• 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

相似文献

1
Decreased RyR2 refractoriness determines myocardial synchronization of aberrant Ca2+ release in a genetic model of arrhythmia.RyR2 不应期缩短决定了心律失常基因模型中心肌异常钙释放的同步性。
Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):10312-7. doi: 10.1073/pnas.1300052110. Epub 2013 Jun 3.
2
Neuronal Na+ channel blockade suppresses arrhythmogenic diastolic Ca2+ release.神经元钠通道阻滞可抑制致心律失常性舒张期钙释放。
Cardiovasc Res. 2015 Apr 1;106(1):143-52. doi: 10.1093/cvr/cvu262. Epub 2014 Dec 23.
3
In situ confocal imaging in intact heart reveals stress-induced Ca(2+) release variability in a murine catecholaminergic polymorphic ventricular tachycardia model of type 2 ryanodine receptor(R4496C+/-) mutation.在完整心脏中的共聚焦成像揭示了 2 型兰尼碱受体(R4496C+/-)突变型儿茶酚胺多形性室性心动过速小鼠模型中应激诱导的 Ca(2+)释放变异性。
Circ Arrhythm Electrophysiol. 2012 Aug 1;5(4):841-9. doi: 10.1161/CIRCEP.111.969733. Epub 2012 Jun 21.
4
Paradoxical effect of increased diastolic Ca(2+) release and decreased sinoatrial node activity in a mouse model of catecholaminergic polymorphic ventricular tachycardia.儿茶酚胺敏感性多形性室性心动过速小鼠模型中舒张期 Ca(2+)释放增加和窦房结活性降低的矛盾现象。
Circulation. 2012 Jul 24;126(4):392-401. doi: 10.1161/CIRCULATIONAHA.111.075382. Epub 2012 Jun 18.
5
Prevention of ventricular arrhythmia and calcium dysregulation in a catecholaminergic polymorphic ventricular tachycardia mouse model carrying calsequestrin-2 mutation.钙释放通道蛋白 2 突变致儿茶酚胺敏感性多形性室性心动过速小鼠模型中心律失常和钙稳态失衡的预防。
J Cardiovasc Electrophysiol. 2011 Mar;22(3):316-24. doi: 10.1111/j.1540-8167.2010.01877.x. Epub 2010 Aug 30.
6
Phospholamban knockout breaks arrhythmogenic Ca²⁺ waves and suppresses catecholaminergic polymorphic ventricular tachycardia in mice.肌浆网磷蛋白敲除可阻断致心律失常性 Ca²⁺波并抑制小鼠儿茶酚胺敏感性多形性室性心动过速。
Circ Res. 2013 Aug 16;113(5):517-26. doi: 10.1161/CIRCRESAHA.113.301678. Epub 2013 Jul 15.
7
RYR2 Channel Inhibition Is the Principal Mechanism of Flecainide Action in CPVT.RYR2 通道抑制是氟卡尼在 CPVT 中作用的主要机制。
Circ Res. 2021 Feb 5;128(3):321-331. doi: 10.1161/CIRCRESAHA.120.316819. Epub 2020 Dec 10.
8
Short communication: flecainide exerts an antiarrhythmic effect in a mouse model of catecholaminergic polymorphic ventricular tachycardia by increasing the threshold for triggered activity.短篇交流:氟卡尼通过增加触发活动的阈值对儿茶酚胺多形性室性心动过速的小鼠模型发挥抗心律失常作用。
Circ Res. 2011 Jul 22;109(3):291-5. doi: 10.1161/CIRCRESAHA.111.247338. Epub 2011 Jun 16.
9
The cardiac ryanodine receptor luminal Ca2+ sensor governs Ca2+ waves, ventricular tachyarrhythmias and cardiac hypertrophy in calsequestrin-null mice.肌质网ryanodine 受体腔钙传感器调控 calsequestrin 敲除小鼠的钙离子波、室性心律失常和心肌肥厚。
Biochem J. 2014 Jul 1;461(1):99-106. doi: 10.1042/BJ20140126.
10
R4496C RyR2 mutation impairs atrial and ventricular contractility.R4496C型兰尼碱受体2(RyR2)突变损害心房和心室收缩力。
J Gen Physiol. 2016 Jan;147(1):39-52. doi: 10.1085/jgp.201511450. Epub 2015 Dec 14.

引用本文的文献

1
Sexual dimorphism in bidirectional SR-mitochondria crosstalk in ventricular cardiomyocytes.心室肌细胞中双向 SR-线粒体串扰的性别二态性。
Basic Res Cardiol. 2023 May 3;118(1):15. doi: 10.1007/s00395-023-00988-1.
2
Genetic Inhibition of Mitochondrial Permeability Transition Pore Exacerbates Ryanodine Receptor 2 Dysfunction in Arrhythmic Disease.遗传抑制线粒体通透性转换孔加剧心律失常疾病中肌浆网钙释放通道 2 功能障碍。
Cells. 2023 Jan 4;12(2):204. doi: 10.3390/cells12020204.
3
Molecular, Subcellular, and Arrhythmogenic Mechanisms in Genetic RyR2 Disease.基因 RyR2 病的分子、亚细胞和心律失常机制。
Biomolecules. 2022 Jul 26;12(8):1030. doi: 10.3390/biom12081030.
4
Simultaneous imaging of calcium and contraction in the beating heart of zebrafish larvae.斑马鱼幼鱼心跳过程中钙离子和收缩的同步成像。
Theranostics. 2022 Jan 1;12(3):1012-1029. doi: 10.7150/thno.64734. eCollection 2022.
5
MCU overexpression evokes disparate dose-dependent effects on mito-ROS and spontaneous Ca release in hypertrophic rat cardiomyocytes.MCU 过表达在肥厚大鼠心肌细胞中线粒体 ROS 和自发性 Ca 释放方面引起不同的剂量依赖性效应。
Am J Physiol Heart Circ Physiol. 2021 Oct 1;321(4):H615-H632. doi: 10.1152/ajpheart.00126.2021. Epub 2021 Aug 20.
6
Local recovery of cardiac calcium-induced calcium release interrogated by ultra-effective, two-photon uncaging of calcium.利用超效、双光子钙光解技术研究钙诱导钙释放的局部恢复。
J Physiol. 2021 Aug;599(16):3841-3852. doi: 10.1113/JP281482. Epub 2021 Aug 2.
7
Multiphoton Imaging of Ca Instability in Acute Myocardial Slices from a Murine Model of Catecholaminergic Polymorphic Ventricular Tachycardia.儿茶酚胺能多形性室性心动过速小鼠模型急性心肌切片中钙不稳定性的多光子成像
J Clin Med. 2021 Jun 26;10(13):2821. doi: 10.3390/jcm10132821.
8
Recent advances in gene therapy for atrial fibrillation.房颤的基因治疗新进展。
J Cardiovasc Electrophysiol. 2021 Oct;32(10):2854-2864. doi: 10.1111/jce.15116. Epub 2021 Jul 6.
9
Mapping Calcium Dynamics in the Heart of Zebrafish Embryos with Ratiometric Genetically Encoded Calcium Indicators.利用比率型基因编码钙指示剂绘制斑马鱼胚胎心脏中的钙动力学图谱。
Int J Mol Sci. 2020 Sep 10;21(18):6610. doi: 10.3390/ijms21186610.
10
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of -Catecholaminergic Polymorphic Ventricular Tachycardia.《儿茶酚胺多形性室性心动过速的遗传模式、心律失常风险和潜在机制的国际多中心评估》。
Circulation. 2020 Sep 8;142(10):932-947. doi: 10.1161/CIRCULATIONAHA.120.045723. Epub 2020 Jul 22.

本文引用的文献

1
Store-dependent deactivation: cooling the chain-reaction of myocardial calcium signaling.依赖储存的失活:冷却心肌钙信号的连锁反应。
J Mol Cell Cardiol. 2013 May;58:77-83. doi: 10.1016/j.yjmcc.2012.10.008. Epub 2012 Oct 27.
2
Ryanodine receptor current amplitude controls Ca2+ sparks in cardiac muscle.肌质网钙释放通道电流幅度控制心肌内钙离子火花。
Circ Res. 2012 Jun 22;111(1):28-36. doi: 10.1161/CIRCRESAHA.112.265652. Epub 2012 May 24.
3
Shortened Ca2+ signaling refractoriness underlies cellular arrhythmogenesis in a postinfarction model of sudden cardiac death.短缩的 Ca2+ 信号不应期是心肌梗死后心源性猝死模型中细胞心律失常发生的基础。
Circ Res. 2012 Feb 17;110(4):569-77. doi: 10.1161/CIRCRESAHA.111.260455. Epub 2012 Jan 5.
4
Dantrolene prevents arrhythmogenic Ca2+ release in heart failure.丹曲林钠可预防心力衰竭中心律失常性 Ca2+释放。
Am J Physiol Heart Circ Physiol. 2012 Feb 15;302(4):H953-63. doi: 10.1152/ajpheart.00936.2011. Epub 2011 Dec 16.
5
Heart disease and stroke statistics--2012 update: a report from the American Heart Association.《2012年心脏病和中风统计数据更新:美国心脏协会报告》
Circulation. 2012 Jan 3;125(1):e2-e220. doi: 10.1161/CIR.0b013e31823ac046. Epub 2011 Dec 15.
6
Calsequestrin 2 deletion shortens the refractoriness of Ca²⁺ release and reduces rate-dependent Ca²⁺-alternans in intact mouse hearts.肌浆网钙结合蛋白 2 缺失缩短了钙离子释放的不应期,并降低了完整小鼠心脏中的钙震荡的时变依赖性。
J Mol Cell Cardiol. 2012 Jan;52(1):21-31. doi: 10.1016/j.yjmcc.2011.09.020. Epub 2011 Sep 29.
7
NCX is an important determinant for premature ventricular activity in a drug-induced model of Andersen-Tawil syndrome.NCX 是 Andersen-Tawil 综合征药物诱导模型中室性早搏活动的重要决定因素。
Cardiovasc Res. 2011 Oct 1;92(1):57-66. doi: 10.1093/cvr/cvr180. Epub 2011 Jun 21.
8
Recovery of cardiac calcium release is controlled by sarcoplasmic reticulum refilling and ryanodine receptor sensitivity.心肌钙释放的恢复受肌浆网再充盈和兰尼碱受体敏感性的控制。
Cardiovasc Res. 2011 Sep 1;91(4):598-605. doi: 10.1093/cvr/cvr143. Epub 2011 May 24.
9
The relationship between arrhythmogenesis and impaired contractility in heart failure: role of altered ryanodine receptor function.心力衰竭中心律失常与收缩功能障碍的关系:兰尼碱受体功能改变的作用。
Cardiovasc Res. 2011 Jun 1;90(3):493-502. doi: 10.1093/cvr/cvr025. Epub 2011 Jan 27.
10
Synchronization of stochastic Ca²(+) release units creates a rhythmic Ca²(+) clock in cardiac pacemaker cells.随机 Ca²(+) 释放单位的同步在心脏起搏细胞中产生节律性 Ca²(+) 时钟。
Biophys J. 2011 Jan 19;100(2):271-83. doi: 10.1016/j.bpj.2010.11.081.

RyR2 不应期缩短决定了心律失常基因模型中心肌异常钙释放的同步性。

Decreased RyR2 refractoriness determines myocardial synchronization of aberrant Ca2+ release in a genetic model of arrhythmia.

机构信息

D. Davis Heart and Lung Research Institute, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.

出版信息

Proc Natl Acad Sci U S A. 2013 Jun 18;110(25):10312-7. doi: 10.1073/pnas.1300052110. Epub 2013 Jun 3.

DOI:10.1073/pnas.1300052110
PMID:23733959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3690898/
Abstract

Dysregulated intracellular Ca(2+) signaling is implicated in a variety of cardiac arrhythmias, including catecholaminergic polymorphic ventricular tachycardia. Spontaneous diastolic Ca(2+) release (DCR) can induce arrhythmogenic plasma membrane depolarizations, although the mechanism responsible for DCR synchronization among adjacent myocytes required for ectopic activity remains unclear. We investigated the synchronization mechanism(s) of DCR underlying untimely action potentials and diastolic contractions (DCs) in a catecholaminergic polymorphic ventricular tachycardia mouse model with a mutation in cardiac calsequestrin. We used a combination of different approaches including single ryanodine receptor channel recording, optical imaging (Ca(2+) and membrane potential), and contractile force measurements in ventricular myocytes and intact cardiac muscles. We demonstrate that DCR occurs in a temporally and spatially uniform manner in both myocytes and intact myocardial tissue isolated from cardiac calsequestrin mutation mice. Such synchronized DCR events give rise to triggered electrical activity that results in synchronous DCs in the myocardium. Importantly, we establish that synchronization of DCR is a result of a combination of abbreviated ryanodine receptor channel refractoriness and the preceding synchronous stimulated Ca(2+) release/reuptake dynamics. Our study reveals how aberrant DCR events can become synchronized in the intact myocardium, leading to triggered activity and the resultant DCs in the settings of a cardiac rhythm disorder.

摘要

细胞内钙离子信号失调与多种心律失常有关,包括儿茶酚胺多形性室性心动过速。自发性舒张期 Ca(2+)释放(DCR)可引起致心律失常的细胞膜去极化,尽管导致异位活动的相邻心肌细胞中 DCR 同步的机制尚不清楚。我们研究了心脏 calsequestrin 突变的儿茶酚胺多形性室性心动过速小鼠模型中,DCR 下不及时动作电位和舒张收缩(DC)的同步机制。我们使用了包括单个ryanodine 受体通道记录、光学成像(Ca(2+)和膜电位)和心室肌细胞和完整心肌组织的收缩力测量在内的不同方法的组合。我们证明 DCR 在心脏 calsequestrin 突变小鼠的心肌细胞和完整心肌组织中以时间和空间均匀的方式发生。这种同步的 DCR 事件产生触发电活动,导致心肌中的同步 DC。重要的是,我们确定 DCR 的同步是缩短ryanodine 受体通道不应期和先前同步刺激 Ca(2+)释放/摄取动力学的组合的结果。我们的研究揭示了异常的 DCR 事件如何在完整的心肌中同步,导致在心脏节律紊乱的情况下触发活动和随后的 DC。