Moreno-Aurioles V R, Sobrino F
Departamento de Bioquímica Médica y Biología Molecular, Facultad de Medicina, Universidad de Sevilla, Spain.
Biochim Biophys Acta. 1991 Jan 10;1091(1):96-100. doi: 10.1016/0167-4889(91)90227-o.
The content of fructose 2,6-bisphosphate (Fru(2,6)P2) and lactate production in triamcinolone acetonide-treated rats thymocytes was studied. The effect in vitro of corticosterone and dexamethasone on normal thymocytes was also examined. Glucocorticoids produced a marked decrease in Fru(2,5)P2 content and lactate production. The largest effect was observed with triamcinolone acetonide (7.5 mg per kg body weight), which after 20 h of treatment produced over 90% of inhibition. This change was accompanied by the decrease of both phosphofructokinase-1 and -2 activities and ATP levels, without modifications of hexoses phosphate content. The inhibitory actions of glucocorticoids were abolished by cycloheximide, an inhibitor of protein synthesis. Furthermore this drug, by itself, increased Fru(2,6)P2 content by more than 50% compared with the controls.
研究了曲安奈德处理的大鼠胸腺细胞中果糖-2,6-二磷酸(Fru(2,6)P2)的含量和乳酸生成情况。还检测了皮质酮和地塞米松对正常胸腺细胞的体外作用。糖皮质激素使Fru(2,5)P2含量和乳酸生成显著降低。曲安奈德(每千克体重7.5毫克)的作用最为明显,处理20小时后产生了超过90%的抑制作用。这种变化伴随着磷酸果糖激酶-1和-2活性以及ATP水平的降低,而磷酸己糖含量没有改变。蛋白质合成抑制剂环己酰亚胺消除了糖皮质激素的抑制作用。此外,与对照组相比,该药物本身使Fru(2,6)P2含量增加了50%以上。