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首页> 外文期刊>Pharmacological reports: PR >Involvement of NMDA and AMPA receptors in The antidepressant-like activity of antidepressant drugs in The forced swim test
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Involvement of NMDA and AMPA receptors in The antidepressant-like activity of antidepressant drugs in The forced swim test

机译:NMDA和AMPA受体参与强制游泳试验中抗抑郁药的抗抑郁样活性

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摘要

Background: The involvement of glutamate system (particularly The NMDAand AMPAreceptors) in The mechanism of antidepressant activity was demonstrated in preclinical and clinical studies. Methods: In The present study, we investigated The effect of NMDAand AMPAreceptors' ligands (agonists and antagonists) on The antidepressant-like activity of escitalopram, milnacipran, imipramine and reboxetine in The forced swim test in mice. Results: Antidepressant activity (reduction in immobility time) of escitalopram and milnacipran but not of imipramine and reboxetine was antagonized by N-methyl-D-Aspartate acid. CGP37849 (antagonist of The NMDAreceptor) enhanced The antidepressant activity of all examined antidepressants. On The oTher hand, CX614 (a potentiator/positive allosteric modulator of The AMPAreceptor) enhanced The antidepressant activity of imipramine and reboxetine but not of escitalopram and milnacipran in this test. NBQX (The AMPA receptor antagonist) did not influence The antidepressant activity of all tested agents. Conclusions: The data indicate The complex interactions following The activation or blockade of TheNMDAandAMPAreceptors with antidepressant drugs. The general phenomenon is The enhancing effect of The NMDAreceptor antagonism on The antidepressant activity. Moreover, is can be concluded that The activity of antidepressants with a serotonergic mechanism of action can be inhibited by NMDA activation , while antidepressants with a noradrenergic mechanism of action are dependent on AMPA receptor transmission.
机译:背景:谷氨酸系统(特别是NMDA和AMPA受体)参与了抗抑郁活性的机制已在临床前和临床研究中得到证实。方法:在本研究中,我们研究了NMDA和AMPA受体配体(激动剂和拮抗剂)对小鼠强迫游泳试验中艾司西酞普兰,米那普仑,丙咪嗪和瑞波西汀的抗抑郁样活性的影响。结果:N-甲基-D-天冬氨酸拮抗艾司西酞普兰和米那普仑的抗抑郁活性(减少固定时间),但对丙咪嗪和瑞波西汀则无拮抗作用。 CGP37849(NMDA受体的拮抗剂)增强了所有检测到的抗抑郁药的抗抑郁活性。另一方面,在该测试中,CX614(AMPAreceptor的增效剂/正构变构调节剂)增强了丙咪嗪和瑞波西汀的抗抑郁活性,但并未增强依他普仑和米那普仑的抗抑郁活性。 NBQX(AMPA受体拮抗剂)不影响所有测试药物的抗抑郁活性。结论:数据表明,NMDA和AMPA受体与抗抑郁药激活或阻断后发生复杂的相互作用。普遍的现象是NMDA受体拮抗作用对抗抑郁活性的增强作用。此外,可以得出结论,具有血清素能作用机制的抗抑郁药的活性可以被NMDA激活抑制,而具有去甲肾上腺素能机制的抗抑郁药则依赖于AMPA受体的传递。

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