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心脏/肌肉特异性锰超氧化物歧化酶缺陷小鼠的心脏电生理改变:膳食抗氧化多酚的预防作用

Cardiac electrophysiological alterations in heart/muscle-specific manganese-superoxide dismutase-deficient mice: prevention by a dietary antioxidant polyphenol.

作者信息

Sunagawa Tadahiro, Shimizu Takahiko, Matsumoto Akio, Tagashira Motoyuki, Kanda Tomomasa, Shirasawa Takuji, Nakaya Haruaki

机构信息

Research Laboratories for Applied Technology of Food, Asahi Group Holdings, Ltd., Moriya, Ibaraki 302-0106, Japan ; Molecular Gerontology, Tokyo Metropolitan Institute of Gerontology, Itabashi-ku, Tokyo 173-0015, Japan.

Molecular Gerontology, Tokyo Metropolitan Institute of Gerontology, Itabashi-ku, Tokyo 173-0015, Japan ; Department of Advanced Aging Medicine, Chiba University Graduate School of Medicine, Chuo-ku, Chiba 260-8670, Japan.

出版信息

Biomed Res Int. 2014;2014:704291. doi: 10.1155/2014/704291. Epub 2014 Mar 19.

DOI:10.1155/2014/704291
PMID:24772433
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3977505/
Abstract

Cardiac electrophysiological alterations induced by chronic exposure to reactive oxygen species and protective effects of dietary antioxidant have not been thoroughly examined. We recorded surface electrocardiograms (ECG) and evaluated cellular electrophysiological abnormalities in enzymatically-dissociated left ventricular (LV) myocytes in heart/muscle-specific manganese-superoxide dismutase-deficient (H/M-Sod2(-/-)) mice, which exhibit dilated cardiomyopathy due to increased oxidative stress. We also investigated the influences of intake of apple polyphenols (AP) containing mainly procyanidins with potent antioxidant activity. The QRS and QT intervals of ECG recorded in H/M-Sod2(-/-) mice were prolonged. The effective refractory period in the LV myocardium of H/M-Sod2(-/-) mice was prolonged, and susceptibility to ventricular tachycardia or fibrillation induced by rapid ventricular pacing was increased. Action potential duration in H/M-Sod2(-/-) LV myocytes was prolonged, and automaticity was enhanced. The density of the inwardly rectifier K(+) current (I K1) was decreased in the LV cells of H/M-Sod2(-/-) mice. The AP intake partially improved these electrophysiological alterations and extended the lifespan in H/M-Sod2(-/-) mice. Thus, chronic exposure of the heart to oxidative stress produces a variety of electrophysiological abnormalities, increased susceptibility to ventricular arrhythmias, and action potential changes associated with the reduced density of I K1. Dietary intake of antioxidant nutrients may prevent oxidative stress-induced electrophysiological disturbances.

摘要

长期暴露于活性氧所诱发的心脏电生理改变以及膳食抗氧化剂的保护作用尚未得到充分研究。我们记录了心脏/肌肉特异性锰超氧化物歧化酶缺陷(H/M-Sod2(-/-))小鼠的体表心电图(ECG),并评估了酶解离的左心室(LV)心肌细胞中的细胞电生理异常,这些小鼠由于氧化应激增加而表现出扩张型心肌病。我们还研究了主要含有具有强大抗氧化活性的原花青素的苹果多酚(AP)摄入的影响。H/M-Sod2(-/-)小鼠记录的ECG的QRS和QT间期延长。H/M-Sod2(-/-)小鼠LV心肌的有效不应期延长,快速心室起搏诱发室性心动过速或颤动的易感性增加。H/M-Sod2(-/-) LV心肌细胞的动作电位时程延长,自律性增强。H/M-Sod2(-/-)小鼠LV细胞内向整流钾电流(I K1)密度降低。AP摄入部分改善了这些电生理改变,并延长了H/M-Sod2(-/-)小鼠的寿命。因此,心脏长期暴露于氧化应激会产生各种电生理异常、室性心律失常易感性增加以及与I K1密度降低相关的动作电位变化。膳食摄入抗氧化营养素可能预防氧化应激诱导的电生理紊乱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/db7a78e72cb8/BMRI2014-704291.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/3156867f5af6/BMRI2014-704291.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/c40138862015/BMRI2014-704291.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/1dd600508422/BMRI2014-704291.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/f37c5f0f85bb/BMRI2014-704291.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/b006efef7fda/BMRI2014-704291.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/db7a78e72cb8/BMRI2014-704291.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/3156867f5af6/BMRI2014-704291.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/c40138862015/BMRI2014-704291.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/1dd600508422/BMRI2014-704291.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/f37c5f0f85bb/BMRI2014-704291.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/b006efef7fda/BMRI2014-704291.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b7/3977505/db7a78e72cb8/BMRI2014-704291.006.jpg

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