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跨膜质子梯度与血小板5-羟色胺转运的偶联。

Coupling of transmembrane proton gradients to platelet serotonin transport.

作者信息

Keyes S R, Rudnick G

出版信息

J Biol Chem. 1982 Feb 10;257(3):1172-6.

PMID:7056713
Abstract

A pH difference (acid inside) across the platelet plasma membrane increases both the rate and extent of serotonin accumulation inside plasma membrane vesicles. Even in the absence of other transmembrane ion gradients, this pH difference (delta pH) serves as the sole driving force for serotonin accumulation, leading to a serotonin concentration 18-fold higher inside the vesicle. This process requires Na+ and is blocked by imipramine, indicating that it is mediated by the serotonin transporter. At physiological pH, internal K+ is counter-transported with serotonin, and high internal K+ stimulates transport maximally. Internal K+ also blocks the delta pH stimulation of serotonin transport. Conversely, low internal pH (5.6) inhibits the ability of internal K+ to stimulate transport. This apparent competition between K+ and protons suggests that delta pH drives serotonin accumulation through counter-transport with protons, and that serotonin is transported in its cationic form.

摘要

血小板质膜两侧的pH差异(内部呈酸性)会增加血清素在质膜囊泡内积累的速率和程度。即使不存在其他跨膜离子梯度,这种pH差异(ΔpH)也作为血清素积累的唯一驱动力,导致囊泡内血清素浓度高出18倍。该过程需要Na+并被丙咪嗪阻断,表明它由血清素转运体介导。在生理pH下,内部K+与血清素进行反向转运,高内部K+能最大程度地刺激转运。内部K+也会阻断ΔpH对血清素转运的刺激。相反,低内部pH(5.6)会抑制内部K+刺激转运的能力。K+与质子之间这种明显的竞争表明,ΔpH通过与质子反向转运来驱动血清素积累,并且血清素以阳离子形式被转运。

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