首页> 美国卫生研究院文献>Frontiers in Behavioral Neuroscience >Mifepristone Treatment during Early Adolescence Fails to Restore Maternal Deprivation-Induced Deficits in Behavioral Inhibition of Adult Male Rats
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Mifepristone Treatment during Early Adolescence Fails to Restore Maternal Deprivation-Induced Deficits in Behavioral Inhibition of Adult Male Rats

机译:青春期早期的米非司酮治疗未能恢复母体剥夺诱导的成年雄性大鼠行为抑制的缺陷。

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摘要

Early life adversity has a profound impact on brain development and later life health. Animal models have provided insight how early life stress programs stress responsiveness and might contribute to the development of psychiatric disorders. In the present study, the long-term effects of maternal deprivation (MD) on behavioral inhibition and attention were examined in adult male Wistar rats. To this end animals were tested in the 5-choice serial reaction time task (5-choice SRTT). We also explored the potential of a 3-day treatment with the glucocorticoid receptor (GR) antagonist mifepristone during early adolescence to normalize putative behavioral effects of early life stress. Deprivation of the mother for 24 h on postnatal day (PND) 3 led to a modest but significant increase in premature responses in the 5-choice SRTT, but did not affect measures of attention. Body weight was lower in deprived animals from weaning until the start of testing. Early adolescent mifepristone treatment (PND 26–28) did not influence performance on the 5-choice SRTT and did not mitigate the deprivation-related impairment in behavioral inhibition. Our results indicate that MD leads to impaired behavioral inhibition, and that mifepristone treatment during early adolescence does not normalize the behavioral changes caused by early life stress.
机译:早期的逆境对大脑的发育和后期的健康有着深远的影响。动物模型提供了洞察力,指出早期生活压力程序如何压力反应能力,并可能有助于精神疾病的发展。在本研究中,在成年雄性Wistar大鼠中检查了母体剥夺(MD)对行为抑制和注意力的长期影响。为此,在5-选择序列反应时间任务(5-选择SRTT)中测试动物。我们还探讨了在青春期早期用糖皮质激素受体(GR)拮抗剂米非司酮治疗3天的潜力,以使早期生活压力的假定行为影响正常化。产后一天(PND)3剥夺母亲24 h导致5选SRTT的早产反应适度但显着增加,但并未影响注意措施。被剥夺动物断奶至测试开始之前的体重较低。青春期早期米非司酮治疗(PND 26–28)不会影响5选择SRTT的性能,也无法减轻行为抑制中与剥夺相关的损害。我们的结果表明,MD会导致行为抑制受损,而米非司酮治疗在青春期早期并不能使早期生活压力引起的行为改变正常化。

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