Sayers L G, Brown G R, Michell R H, Michelangeli F
School of Biochemistry, University of Birmingham, Edgbaston, UK.
Biochem J. 1993 Feb 1;289 ( Pt 3)(Pt 3):883-7. doi: 10.1042/bj2890883.
Thimerosal inhibits calcium uptake in skeletal muscle sarcoplasmic reticulum and rat cerebellar microsomes by inhibiting the Ca(2+)-ATPase. In the presence of 5 mM dithiothreitol (DTT), Ca2+ uptake and ATPase activity were not inhibited by thimerosal, indicating that thimerosal modifies cysteine residues of the Ca(2+)-ATPase. Low thimerosal concentrations (2 microM) sensitize the inositol 1,4,5-trisphosphate (InsP3)-sensitive Ca2+ channel, making it open at lower InsP3 concentrations. Higher concentrations of thimerosal, however, cause inhibition of InsP3-induced Ca2+ release. Both sensitization and inhibition of the InsP3 receptor by thimerosal can be prevented by DTT. The binding and metabolism of InsP3 by cerebellar microsomes is not affected by thimerosal. The amount of InsP3-induced Ca2+ release is co-operatively linked to the InsP3 concentration with a Hill coefficient of 2.0 +/- 0.3. This is decreased to 1.0 +/- 0.2 at inhibitory concentrations of thimerosal. Under our experimental conditions, we observed no dependence of quantal Ca2+ release on intraluminal Ca2+ concentration.
硫柳汞通过抑制Ca(2+)-ATP酶来抑制骨骼肌肌浆网和大鼠小脑微粒体对钙的摄取。在存在5 mM二硫苏糖醇(DTT)的情况下,硫柳汞不会抑制Ca2+摄取和ATP酶活性,这表明硫柳汞会修饰Ca(2+)-ATP酶的半胱氨酸残基。低浓度的硫柳汞(2 microM)会使肌醇1,4,5-三磷酸(InsP3)敏感的Ca2+通道敏感化,使其在较低的InsP3浓度下打开。然而,较高浓度的硫柳汞会抑制InsP3诱导的Ca2+释放。DTT可以防止硫柳汞对InsP3受体的敏感化和抑制作用。硫柳汞不会影响小脑微粒体对InsP3的结合和代谢。InsP3诱导的Ca2+释放量与InsP3浓度协同相关,希尔系数为2.0±0.3。在硫柳汞的抑制浓度下,该系数降至1.0±0.2。在我们的实验条件下,我们未观察到量子Ca2+释放对管腔内Ca2+浓度的依赖性。