Balestrero F, Morelli A, Damonte G, Voci A, Orunesu M
Istituto di Fisiologia Generale, Università, Genova.
Ital J Biochem. 1990 Jul-Aug;39(4):250-7.
T3 administration to rats exerts quite different effects on enzyme activities associated to liver microsomal membranes such as G-6-Pase, Mg ATPase and Ca2(+)-dependent ATPase: in fact G-6-Pase activity is significantly enhanced, Mg ATPase is not affected whereas Ca2(+)-dependent ATPase is drastically inhibited. The T3 induced decrease in Ca2(+)-dependent ATPase activity is associated with a net reduction (to about 50% with respect to controls) of the Ca2+ sequestration in liver microsomal vesicles. The enhanced level of inorganic phosphate in the endoplasmic reticulum due to the stimulation of G-6-Pase activity does not significantly affect the uptake of calcium in microsomal vesicles. The decreased Ca2(+)-dependent ATPase activity is associated to an enhanced level of the enzyme in the phosphorylated form (E-P). This suggests that in liver preparations from T3 treated rats the turnover of ATP and cleavage of E-P is reduced, thus resulting in the accumulation of the phosphorylated intermediate. The accumulation of E-P is in agreement with the inhibition of the calcium sequestration since the active transport of this cation in microsomal membranes requires the hydrolysis of the E-P complex.
给大鼠注射T3对与肝微粒体膜相关的酶活性,如葡萄糖-6-磷酸酶、镁ATP酶和钙依赖性ATP酶,产生截然不同的影响:实际上,葡萄糖-6-磷酸酶活性显著增强,镁ATP酶不受影响,而钙依赖性ATP酶则受到强烈抑制。T3诱导的钙依赖性ATP酶活性降低与肝微粒体囊泡中钙螯合作用的净减少(相对于对照组减少约50%)相关。由于葡萄糖-6-磷酸酶活性的刺激,内质网中无机磷酸盐水平的升高并未显著影响微粒体囊泡对钙的摄取。钙依赖性ATP酶活性的降低与磷酸化形式(E-P)的酶水平升高相关。这表明,在T3处理大鼠的肝脏制剂中,ATP的周转和E-P的裂解减少,从而导致磷酸化中间体的积累。E-P的积累与钙螯合作用的抑制一致,因为该阳离子在微粒体膜中的主动转运需要E-P复合物的水解。