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在自由活动大鼠中,通过体内伏安法测量,噻奈普汀对5-羟吲哚以及对吗啡诱导的延髓背角水平5-羟色胺(5-HT)代谢增加的影响。

Effects of tianeptine on 5-hydroxyindoles and on the morphine-induced increase in 5-HT metabolism at the medullary dorsal horn level as measured by in vivo voltammetry in freely moving rats.

作者信息

Puig S, Rivot J P, Besson J M

机构信息

Unité de Recherches de Physiopharmacologie du Système Nerveux, INSERM, U. 161, Paris, France.

出版信息

Brain Res. 1993 Jan 15;600(2):219-24. doi: 10.1016/0006-8993(93)91376-4.

Abstract

The present study, by the use of in vivo electrochemical detection of 5-hydroxyindole (peak '3') in the bulbo spinal serotonergic system at the medullary dorsal horn (MDH) level, investigated the effects of the new tricyclic antidepressant (TCA) tianeptine, which has been shown to be a specific serotonin (5-HT) uptake enhancer. It was found that acutely administered tianeptine (10 mg/kg, i.p.) induced a marked significant increase in peak 3 within the dorsal horn, an in vivo observation which is in accordance with the biochemical properties of tianeptine as studied in forebrain structures. In addition, the effect of tianeptine on the morphine-induced increase in 5-HT metabolism was investigated, by comparison with the previous data obtained with the specific 5-HT uptake inhibitor femoxetine in the MDH. It was shown that tianeptine can display additive effect with morphine (10 mg/kg, i.p.) on 5-HT metabolism at the MDH level. These results are discussed in relation to the effects of classical TCAs and the particular properties of tianeptine.

摘要

本研究通过在延髓背角(MDH)水平对延髓-脊髓5-羟色胺能系统中的5-羟吲哚(峰“3”)进行体内电化学检测,研究了新型三环类抗抑郁药(TCA)噻奈普汀的作用,噻奈普汀已被证明是一种特异性5-羟色胺(5-HT)摄取增强剂。研究发现,急性给予噻奈普汀(10mg/kg,腹腔注射)可使背角内的峰3显著明显增加,这一体内观察结果与在前脑结构中研究的噻奈普汀的生化特性一致。此外,通过与先前在MDH中使用特异性5-HT摄取抑制剂非莫西汀获得的数据进行比较,研究了噻奈普汀对吗啡诱导的5-HT代谢增加的影响。结果表明,噻奈普汀在MDH水平上可与吗啡(10mg/kg,腹腔注射)对5-HT代谢产生相加作用。结合经典三环类抗抑郁药的作用和噻奈普汀的特殊性质对这些结果进行了讨论。

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