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肌浆网Ca2+转运的瞬态动力学。心肌与骨骼肌的比较。

Transient kinetics of Ca2+ transport of sarcoplasmic reticulum. A comparison of cardiac and skeletal muscle.

作者信息

Sumida M, Wang T, Mandel F, Froehlich J P, Schwartz A

出版信息

J Biol Chem. 1978 Dec 25;253(24):8772-7.

PMID:721812
Abstract

Current evidence supports similar functions and mechanisms for cardiac sarcoplasmic reticulum (CSR) as for skeletal sarcoplasmic reticulum (SSR). It is thought that the slower relaxation rate of cardiac muscle compared to fast skeletal muscle reflects the lower ATPase activity and calcium transport of CSR. Possible quantitative differences is phosphorylation, dephosphorylation, and calcium transport of the isolated preparations are studied using a quench-flow apparatus. The results show that both CSR and SSR bind calcium tightly in the absence of ATP, and coupling of E approximately P formation and calcium transport occurs in the transient phase of ATP hydrolysis. The rate of phosphorylation (t-1/2 - 10 ms) of sarcoplasmic reticulum (SR) preloaded with calcium is the same for cardiac and skeletal preparations. However, the rates of dissociation of extra vesicular calcium (10 s-1 versus 15 s-1), phosphorylation of calcium-free SR, and dephosphorylation of E approximately P (8 s-1 versus 12 s-1) are lower for CSR than for SSR. By computer simulation, the apparent rate constants associated with the reduced rates of phosphorylation of calcium-free SR were: 12 s-1 for CSR and 63 s-1 for SSR in the presence of high Mg2+. The difference in the rates may be partly responsible for the lower levels of ATPase and calcium transport activity with characterize cardiac muscle preparations.

摘要

目前的证据支持心脏肌浆网(CSR)与骨骼肌肌浆网(SSR)具有相似的功能和机制。据认为,与快速骨骼肌相比,心肌较慢的舒张速率反映了CSR较低的ATP酶活性和钙转运能力。使用淬灭流动装置研究了分离制剂在磷酸化、去磷酸化和钙转运方面可能存在的定量差异。结果表明,在没有ATP的情况下,CSR和SSR都能紧密结合钙,并且在ATP水解的瞬态阶段发生E~P形成与钙转运的偶联。预加载钙的肌浆网(SR)的磷酸化速率(t-1/2 - 10毫秒)在心脏和骨骼肌制剂中是相同的。然而,CSR的细胞外钙解离速率(10 s-1对15 s-1)、无钙SR的磷酸化速率以及E~P的去磷酸化速率(8 s-1对12 s-1)均低于SSR。通过计算机模拟,在高Mg2+存在下,与无钙SR磷酸化速率降低相关的表观速率常数为:CSR为12 s-1,SSR为63 s-1。速率差异可能部分导致了心肌制剂中ATP酶和钙转运活性水平较低。

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