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人淋巴细胞中高亲和力5-羟色胺转运体的表达

Expression of a high-affinity serotonin transporter in human lymphocytes.

作者信息

Faraj B A, Olkowski Z L, Jackson R T

机构信息

Department of Radiology (Division of Nuclear Medicine), Emory University School of Medicine, Atlanta, GA 30322.

出版信息

Int J Immunopharmacol. 1994 Jul;16(7):561-7. doi: 10.1016/0192-0561(94)90107-4.

Abstract

This study was undertaken to assess the capability of lymphocytes to actively transport serotonin (5-HT). The data we obtained showed that lymphocytes isolated from the blood of normal human subjects contained a high-affinity uptake system for [3H]5-HT. Kinetic analysis of the uptake data as computed by regression analysis from Lineweaver--Burk plots, yielded a Km of 180 +/- 20 nM and Vmax of 94 +/- pmole/10(7) cells. The uptake of [3H]5-HT was temperature, sodium and chloride dependent and was potently inhibited by the antidepressants clomipramine, imipramine, fluoxetine and fluvoxamine, which are specific for the 5-HT transporter. Compounds that are more selective for norepinephrine and dopamine transporters such as mazindol, desipramine, and GBR 19209 had a lower inhibitory effect on the uptake of [3H]5-HT in human lymphocytes. The expression of a 5-HT transporter in human lymphocytes that resembles 5-HT uptake by platelets and brain synaptosomes may provide insights into the potential role of 5-HT in immune function and its relationship to the neurobiology of affective and addictive disorders.

摘要

本研究旨在评估淋巴细胞主动转运血清素(5-羟色胺,5-HT)的能力。我们获得的数据表明,从正常人类受试者血液中分离出的淋巴细胞含有一个针对[3H]5-HT的高亲和力摄取系统。通过对Lineweaver-Burk图进行回归分析计算摄取数据的动力学分析,得出Km为180±20 nM,Vmax为94±pmole/10(7)个细胞。[3H]5-HT的摄取依赖于温度、钠和氯,并且被抗抑郁药氯米帕明、丙咪嗪、氟西汀和氟伏沙明强烈抑制,这些药物对5-HT转运体具有特异性。对去甲肾上腺素和多巴胺转运体更具选择性的化合物,如马吲哚、地昔帕明和GBR 19209,对人淋巴细胞中[3H]5-HT摄取的抑制作用较低。人淋巴细胞中5-HT转运体的表达类似于血小板和脑突触体对5-HT的摄取,这可能为5-HT在免疫功能中的潜在作用及其与情感和成瘾性障碍神经生物学的关系提供见解。

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