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氟烷抑制大鼠脑突触体对5-羟色胺的摄取。

Halothane inhibits 5-hydroxytryptamine uptake by synaptosomes from rat brain.

作者信息

Martin D C, Adams R J, Introna R P

机构信息

Department of Anesthesiology and Physiology and Endocrinology, Medical College of Georgia, Augusta 30912.

出版信息

Neuropharmacology. 1990 Jan;29(1):9-16. doi: 10.1016/0028-3908(90)90077-5.

Abstract

The activity of 5-hydroxytryptamine (serotonin; 5-HT) in the central nervous system modulates sleep, the perception of pain and other functions of the body which might possibly relate to mechanisms of general anesthetic action. While administration of anesthetics has inconsistent effects on the content of 5-HT in brain, in vivo, accumulated data suggest that anesthetic drugs alter 5-HT homeostasis in the central nervous system. In an effort to identify one possible site of anesthetic action, the effect of halothane on the uptake of 5-HT was studied in synaptosomes isolated from the brain of rat. Established techniques were used to prepare the synaptosomal fractions and measure high affinity transport of radiolabelled 5-HT. Halothane inhibited synaptosomal accumulation of 5HT in a concentration-dependent manner, but had little effect on the passive or spontaneous release of the accumulated 5-HT. Rates of uptake of 5HT were inhibited by 43% in the presence of 1 mM halothane and by 75% of control in the presence of 5 mM halothane; the apparent I50 for halothane was 1.0 +/- 0.1 mM and Lineweaver-Burk analysis indicated the inhibition to be competitive at concentrations around the I50.

摘要

5-羟色胺(血清素;5-HT)在中枢神经系统中的活性调节睡眠、痛觉感知以及身体的其他功能,这些功能可能与全身麻醉作用机制有关。虽然麻醉药对脑内5-HT含量的影响并不一致,但体内积累的数据表明麻醉药物会改变中枢神经系统中5-HT的稳态。为了确定麻醉作用的一个可能位点,研究了氟烷对从大鼠脑部分离的突触体摄取5-HT的影响。采用既定技术制备突触体组分并测量放射性标记的5-HT的高亲和力转运。氟烷以浓度依赖性方式抑制突触体对5-HT的积累,但对积累的5-HT的被动或自发释放影响很小。在1 mM氟烷存在下,5-HT的摄取速率被抑制43%,在5 mM氟烷存在下被抑制至对照的75%;氟烷的表观半数抑制浓度(I50)为1.0±0.1 mM,Lineweaver-Burk分析表明在I50附近浓度下的抑制作用为竞争性抑制。

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