Tobin R B, Berdanier C D, Ecklund R E
J Environ Pathol Toxicol. 1979 Jul-Aug;2(6):1247-66.
The effect of thyroxine administration upon ATPase activity of several subcellular fractions of livers from rats and guinea pigs has been studied. To determine a patho-physiological dose of levo thyroxine [T4] for guinea pigs, a dose-response curve was examined of T4 effect upon oxidative phosphorylatin of guinea pig liver mitochondria. Maximum stimulation of mitochondrial respiration without uncoupling of oxidative phosphorylation was found with 15 microgram of T4 per 100 g body weight per day. This dose of T4 stimulated Mg++ activated ATPase of plasma membranes of guinea pigs and slightly stimulated Mg++ activated ATPase of guinea pig liver nuclear membranes. Rat liver nuclear membrane ATPase was not responsive to thyroxine at doses from 5 to 150 microgram per 100 g body weight. T4 significantly stimulated Ca++ or Mg++ ATPase of mitochondria and microsomes from both rat and guinea pig liver. Microsomes from both species were maximally activated by Mg++ and no significant additional stimulation with Ca++ was found. Mitochondrial ATPase from both species showed significantly greater Ca++ plus Mg++ ATPase activity than did Mg++ alone. Ca++ activated ATPase was approximately equal to dinitrophenol stimulated mitochondrial ATPase. Maximum activation of microsomal ATPase in both species was found with 1 mM calcium. We conclude that at physiological-intracellular concentrations of Ca++ and Mg++, thyroxine probably stimulates Mg++ activated microsomal ATPase and Ca++ activated mitochondrial ATPase. A potential role of Ca++ as a moderator of thyroxine stimulated activity in mitochondria and the relation of calcium to other metabolic reactions that are thyroxine sensitive is discussed.
已经研究了给予甲状腺素对大鼠和豚鼠肝脏几种亚细胞组分的ATP酶活性的影响。为了确定豚鼠左甲状腺素[T4]的病理生理剂量,检测了T4对豚鼠肝线粒体氧化磷酸化作用的剂量反应曲线。发现每天每100克体重给予15微克T4时,线粒体呼吸有最大刺激且氧化磷酸化未解偶联。该剂量的T4刺激了豚鼠质膜的Mg++激活的ATP酶,并轻微刺激了豚鼠肝核膜的Mg++激活的ATP酶。每100克体重给予5至150微克剂量的甲状腺素时,大鼠肝核膜ATP酶对其无反应。T4显著刺激大鼠和豚鼠肝脏线粒体及微粒体的Ca++或Mg++ATP酶。两种动物的微粒体均被Mg++最大程度激活,未发现Ca++有明显的额外刺激作用。两种动物的线粒体ATP酶显示出的Ca++加Mg++ATP酶活性明显高于单独的Mg++。Ca++激活的ATP酶约等于二硝基苯酚刺激的线粒体ATP酶。两种动物的微粒体ATP酶在1 mM钙浓度下均有最大激活。我们得出结论,在生理细胞内Ca++和Mg++浓度下,甲状腺素可能刺激Mg++激活的微粒体ATP酶和Ca++激活的线粒体ATP酶。讨论了Ca++作为甲状腺素刺激线粒体活性的调节剂的潜在作用以及钙与其他对甲状腺素敏感的代谢反应的关系。