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纳洛酮急性给药可促进清醒,抑制 REM 睡眠。

Noribogaine acute administration in rats promotes wakefulness and suppresses REM sleep.

机构信息

Departamento de Fisiología, Facultad de Medicina, Universidad de la República, Montevideo, 11800, Uruguay.

Laboratorio de Síntesis Orgánica, Departamento de Química Orgánica, Facultad de Química, Universidad de la República, Montevideo, 11800, Uruguay.

出版信息

Psychopharmacology (Berl). 2024 Jul;241(7):1417-1426. doi: 10.1007/s00213-024-06572-2. Epub 2024 Mar 12.

Abstract

Ibogaine is a potent atypical psychedelic that has gained considerable attention due to its antiaddictive and antidepressant properties in preclinical and clinical studies. Previous research from our group showed that ibogaine suppresses sleep and produces an altered wakefulness state, which resembles natural REM sleep. However, after systemic administration, ibogaine is rapidly metabolized to noribogaine, which also shows antiaddictive effects but with a distinct pharmacological profile, making this drug a promising therapeutic candidate. Therefore, we still ignore whether the sleep/wake alterations depend on ibogaine or its principal metabolite noribogaine. To answer this question, we conducted polysomnographic recordings in rats following the administration of pure noribogaine. Our results show that noribogaine promotes wakefulness while reducing slow-wave sleep and blocking REM sleep, similar to our previous results reported for ibogaine administration. Thus, we shed new evidence on the mechanisms by which iboga alkaloids work in the brain.

摘要

伊博加因是一种有效的非典型迷幻剂,由于其在临床前和临床研究中的抗成瘾和抗抑郁特性而引起了相当大的关注。我们小组的先前研究表明,伊博加因抑制睡眠并产生改变的觉醒状态,类似于自然 REM 睡眠。然而,在全身给药后,伊博加因迅速代谢为去甲伊博加因,它也显示出抗成瘾作用,但具有明显的药理学特征,使这种药物成为一种有前途的治疗候选药物。因此,我们仍然不知道睡眠/觉醒的改变是依赖于伊博加因还是它的主要代谢物去甲伊博加因。为了回答这个问题,我们在大鼠中进行了多导睡眠描记术记录,以观察纯去甲伊博加因的给药情况。我们的结果表明,去甲伊博加因促进觉醒,同时减少慢波睡眠并阻断 REM 睡眠,这与我们之前报道的伊博加因给药的结果相似。因此,我们为伊博加因类生物碱在大脑中的作用机制提供了新的证据。

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