Foster J D, Bode A M, Nordlie R C
Department of Biochemistry and Molecular Biology, University of North Dakota School of Medicine, Grand Forks 58202.
Biochim Biophys Acta. 1994 Oct 19;1208(2):222-8. doi: 10.1016/0167-4838(94)90107-4.
3-Mercaptopicolinate (3-MP) inhibits D-glucose-6-phosphate (G6P) phosphohydrolase activity of the glucose-6-phosphatase system (Bode et al. (1993) Biochem. Cell Biol. 71, 113-121). We therefore attempted to maximize the inhibition by varying the physical state of microsomes, the concentration of 3-MP, and the time of preliminary incubation of 3-MP with the enzyme. The inhibition was irreversible and time- and inhibitor-concentration-dependent, with G6P phosphohydrolase activity of intact rat liver microsomes, but there was no inhibition with detergent-treated microsomes. The effectiveness of 3-MP as a time-dependent inhibitor of glucose 6-phosphatase was demonstrated in situ by measuring glycogenolysis in isolated, perfused livers from fed rats. We first exposed the livers to 2 mM 3-MP for 40 min, and then assessed the inhibitory effects on glycogenolysis. It was lowered by 50%. These observations establish that 3-MP at the mM level may be useful as an experimental probe in the study of the role(s) of G6P in the regulation of glycogenolysis as well as glycogenesis. Further, they validate the use of much lower (microM) concentrations of 3-MP to block gluconeogenesis (at the phosphoenolpyruvate carboxykinase step) without interfering with glucose 6-phosphatase. We also explored the mechanism of 3-MP inhibition. The time-dependent inhibition of carbamoyl-phosphate:glucose phosphotransferase activity with microsomes incubated with 1 mM 3-MP for 60 or 90 min and then assayed with 1 mM carbamoyl phosphate and 180 mM glucose was modest compared with inhibition of G6P phosphohydrolase. When G6P production by carbamoyl-phosphate:glucose phosphotransferase was reduced by decreasing glucose concentration to 60 mM, no inhibition by 3-MP was discernible. There was no inhibition of inorganic pyrophosphatase activity. These studies support the model of time-dependent, irreversible reaction of 3-MP with the G6P translocase component of the glucose-6-phosphatase system.
3-巯基吡啶甲酸酯(3-MP)可抑制葡萄糖-6-磷酸酶系统的D-葡萄糖-6-磷酸(G6P)磷酸水解酶活性(博德等人,《生物化学与细胞生物学》,1993年,第71卷,第113 - 121页)。因此,我们试图通过改变微粒体的物理状态、3-MP的浓度以及3-MP与酶的预孵育时间来使抑制作用最大化。这种抑制作用是不可逆的,且与时间和抑制剂浓度相关,对完整大鼠肝微粒体的G6P磷酸水解酶活性有抑制作用,但对用去污剂处理过的微粒体则没有抑制作用。通过测量喂食大鼠分离灌注肝脏中的糖原分解,在原位证明了3-MP作为葡萄糖6-磷酸酶的时间依赖性抑制剂的有效性。我们首先将肝脏暴露于2 mM的3-MP中40分钟,然后评估其对糖原分解的抑制作用。糖原分解降低了50%。这些观察结果表明,毫摩尔水平的3-MP可用作研究G6P在糖原分解以及糖原合成调节中的作用的实验探针。此外,它们验证了使用低得多(微摩尔)浓度的3-MP来阻断糖异生(在磷酸烯醇式丙酮酸羧激酶步骤)而不干扰葡萄糖6-磷酸酶的方法。我们还探究了3-MP抑制的机制。与G6P磷酸水解酶的抑制相比,用1 mM 3-MP孵育微粒体60或90分钟,然后用1 mM氨基甲酰磷酸和180 mM葡萄糖进行测定时,氨基甲酰磷酸:葡萄糖磷酸转移酶活性的时间依赖性抑制作用较小。当通过将葡萄糖浓度降低至60 mM来降低氨基甲酰磷酸:葡萄糖磷酸转移酶产生的G6P时,未观察到3-MP的抑制作用。无机焦磷酸酶活性未受到抑制。这些研究支持了3-MP与葡萄糖-6-磷酸酶系统的G6P转位酶成分发生时间依赖性、不可逆反应的模型。