Jensen C B, Sistare F D, Hamman H C, Haynes R C
Biochem J. 1983 Mar 15;210(3):819-27. doi: 10.1042/bj2100819.
(1) Activation of rat liver mitochondrial functions following glucagon treatment was demonstrated in mitochondria that had not been isolated by the conventional technique of differential centrifugation and washing in sucrose solutions. Crude liver homogenates in 0.3 M-sucrose or 0.15 M-KCl prepared from rats treated with glucagon showed stimulation of State-3 and uncoupled respiration, carboxylation of pyruvate, and citrulline synthesis comparable with those previously reported in isolated mitochondria. (2) During the isolation procedure of mitochondria the hormonal stimulations of pyruvate carboxylation and citrulline formation were shown not to be enhanced by sequential washing. (3) Mitochondria isolated from glucagon-treated rats by differential centrifugation and washing in 0.3 M-mannitol/1 mM-EGTA, pH 7.0, exhibited a mean rate of citrulline synthesis that was greater than twice that of the control. Liver homogenates prepared in 0.3 M-sucrose or 0.3 M-mannitol showed identical rates of State-3 respiration and percentage stimulations of respiration by glucagon treatment. (4) Addition of glucagon led to a rapid accumulation of malate and aspartate and decreased the amounts of glutamate and citrate in isolated hepatocytes incubated with L-lactate. When gluconeogenesis was inhibited at the phosphoenolpyruvate carboxykinase (EC 4.1.1.32) reaction these phenomena were accentuated, lending support to the interpretation that they are the direct result of stimulation of carboxylation and oxidation reactions in the mitochondria. These results do not support the proposal [Siess, Fahimi & Wieland (1981) Hoppe-Seyler's Z. Physiol. Chem. 362. 1643-1651] that the mitochondrial effects of glucagon treatment result from a stabilization of mitochondria to detrimental effects of sucrose during their isolation. (5) The mean hormonal stimulation of pyruvate carboxylation in mitochondria isolated in 0.3 M-sucrose was shown to be approx. 2.5-fold when assayed either at 37 degrees C or 25 degrees C. In contrast, on the basis of similar experiments, Siess et al. (1981) concluded that the effects of glucagon on hepatic mitochondria are not characteristic of a true hormonal stimulation. Our data indicate this conclusion to be unjustified.
(1) 在未采用常规差速离心和蔗糖溶液洗涤技术分离的线粒体中,证明了胰高血糖素处理后大鼠肝脏线粒体功能的激活。用胰高血糖素处理的大鼠制备的0.3M蔗糖或0.15M氯化钾中的粗肝匀浆显示,状态3呼吸和非偶联呼吸、丙酮酸羧化以及瓜氨酸合成受到刺激,与先前在分离的线粒体中报道的情况相当。(2) 在分离线粒体的过程中,丙酮酸羧化和瓜氨酸形成的激素刺激并未因顺序洗涤而增强。(3) 通过差速离心并用0.3M甘露醇/1mM乙二醇双乙醚四乙酸(EGTA),pH7.0洗涤从用胰高血糖素处理的大鼠中分离的线粒体,其瓜氨酸合成的平均速率大于对照的两倍以上。在0.3M蔗糖或0.3M甘露醇中制备的肝匀浆显示,状态3呼吸速率以及胰高血糖素处理对呼吸的刺激百分比相同。(4) 添加胰高血糖素导致在与L-乳酸一起孵育的分离肝细胞中苹果酸和天冬氨酸迅速积累,并降低了谷氨酸和柠檬酸的量。当在磷酸烯醇丙酮酸羧激酶(EC 4.1.1.32)反应处抑制糖异生时,这些现象会加剧,这支持了它们是线粒体中羧化和氧化反应刺激的直接结果的解释。这些结果不支持[西尔斯、法希米和维兰德(1981年)《霍佩-赛勒生理化学杂志》362卷。1643 - 1651页]的提议,即胰高血糖素处理的线粒体效应是由于线粒体在分离过程中对蔗糖有害作用的稳定化所致。(5) 在0.3M蔗糖中分离的线粒体中,丙酮酸羧化的平均激素刺激在37℃或25℃测定时显示约为2.5倍。相比之下,基于类似实验,西尔斯等人(1981年)得出结论,胰高血糖素对肝脏线粒体的作用不是真正激素刺激的特征。我们的数据表明这一结论是不合理的。