López-Arnau Raúl, Martínez-Clemente José, Abad Sonia, Pubill David, Camarasa Jorge, Escubedo Elena
Department of Pharmacology and Therapeutic Chemistry (Pharmacology Section) and Institute of Biomedicine (IBUB), Faculty of Pharmacy, University of Barcelona, Av. Joan XXIII s/n, 08028, Barcelona, Spain.
Psychopharmacology (Berl). 2014 Aug;231(16):3119-29. doi: 10.1007/s00213-014-3493-6. Epub 2014 Apr 5.
Methylone, a new drug of abuse sold as "bath salts," has similar effects to ecstasy or cocaine.
We have investigated changes in dopaminergic and serotoninergic markers, indicative of neuronal damage induced by methylone in the frontal cortex, hippocampus, and striatum of mice, according to two different treatment schedules.
Methylone was given subcutaneously to male Swiss CD1 mice at an ambient temperature of 26 °C. Treatment A consisted of three doses of 25 mg/kg at 3.5-h intervals between doses for two consecutive days, and treatment B consisted of four doses of 25 mg/kg at 3-h intervals in 1 day.
Repeated methylone administration induced hyperthermia and a significant loss in body weight. Following treatment A, methylone induced transient dopaminergic (frontal cortex) and serotoninergic (hippocampus) impairment. Following treatment B, transient dopaminergic (frontal cortex) and serotonergic (frontal cortex and hippocampus) changes 7 days after treatment were found. We found evidence of astrogliosis in the CA1 and the dentate gyrus of the hippocampus following treatment B. The animals also showed an increase in immobility time in the forced swim test, pointing to a depressive-like behavior. In cultured cortical neurons, methylone (for 24 and 48 h) did not induce a remarkable cytotoxic effect.
The neural effects of methylone differ depending upon the treatment schedule. Neurochemical changes elicited by methylone are apparent when administered at an elevated ambient temperature, four times per day at 3-h intervals, which is in accordance with its short half-life.
甲酮是一种作为“浴盐”出售的新型滥用药物,其效果与摇头丸或可卡因相似。
我们根据两种不同的治疗方案,研究了甲酮对小鼠额叶皮质、海马体和纹状体中多巴胺能和5-羟色胺能标志物的影响,这些标志物表明了甲酮诱导的神经元损伤。
在26℃的环境温度下,将甲酮皮下注射给雄性瑞士CD1小鼠。治疗A包括连续两天,每隔3.5小时注射三剂25mg/kg;治疗B包括在一天内每隔3小时注射四剂25mg/kg。
重复给予甲酮会导致体温过高和体重显著下降。治疗A后,甲酮诱导了短暂的多巴胺能(额叶皮质)和5-羟色胺能(海马体)损伤。治疗B后,在治疗7天后发现了短暂的多巴胺能(额叶皮质)和5-羟色胺能(额叶皮质和海马体)变化。我们发现治疗B后海马体CA1区和齿状回有星形胶质细胞增生的证据。在强迫游泳试验中,这些动物的不动时间也增加了,表明存在类似抑郁的行为。在培养的皮质神经元中,甲酮(作用24和48小时)未诱导明显的细胞毒性作用。
甲酮的神经效应因治疗方案而异。当在较高的环境温度下,每天四次、每隔3小时给药时,甲酮引起的神经化学变化很明显,这与其短半衰期一致。