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麻醉剂对大鼠脑突触体摄取5-羟色胺的影响。

Anesthetic effects on 5-hydroxytryptamine uptake by rat brain synaptosomes.

作者信息

Martin D C, Watkins C A, Adams R J, Nason L A

机构信息

Department of Anesthesiology, Medical College of Georgia, Augusta 30912-2277.

出版信息

Brain Res. 1988 Jul 12;455(2):360-5. doi: 10.1016/0006-8993(88)90095-9.

Abstract

As a neurotransmitter involved in modulating central nervous system nociception and awareness, 5-hydroxytryptamine (5-HT) may play an important role in the clinical sequelae of certain anesthetic compounds. Anesthetic agents are known to affect peripheral, non-neuronal 5-HT uptake but little is known about their effects on 5-HT metabolism in the central nervous system. The effects of several anesthetic compounds on 5-HT uptake were examined in synaptosomes isolated from rat brain cortex. Inhibition of this uptake process was observed by exposure to clinically relevant concentrations of the volatile anesthetics halothane, isoflurane, and enflurane. The non-volatile agent, ketamine also inhibited uptake while the narcotic fentanyl had an effect only at the highest concentrations tested. Non-volatile agents which had neither a consistent nor significant effect on synaptosomal 5-HT uptake included pentobarbital, sufentanil, and etomidate. These alterations of 5-HT metabolism could represent a mechanism that contributes to anesthetic action.

摘要

作为一种参与调节中枢神经系统伤害感受和意识的神经递质,5-羟色胺(5-HT)可能在某些麻醉化合物的临床后遗症中发挥重要作用。已知麻醉剂会影响外周非神经元5-HT的摄取,但它们对中枢神经系统中5-HT代谢的影响却知之甚少。在从大鼠大脑皮层分离出的突触体中检测了几种麻醉化合物对5-HT摄取的影响。通过暴露于临床相关浓度的挥发性麻醉剂氟烷、异氟烷和恩氟烷,观察到了这种摄取过程的抑制。非挥发性药物氯胺酮也抑制摄取,而麻醉性镇痛药芬太尼仅在测试的最高浓度时有作用。对突触体5-HT摄取既无一致影响也无显著影响的非挥发性药物包括戊巴比妥、舒芬太尼和依托咪酯。5-HT代谢的这些改变可能代表了一种促成麻醉作用的机制。

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