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Effects of environmental enrichment on ERK1/2 phosphorylation in the rat prefrontal cortex following nicotine-induced sensitization or nicotine self-administration

机译:尼古丁诱导致敏或尼古丁自我施用后大鼠前额叶皮质ERK1 / 2磷酸化对ERK1 / 2磷酸化的影响

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Rats raised in an enriched condition (EC) exhibit alterations in the neurobiological and behavioral response to nicotine compared with rats reared in an impoverished condition (IC) or a standard condition (SC). The current study determined whether environmental enrichment differentially regulates extracellular signal-regulated kinase1/2 (ERK1/2) activity in the prefrontal cortex in rats following nicotine sensitization or nicotine self-administration. Under the saline control condition, EC rats displayed diminished baseline activity and greater sensitization to repeated administration of nicotine compared with IC and SC rats. After repeated saline injections, the basal levels of phosphorylated ERK1/2 (pERK1/2) were higher in EC compared with IC and SC rats, which was negatively correlated with their respective baseline activities. Repeated nicotine (0.35mg/kg) injections induced pERK1/2 to similar levels in SC and IC rats; however, the induction of pERK1/2 in EC rats by nicotine was not significantly different from saline controls, owing to their high baseline. In the self-administration paradigm, EC rats self-administered less nicotine (0.03mg/kg/infusion) relative to IC or SC rats on a fixed ratio-1 schedule of reinforcement. Accordingly, no differences in pERK1/2 were found between EC and IC rats self-administering saline, whereas nicotine self-administration resulted in an increase in pERK1/2 in IC rats but not in EC rats. Furthermore, the levels of pERK1/2 in EC and IC rats were positively correlated with their respective total number of nicotine infusions. Thus, these findings suggest that environmental enrichment alters the basal and nicotine-mediated pERK1/2, which may contribute to enrichment-induced behavioral alterations in response to nicotine.
机译:与贫困条件(IC)或标准条件(SC)中饲养的大鼠相比,在富集的病症(EC)中提出的大鼠表现出对尼古丁的神经生物学和行为应答的改变。目前的研究确定了尼古丁致敏或尼古丁自我给药后大鼠前额叶皮质中的细胞外信号调节激酶1/2(ERK1 / 2)活性。在盐水控制条件下,与IC和SC大鼠相比,EC大鼠展示了基线活动和对重复尼古丁的敏感性更大。在重复盐水注射后,与IC和SC大鼠相比,EC的磷酸化ERK1 / 2(PERK1 / 2)的基础水平较高,与其各自的基线活动呈负相关。重复的尼古丁(0.35mg / kg)注射诱导SC和IC大鼠的Perk1 / 2至相似的水平;然而,由于它们的高基线,尼古丁EC大鼠中的EC大鼠诱导肠道大鼠的诱导与盐水对照没有显着差异。在自我管理范式中,EC大鼠相对于IC或SC大鼠在固定比例的增强时间表上自我施用较少的尼古丁(0.03mg / kg /输注)。因此,EC和IC大鼠自我施用盐水之间没有发现Perk1 / 2的差异,而尼古丁自我给药导致IC大鼠中的Perk1 / 2增加,但不在EC大鼠中增加。此外,EC和IC大鼠的PERK1 / 2水平与其各自的尼古丁输注总数呈正相关。因此,这些研究结果表明,环境富集改变了基础和尼古丁介导的PERK1 / 2,这可能有助于富集诱导的行为改变响应尼古丁。

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