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通过对分离的大鼠脂肪细胞中己糖转运的动力学研究对易位假说进行重新评估。

Reassessment of the translocation hypothesis by kinetic studies on hexose transport in isolated rat adipocytes.

作者信息

Suzuki K

机构信息

Division of Endocrinology and Metabolism, Asahi Life Foundation, Tokyo, Japan.

出版信息

J Biol Chem. 1988 Sep 5;263(25):12247-52.

PMID:3045114
Abstract

The effect of insulin and factors which have insulin-like activity on the kinetic parameters of 3-O-methyl-D-glucose (MeGlc) transport in rat adipocytes were assessed. Carrier-mediated uptake of MeGlc was estimated by the difference in the amounts of [14C]MeGlc and L-[3H]glucose taken up in cells under equilibrium exchange conditions at 37 degrees C. The Km and Vmax values in basal cells were 17.4 mM and 0.24 nmol/10(6) cells/s, respectively. Removal of endogenous adenosine by adenosine deaminase resulted in a 26% decrease in the basal rate due to a slight increase in the Km (19.6 mM) and a decrease in the Vmax value (0.20 nmol/10(6) cells/s). The maximum concentration (10 nM) of insulin decreased the Km to approximately one-half of the basal (7.1 mM) concomitant with an 8.5-fold increase in the Vmax value (2.04 nmol/10(6) cells/s). Submaximal concentrations (50 and 150 pM) of insulin, N6-phenylisopropyladenosine (1 microM), mechanical agitation of cells by centrifugal force (160 x g), low temperature (15 degrees C), 12-O-tetradecanoylphorbol-13-acetate (1 microM), and hydrogen peroxide (10 mM) all decreased the basal Km value to a range of 13.5-7.3 mM, concomitant with a 1.7-7.4-fold increase in the Vmax. A possible explanation for the alterations in the kinetic parameters may be that insulin and other factors cause the translocation of the mobile low-Km glucose transporters from an intracellular site to the cell surface, where the stationary high-Km transporters are located. Thus, when the Km and Vmax values of the hypothetical high-Km transporters were assumed to be 20 mM and 0.20 nmol/10(6) cells/s, respectively, and the Km of the low-Km transporters was assumed to be 7 mM, the theoretical Km decreased from 20 to 7.5 mM as the Vmax of the low-Km transporters increased from near 0 to 2.0 nmol/10(6) cells/s. The relation between empirical Km and Vmax values as affected by several agents and conditions followed closely the relation predicted by the above two-transporter model.

摘要

评估了胰岛素及具有胰岛素样活性的因子对大鼠脂肪细胞中3-O-甲基-D-葡萄糖(MeGlc)转运动力学参数的影响。在37℃平衡交换条件下,通过细胞摄取的[14C]MeGlc和L-[3H]葡萄糖量的差异来估计载体介导的MeGlc摄取。基础细胞中的Km和Vmax值分别为17.4 mM和0.24 nmol/10(6)细胞/秒。用腺苷脱氨酶去除内源性腺苷导致基础速率下降26%,这是由于Km略有增加(19.6 mM)和Vmax值降低(0.20 nmol/10(6)细胞/秒)。胰岛素的最大浓度(10 nM)使Km降至基础值的约一半(7.1 mM),同时Vmax值增加8.5倍(2.04 nmol/10(6)细胞/秒)。亚最大浓度(50和150 pM)的胰岛素、N6-苯基异丙基腺苷(1 microM)、通过离心力(160 x g)对细胞进行机械搅拌、低温(15℃)、12-O-十四烷酰佛波醇-13-乙酸酯(1 microM)和过氧化氢(10 mM)均使基础Km值降至13.5 - 7.3 mM范围,同时Vmax增加1.7 - 7.4倍。动力学参数改变的一个可能解释是胰岛素和其他因子导致可移动的低Km葡萄糖转运体从细胞内位点转运至细胞表面,即固定的高Km转运体所在的位置。因此,假设高Km转运体的Km和Vmax值分别为20 mM和0.20 nmol/10(6)细胞/秒,低Km转运体的Km为7 mM,随着低Km转运体的Vmax从接近0增加到2.0 nmol/10(6)细胞/秒,理论Km从20 mM降至7.5 mM。几种试剂和条件影响下的经验Km和Vmax值之间的关系与上述双转运体模型预测的关系密切相符。

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