Kuo T H, Tsang W, Wang K K, Carlock L
Department of Pathology, Wayne State University, School of Medicine, Detroit, MI 48201.
Biochim Biophys Acta. 1992 Apr 14;1138(4):343-9. doi: 10.1016/0925-4439(92)90013-d.
Altered calcium regulation is a prominent feature in the hereditary cardiomyopathy of the Syrian hamster. However, the activity of the two systems necessary for intracellular calcium homeostasis in the heart, the sarcolemmal and sarcoplasmic reticulum calcium ATPase pumps, have not been correlated. Using age- and pair-matched myopathic and control hamsters, a simultaneous reduction in gene expression and enzyme activity for these two pumps has been demonstrated. The concomitant alteration in gene expression as early as 1 month of age, preceding noticeable myocytolysis suggests that the depressed activity in these two calcium ATPase systems is not due to cell necrosis but at least in part due to reduction in their mRNA levels. Reduced capacity of the calcium pumps would result in calcium overload as well as impaired contractility that leads to the eventual heart failure in this animal model.
钙调节异常是叙利亚仓鼠遗传性心肌病的一个显著特征。然而,心脏中细胞内钙稳态所需的两个系统,即肌膜和肌浆网钙ATP酶泵的活性,尚未得到关联研究。使用年龄和配对匹配的肌病仓鼠和对照仓鼠,已证明这两种泵的基因表达和酶活性同时降低。早在1月龄时,在明显的肌细胞溶解之前就出现了基因表达的伴随变化,这表明这两个钙ATP酶系统的活性降低并非由于细胞坏死,而是至少部分由于其mRNA水平的降低。钙泵能力的降低将导致钙超载以及收缩力受损,进而导致该动物模型最终发生心力衰竭。