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镉对大鼠肝线粒体中琥珀酸和NADH相关底物氧化的影响。

The effects of cadmium on succinate and NADH-linked substrate oxidations in rat hepatic mitochondria.

作者信息

Cameron I, McNamee P M, Markham A, Morgan R M, Wood M

出版信息

J Appl Toxicol. 1986 Oct;6(5):325-30. doi: 10.1002/jat.2550060505.

Abstract

Low concentrations of cadmium (3.3-40 microM) inhibited State 3 NADH-linked respiration in rat hepatic mitochondria, but failed to release oligomycin (1 microgram) inhibited State 3 respiration, or to significantly change the State 4 rate. In the presence of succinate, 40 microM cadmium inhibited State 3 respiration by 89%, while concentrations between 3.3 and 13.3 microM stimulated State 4 respiration. Higher concentrations caused marked inhibition. In the presence of succinate, cadmium released oligomycin inhibited State 3 respiration. Cadmium (0.001-1.0 mM) did not stimulate mitochondrial ATPase activity or inhibit ferricyanide reduction, but stimulated NAD+ linked mitochondrial dehydrogenase activities and NADH oxidation. These results indicate that cadmium interacts with either the NADH dehydrogenase complex or other NADH-dependent enzymes and not solely by an uncoupling action.

摘要

低浓度的镉(3.3 - 40微摩尔)抑制大鼠肝脏线粒体中与NADH相关的状态3呼吸作用,但未能释放寡霉素(1微克)抑制的状态3呼吸作用,也未显著改变状态4的速率。在琥珀酸存在的情况下,40微摩尔的镉抑制状态3呼吸作用达89%,而浓度在3.3至13.3微摩尔之间则刺激状态4呼吸作用。更高浓度会导致显著抑制。在琥珀酸存在的情况下,镉能释放被寡霉素抑制的状态3呼吸作用。镉(0.001 - 1.0毫摩尔)不会刺激线粒体ATP酶活性或抑制铁氰化物还原,但会刺激与NAD⁺相关的线粒体脱氢酶活性和NADH氧化。这些结果表明,镉与NADH脱氢酶复合物或其他NADH依赖性酶相互作用,而不仅仅是通过解偶联作用。

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