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一种间苯三酚单宁提取物对阿霉素诱导的大鼠模型心脏毒性的心脏保护作用

Cardioprotective Effects of a Phlorotannin Extract Against Doxorubicin-Induced Cardiotoxicity in a Rat Model.

作者信息

Ahn Hyo-Suk, Lee Dong-Hyeon, Kim Tae-Jung, Shin Hyeon-Cheol, Jeon Hui-Kyung

机构信息

1 Division of Cardiology, Department of Internal Medicine, The Catholic University of Korea, Uijeongbu St. Mary's Hospital , Uijeongbu, Korea.

2 Division of Cardiology, Department of Internal Medicine, The Catholic University of Korea, Seoul St. Mary's Hospital , Seoul, Korea.

出版信息

J Med Food. 2017 Oct;20(10):944-950. doi: 10.1089/jmf.2017.3919. Epub 2017 Aug 17.

DOI:10.1089/jmf.2017.3919
PMID:28816580
Abstract

Long-term therapy with doxorubicin (DOX) is associated with high incidence of cumulative and irreversible dilated cardiomyopathy. The goal of this study was to evaluate the cardioprotective effects and safety of a phlorotannin extract from a brown algae Ecklonia cava (Seapolynol™, SPN) against DOX-induced cardiotoxicity in a rat model. A total of 42 rats were divided into six groups: control, low-dose SPN (LDS), high-dose SPN (HDS), DOX, DOX with low-dose SPN (DOX+LDS), and DOX with high-dose SPN (DOX+HDS). Echocardiography was performed at baseline and after 6 weeks. In left ventricular (LV) ejection fraction, DOX and DOX+LDS groups showed significant decreases (P < .001), while LDS, HDS, and DOX+HDS groups showed no significant change compared with control group. In LV mass index, DOX and DOX+LDS groups showed significant increases (P < .001 and P = .013), while LDS, HDS, and DOX+HDS groups showed no significant change compared with control group. In electron microscopy of the LV wall tissue, DOX+HDS group showed markedly less impaired myofibrils and mitochondria compared with both DOX and DOX+LDS groups. On the findings in echocardiography and electron microscopy, 6-week oral administration of SPN was safe and cardioprotective in a DOX-induced rat cardiotoxicity model in a dose-dependent manner.

摘要

长期使用阿霉素(DOX)治疗会导致累积性和不可逆性扩张型心肌病的高发病率。本研究的目的是评估一种从褐藻海蕴中提取的间苯三酚单宁(Seapolynol™,SPN)对大鼠模型中DOX诱导的心脏毒性的心脏保护作用和安全性。总共42只大鼠被分为六组:对照组、低剂量SPN组(LDS)、高剂量SPN组(HDS)、DOX组、DOX与低剂量SPN联合组(DOX+LDS)以及DOX与高剂量SPN联合组(DOX+HDS)。在基线和6周后进行超声心动图检查。在左心室(LV)射血分数方面,DOX组和DOX+LDS组显著降低(P < 0.001),而LDS组、HDS组和DOX+HDS组与对照组相比无显著变化。在LV质量指数方面,DOX组和DOX+LDS组显著增加(P < 0.001和P = 0.013),而LDS组、HDS组和DOX+HDS组与对照组相比无显著变化。在LV壁组织的电子显微镜检查中,与DOX组和DOX+LDS组相比,DOX+HDS组的肌原纤维和线粒体受损明显较少。基于超声心动图和电子显微镜的结果,在DOX诱导的大鼠心脏毒性模型中,6周口服SPN以剂量依赖的方式具有安全性和心脏保护作用。

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