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抗抑郁药物作用下光敏狒狒的癫痫发作活动及5-羟色胺能机制的作用。

Seizure activity in photosensitive baboons following antidepressant drugs and the role of serotoninergic mechanisms.

作者信息

Trimble M, Anlezark G, Meldrum B

出版信息

Psychopharmacology (Berl). 1977 Jan 31;51(2):159-64. doi: 10.1007/BF00431733.

Abstract

Laboratroy and clinical evidence indicates that tricyclic antidepressants lower seizure threshold and in high doses may induce generalised seizures. In baboons with photosensitive epilepsy (Papio papio) the effects of 2 tricyclic antidepressants (imipramine and chlorimipramine) and of maprotiline and Nomi fensine have been studied (i.v. dose range 1-20 mg/kg. Imipramine, chlorimipramine and maprotiline (10 mg/kg i.v.) lowered seizure threshold to a comparable extent, whereas Nomifensine (10 mg/kg i.v-) did not enhance myoclinic responses to photic stimulation. Generalised seizures were seen 15-30 min after imipramine or chlorimipramine (20 mg/kg), and these two drugs showed no difference in their epileptogenicity. Administration of 5-hydroxytryptophan (25 mg/kg i.v.) 90 min before chlorimipramine or imipramine (10 mg/kg) completely blocked the usual augmentation of photically-induced epileptic responses. It is concluded that enhancement of serotoninergic activity following blockade of 5-HT re-uptake within the brain is unlikely to be responsible for enhanced myoclonic responses and epileptogenic seizures seen after tricyclic antidepressants. Nomifensine is significantly less epileptogenic than imipramine or chlorimipramine.

摘要

实验室和临床证据表明,三环类抗抑郁药会降低癫痫发作阈值,高剂量时可能诱发全身性癫痫发作。在患有光敏性癫痫的狒狒(巴氏狒狒)中,研究了两种三环类抗抑郁药(丙咪嗪和氯丙咪嗪)、马普替林和诺米芬辛的作用(静脉注射剂量范围为1 - 20毫克/千克)。丙咪嗪、氯丙咪嗪和马普替林(静脉注射10毫克/千克)降低癫痫发作阈值的程度相当,而诺米芬辛(静脉注射10毫克/千克)并未增强对光刺激的肌阵挛反应。在丙咪嗪或氯丙咪嗪(20毫克/千克)注射后15 - 30分钟出现全身性癫痫发作,且这两种药物的致癫痫性无差异。在氯丙咪嗪或丙咪嗪(10毫克/千克)注射前90分钟静脉注射5 - 羟色氨酸(25毫克/千克)可完全阻断通常由光诱导的癫痫反应增强。结论是,脑内5 - 羟色胺再摄取被阻断后血清素能活性增强不太可能是三环类抗抑郁药后出现的肌阵挛反应增强和致癫痫性发作的原因。诺米芬辛的致癫痫性明显低于丙咪嗪或氯丙咪嗪。

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