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经苯巴比妥预处理的大鼠肝脏蛋白激酶C的昼夜节律

Circadian-time rhythm of hepatic protein kinase C of rats pretreated with phenobarbital.

作者信息

Möritz K U, Walter R, Franke G, Siegmund W

机构信息

Institut für Pharmakologie, Medizinische Fakultät, Ernst-Moritz-Arndt- Universität Greifswald.

出版信息

Pharmazie. 1995 Mar;50(3):211-3.

PMID:7732053
Abstract

Circadian-time dependent differences of protein kinase C (PKC) activities as well as its susceptibility to a phenobarbital caused suppression in vivo (40 mg/kg b.i.d. for 3 days) were studied in outbred male Wistar rats weighing 280-360 g. The well-known phenobarbital induction of cytochrome P-450 and 7-pentylresorufin-O-depentylase (PROD) was associated with inhibition of the hepatic PKC. The activities of the cytosolic and membrane-bound PKC were significantly lower than in the respective controls. Statistically significant circadian-time differences were found. The activities of both cytosolic and membrane-bound PKC of control rats were highest in the evening (158% and 131%, respectively, of the morning values). Furthermore, phenobarbital inhibited the enzyme more strongly at 19.00 h than at 07.00 h. Our results suggest that increase of hepatic cytochrome P-450 content as well as induction of PROD are inversely related with the function of PKC.

摘要

在体重为280 - 360克的远交系雄性Wistar大鼠中,研究了蛋白激酶C(PKC)活性的昼夜时间依赖性差异及其在体内对苯巴比妥所致抑制作用(40毫克/千克,每日两次,共3天)的敏感性。众所周知,苯巴比妥诱导细胞色素P - 450和7 - 戊基试卤灵 - O - 脱戊基酶(PROD)与肝PKC的抑制有关。胞质和膜结合PKC的活性显著低于各自的对照组。发现了具有统计学意义的昼夜时间差异。对照大鼠的胞质和膜结合PKC活性在傍晚最高(分别为早晨值的158%和131%)。此外,苯巴比妥在19:00时比在07:00时更强烈地抑制该酶。我们的结果表明,肝细胞色素P - 450含量的增加以及PROD的诱导与PKC的功能呈负相关。

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