Department of Experimental and Clinical Pharmacology, Medical University, Jaczewskiego 8b, 20-090 Lublin, Poland.
Department of Nephrology, Medical University, Jaczewskiego 8, 20-090 Lublin, Poland.
Toxicol Appl Pharmacol. 2022 Nov 1;454:116216. doi: 10.1016/j.taap.2022.116216. Epub 2022 Aug 31.
While mephedrone (4-methylmethcathinone), a synthetic cathinone derivative, is widely abused by adolescents and young adults, the knowledge about its long-term effects on memory processes is limited. Kynurenic acid (KYNA) is a neuroactive metabolite of the kynurenine pathway of tryptophan degradation. KYNA is considered an important endogenous modulator influencing physiological and pathological processes, including learning and memory processes. The aim of this study was to determine whether (A) binge-like mephedrone administration (10.0 and 30.0 mg/kg, intraperitoneally, in 4 doses separated by 2 h) induces memory impairments, assessed 2, 8 and 15 days after mephedrone cessation in the passive avoidance test in mice, and whether (B) KYNA is involved in these memory processes. To clarify the role of KYNA in the mephedrone effects, its production in the murine brain in vivo, and in cortical slices in vitro, as well as the activities of kynurenine aminotransferases (KATs) I and II were assessed. Furthermore, cell line experiments were conducted to investigate the effects of mephedrone on normal human brain cells. Our results showed memory impairments 8 and 15 days after binge-like mephedrone administration. At the same time, reduction in the KYNA level in the murine brain was noted. In vitro studies showed no effect of mephedrone on the production of KYNA in cortical slices or on the activity of the KAT I and II enzymes. Finally, exposure of normal cells to mephedrone in vitro resulted in a modest reduction of cell viability and proliferation.
虽然甲卡西酮(4-甲基甲卡西酮)作为一种合成卡西酮衍生物,被青少年和年轻人广泛滥用,但关于其对记忆过程的长期影响的知识有限。犬尿酸(KYNA)是色氨酸降解犬尿氨酸途径的一种神经活性代谢物。KYNA 被认为是一种重要的内源性调节剂,影响包括学习和记忆过程在内的生理和病理过程。本研究旨在确定:(A) binge-like 甲卡西酮给药(10.0 和 30.0 mg/kg,腹膜内,每 2 小时分 4 次给药)是否会导致小鼠被动回避测试中的记忆障碍,并在甲卡西酮停药后 2、8 和 15 天进行评估,以及(B)KYNA 是否参与这些记忆过程。为了阐明 KYNA 在甲卡西酮作用中的作用,评估了其在体内小鼠脑中的产生以及在体外皮质切片中的产生,以及犬尿氨酸氨基转移酶(KAT)I 和 II 的活性。此外,还进行了细胞系实验,以研究甲卡西酮对正常人类脑细胞的影响。我们的结果表明,binge-like 甲卡西酮给药后 8 天和 15 天出现记忆障碍。同时,注意到小鼠脑中 KYNA 水平降低。体外研究表明,甲卡西酮对皮质切片中 KYNA 的产生或 KAT I 和 II 酶的活性没有影响。最后,体外暴露于甲卡西酮的正常细胞导致细胞活力和增殖适度降低。