MacDonald E, Rubinow D, Linnoila M
Arch Gen Psychiatry. 1984 May;41(5):487-93. doi: 10.1001/archpsyc.1984.01790160073009.
The sensitivity of RBC membrane (RBCM) Ca2+-adenosine triphosphatase (Ca2+-ATPase) to calmodulin stimulation was repeatedly studied in healthy volunteers and in 12 patients with affective disorders. Whereas control response was relatively stable, the patients showed great variability. This phenomenon was not due to formation of resealed vesicles in the RBCM nor to the quantity of calmodulin remaining in the RBCM preparations present in the cells before hemolysis. Changes in calmodulin sensitivity did not correlate with changes of mood or of drug treatment. When Ca2+-ATPase was relatively unresponsive to calmodulin, considerable enzyme activity was maintained at low calcium concentrations without calmodulin. In samples showing a large response to calmodulin, virtually no enzyme activity was detected at low calcium concentrations without exogenous calmodulin. Thus, calcium dependence and calmodulin sensitivity of the Ca2+-ATPase appeared to correlate positively with each other. As a similar phenomenon has been linked to changes in the composition of membrane phospholipids responsible for the regulation of Ca2+-ATPase activity, variations in baseline activity and calmodulin-induced stimulation of this enzyme may represent a fundamental defect in systems regulating membrane phospholipid composition.
在健康志愿者和12名情感障碍患者中,对红细胞膜(RBCM)钙 - 三磷酸腺苷酶(Ca2 + -ATPase)对钙调蛋白刺激的敏感性进行了反复研究。对照反应相对稳定,而患者表现出很大的变异性。这种现象既不是由于RBCM中重新封闭的囊泡形成,也不是由于溶血前细胞中RBCM制剂中残留的钙调蛋白量所致。钙调蛋白敏感性的变化与情绪变化或药物治疗无关。当Ca2 + -ATPase对钙调蛋白相对无反应时,在没有钙调蛋白的低钙浓度下仍保持相当的酶活性。在对钙调蛋白有较大反应的样品中,在没有外源性钙调蛋白的低钙浓度下几乎检测不到酶活性。因此,Ca2 + -ATPase的钙依赖性和钙调蛋白敏感性似乎呈正相关。由于类似的现象与负责调节Ca2 + -ATPase活性的膜磷脂组成变化有关,该酶的基线活性和钙调蛋白诱导的刺激变化可能代表调节膜磷脂组成系统中的基本缺陷。