Murono E P, Lin T, Osterman J
Andrologia. 1986 Nov-Dec;18(6):587-94. doi: 10.1111/j.1439-0272.1986.tb01836.x.
The present study examines several aspects of [14C]-2-deoxyglucose uptake by rat Leydig cells: the characteristics of uptake by Leydig cells and type of inhibition by cytochalasin B, the effect of other drugs on [14C]-2-deoxyglucose uptake, the specificity of the glucose transporter for other substrates and the effect of various hormones. The apparent Km and V for [14C]-2-deoxyglucose were 0.4 mM and 0.17 mumol/min/10(6) cells, respectively. The inhibition of [14C]-2-deoxyglucose by cytochalasin B was competitive in nature, with an apparent Ki of 0.28 microM. Both phloretin and phlorizin (1.0-50 microM) inhibited [14C]-2-deoxyglucose uptake in a dose-dependent manner. Although D-glucose inhibited [14C]-2-deoxyglucose uptake by Leydig cells, L-glucose was ineffective, reflecting the stereospecificity of the glucose transporter for the former substrate. Various hormones, including: insulin, LH, 17 beta-estradiol or growth hormone which have been reported to stimulate glucose uptake in cells from other tissues, had no effect on [14C]-2-deoxyglucose uptake in Leydig cells under the current conditions. It remains to be determined how glucose uptake in Leydig cells is regulated.
本研究考察了大鼠睾丸间质细胞对[14C]-2-脱氧葡萄糖摄取的几个方面:睾丸间质细胞摄取的特征及细胞松弛素B的抑制类型、其他药物对[14C]-2-脱氧葡萄糖摄取的影响、葡萄糖转运体对其他底物的特异性以及各种激素的作用。[14C]-2-脱氧葡萄糖的表观Km和V分别为0.4 mM和0.17 μmol/分钟/10(6)个细胞。细胞松弛素B对[14C]-2-脱氧葡萄糖的抑制本质上是竞争性的,表观Ki为0.28 μM。根皮素和根皮苷(1.0 - 50 μM)均以剂量依赖性方式抑制[14C]-2-脱氧葡萄糖的摄取。虽然D-葡萄糖抑制睾丸间质细胞对[14C]-2-脱氧葡萄糖的摄取,但L-葡萄糖无效,这反映了葡萄糖转运体对前一种底物的立体特异性。各种激素,包括:胰岛素、促黄体生成素、17β-雌二醇或生长激素,据报道它们可刺激其他组织细胞的葡萄糖摄取,但在当前条件下对睾丸间质细胞摄取[14C]-2-脱氧葡萄糖没有影响。睾丸间质细胞中葡萄糖摄取是如何调节的仍有待确定。