首页> 外文期刊>Neuropharmacology >Involvement of extracellular signal-regulated kinase (ERK) in the short and long-lasting antidepressant-like activity of NMDA receptor antagonists (zinc and Ro 25-6981) in the forced swim test in rats
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Involvement of extracellular signal-regulated kinase (ERK) in the short and long-lasting antidepressant-like activity of NMDA receptor antagonists (zinc and Ro 25-6981) in the forced swim test in rats

机译:细胞外信号调节激酶(ERK)在大鼠强制游泳试验中NMDA受体拮抗剂(锌和RO 25-6981)的短期和长持续的抗抑郁药活性

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摘要

Abstract Short and long acting NMDA receptor (NMDAR) antagonists exert their antidepressant-like effects by activating signaling pathways involved in the synthesis of synaptic proteins and formation of new synaptic connections in the prefrontal cortex (PFC) of rats. The blockade of the ERK pathway abolishes ketamine and Ro 25-6981 antidepressant potency. However, the role of ERK in the antidepressant-like activity of short acting NMDAR antagonists is still unclear. More puzzling is the fact that the precise role of ERK in the short and long lasting effects of long-acting NMDAR antagonists is unknown. In this study, we show that zinc, (Zn) a short-acting NMDAR antagonist evokes only transient ERK activation, which is observed 7?min after its administration in the PFC of rats. In contrast to Zn, the long acting NMDAR antagonist Ro 25-6981 produces persistent ERK activation lasting up to 24?h. Pretreatment with the MAPK/ERK inhibitor (U0126) totally abolished Zn and Ro 25-6981 antidepressant-like activities in the forced swim test in rats. However, when U0126 is administered 15?min after Zn or Ro 25-6981 both compounds maintain their short-lasting antidepressant-like activity. On the other hand, posttreatment with U0126 significantly attenuated the long lasting antidepressant-like activity of Ro 25-6981. These results indicate that the activation of ERK is crucial for the short- and long lasting antidepressant-like activity observed in the FST in rats. Highlights ? U0126 blocked the antidepressant-like effect of Zn and Ro 25-6981 in FST. ? Zn increased the p-ERK/ERK ratio 7?min after the treatment. ? NMDA reversed increase in p-ERK/ERK ratio induced by Zn treatment. ? Ro 25-6981 increased the p-ERK/ERK ratio 7, 15, 60?min and 24?h after the treatment. ? U0126 administered after Ro 25-6981 attenuates its long-lasting effect in FST.
机译:摘要短期和长效的NMDA受体(NMDAR)拮抗剂通过激活突触蛋白合成中涉及的信号传导途径和在大鼠前额叶皮质(PFC)中的新突触连接的形成和形成新的突触连接来发挥抗抑郁药物。 ERK途径阻止了氯胺酮和RO 25-6981抗抑郁症效力。然而,ERK在抗抑郁药物的抗抑郁症拮抗剂的抗抑郁药活性中的作用仍然不清楚。更令人费解的是,ERK在长效的NMDAR拮抗剂的短期和长期效果中的确切作用是未知的。在这项研究中,我们表明锌,(Zn)仅仅是瞬时ERK激活的短作用NMDAR拮抗剂,其在其在大鼠PFC的施用后观察到7?min。与Zn相比,长效的NMDAR拮抗剂RO 25-6981产生持续的ERK激活持续到24℃。用MAPK / ERK抑制剂(U0126)预处理(U0126)在大鼠强制游泳试验中完全废除Zn和RO 25-6981抗抑郁药物。然而,当Zn或RO 25-6981之后施用U0126 15?分钟,两种化合物保持其持久的抗抑郁药物的活性。另一方面,与U0126的后处理显着减弱了RO 25-6981的持久抗抑郁药活性。这些结果表明,ERK的激活对于在大鼠FST中观察到的短期和长期持久的抗抑郁药活性至关重要。强调 ? U0126在FST中阻断了Zn和Ro 25-6981的抗抑郁药物。还Zn在治疗后增加了P-ERK / ERK比例7?分钟。还NMDA逆转Zn处理诱导的P-ERK / ERK比率的增加。还RO 25-6981在治疗后增加了P-ERK / ERK比例7,15,60?min和24℃。还RO 25-6981后施用U0126,在FST中衰减其长期效果。

著录项

  • 来源
    《Neuropharmacology》 |2017年第2017期|共10页
  • 作者单位

    Institute of Pharmacology Polish Academy of Sciences Department of Neurobiology;

    Institute of Pharmacology Polish Academy of Sciences Department of Neurobiology;

    Institute of Pharmacology Polish Academy of Sciences Department of Neurobiology;

    Institute of Pharmacology Polish Academy of Sciences Department of Neurobiology;

    Institute of Pharmacology Polish Academy of Sciences Department of Neurobiology;

    Institute of Pharmacology Polish Academy of Sciences Department of Neurobiology;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
  • 关键词

    Zinc; Ro 25-6981; NMDA; ERK; Depression;

    机译:锌;ro 25-6981;nmda;erk;抑郁症;
  • 入库时间 2022-08-20 04:36:04

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