• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

慢性间歇性低强度经皮迷走神经耳支电刺激可改善心肌梗死愈合的清醒犬左心室重构。

Chronic intermittent low-level transcutaneous electrical stimulation of auricular branch of vagus nerve improves left ventricular remodeling in conscious dogs with healed myocardial infarction.

作者信息

Wang Zhuo, Yu Lilei, Wang Songyun, Huang Bing, Liao Kai, Saren Gaowa, Tan Tuantuan, Jiang Hong

机构信息

From the Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Circ Heart Fail. 2014 Nov;7(6):1014-21. doi: 10.1161/CIRCHEARTFAILURE.114.001564. Epub 2014 Oct 20.

DOI:10.1161/CIRCHEARTFAILURE.114.001564
PMID:25332149
Abstract

BACKGROUND

Vagus nerve stimulation attenuates left ventricular (LV) remodeling after myocardial infarction (MI). Our previous study found a noninvasive approach to deliver vagus nerve stimulation by transcutaneous electric stimulation of auricular branch of vagus nerve. So we hypothesize that chronic intermittent low-level tragus stimulation (LL-TS) could attenuate LV remodeling in conscious dogs with healed MI.

METHODS AND RESULTS

Thirty beagle dogs were randomly divided into 3 groups, MI group (left anterior descending artery and major diagonal branches ligation to introduce MI, n=10), LL-TS group (MI plus chronic intermittent LL-TS, n=10), and control group (sham surgery without stimulation, n=10). Tragus stimulation was delivered to bilateral tragus with ear-clips connected to a custom-made stimulator. The voltage slowing sinus rate was used as the threshold for setting LL-TS at 80% below that. LL-TS group was given 4 hours stimulation at 7-9 am and 4-6 pm on conscious dogs. At the end of 90-day follow-up, LL-TS group significantly reduced LA and LV dilatation, improved LV contractile and diastolic function, reduced infarct size by ≈50% compared with MI group. LL-TS treatment alleviated cardiac fibrosis and significantly decreased protein expression level of collagen I, collagen III, transforming growth factor β1, and matrix metallopeptidase 9 in LV tissues. The plasma level of high-specific C-reactive protein, norepinephrine, N-terminal pro-B-type-natriuretic peptide in LL-TS group was significantly lower than those in MI group from the 7th day to the end of follow-up.

CONCLUSIONS

Chronic intermittent low-level transcutaneous electric stimulation of auricular branch of vagus nerve can attenuate LV remodeling in conscious dogs with healed MI.

摘要

背景

迷走神经刺激可减轻心肌梗死(MI)后的左心室(LV)重构。我们之前的研究发现了一种通过经皮电刺激迷走神经耳支来进行迷走神经刺激的非侵入性方法。因此,我们假设慢性间歇性低强度耳屏刺激(LL-TS)可减轻心肌梗死愈合的清醒犬的左心室重构。

方法与结果

30只比格犬随机分为3组,心肌梗死组(结扎左前降支和主要对角支以诱导心肌梗死,n = 10),LL-TS组(心肌梗死加慢性间歇性LL-TS,n = 10),对照组(假手术不刺激,n = 10)。通过连接到定制刺激器的耳夹对双侧耳屏进行刺激。将使窦性心率减慢的电压作为阈值,将LL-TS设置为低于该阈值80%。LL-TS组在清醒犬上午7 - 9点和下午4 - 6点给予4小时刺激。在90天随访结束时,与心肌梗死组相比,LL-TS组显著减轻了左心房和左心室扩张,改善了左心室收缩和舒张功能,梗死面积缩小约5​​0%。LL-TS治疗减轻了心脏纤维化,并显著降低了左心室组织中I型胶原、III型胶原、转化生长因子β1和基质金属蛋白酶9的蛋白表达水平。从第7天到随访结束时,LL-TS组的高特异性C反应蛋白、去甲肾上腺素、N末端B型利钠肽原的血浆水平显著低于心肌梗死组。

结论

慢性间歇性经皮电刺激迷走神经耳支可减轻心肌梗死愈合的清醒犬的左心室重构。

相似文献

1
Chronic intermittent low-level transcutaneous electrical stimulation of auricular branch of vagus nerve improves left ventricular remodeling in conscious dogs with healed myocardial infarction.慢性间歇性低强度经皮迷走神经耳支电刺激可改善心肌梗死愈合的清醒犬左心室重构。
Circ Heart Fail. 2014 Nov;7(6):1014-21. doi: 10.1161/CIRCHEARTFAILURE.114.001564. Epub 2014 Oct 20.
2
Low-level transcutaneous electrical stimulation of the auricular branch of vagus nerve ameliorates left ventricular remodeling and dysfunction by downregulation of matrix metalloproteinase 9 and transforming growth factor β1.迷走神经耳支的低强度经皮电刺激通过下调基质金属蛋白酶9和转化生长因子β1改善左心室重构和功能障碍。
J Cardiovasc Pharmacol. 2015 Apr;65(4):342-8. doi: 10.1097/FJC.0000000000000201.
3
Low-level transcutaneous electrical stimulation of the auricular branch of the vagus nerve: a noninvasive approach to treat the initial phase of atrial fibrillation.低强度经皮迷走神经耳支电刺激:一种治疗心房颤动初始期的非侵入性方法。
Heart Rhythm. 2013 Mar;10(3):428-35. doi: 10.1016/j.hrthm.2012.11.019. Epub 2012 Nov 24.
4
Non-invasive tragus stimulation improves cardiac post-ischemic remodeling by regulating cardiac parasympathetic activity.无创耳甲刺激通过调节心脏副交感神经活性改善缺血后心脏重构。
ESC Heart Fail. 2022 Dec;9(6):4129-4138. doi: 10.1002/ehf2.14146. Epub 2022 Sep 9.
5
Low-Level Tragus Stimulation for the Treatment of Ischemia and Reperfusion Injury in Patients With ST-Segment Elevation Myocardial Infarction: A Proof-of-Concept Study.低位耳屏刺激治疗 ST 段抬高型心肌梗死患者的缺血再灌注损伤:概念验证研究。
JACC Cardiovasc Interv. 2017 Aug 14;10(15):1511-1520. doi: 10.1016/j.jcin.2017.04.036.
6
Chronic Intermittent Low-Level Stimulation of Tragus Reduces Cardiac Autonomic Remodeling and Ventricular Arrhythmia Inducibility in a Post-Infarction Canine Model.慢性间歇性低强度刺激耳屏可减轻心肌梗死后犬模型的心脏自主神经重塑和室性心律失常的易感性。
JACC Clin Electrophysiol. 2016 Jun;2(3):330-339. doi: 10.1016/j.jacep.2015.11.006. Epub 2015 Dec 9.
7
Atrial Fibrillation in Acute Obstructive Sleep Apnea: Autonomic Nervous Mechanism and Modulation.急性阻塞性睡眠呼吸暂停中的心房颤动:自主神经机制与调节。
J Am Heart Assoc. 2017 Sep 13;6(9):e006264. doi: 10.1161/JAHA.117.006264.
8
Left-sided Noninvasive Vagus Nerve Stimulation Suppresses Atrial Fibrillation by Upregulating Atrial Gap Junctions in Canines.左侧非侵入性迷走神经刺激通过上调犬心房缝隙连接抑制心房颤动。
J Cardiovasc Pharmacol. 2015 Dec;66(6):593-9. doi: 10.1097/FJC.0000000000000309.
9
Chronic vagus nerve stimulation improves left ventricular function in a canine model of chronic mitral regurgitation.慢性迷走神经刺激可改善慢性二尖瓣反流犬模型的左心室功能。
J Transl Med. 2014 Nov 4;12:302. doi: 10.1186/s12967-014-0302-2.
10
Low-Level Vagus Nerve Stimulation Attenuates Myocardial Ischemic Reperfusion Injury by Antioxidative Stress and Antiapoptosis Reactions in Canines.低水平迷走神经刺激通过抗氧化应激和抗凋亡反应减轻犬心肌缺血再灌注损伤
J Cardiovasc Electrophysiol. 2016 Feb;27(2):224-31. doi: 10.1111/jce.12850. Epub 2015 Nov 6.

引用本文的文献

1
The efficacy of transcutaneous vagus nerve stimulation in heart failure management - a systematic review and meta-analysis.经皮迷走神经刺激在心力衰竭管理中的疗效——一项系统评价和荟萃分析。
BMC Cardiovasc Disord. 2025 Jul 4;25(1):481. doi: 10.1186/s12872-025-04919-x.
2
Pocking the Ear for HFpEF?通过掏耳朵来诊断射血分数保留的心力衰竭?
Cardiovasc Drugs Ther. 2025 Apr 30. doi: 10.1007/s10557-025-07712-2.
3
Recent advances in targeting obesity, with a focus on TGF-β signaling and vagus nerve innervation.针对肥胖症的最新进展,重点关注转化生长因子-β信号传导和迷走神经支配。
Bioelectron Med. 2025 Apr 30;11(1):10. doi: 10.1186/s42234-025-00172-x.
4
Acute right-sided transcutaneous vagus nerve stimulation improves cardio-vagal baroreflex gain in patients with chronic heart failure.急性右侧经皮迷走神经刺激可改善慢性心力衰竭患者的心肺迷走神经压力反射增益。
Clin Auton Res. 2025 Feb;35(1):75-85. doi: 10.1007/s10286-024-01074-9. Epub 2024 Oct 14.
5
Research hotspots and trends of non-invasive vagus nerve stimulation: a bibliometric analysis from 2004 to 2023.非侵入性迷走神经刺激的研究热点与趋势:2004年至2023年的文献计量分析
Front Neurol. 2024 Sep 19;15:1429506. doi: 10.3389/fneur.2024.1429506. eCollection 2024.
6
Vagal nerve stimulation in myocardial ischemia/reperfusion injury: from bench to bedside.迷走神经刺激在心肌缺血/再灌注损伤中的应用:从实验台到临床应用
Bioelectron Med. 2024 Sep 13;10(1):22. doi: 10.1186/s42234-024-00153-6.
7
Highly-stable, injectable, conductive hydrogel for chronic neuromodulation.用于慢性神经调节的高稳定、可注射、导电水凝胶。
Nat Commun. 2024 Sep 12;15(1):7993. doi: 10.1038/s41467-024-52418-y.
8
Treating heart failure by targeting the vagus nerve.通过靶向迷走神经治疗心力衰竭。
Heart Fail Rev. 2024 Nov;29(6):1201-1215. doi: 10.1007/s10741-024-10430-w. Epub 2024 Aug 9.
9
The protective role of vagus nerve stimulation in ischemia-reperfusion injury.迷走神经刺激在缺血再灌注损伤中的保护作用。
Heliyon. 2024 May 9;10(10):e30952. doi: 10.1016/j.heliyon.2024.e30952. eCollection 2024 May 30.
10
Transcutaneous auricular vagus nerve stimulation as a novel therapy connecting the central and peripheral systems: a review.经皮耳迷走神经刺激作为一种连接中枢和外周系统的新型治疗方法:综述。
Int J Surg. 2024 Aug 1;110(8):4993-5006. doi: 10.1097/JS9.0000000000001592.