardiac hypertrophy and fibrosis.

摘要

心力衰竭是一个主要的公共卫生问题,通常源于心肌的长期压力或损伤,导致心肌肥厚。这可能会发展为心力衰竭和其他心血管问题。多柔比星(DOX)是一种常用的化疗药物,异丙肾上腺素(ISO)是一种β-肾上腺素能激动剂,它们通过不同的机制诱导心肌肥厚。本研究探讨了通冠丸(TGW)作为一种传统的草药疗法,对 DOX 诱导的 H9c2 细胞和 ISO 诱导的小鼠模型中心肌肥厚和纤维化的影响。研究发现,TGW 可以对抗 DOX 诱导的 H9c2 细胞表面积增加( = 8, < 0.01),并改善心钠肽(ANP)( = 3, < 0.01)和脑钠肽(BNP)( = 3, < 0.01)等生物标志物。它抑制了 MAPK 途径( = 4, < 0.01)和 GATA-4/钙调神经磷酸酶/NFAT-3 信号,通过减少 NF-κB p65 易位减少炎症,并增强凋亡相关因子,如半胱天冬酶-3( = 3, < 0.01)、半胱天冬酶-9( = 3, < 0.01)、Bax( = 3, < 0.01)和 Bcl-2( = 3, < 0.01)。流式细胞术显示 TGW 减少了凋亡细胞群。在体内,TGW 降低了 ISO 诱导的小鼠心脏( = 810, < 0.01)和左心室重量( = 67)、心肌肥厚标志物( = 3, < 0.01)和血管周围纤维化,Western blot 分析证实纤维化相关因子如纤连蛋白、α-SMA( = 3, < 0.05)和 I 型胶原( = 3, < 0.05)的水平降低。这些发现表明 TGW 可能是治疗心肌肥厚和纤维化的一种选择。

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