Laychock S G
Department of Pharmacology, and Toxicology, State University of New York at Buffalo 14214, USA.
Biochem Pharmacol. 1996 Sep 13;52(5):793-9. doi: 10.1016/0006-2952(96)00391-7.
Culture of isolated rat islets at either 5.5 or 11 mM glucose for up to 6 days was associated with significant time-dependent increases in glyceraldehyde 3-phosphate dehydrogenase (G3PD) activity of islet homogenates compared with freshly isolated islet G3PD activity. In addition, after 6 days of culture of islets at 11 mM glucose, there was a significant increase in G3PD activity compared with the enzyme activity of islets cultured at 5.5 mM glucose. Culture of islets at 5.5 mM glucose for 2 days in the presence of forskolin, 3-isobutylmethylxanthine (IBMX), and 8-bromo-cyclic AMP also significantly increased G3PD activity compared with control islets, although there was no change in enzyme activity after only 1 day of culture with forskolin. Treatment with forskolin was associated with an increase in the Vmax of G3PD, but no change was observed in the apparent K(m) with NAD. IBMX and 8-bromo-cyclic AMP also increased G3PD activity in islets cultured at 11 mM glucose for 2 days. 8-Bromo-cyclic AMP did not affect or inhibit G3PD activity when added directly to islet homogenates. Islets cultured with 8-bromo-cyclic GMP for 2 days at 5.5 or 11 mM glucose did not show changes in G3PD activity. Increases in G3PD activity did not correlate with significant changes in islet glucose utilization. Thus, G3PD activity is modulated by the duration of glucose stimulation in cultured islets, and cyclic AMP may mediate changes in G3PD activity in islet cells.
将分离的大鼠胰岛分别在5.5 mM或11 mM葡萄糖浓度下培养长达6天,与新鲜分离的胰岛甘油醛-3-磷酸脱氢酶(G3PD)活性相比,胰岛匀浆中的G3PD活性随时间显著增加。此外,在11 mM葡萄糖浓度下培养6天后,与在5.5 mM葡萄糖浓度下培养的胰岛的酶活性相比,G3PD活性显著增加。在5.5 mM葡萄糖存在下,用福斯可林、3-异丁基-1-甲基黄嘌呤(IBMX)和8-溴环磷酸腺苷培养胰岛2天,与对照胰岛相比,也显著增加了G3PD活性,尽管用福斯可林培养仅1天后酶活性没有变化。福斯可林处理使G3PD的Vmax增加,但未观察到与NAD的表观K(m)有变化。IBMX和8-溴环磷酸腺苷也增加了在11 mM葡萄糖浓度下培养2天的胰岛中的G3PD活性。直接添加到胰岛匀浆中时,8-溴环磷酸腺苷不影响或抑制G3PD活性。在5.5 mM或l1 mM葡萄糖浓度下用8-溴环磷酸鸟苷培养胰岛2天,G3PD活性没有变化。G3PD活性的增加与胰岛葡萄糖利用的显著变化无关。因此,培养的胰岛中G3PD活性受葡萄糖刺激持续时间的调节,环磷酸腺苷可能介导胰岛细胞中G3PD活性的变化。