Thompson Institute, University of the Sunshine Coast, 12 Innovation Parkway, Birtinya, QLD, 4575, Australia.
Psychopharmacology (Berl). 2023 Dec;240(12):2483-2497. doi: 10.1007/s00213-023-06480-x. Epub 2023 Oct 26.
Ketamine has received considerable attention for its rapid and robust antidepressant response over the past decade. Current evidence, in clinical populations, predominantly relates to parenterally administered ketamine, which is reported to produce significant undesirable side effects, with additional concerns regarding long-term safety and abuse potential. Attempts to produce a similar drug to ketamine, without the psychotomimetic side effects, have proved elusive. Orally administered ketamine has a different pharmacological profile to parentally administered ketamine, suggesting it may be a viable alternative. Emerging evidence regarding the efficacy and tolerability of oral ketamine suggests that it may be a favourable route of administration, as it appears to obtain similarly beneficial treatment effects, but without the cost and medical resources required in parenteral dosing. The pharmacological effects may be due to the active metabolite norketamine, which has been found to be at substantially higher levels via oral dosing, most likely due to first-pass clearance. Despite bioavailability and peak plasma concentrations both being lower than when administered parenterally, evidence suggests that low-dose oral ketamine is clinically effective in treating pain. This may also be due to the actions of norketamine and therefore, its relevance to the mental health context is explored in this narrative review.
在过去十年中,氯胺酮因其快速而强大的抗抑郁反应而受到广泛关注。目前的证据主要与静脉注射氯胺酮有关,据报道,它会产生显著的不良副作用,此外还存在长期安全性和滥用潜力方面的担忧。人们试图制造一种类似氯胺酮的药物,但没有致幻副作用,但一直未能成功。与静脉注射氯胺酮相比,口服氯胺酮具有不同的药理学特征,这表明它可能是一种可行的替代药物。关于口服氯胺酮疗效和耐受性的新证据表明,它可能是一种更有利的给药途径,因为它似乎能获得类似的有益治疗效果,而无需静脉注射所需的成本和医疗资源。药理学作用可能是由于活性代谢物去甲氯胺酮的存在,通过口服给药发现去甲氯胺酮的水平要高得多,这很可能是由于首过清除。尽管口服给药的生物利用度和血浆峰浓度均低于静脉给药,但有证据表明,低剂量口服氯胺酮在治疗疼痛方面具有临床疗效。这也可能是由于去甲氯胺酮的作用,因此,本文探讨了其与心理健康领域的相关性。