Storm H, van Hardeveld C
Biochim Biophys Acta. 1985 Aug 30;846(2):275-85. doi: 10.1016/0167-4889(85)90075-8.
The relation between Ca2+ efflux, Ca2+ mobilization from mitochondria and glycogenolysis was studied in perfused euthyroid and hypothyroid rat livers stimulated by Ca2+-mobilizing hormones. Ca2+ efflux, induced by noradrenaline (1 microM) in the absence or presence of DL-propranolol (10 microM) from livers perfused with medium containing a low concentration of Ca2+ (approx. 24 microM), was decreased by more than 50% in hypothyroidism. This correlated with an equal decrease of the fractional mobilization of mitochondrial Ca2+, which could account for 65% of the difference between the net amounts of Ca2+ expelled from the euthyroid and hypothyroid livers. With vasopressin (10 nM) similar results were found, suggesting that hypothyroidism has a general effect on mobilization of internal Ca2+. In normal Ca2+ medium (1300 microM), however, the effect of vasopressin on net Ca2+ fluxes and phosphorylase activation was not impaired in hypothyroidism, indicating that Ca2+ mobilization from the mitochondria in this case plays a minor role in phosphorylase activation. The alpha 1-adrenergic responses of Ca2+ efflux, phosphorylase activation and glucose output, glucose-6-phosphatase activity and oxygen consumption in hypothyroid rat liver were completely restored by in vivo T3 injections (0.5 micrograms per 100 g body weight, daily during 3 days). Perfusion with T3 (100 pM) during 19 min did not influence hypothyroid rat liver oxygen consumption and alpha 1-receptor-mediated Ca2+ efflux. However, this in vitro T3 treatment showed a completely recovered alpha 1-adrenergic response of phosphorylase and a partly restored glucose-6-phosphatase activity and glucose output. The results indicate that thyroid hormones may control alpha 1-adrenergic stimulation of glycogenolysis by at least two mechanisms, i.e., a long-term action on Ca2+ mobilization, and a short-term action on separate stages of the glycogenolytic process.
在灌注的正常甲状腺和甲状腺功能减退大鼠肝脏中,研究了由钙动员激素刺激引起的钙离子外流、线粒体钙离子动员与糖原分解之间的关系。在灌注含低浓度钙离子(约24微摩尔)的培养基的肝脏中,去甲肾上腺素(1微摩尔)在不存在或存在DL-普萘洛尔(10微摩尔)时诱导的钙离子外流,在甲状腺功能减退时降低了50%以上。这与线粒体钙离子的分数动员的同等降低相关,这可以解释正常甲状腺和甲状腺功能减退肝脏排出的钙离子净量之间差异的65%。对于血管加压素(10纳摩尔),发现了类似的结果,表明甲状腺功能减退对细胞内钙离子的动员有普遍影响。然而,在正常钙离子培养基(1300微摩尔)中,血管加压素对钙离子净通量和磷酸化酶激活的作用在甲状腺功能减退时并未受损,表明在这种情况下,线粒体钙离子的动员在磷酸化酶激活中起次要作用。通过体内注射T3(每100克体重0.5微克,连续3天每天注射),甲状腺功能减退大鼠肝脏中钙离子外流、磷酸化酶激活、葡萄糖输出、葡萄糖-6-磷酸酶活性和耗氧量的α1-肾上腺素能反应完全恢复。用T3(100皮摩尔)灌注19分钟对甲状腺功能减退大鼠肝脏的耗氧量和α1-受体介导的钙离子外流没有影响。然而,这种体外T3处理显示磷酸化酶的α1-肾上腺素能反应完全恢复,葡萄糖-6-磷酸酶活性和葡萄糖输出部分恢复。结果表明,甲状腺激素可能通过至少两种机制控制α1-肾上腺素能刺激的糖原分解,即对钙离子动员的长期作用,以及对糖原分解过程不同阶段的短期作用。