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存活和非存活心肌细胞对底物氧化的贡献。

Contribution of viable and nonviable heart myocytes to substrate oxidation.

作者信息

Long W M, Bagby G J, Spitzer J J

出版信息

Am J Physiol. 1980 May;238(5):H740-4. doi: 10.1152/ajpheart.1980.238.5.H740.

DOI:10.1152/ajpheart.1980.238.5.H740
PMID:7377369
Abstract

An approach is described that allows metabolic data obtained from a mixture of vital dye-excluding (T-) and nonexcluding (T+) myocytes to be extrapolated to a homogeneous cell population. Myocytes from adult dog hearts were dispersed by enzymatic treatment and separated into two fractions: one containing predominantly T-, and the other containing predominately T+ cells. Measuring the oxidation rate and viability of each fraction allows the determination of the rate of oxidation of a homogeneous cell population when palmitate, glucose, or lactate is the oxidizable substrate. The calculated rate of oxidation of these substrates by 100% T- cells was: 0.15, 0.46, and 2.99 nmol . mg protein-1 . min-1, respectively. Oxidation of palmitate and lactate by T+ cells was one-fifth of the T-cell rate. Glucose oxidation of T+ cells was not significantly different from zero. Use of this procedure will permit study of myocardial metabolism when experimental procedures may cause altered cell viability.

摘要

本文描述了一种方法,该方法可将从活力染料排斥(T-)和非排斥(T+)心肌细胞混合物中获得的代谢数据外推至同质细胞群体。成年犬心脏的心肌细胞经酶处理后分散,并分为两部分:一部分主要包含T-细胞,另一部分主要包含T+细胞。测量每一部分的氧化速率和活力,可确定以棕榈酸、葡萄糖或乳酸作为可氧化底物时同质细胞群体的氧化速率。计算得出,100% T-细胞对这些底物的氧化速率分别为:0.15、0.46和2.99 nmol·mg蛋白-1·min-1。T+细胞对棕榈酸和乳酸的氧化速率是T-细胞的五分之一。T+细胞对葡萄糖的氧化与零无显著差异。当实验操作可能导致细胞活力改变时,使用该程序将有助于研究心肌代谢。

相似文献

1
Contribution of viable and nonviable heart myocytes to substrate oxidation.存活和非存活心肌细胞对底物氧化的贡献。
Am J Physiol. 1980 May;238(5):H740-4. doi: 10.1152/ajpheart.1980.238.5.H740.
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Exogenous substrate utilization in Ca2+-tolerant myocytes from adult rat hearts.成年大鼠心脏耐钙心肌细胞中外源底物的利用
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Relation between cytosolic free Ca2+ concentration and the control of pyruvate dehydrogenase in isolated cardiac myocytes.离体心肌细胞中胞质游离钙离子浓度与丙酮酸脱氢酶调控之间的关系
Biochem J. 1987 Jan 1;241(1):145-51. doi: 10.1042/bj2410145.