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调钙素调节激素对大鼠肝细胞膜中(钙 - 镁)-ATP酶活性的影响。

Regucalcin modulates hormonal effect on (Ca(2+)-Mg2+)-ATPase activity in rat liver plasma membranes.

作者信息

Takahashi H, Yamaguchi M

机构信息

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

出版信息

Mol Cell Biochem. 1993 Aug 25;125(2):171-7. doi: 10.1007/BF00936446.

Abstract

The interaction of various hormones and regucalcin on (Ca(2+)-Mg2+)-ATPase activity in rat liver plasma membranes was investigated. The presence of epinephrine (10(-6)-10(-4) M), phenylephrine (10(-6)-10(-4) M), and insulin (10(-8)-10(-7) M) in the reaction mixture produced a significant increase in (Ca(2+)-Mg7+)-ATPase activity, while the enzyme activity was decreased significantly by calcitonin (3 x 10(-8)-3 x 10(-6) M). These hormonal effects, except for calcitonin, were clearly inhibited by the presence of vanadate (10(-4) M) which can inhibit the Ca(2+)-dependent phosphorylation of enzyme. Meanwhile, regucalcin (0.25 and 0.50 microM), isolated from rat liver cytosol, elevated significantly (Ca(2+)-Mg2+)-ATPase activity in the plasma membranes, although this elevation was not inhibited by vanadate (10(-4) M). The epinephrine (10(-5) M) or phenylephrine (10(-4) M)-induced increase in (Ca(2+)-Mg2+)-ATPase activity was disappeared in the presence of regucalcin; in this case the effect of regucalcin was also weakened. However, the inhibitory effect of calcitonin (3 x 10(-6) M) was not weakened by the presence of regucalcin (0.5 microM). Moreover, GTP (10(-5) and 10(-4) M)-induced increase in (Ca(2+)-Mg2+)-ATPase activity was not seen in the presence of regucalcin (0.25 microM). The present finding suggests that the activating mechanism of regucalcin on (Ca(2+)-Mg2+)-ATPase is not involved on GTP-binding protein which modulates the receptor-mediated hormonal effect in rat liver plasma membranes.

摘要

研究了大鼠肝细胞膜中各种激素与调钙素对(Ca(2 +)-Mg2 +)-ATP酶活性的相互作用。反应混合物中存在肾上腺素(10(-6)-10(-4) M)、去氧肾上腺素(10(-6)-10(-4) M)和胰岛素(10(-8)-10(-7) M)时,(Ca(2 +)-Mg7 +)-ATP酶活性显著增加,而降钙素(3×10(-8)-3×10(-6) M)则使该酶活性显著降低。除降钙素外,这些激素效应均被钒酸盐(10(-4) M)明显抑制,钒酸盐可抑制酶的Ca(2 +)依赖性磷酸化。同时,从大鼠肝细胞溶质中分离出的调钙素(0.25和0.50 microM)可显著提高细胞膜中(Ca(2 +)-Mg2 +)-ATP酶活性,尽管这种提高不受钒酸盐(10(-4) M)抑制。在存在调钙素的情况下,肾上腺素(10(-5) M)或去氧肾上腺素(10(-4) M)诱导的(Ca(2 +)-Mg2 +)-ATP酶活性增加消失;在这种情况下,调钙素的作用也减弱。然而,降钙素(3×10(-6) M)的抑制作用不受调钙素(0.5 microM)存在的影响。此外,在存在调钙素(0.25 microM)的情况下,未观察到GTP(10(-5)和10(-4) M)诱导的(Ca(2 +)-Mg2 +)-ATP酶活性增加。目前的发现表明,调钙素对(Ca(2 +)-Mg2 +)-ATP酶的激活机制不涉及在大鼠肝细胞膜中调节受体介导的激素效应的GTP结合蛋白。

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