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本文引用的文献

1
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.
2
Local control in cardiac E-C coupling.心脏电偶联中的局部控制。
J Mol Cell Cardiol. 2012 Feb;52(2):298-303. doi: 10.1016/j.yjmcc.2011.04.014. Epub 2011 May 14.
3
Dynamic calcium movement inside cardiac sarcoplasmic reticulum during release.心脏肌浆网内钙离子的动态运动在释放过程中。
Circ Res. 2011 Apr 1;108(7):847-56. doi: 10.1161/CIRCRESAHA.111.240234. Epub 2011 Feb 10.
4
Complex and rate-dependent beat-to-beat variations in Ca2+ transients of canine Purkinje cells.犬浦肯野细胞钙离子瞬变的复杂且速率依赖的拍间变化。
J Mol Cell Cardiol. 2011 Apr;50(4):662-9. doi: 10.1016/j.yjmcc.2010.12.023. Epub 2011 Jan 11.
5
Alternans and arrhythmias: from cell to heart.交替和心律失常:从细胞到心脏。
Circ Res. 2011 Jan 7;108(1):98-112. doi: 10.1161/CIRCRESAHA.110.223586.
6
Quarky calcium release in the heart.心脏中的点状钙释放。
Circ Res. 2011 Jan 21;108(2):210-8. doi: 10.1161/CIRCRESAHA.110.231258. Epub 2010 Dec 9.
7
Dyssynchrony of Ca2+ release from the sarcoplasmic reticulum as subcellular mechanism of cardiac contractile dysfunction.肌浆网钙离子释放不同步作为心肌收缩功能障碍的亚细胞机制。
J Mol Cell Cardiol. 2011 Mar;50(3):390-400. doi: 10.1016/j.yjmcc.2010.11.008. Epub 2010 Nov 12.
8
Numerical analysis of Ca2+ signaling in rat ventricular myocytes with realistic transverse-axial tubular geometry and inhibited sarcoplasmic reticulum.具有真实的横向轴管状几何形状和抑制的肌浆网的大鼠心室肌细胞中 Ca2+信号的数值分析。
PLoS Comput Biol. 2010 Oct 28;6(10):e1000972. doi: 10.1371/journal.pcbi.1000972.
9
Spontaneous Ca2+ sparks and Ca2+ homeostasis in a minimal model of permeabilized ventricular myocytes.在渗透的心室肌细胞的最小模型中,自发的 Ca2+火花和 Ca2+动态平衡。
Am J Physiol Heart Circ Physiol. 2010 Dec;299(6):H1996-2008. doi: 10.1152/ajpheart.00293.2010. Epub 2010 Sep 17.
10
Na+ currents are required for efficient excitation-contraction coupling in rabbit ventricular myocytes: a possible contribution of neuronal Na+ channels.钠离子电流对于兔心室肌细胞有效的兴奋-收缩耦联是必需的:神经元钠离子通道的一种可能贡献。
J Physiol. 2010 Nov 1;588(Pt 21):4249-60. doi: 10.1113/jphysiol.2010.194688.

肌浆网钙离子的动态局部变化:生理和病理生理作用。

Dynamic local changes in sarcoplasmic reticulum calcium: physiological and pathophysiological roles.

机构信息

Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, New York, NY, USA.

出版信息

J Mol Cell Cardiol. 2012 Feb;52(2):304-11. doi: 10.1016/j.yjmcc.2011.06.024. Epub 2011 Jul 13.

DOI:10.1016/j.yjmcc.2011.06.024
PMID:21767546
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3217160/
Abstract

Evidence obtained in recent years indicates that, in cardiac myocytes, release of Ca(2+) from the sarcoplasmic reticulum (SR) is regulated by changes in the concentration of Ca(2+) within the SR. In this review, we summarize recent advances in our understanding of this regulatory role, with a particular emphasis on dynamic and local changes in SR [Ca(2+)]. We focus on five important questions that are to some extent unresolved and controversial. These questions concern: (1) the importance of SR [Ca(2+)] depletion in the termination of Ca(2+) release; (2) the quantitative extent of depletion during local release events such as Ca(2+) sparks; (3) the influence of SR [Ca(2+)] refilling on release refractoriness and the propensity for pathological Ca(2+) release; (4) dynamic changes in SR [Ca(2+)] during propagating Ca(2+) waves; and (5) the speed of Ca(2+) diffusion within the SR. With each issue, we discuss data supporting alternative viewpoints, and we identify fundamental questions that are being actively investigated. We conclude with a discussion of experimental and computational advances that will help to resolve controversies. This article is part of a special issue entitled "Local Signaling in Myocytes."

摘要

近年来的证据表明,在心肌细胞中,肌浆网 (SR) 中 Ca(2+) 的释放受 SR 内 Ca(2+) 浓度变化的调节。在这篇综述中,我们总结了对这种调节作用的最新理解进展,特别强调了 SR [Ca(2+)] 的动态和局部变化。我们重点关注了五个在某种程度上尚未解决且存在争议的重要问题。这些问题涉及:(1) SR [Ca(2+)] 耗竭在终止 Ca(2+) 释放中的重要性;(2) 局部释放事件(如 Ca(2+) 火花)期间的耗竭程度;(3) SR [Ca(2+)] 再填充对释放不应期和病理性 Ca(2+) 释放倾向的影响;(4) 传播 Ca(2+) 波期间 SR [Ca(2+)] 的动态变化;以及 (5) SR 内 Ca(2+) 的扩散速度。对于每个问题,我们讨论了支持替代观点的数据,并确定了正在积极研究的基本问题。最后,我们讨论了有助于解决争议的实验和计算进展。本文是题为“心肌细胞中的局部信号转导”的特刊的一部分。