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牛嗜铬粒细胞膜对间碘苄胍的摄取

Uptake of meta-iodobenzylguanidine by bovine chromaffin granule membranes.

作者信息

Gasnier B, Roisin M P, Scherman D, Coornaert S, Desplanches G, Henry J P

出版信息

Mol Pharmacol. 1986 Mar;29(3):275-80.

PMID:3951433
Abstract

meta-Iodobenzylguanidine, an adrenal imaging agent used for the scintigraphic detection of human pheochromocytoma, is a substrate for the monoamine uptake system of chromaffin granules. It is accumulated by bovine chromaffin granule membrane vesicles in the presence of ATP, and it can be released by an osmotic shock. The uptake is dependent upon the generation of an H+-electrochemical gradient by an ATP-dependent H+ pump since it is blocked by an H+ ionophore and since meta-iodobenzylguanidine uptake can be driven by imposing an artificial pH gradient (inside acidic) on the membrane vesicles. The transport is saturable and its Km value (2.0 microM at pH 8.0) is similar to that of noradrenaline (5.3 microM). Transport occurs through the monoamine transporter since it is blocked by the same inhibitors, tetrabenazine and reserpine, and also by the transporter substrates noradrenaline and serotonin. Noradrenaline inhibits meta-iodobenzylguanidine uptake competitively (Ki = 13 microM). In addition, meta-iodobenzylguanidine displaces dihydrotetrabenazine and reserpine from their binding sites on chromaffin granule membranes. It is thus likely that, after in vivo administration, [131I] meta-iodobenzylguanidine is ultimately stored in chromaffin granules and that it is translocated by the monoamine transporter.

摘要

间碘苄胍是一种用于人体嗜铬细胞瘤闪烁显像检测的肾上腺显像剂,是嗜铬粒蛋白单胺摄取系统的底物。在ATP存在的情况下,它可被牛嗜铬粒蛋白膜囊泡摄取,并可通过渗透压休克释放出来。摄取依赖于由ATP依赖性H⁺泵产生的H⁺电化学梯度,因为它被H⁺离子载体阻断,并且由于在膜囊泡上施加人工pH梯度(内部呈酸性)可驱动间碘苄胍的摄取。这种转运是可饱和的,其Km值(pH 8.0时为2.0 μM)与去甲肾上腺素的Km值(5.3 μM)相似。转运通过单胺转运体进行,因为它被相同的抑制剂丁苯那嗪和利血平阻断,也被转运体底物去甲肾上腺素和5-羟色胺阻断。去甲肾上腺素竞争性抑制间碘苄胍的摄取(Ki = 13 μM)。此外,间碘苄胍可将二氢丁苯那嗪和利血平从它们在嗜铬粒蛋白膜上的结合位点置换下来。因此,体内给药后,[¹³¹I]间碘苄胍很可能最终储存在嗜铬粒蛋白中,并通过单胺转运体转运。

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