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哌甲酯对青春期大鼠前额叶皮质具有持久的可塑性变化效应。

Methylphenidate has long-lasting metaplastic effects in the prefrontal cortex of adolescent rats.

作者信息

Burgos H, Cofré C, Hernández A, Sáez-Briones P, Agurto R, Castillo A, Morales B, Zeise M L

机构信息

Laboratorio de Biopsicología, Escuela de Psicología, FAHU, USACH, Chile; Escuela de Psicología, FACSO, Universidad Central de Chile, FAHU, USACH, Chile.

Laboratorio de Biopsicología, Escuela de Psicología, FAHU, USACH, Chile.

出版信息

Behav Brain Res. 2015 Sep 15;291:112-117. doi: 10.1016/j.bbr.2015.05.009. Epub 2015 May 18.

Abstract

Methylphenidate (MPH) is widely used as a "nootropic" agent and in the treatment of disorders of attention, and has been shown to modulate synaptic plasticity in vitro. Here we present in vivo evidence that this MPH-induced metaplasticity can last long after the end of treatment. MPH (0, 0.2, 1 and 5mg/kg) was administered daily to male rats from postnatal day 42 for 15 days. The animals were tested daily in a radial maze. Long-term potentiation (LTP), a marker of neural plasticity, was induced in vivo in the prefrontal cortex after 2-3h, 15-18 days or 5 months without treatment. The behavioral performance of the 1mg/kg group improved, while that of animals that had received 5mg/kg deteriorated. In the 1 and 5mg/kg groups LTP induced 2-3h after the last MPH treatment was twice as large as in the controls. Further, 15-18 days after the last MPH administration, in groups receiving 1 and 5mg/kg, LTP was about fourfold higher than in controls. However, 5 months later, LTP in the 1mg/kg group was similar to controls and in the 5mg/kg group LTP could not be induced at all. No significant changes of LTP were seen in the low-dose group of animals (0.2mg/kg). Thus, firstly, doses of MPH that improve learning coincide approximately with those that augment LTP. Secondly, MPH-induced increases in LTP can last for several weeks, but these may disappear over longer periods or deteriorate at high doses.

摘要

哌甲酯(MPH)作为一种“益智”药物被广泛使用,并用于治疗注意力障碍,且已在体外实验中显示出可调节突触可塑性。在此,我们提供体内实验证据,表明这种由MPH诱导的元可塑性在治疗结束后仍能持续很长时间。从出生后第42天起,每天给雄性大鼠注射MPH(0、0.2、1和5mg/kg),持续15天。每天在放射状迷宫中对动物进行测试。在停止治疗2 - 3小时、15 - 18天或5个月后,在体内前额叶皮质诱导出神经可塑性标志物——长时程增强(LTP)。1mg/kg组的行为表现有所改善,而接受5mg/kg的动物行为表现则变差。在1mg/kg和5mg/kg组中,最后一次MPH治疗后2 - 3小时诱导出的LTP是对照组的两倍。此外,在最后一次给予MPH 15 - 18天后,接受1mg/kg和5mg/kg的组中,LTP比对照组高约四倍。然而,5个月后,1mg/kg组的LTP与对照组相似,而5mg/kg组根本无法诱导出LTP。在低剂量组动物(0.2mg/kg)中未观察到LTP有显著变化。因此,首先,改善学习的MPH剂量大致与增强LTP的剂量相符。其次,MPH诱导的LTP增加可持续数周,但在更长时间内可能消失,或在高剂量时变差。

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