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六(2-甲氧基异丁基异腈)锝-99m与氯化铊-201:在培养心肌细胞中的摄取与释放

Hexakis (2-methoxy isobutylisonitrile) technetium-99m and thallium-201 chloride: uptake and release in cultured myocardial cells.

作者信息

Maublant J C, Gachon P, Moins N

机构信息

Div. of Nuclear Medicine, Centre Jean Perrin, Clermont-Ferrand, France.

出版信息

J Nucl Med. 1988 Jan;29(1):48-54.

PMID:3335927
Abstract

Hexakis (2-methoxy isobutylisonitrile) technetium-99m [(99mTc]MIBI), a new tracer of myocardial blood flow, was compared with 201TI CI in cultures of myocardial cells of newborn rats. The kinetics of uptake and release of both tracers were assessed in basal conditions and in the presence of 5 mM cyanide, an inhibitor of the respiratory chain, 0.1 mM iodoacetate, an inhibitor of glycolysis, 10 microM ouabain, an inhibitor of the Na-K ATPase, or with various pH values. The amplitude and frequency of contractions of the cells were also monitored in the same conditions. Results show that the washin and washout kinetics of [99mTc]MIBI are slower than 201TI(T1/2) of the washout curves were, respectively, of 28 min and 6 min). The kinetics of release of both tracers were not influenced by any of the inhibitors. There was a strong effect of the pH on the 201TI uptake only. Moreover 201TI uptake was decreased by 34% in the presence of cyanide plus iodoacetate. Otherwise the uptakes of 201TI and [99mTc]MIBI were not decreased by any of the drugs. The cellular contractility was significantly diminished by cyanide and it was abolished by cyanide plus iodoacetate. It is concluded that (a) impaired contractility can be associated with normal 201TI and [99mTc]MIBI kinetics in myocardial cells in culture, (b) that 201TI uptake may depend on the level of ATP devoted to the maintenance of membrane integrity, (c) that [99mTc]MIBI shows slower kinetics but is less sensitive to metabolic inhibitors than 201TI.

摘要

六甲基异丁基异腈-锝99m[(99mTc)MIBI],一种新型心肌血流示踪剂,在新生大鼠心肌细胞培养物中与铊201(201TI)进行了比较。在基础条件下以及存在5 mM氰化物(呼吸链抑制剂)、0.1 mM碘乙酸盐(糖酵解抑制剂)、10 microM哇巴因(钠钾ATP酶抑制剂)或不同pH值的情况下,评估了两种示踪剂的摄取和释放动力学。在相同条件下还监测了细胞收缩的幅度和频率。结果表明,[99mTc]MIBI的洗入和洗出动力学比201TI慢(洗出曲线的T1/2分别为28分钟和6分钟)。两种示踪剂的释放动力学均不受任何抑制剂的影响。pH值仅对201TI的摄取有强烈影响。此外,在氰化物加碘乙酸盐存在的情况下,201TI摄取降低了34%。否则,201TI和[99mTc]MIBI的摄取均未因任何药物而降低。氰化物显著降低了细胞收缩力,而氰化物加碘乙酸盐则使其消失。结论是:(a)在培养的心肌细胞中,收缩力受损可能与正常的201TI和[99mTc]MIBI动力学相关;(b)201TI摄取可能取决于用于维持膜完整性的ATP水平;(c)[99mTc]MIBI显示出较慢的动力学,但比201TI对代谢抑制剂的敏感性更低。

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