Jaques S, Tobes M C, Sisson J C, Baker J A, Wieland D M
Mol Pharmacol. 1984 Nov;26(3):539-46.
Radioiodinated meta-iodobenzylguanidine (MIBG), a scintigraphic agent used for the detection of human pheochromocytomas, is thought to utilize the same uptake and retention mechanism(s) as norepinephrine (NE). Using cultured bovine adrenomedullary cells, we compared the mechanism(s) of uptake of MIBG to that of NE. Two different uptake systems were identified. NE and MIBG were taken up by a sodium-dependent system that was characterized by: 1) temperature dependency; 2) high affinity: Km of 1.22 +/- 0.12 microM for MIBG and 1.41 +/- 0.50 microM for NE; 3) low capacity: Vm (picomoles/10(6) cells/10 min) of 64.3 +/- 3.3 for MIBG and 36.6 +/- 7.2 for NE; 4) saturability; 5) ouabain sensitivity; and 6) energy dependency. However, NE and MIBG also were taken up by a temperature-dependent, sodium-independent, apparently unsaturable, and energy-independent system. The sodium-dependent uptake system fulfills many of the criteria for Uptake1 whereas the sodium-independent uptake system is most likely a passive diffusion process. NE uptake proceeded predominantly by the sodium-dependent process. Uptake of MIBG occurred by both pathways at low concentrations, but at high concentrations (greater than 10 microM) uptake was predominantly (75 to 100%) by the sodium-independent process. Inhibition studies suggest that MIBG and NE are transported by the same carrier involved in the sodium-dependent system. Scintiscans of the human adrenals and pheochromocytomas appear to reflect uptake of [131I]MIBG by the sodium-dependent system.
放射性碘标记的间碘苄胍(MIBG)是一种用于检测人类嗜铬细胞瘤的闪烁显像剂,被认为与去甲肾上腺素(NE)利用相同的摄取和保留机制。我们使用培养的牛肾上腺髓质细胞,比较了MIBG与NE的摄取机制。确定了两种不同的摄取系统。NE和MIBG通过一种钠依赖性系统摄取,其特点为:1)温度依赖性;2)高亲和力:MIBG的Km为1.22±0.12微摩尔,NE的Km为1.41±0.50微摩尔;3)低容量:MIBG的Vm(皮摩尔/10⁶细胞/10分钟)为64.3±3.3,NE的Vm为36.6±7.2;4)可饱和性;5)哇巴因敏感性;6)能量依赖性。然而,NE和MIBG也通过一种温度依赖性、钠非依赖性、明显不饱和且能量非依赖性的系统摄取。钠依赖性摄取系统满足摄取1的许多标准,而钠非依赖性摄取系统很可能是一个被动扩散过程。NE摄取主要通过钠依赖性过程进行。低浓度时,MIBG通过两条途径摄取,但高浓度(大于10微摩尔)时,摄取主要(75%至100%)通过钠非依赖性过程。抑制研究表明,MIBG和NE由参与钠依赖性系统的同一载体转运。人类肾上腺和嗜铬细胞瘤的闪烁扫描似乎反映了[¹³¹I]MIBG通过钠依赖性系统的摄取。