用n -甲基- d -天冬氨酸受体(nmdar)阻滞剂预处理小鼠左乙拉西坦可阻断抑郁样作用

A. Mesripour, T. Ahmadi
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引用次数: 1

摘要

n -甲基- d -天冬氨酸受体(NMDAR)刺激可能是左乙拉西坦(Lev)诱导抑郁的原因。本研究的目的是评估非竞争性NMDAR阻滞剂右美沙芬(Dxt)和地唑西平(MK801)对小鼠肾上腺素诱导抑郁症的影响。雄性NMRI小鼠每天注射Lev,持续14天。在给药前30分钟用Dxt或MK801进行预处理。进行运动测试、强迫游泳测试(FST)和新颖性抑制进食测试(NSFT)。经Dxt或MK801预处理后,FST的静止时间比单独Lev短。运动活动没有变化。在NSFT期间,Lev增加了潜伏期,减少了食物摄入量;而Dxt或MK801预处理可逆转这些效应。据我们所知,这是第一个表明NMDAR阻滞剂可以阻止Lev在小鼠中引起的抑郁样行为的研究。并且证明了NMDAR的部分激活是Lev诱发抑郁症的原因,这值得进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DEPRESSION-LIKE EFFECTS OF LEVETIRACETAM WAS HALTED BY PRETREATMENT WITH N-METHYL-D-ASPARTATE RECEPTOR (NMDAR) BLOCKERS IN MICE
N-methyl-D-aspartate receptor (NMDAR) stimulation might be responsible for levetiracetam -(Lev) induced depression. The aim of our study is to evaluate the effect of noncompetitive NMDAR blockers, dextromethorphan (Dxt) and dizocilpine (MK801), on Lev-induced depression in mice. Male NMRI mice were daily injected with Lev for 14 days. Pretreatments with Dxt, or MK801 were performed 30 min prior to Lev administration. The locomotor test and the forced swimming test (FST) and the novelty suppressed feeding test (NSFT) were performed. Following Dxt or MK801 pretreatment immobility time during FST was lower than Lev alone. There was no change in the locomotor activity. During NSFT, Lev increased latency, and decreased food intake; while, pretreatment with Dxt or MK801 reversed these effects. To our knowledge this is the first study showing that NMDAR blockers prevented the depressive-like behavior induced by Lev in mice. And proved that, at least in part activation of NMDAR is responsible for Lev induced depression, that warrants further research.
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