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二磷酸腺苷抑制血清素转运体。

Adenosine diphosphate inhibits the serotonin transporter.

作者信息

Anderson G M, Hall L M, Horne W C, Yang J X

机构信息

Child Study Center, Yale University School of Medicine, New Haven, CT 06520-7900, USA.

出版信息

Biochim Biophys Acta. 1996 Aug 14;1283(1):14-20. doi: 10.1016/0005-2736(96)00073-9.

DOI:10.1016/0005-2736(96)00073-9
PMID:8765089
Abstract

Adenosine 5'-diphosphate (ADP) caused rapid and significant reductions in the rates of [3H]serotonin uptake observed for human platelets, human platelet vesicles, and rat brain synaptic vesicles. Estimated Vmax values in platelets (N = 15). platelet vesicles (N = 3), and synaptic vesicles (N = 3) exposed to 100 microM ADP were 42.3 +/- 11.4%, 78.8 +/- 1.4%, and 56.8 +/- 9.9% of control values, respectively. The EC50 values observed for ADP in platelets and platelet vesicles were 10-24 microM. Exposure to 100 microM ADP had small, inconsistent effects on KM values observed for the platelet transporter. ADP (100 microM) caused only a slight competitive inhibition of the platelet membrane binding of [3H]citalopram, a ligand for the 5HT uptake site of the transporter (5.0% displacement of 1.0 nM [3H]citalopram, 13% increase in apparent KD). The ADP analogue 2-methylthioADP caused similar decreases in the rates of platelet [3H]serotonin uptake, while a number of other related compounds had little or no effect on rates of platelet uptake. The ADP-effect on uptake was rapid, occurring in less than 2.5 s. and was additive with reductions produced by protein kinase C (PKC) activation. The ADP-induced decreases in uptake did not appear to occur through the ADP receptor or known platelet second messenger systems. The exact mechanism of the ADP-effect and its functional significance remain to be determined.

摘要

5'-二磷酸腺苷(ADP)可使人类血小板、人类血小板囊泡及大鼠脑突触囊泡对[3H]5-羟色胺的摄取速率迅速且显著降低。暴露于100微摩尔/升ADP的血小板(N = 15)、血小板囊泡(N = 3)及突触囊泡(N = 3)的最大反应速度(Vmax)估计值分别为对照值的42.3±11.4%、78.8±1.4%及56.8±9.9%。ADP在血小板及血小板囊泡中的半数有效浓度(EC50)值为10 - 24微摩尔/升。暴露于100微摩尔/升ADP对血小板转运体的米氏常数(KM)值影响较小且不一致。100微摩尔/升的ADP仅对[3H]西酞普兰(转运体5-羟色胺摄取位点的配体)与血小板膜的结合产生轻微的竞争性抑制(1.0纳摩尔[3H]西酞普兰的置换率为5.0%,表观解离常数[KD]增加13%)。ADP类似物2-甲硫基ADP可使血小板对[3H]5-羟色胺的摄取速率产生类似的降低,而其他一些相关化合物对血小板摄取速率几乎没有影响。ADP对摄取的作用迅速,在不到2.5秒内即可发生,且与蛋白激酶C(PKC)激活所导致的摄取降低具有相加作用。ADP诱导的摄取降低似乎并非通过ADP受体或已知的血小板第二信使系统发生。ADP作用的确切机制及其功能意义仍有待确定。

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