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鸟类红细胞代谢研究。第十七部分:鸡网织红细胞中肌醇的动力学和转运特性。

Studies on avian erythrocyte metabolism. XVII. Kinetics and transport properties of myo-inositol in chicken reticulocytes.

作者信息

Isaacks R E, Lai L L, Kim C Y, Goldman P H, Kim H D

机构信息

Research Laboratory, Veterans Administration Medical Center, Miami, Florida.

出版信息

Arch Biochem Biophys. 1989 Nov 1;274(2):564-73. doi: 10.1016/0003-9861(89)90471-2.

Abstract

The uptake of myo-inositol was determined in a reticulocyte-enriched fraction prepared from chicken blood and compared with uptake in mature erythrocytes. While reticulocytes accumulated inositol at levels more than threefold that of the plasma concentration, erythrocyte levels were only slightly higher than that of the plasma concentration. The rate of uptake in reticulocytes was approximately 66 mumol/ml rbc/h compared to 5 mumol/ml rbc/h in mature erythrocytes when measured at an inositol medium concentration of 250 microM. The kinetic analysis of inositol influx by reticulocytes reveals a two component system: saturable and nonsaturable. The saturable component, which has a Km for inositol of approximately 222 microM, is Na-dependent. This Na-dependent saturable component, which presumably reflects active transport of inositol, accounts for 30-35% of the transport process. The saturable component is completely inhibited by amiloride but to a lesser extent by ouabain and bumetanide. Moreover, in the course of reticulocyte maturation, the saturable component is lost concomitantly with the completion of the synthesis of myo-inositol pentakisphosphate and the drastic decrease in the membrane permeability to inositol. In addition, phloretin and cytochalasin B, which bind to hexose carriers and inhibit hexose sugar transport, also inhibited inositol transport. The uptake of inositol was not affected by excesses of 3-O-methylglucose (100 mM) or by physiological concentrations of D-glucose. Thus, the transport mechanism of myo-inositol appears distinct from that of D-glucose.

摘要

测定了从鸡血中制备的富含网织红细胞的部分对肌醇的摄取,并与成熟红细胞中的摄取情况进行了比较。网织红细胞积累肌醇的水平是血浆浓度的三倍多,而红细胞中的水平仅略高于血浆浓度。当在250微摩尔的肌醇培养基浓度下测量时,网织红细胞的摄取速率约为66微摩尔/毫升红细胞/小时,而成熟红细胞的摄取速率为5微摩尔/毫升红细胞/小时。网织红细胞对肌醇流入的动力学分析揭示了一个双组分系统:可饱和和不可饱和。可饱和组分对肌醇的Km约为222微摩尔,是钠依赖性的。这种钠依赖性可饱和组分可能反映了肌醇的主动转运,占转运过程的30-35%。可饱和组分被阿米洛利完全抑制,但被哇巴因和布美他尼抑制的程度较小。此外,在网织红细胞成熟过程中,可饱和组分随着肌醇五磷酸合成的完成和膜对肌醇通透性的急剧下降而消失。此外,与己糖载体结合并抑制己糖转运的根皮素和细胞松弛素B也抑制了肌醇转运。肌醇的摄取不受过量3-O-甲基葡萄糖(100毫摩尔)或生理浓度的D-葡萄糖的影响。因此,肌醇的转运机制似乎与D-葡萄糖的不同。

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