Jornet-Plaza Jordi, Ledesma-Corvi Sandra, García-Fuster M Julia
IUNICS, University of the Balearic Islands, Palma, Spain; Health Research Institute of the Balearic Islands (IdISBa), Palma, Spain.
IUNICS, University of the Balearic Islands, Palma, Spain; Health Research Institute of the Balearic Islands (IdISBa), Palma, Spain; Department of Medicine, University of the Balearic Islands, Palma, Spain.
Biomed Pharmacother. 2025 Jan;182:117781. doi: 10.1016/j.biopha.2024.117781. Epub 2024 Dec 25.
While ketamine was approved for treatment-resistant depression in adult patients, its efficacy and safety profile for adolescence still requires further characterization. In this context, prior preclinical studies have shown that sub-anesthetic doses of ketamine during adolescence exert antidepressant-like effects in rodents in a dose- and sex-dependent manner. However, additional studies evaluating the short- and long-term safety profile of ketamine at the doses necessary to induce antidepressant-like effects are needed. The present study aimed at validating the dose- and sex-dependent antidepressant-like responses of adolescent ketamine while evaluated its safety profile in rats of both sexes. To do so, ketamine was administered (1, 5 or 10 mg/kg; vs. vehicle; 1 vs. 7 days) during adolescence in naïve or early-life stressed (i.e., maternal deprivation) rats of both sexes. Antidepressant-like responses were scored in the forced-swim or novelty-suppressed feeding tests, and safety was evaluated by measuring psychomotor- and reinforcing-like responses induced by ketamine. In addition, long-term safety was assessed in adulthood through cognitive performance, or addiction liability (induced by ketamine re-exposure in rats treated with ketamine in adolescence). The main results validated the potential use of ketamine as an antidepressant for adolescence, but at different dose ranges for each sex. However, some safety concerns emerged in adolescent female rats (i.e., signs of sensitization at the dose used as antidepressant) or adult male rats (i.e., addiction liability when re-exposed to ketamine in adulthood), suggesting that caution and further research are needed before ketamine could be safely used in the clinic as an antidepressant for adolescents.
虽然氯胺酮已被批准用于治疗成年患者的难治性抑郁症,但其对青少年的疗效和安全性仍需进一步明确。在此背景下,先前的临床前研究表明,青春期给予亚麻醉剂量的氯胺酮会以剂量和性别依赖的方式在啮齿动物中产生抗抑郁样作用。然而,还需要更多研究来评估氯胺酮在诱导抗抑郁样作用所需剂量下的短期和长期安全性。本研究旨在验证青春期氯胺酮剂量和性别依赖性的抗抑郁样反应,同时评估其在两性大鼠中的安全性。为此,在青春期对未处理或早年应激(即母婴分离)的两性大鼠给予氯胺酮(1、5或10mg/kg;与溶剂对照;给药1天或7天)。在强迫游泳或新奇抑制摄食试验中对抗抑郁样反应进行评分,并通过测量氯胺酮诱导的精神运动和强化样反应来评估安全性。此外,在成年期通过认知能力或成瘾倾向(青春期接受氯胺酮治疗的大鼠再次接触氯胺酮诱导)评估长期安全性。主要结果验证了氯胺酮作为青少年抗抑郁药的潜在用途,但两性的有效剂量范围不同。然而,在青春期雌性大鼠(即用作抗抑郁药的剂量出现敏感化迹象)或成年雄性大鼠(即成年期再次接触氯胺酮时的成瘾倾向)中出现了一些安全问题,这表明在氯胺酮能够安全地在临床上用作青少年抗抑郁药之前,需要谨慎并进行进一步研究。