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大鼠经四氯化碳给药致肝损伤后,钙网蛋白对肝细胞膜(Ca²⁺-Mg²⁺)-ATP酶的激活作用受损。

Activatory effect of regucalcin on hepatic plasma membrane (Ca(2+)-Mg2+)-ATPase is impaired by liver injury with carbon tetrachloride administration in rats.

作者信息

Takahashi H, Yamaguchi M

机构信息

Laboratory of Endocrinology and Molecular Metabolism, Graduate School of Nutritional Sciences, University of Shizuoka, Japan.

出版信息

Mol Cell Biochem. 1996 May 10;158(1):9-16. doi: 10.1007/BF00225877.

Abstract

The alteration of the plasma membrane (Ca(2+)-Mg2+)-ATPase activity in the liver of rats administered orally carbon tetrachloride (CCl4) solution was investigated. Rats received a single oral administration of CCl4 (10, 25 and 50%, 1.0 ml/100 g body weight), and 3 or 24 h later they were sacrificed. CCl4 administration caused a remarkable elevation of liver calcium content and a corresponding increase in liver plasma membrane (Ca(2+)-Mg2+)-ATPase activity, indicating that the increased Ca2+ pump activity is partly involved in calcium accumulation in liver cells. Moreover, the participation in regucalcin, which is an intracellular activating factor on the enzyme, was examined by using anti-regucalcin IgG. The plasma membrane (Ca(2+)-Mg2+)-ATPase activity increased by CCl4 administration was not entirely inhibited by the presence of anti-regucalcin IgG (1.0 and 2.5 ug/ml) in the enzyme reaction mixture. However, the effect of regucalcin (0.25-1.0 uM) to activate (Ca(2+)-Mg2+)-ATPase in the liver plasma membranes of normal rats was not revealed in the liver plasma membranes obtained from CCl4-administered rats. Also, the effect of regucalcin was not seen when the plasma membranes were washed with 1.0 mM EGTA, indicating that the disappearance of regucalcin effect is not dependent on calcium binding to the plasma membranes due to liver calcium accumulation. Now, the presence of dithiothreitol (5 mM) or heparin (20 ug/ml) caused a remarkable elevation of the plasma membrane (Ca(2+)-Mg2+)-ATPase activity in the liver obtained from CCl4-administered rats. Thus, the regucalcin effect differed from that of dithiothreitol or heparin. The present study suggests that the impairment of regucalcin effect on Ca2+ pump activity in liver plasma membranes is partly contribute to hepatic calcium accumulation induced by liver injury with CCl4 administration.

摘要

研究了口服四氯化碳(CCl4)溶液的大鼠肝脏中质膜(Ca(2+)-Mg2+)-ATP酶活性的变化。大鼠单次口服给予CCl4(10%、25%和50%,1.0 ml/100 g体重),3或24小时后处死。给予CCl4导致肝脏钙含量显著升高,同时肝脏质膜(Ca(2+)-Mg2+)-ATP酶活性相应增加,表明Ca2+泵活性增加部分参与了肝细胞内钙的积累。此外,通过使用抗调节钙蛋白IgG检测了调节钙蛋白(一种该酶的细胞内激活因子)的参与情况。在酶反应混合物中存在抗调节钙蛋白IgG(1.0和2.5 μg/ml)时,给予CCl4后增加的质膜(Ca(2+)-Mg2+)-ATP酶活性并未被完全抑制。然而,在给予CCl4的大鼠获得的肝脏质膜中未发现调节钙蛋白(0.25 - 1.0 μM)对正常大鼠肝脏质膜中(Ca(2+)-Mg2+)-ATP酶的激活作用。而且,当质膜用1.0 mM EGTA洗涤时未观察到调节钙蛋白的作用,这表明调节钙蛋白作用的消失并非由于肝脏钙积累导致钙与质膜结合所致。现在,二硫苏糖醇(5 mM)或肝素(20 μg/ml)的存在导致给予CCl4的大鼠肝脏中质膜(Ca(2+)-Mg2+)-ATP酶活性显著升高。因此,调节钙蛋白的作用不同于二硫苏糖醇或肝素的作用。本研究表明,调节钙蛋白对肝脏质膜Ca2+泵活性的作用受损部分导致了CCl4给药引起的肝损伤诱导的肝脏钙积累。

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