Goreisan通过调节ICAT-β-catenin/ERK轴,减轻HFD/L-NAME诱导的保留射血分数心衰患者心脏肥厚和舒张功能障碍。

IF 4.6 2区 医学 Q1 PERIPHERAL VASCULAR DISEASE
Yoko Shojima Isayama, Shouji Matsushima, Keisuke Shinohara, Koichi Isayama, Nobuyuki Enzan, Taishi Yamamoto, Masashi Sada, Ryo Miyake, Yoshitomo Tsutsui, Takayuki Toyohara, Ryohei Nishimura, Yuki Ikeda, Eri Noda, Wataru Otsuru, Shuya Tokumoto, Masatsugu Watanabe, Masataka Ikeda, Toru Hashimoto, Shintaro Kinugawa, Hiroyuki Tsutsui, Kohtaro Abe
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引用次数: 0

摘要

以心脏肥厚和舒张功能障碍为特征的保留射血分数心力衰竭(HFpEF)在世界范围内日益增加。葛丽珊(GRS)是一种传统的草药配方;其成分减轻心肌细胞肥大。本研究旨在探讨GRS对HFpEF病理生理的影响。高脂肪饮食(HFD, 60%脂肪)和n -硝基-L-精氨酸甲基lester (L- name,饮用水中0.5 g/L)增加了C57BL/6小鼠的心肺重量,GRS (5.9 mg/kcal)减少了它们,但血压没有变化。GRS可减轻HFD/ l - name引起的左室壁厚度和舒张功能障碍指标E/A和E/E′的增加。GRS降低HFD/ l - name处理小鼠心肌细胞横截面积。在机制上,它抑制了HFD/ l- name处理心脏中丝裂原活化蛋白激酶(MAPKs)的磷酸化,如细胞外信号调节激酶(ERK)。此外,液相色谱/质谱分析显示心脏中HFD/L-NAME降低,GRS增加73个蛋白。其中,GRS可抑制HFD/ l - name诱导的心肌肥厚负调节因子β-catenin和t细胞因子(ICAT)抑制剂的降低。与此一致的是,ICAT靶标β-catenin表现出相反的变化。在体外实验中,GRS直接降低异丙肾上腺素(ISO)处理的心肌细胞中β-catenin,并伴有心肌细胞表面积的减少。ICAT的过表达也抑制了iso诱导的β-连环蛋白、磷酸化ERK和心肌细胞表面积的增加。在GRS成分中,肉桂醛和茴香醇b23 -醋酸酯可减弱iso诱导的β-连环蛋白和心肌细胞表面积的增加。综上所述,GRS通过ICAT-β-catenin/ERK轴减轻心肌肥厚和舒张功能障碍。GRS是治疗HFpEF的潜在草药配方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Goreisan attenuates cardiac hypertrophy and diastolic dysfunction in heart failure with preserved ejection fraction induced by HFD/L-NAME via regulation of ICAT-β-catenin/ERK axis.

Heart failure with preserved ejection fraction (HFpEF), characterized by cardiac hypertrophy and diastolic dysfunction, is increasing worldwide. Goreisan (GRS) is a traditional herbal formulation; its component attenuates cardiomyocyte hypertrophy. This study aimed to investigate the effect of GRS on the pathophysiology of HFpEF. Administration of a high fat diet (HFD, 60% fat) and N-nitro-L-arginine methylester (L-NAME, 0.5 g/L in drinking water) increased heart and lung weights in C57BL/6 mice and GRS (5.9 mg/kcal) reduced them without changes in blood pressure. GRS attenuated HFD/L-NAME-induced increases in left ventricular wall thickness and E/A and E/E', indices of diastolic dysfunction. GRS decreased cardiomyocyte cross-sectional area in HFD/L-NAME-treated mice. Mechanistically, it suppressed the phosphorylation of mitogen-activated protein kinases (MAPKs), such as extracellular signal-regulated kinase (ERK), in HFD/L-NAME-treated hearts. In addition, liquid chromatography/mass spectrometry demonstrated that HFD/L-NAME decreased and GRS increased 73 proteins in the heart. Among them, GRS prevented HFD/L-NAME-induced decrease in inhibitor of β-catenin and T-cell factor (ICAT), a negative regulator of cardiac hypertrophy. Consistently, β-catenin, an ICAT target, exhibited the opposite change. In in vitro experiments, GRS directly decreased β-catenin in isoproterenol (ISO)-treated cardiomyocytes, accompanied by a decrease in cardiomyocyte surface area. Overexpression of ICAT also suppressed ISO-induced increases in β-catenin, phosphorylated ERK, and cardiomyocyte surface area. Among GRS ingredients, cinnamaldehyde and alisol B 23-acetate attenuated ISO-induced increases in β-catenin and cardiomyocyte surface area. In conclusion, GRS attenuates cardiac hypertrophy and diastolic dysfunction via ICAT-β-catenin/ERK axis. GRS is a potential herbal formulation for the treatment of HFpEF.

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来源期刊
Hypertension Research
Hypertension Research 医学-外周血管病
CiteScore
7.40
自引率
16.70%
发文量
249
审稿时长
3-8 weeks
期刊介绍: Hypertension Research is the official publication of the Japanese Society of Hypertension. The journal publishes papers reporting original clinical and experimental research that contribute to the advancement of knowledge in the field of hypertension and related cardiovascular diseases. The journal publishes Review Articles, Articles, Correspondence and Comments.
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