Simpkins C, Balderman S, Mensah E
Department of Surgery, University at Buffalo School of Medicine, Buffalo, New York, 14215, USA.
J Surg Res. 1998 Nov;80(1):16-21. doi: 10.1006/jsre.1998.5383.
To determine the combined effect of metallothionein and calcium on the oxygen consumption of mitochondria.
We previously showed that mitochondrial oxygen consumption was inhibited by the intracellular acute-phase reactant, metallothionein, which is rapidly induced by nearly all stressed cells. Other investigators have demonstrated that calcium also inhibited oxygen consumption. However, the calcium concentrations used in their experiments were supraphysiologic. Our hypothesis was that metallothionein would enhance the effect of calcium.
We conducted these experiments, of a paired design, on the effects of combinations of metallothionein and calcium using mitochondria isolated from rat liver. An oxygen electrode implanted into a 600-microliter chamber with a stir bar was used to measure oxygen consumption. Various concentrations of calcium, metallothionein, and other reagents were added while oxygen consumption was being continuously recorded. Metals were removed from metallothionein by gel filtration to produce apometallothionein.
Physiological levels of metallothionein synergistically enhanced the inhibitory effect of calcium so that its action occurred at physiological concentrations. Metallothionein devoid of its metals, zinc and cadmium, had no effect on oxygen consumption.
In isolated mitochondria metallothionein inhibits ADP-initiated oxygen consumption. This effect is synergistic with the inhibitory action of calcium. These observations suggest a possible enhancement by metallothionein of the effect of fluxes in intracellular calcium in stressed cells.
确定金属硫蛋白和钙对线粒体氧消耗的联合作用。
我们之前发现,细胞内急性期反应物金属硫蛋白可抑制线粒体氧消耗,几乎所有应激细胞都会迅速诱导产生该蛋白。其他研究人员已证明,钙也会抑制氧消耗。然而,他们实验中使用的钙浓度高于生理水平。我们的假设是,金属硫蛋白会增强钙的作用。
我们采用配对设计进行了这些实验,研究金属硫蛋白和钙的组合对从大鼠肝脏分离的线粒体的影响。将一个带有搅拌棒的氧电极植入一个600微升的反应室中,用于测量氧消耗。在持续记录氧消耗的同时,加入不同浓度的钙、金属硫蛋白和其他试剂。通过凝胶过滤从金属硫蛋白中去除金属,以产生脱金属硫蛋白。
生理水平的金属硫蛋白协同增强了钙的抑制作用,使其在生理浓度下即可发挥作用。不含锌和镉等金属的金属硫蛋白对氧消耗没有影响。
在分离的线粒体中,金属硫蛋白抑制由二磷酸腺苷引发的氧消耗。这种作用与钙的抑制作用具有协同性。这些观察结果表明,金属硫蛋白可能增强应激细胞内钙通量的作用。