Suppr超能文献

镉诱导的离体肝细胞能量水平改变。

Cadmium-induced alteration of the energy level in isolated hepatocytes.

作者信息

Müller L, Ohnesorge F K

出版信息

Toxicology. 1984 Jun;31(3-4):297-306. doi: 10.1016/0300-483x(84)90110-0.

Abstract

The incubation of isolated hepatocytes with 10-100 microM cadmium (Cd) decreased the ATP/ADP-ratio, the ATP/AMP-ratio and the adenylate energy charge and enhanced the lactate/pyruvate-ratio in a time- and concentration-dependent manner. Likewise, the cellular oxygen-consumption was decreased at early incubation times, when the cell membrane was still intact, as judged by the Trypan Blue-exclusion test. Similarly, Cd-concentrations above 0.3 nmol/mg mitochondrial protein inhibited the succinate- and malate/pyruvate-stimulated respiration of isolated mitochondria. This critical concentration was also reached in mitochondria of hepatocytes, when exposed to 25 microM Cd for less than 30 min. We therefore suggest that the inhibition of cellular respiration and the breakdown of cellular energy generation is mediated by a severe disturbance of mitochondrial respiratory functions due to Cd. This effect seems to be an early event in Cd-toxicity in isolated hepatocytes.

摘要

将分离的肝细胞与10 - 100微摩尔镉(Cd)一起孵育,会使ATP/ADP比值、ATP/AMP比值和腺苷酸能荷降低,并使乳酸/丙酮酸比值以时间和浓度依赖的方式升高。同样,在孵育早期,当通过台盼蓝排斥试验判断细胞膜仍完整时,细胞耗氧量会降低。类似地,当线粒体蛋白中Cd浓度高于0.3纳摩尔/毫克时,会抑制分离线粒体的琥珀酸和苹果酸/丙酮酸刺激的呼吸作用。当肝细胞线粒体暴露于25微摩尔Cd少于30分钟时,也会达到这一临界浓度。因此,我们认为细胞呼吸的抑制和细胞能量产生的破坏是由Cd导致的线粒体呼吸功能严重紊乱介导的。这种效应似乎是分离的肝细胞中Cd毒性的早期事件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验