首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Effects of Mephedrone and Amphetamine Exposure during Adolescence on Spatial Memory in Adulthood: Behavioral and Neurochemical Analysis
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Effects of Mephedrone and Amphetamine Exposure during Adolescence on Spatial Memory in Adulthood: Behavioral and Neurochemical Analysis

机译:青春期乳头和疗法暴露在成年期间空间记忆中的影响:行为和神经化学分析

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摘要

A synthetic cathinone, mephedrone is widely abused by adolescents and young adults. Despite its widespread use, little is known regarding its long-term effects on cognitive function. Therefore, we assessed, for the first time, whether (A) repeated mephedrone (30 mg/kg, i.p., 10 days, once a day) exposure during adolescence (PND 40) induces deleterious effects on spatial memory and reversal learning (Barnes maze task) in adult (PND 71–84) rats and whether (B) these effects were comparable to amphetamine (2.5 mg/kg, i.p.). Furthermore, the influence of these drugs on MMP-9, NMDA receptor subunits (GluN1, GluN2A/2B) and PSD-95 protein expression were assessed in adult rats. The drug effects were evaluated at doses that per se induce rewarding/reinforcing effects in rats. Our results showed deficits in spatial memory (delayed effect of amphetamine) and reversal learning in adult rats that received mephedrone/amphetamine in adolescence. However, the reversal learning impairment may actually have been due to spatial learning rather than cognitive flexibility impairments. Furthermore, mephedrone, but not amphetamine, enhanced with delayed onset, MMP-9 levels in the prefrontal cortex and the hippocampus. Mephedrone given during adolescence induced changes in MMP-9 level and up-regulation of the GluN2B-containing NMDA receptor (prefrontal cortex and hippocampus) in young adult (PND 63) and adult (PND 87) rats. Finally, in adult rats, PSD-95 expression was increased in the prefrontal cortex and decreased in the hippocampus. In contrast, in adult rats exposed to amphetamine in adolescence, GluN2A subunit and PSD-95 expression were decreased (down-regulated) in the hippocampus. Thus, in mephedrone—but not amphetamine-treated rats, the deleterious effects on spatial memory were associated with changes in MMP-9 level. Because the GluN2B-containing NMDA receptor dominates in adolescence, mephedrone seems to induce more harmful effects on cognition than amphetamine does during this period of life.
机译:合成的Cathinone,Mephedrone被青少年和年轻成年人受到广泛滥用。尽管它广泛使用,但对其对认知功能的长期影响很少。因此,我们首次评估了(a)反复米飞酮(30mg / kg,IP,10天,每天一次)暴露在青春期(pnd 40)对空间记忆和逆转学习引起有害影响(Barnes迷宫任务)在成人(PND 71-84)大鼠和是否(b)这些效果与amphetamine(2.5mg / kg,IP)相当。此外,在成年大鼠中评估这些药物对MMP-9,NMDA受体亚基(GLUN1,GLUN2A / 2B)和PSD-95蛋白表达的影响。以剂量评估药物效应,以诱导大鼠的奖励/增强效应。我们的结果表明,在青春期接受Mephedrone / Amphetamine的成年大鼠中的空间记忆(延迟效果)和逆转学习的缺陷。然而,逆转学习障碍实际上可能是由于空间学习而不是认知灵活性障碍。此外,Mephedrone,但不是疗法,增强了前额叶皮质和海马的延迟发作,MMP-9水平。在青春期诱导期间给予的Mephedrone在年轻成人(PND 63)和成人(PND 87)大鼠中MMP-9水平和上调的含有NMDA受体(前额甲酯皮层和海马)的升高调节。最后,在成年大鼠中,PSD-95表达在前额叶皮质中增加并在海马中减少。相反,在暴露于青春期的含量的成年大鼠中,在海马中,GLUN2A亚基和PSD-95表达下降(下调)。因此,在Mephedrone-an但不是疗法处理的大鼠中,对空间记忆的有害影响与MMP-9水平的变化有关。因为含有GluN2B的NMDA受体在青春期占主导地位,所以Mephedrone似乎对认知的影响比Amphetamine在这段时间内诱导更有害的影响。

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