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通过19F核磁共振测量用1,2-双(2-氨基-5,6-二氟苯氧基)乙烷-N,N,N',N'-四乙酸负载的灌注兔心脏肌浆网中的游离Ca2+ 。

Measurement of free Ca2+ in sarcoplasmic reticulum in perfused rabbit heart loaded with 1,2-bis(2-amino-5,6-difluorophenoxy)ethane-N,N,N',N'-tetraacetic acid by 19F NMR.

作者信息

Chen W, Steenbergen C, Levy L A, Vance J, London R E, Murphy E

机构信息

Laboratory of Molecular Biophysics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.

出版信息

J Biol Chem. 1996 Mar 29;271(13):7398-403.

PMID:8631764
Abstract

Measurements of free calcium ion concentration in the sarcoplasmic reticulum ([Ca2+]SR) and an evaluation of its relationship to changes in cytosolic free calcium and energy state of the cell, as well as heterogeneity of the SR calcium pool, were performed using 19F NMR in Langendorff perfused rabbit hearts loaded with acetoxymethyl ester of 1,2-bis(2-amino-5,6-difluorophenoxy)ethane-N,N,N',N'-tetraacetic acid. We report a base-line time-average [Ca2+]SR value of 1.5 mM (n = 13) in the beating heart, similar to the value measured at diastole. We further report that [Ca2+]SR decreases by approximately 30% at the start of systole and that there is no evidence of spacial heterogeneity in [Ca2+]SR during the contraction cycle. However, there appears to be a heterogeneous response to SR calcium channel release activator (caffeine) and SR calcium-ATPase inhibitor (cyclopiazonic acid), consistent with studies suggesting that there are subpopulations of SR. Raising cytosolic free calcium by depolarizing the cell with 30 mM extracellular KCl, resulted in an increase in [Ca2+]SR; however, the calcium gradient was unchanged. Lowering cell phosphorylation potential, which would reduce the free energy available for the SR Ca2+-ATPase, leads to a decrease in the calcium gradient across the SR, but this reduced gradient was primarily due to an increase in cytosolic free calcium and not a net release of SR calcium.

摘要

使用19F核磁共振技术,对用1,2-双(2-氨基-5,6-二氟苯氧基)乙烷-N,N,N',N'-四乙酸乙酰氧基甲酯负载的Langendorff灌注兔心脏进行肌浆网中游离钙离子浓度([Ca2+]SR)的测量,并评估其与胞质游离钙变化和细胞能量状态以及肌浆网钙池异质性的关系。我们报告了跳动心脏中基线时间平均[Ca2+]SR值为1.5 mM(n = 13),与舒张期测量值相似。我们进一步报告,在收缩期开始时[Ca2+]SR下降约30%,并且在收缩周期中[Ca2+]SR没有空间异质性的证据。然而,对肌浆网钙通道释放激活剂(咖啡因)和肌浆网钙-ATP酶抑制剂(环匹阿尼酸)似乎存在异质性反应,这与表明存在肌浆网亚群的研究一致。通过用30 mM细胞外KCl使细胞去极化来提高胞质游离钙,导致[Ca2+]SR增加;然而,钙梯度没有变化。降低细胞磷酸化电位,这将减少肌浆网钙-ATP酶可用的自由能,导致跨肌浆网的钙梯度降低,但这种降低的梯度主要是由于胞质游离钙增加,而不是肌浆网钙的净释放。

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