同型半胱氨酸硫内酯心脏毒性作用的器官型组织培养研究。

Ekaterina V Lopatina, A V Kipenko, V A Penniyaynen, N A Pasatetskaya, D Djuric, B V Krylov
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引用次数: 5

摘要

经证实,同型半胱氨酸硫内酯在7 × 10- 9 -1 × 10⁻³浓度下,以剂量依赖的方式抑制10-12日龄鸡胚胎心脏组织外植体的生长。同型半胱氨酸硫内酯的最大心脏毒性作用在1 × 10⁻³M,这对应于严重的高同型半胱氨酸血症。在含有同型半胱氨酸硫内酯(1 × 10⁻m3)和华巴因的培养基中培养心脏组织外植体,以调节Na +、K + - atp酶的信号转导(1 × 10⁻m3)和泵送(1 × 10⁻m3)功能的实验结果表明,同型半胱氨酸硫内酯的心脏毒性作用可能是由于抑制了Na +、K + - atp酶的泵送功能。
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Organotypic tissue culture investigation of homocysteine thiolactone cardiotoxic effect.

Homocysteine thiolactone was demonstrated to inhibit the growth of 10-12-day-old chicken embryo cardiac tissue explants at 7 × 10⁻⁹ -1 × 10⁻³ M concentrations in a dose-dependent manner. The maximal cardiotoxic effect of homocysteine thiolactone was detected at 1 × 10⁻³ M, which corresponds to severe hyperhomocysteinemia. The results of experiments on culturing of cardiac tissue explants in the medium containing homocysteine thiolactone (1 × 10⁻³ M) and ouabain at concentrations regulating the signal-transducing (1 × 10⁻¹⁰ M) and pumping (1 × 10⁻⁸ M) functions of Na⁺,K⁺ -ATPase indicate that the cardiotoxic effect of homocysteine thiolactone is supposed to result from inhibition of the Na⁺,K⁺ -ATPase pumping function.

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来源期刊
Acta physiologica Hungarica
Acta physiologica Hungarica 医学-生理学
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