Németh S, Viskupic E, Murgas K
Endocrinol Exp. 1985 Jun;19(2):91-5.
Glycogen phosphorylase activity was determined in rat livers obtained by laparotomy in thiobarbital (Inactin, PROMONTA) anaesthesia induced by injection of the drug via a polyethylene catheter into a jugular vein as described previously [Németh et al. 1983a]. Intact rats and animals exposed to open field stress without or after i.p. injection of the alpha blocker phentolamine (Regitine, CIBA; 20 mg kg-1, 90 min before stress) or the beta blocker propranolol (Inderal, ICI; 2 mg kg-1, 30 min before stress) were studied. In stressed animals a net increase of phosphorylase activity was observed. This response was abolished after alpha blockade, while after beta blockade it was potentiated. In a further series on animals subjected to the same type of anaesthesia, the activating effect of immobilization stress on phosphorylase activity was confirmed in both fed and fasted animals, the response of the latter issuing from a lower initial level but being of the same extent as in the fed rats.
糖原磷酸化酶活性的测定是在通过硫喷妥(因纳克,普罗蒙塔)麻醉后剖腹获得的大鼠肝脏中进行的,麻醉药物通过聚乙烯导管经颈静脉注射,如先前所述[内梅特等人,1983a]。研究了完整大鼠以及在腹腔注射α受体阻滞剂酚妥拉明(利其丁,汽巴;20毫克/千克,应激前90分钟)或β受体阻滞剂普萘洛尔(心得安,帝国化学工业公司;2毫克/千克,应激前30分钟)后暴露于旷场应激的动物。在应激动物中观察到磷酸化酶活性净增加。α受体阻断后这种反应消失,而β受体阻断后反应增强。在另一组接受相同类型麻醉的动物中,在喂食和禁食的动物中均证实了固定应激对磷酸化酶活性的激活作用,禁食动物的反应起始水平较低,但程度与喂食大鼠相同。