Pyne N J, Houslay M D
Department of Biochemistry, University of Glasgow, Scotland, U.K.
Biochem Biophys Res Commun. 1988 Oct 14;156(1):290-6. doi: 10.1016/s0006-291x(88)80838-6.
An insulin mediator preparation was obtained from rat hepatocytes which had been treated with insulin. This preparation inhibited adenylate cyclase activity. It stimulated the activity of homogeneous preparations of both the cytosolic and membrane-bound forms of rat liver cyclic GMP-activated cyclic AMP phosphodiesterase. It failed to activate homogeneous preparations of both the peripheral plasma membrane and 'dense-vesicle' cyclic AMP phosphodiesterases. The insulin mediator preparation stimulated cyclic GMP-activated cyclic AMP phosphodiesterase activity in a dose-dependent fashion with a hill coefficient of 0.46. Insulin caused the dose-dependent production of mediator activity in intact hepatocytes with a Ka of 9 pM, although concentrations of insulin greater than 10 nM progressively reduced stimulatory activity.
从经胰岛素处理的大鼠肝细胞中获得了一种胰岛素介质制剂。该制剂抑制腺苷酸环化酶活性。它刺激了大鼠肝脏环鸟苷酸激活的环磷酸腺苷磷酸二酯酶的胞质和膜结合形式的均一制剂的活性。它未能激活外周质膜和“致密囊泡”环磷酸腺苷磷酸二酯酶的均一制剂。胰岛素介质制剂以剂量依赖性方式刺激环鸟苷酸激活的环磷酸腺苷磷酸二酯酶活性,希尔系数为0.46。胰岛素在完整肝细胞中以剂量依赖性方式产生介质活性,Ka为9 pM,尽管胰岛素浓度大于10 nM会逐渐降低刺激活性。