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噻嗪类利尿剂对条件性焦虑大鼠模型具有抗焦虑作用。

Loop diuretics have anxiolytic effects in rat models of conditioned anxiety.

机构信息

Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina, United States of America.

出版信息

PLoS One. 2012;7(4):e35417. doi: 10.1371/journal.pone.0035417. Epub 2012 Apr 13.

Abstract

A number of antiepileptic medications that modulate GABA(A) mediated synaptic transmission are anxiolytic. The loop diuretics furosemide (Lasix) and bumetanide (Bumex) are thought to have antiepileptic properties. These drugs also modulate GABA(A) mediated signalling through their antagonism of cation-chloride cotransporters. Given that loop diuretics may act as antiepileptic drugs that modulate GABAergic signalling, we sought to investigate whether they also mediate anxiolytic effects. Here we report the first investigation of the anxiolytic effects of these drugs in rat models of anxiety. Furosemide and bumetanide were tested in adult rats for their anxiolytic effects using four standard anxiety models: 1) contextual fear conditioning; 2) fear-potentiated startle; 3) elevated plus maze, and 4) open-field test. Furosemide and bumetanide significantly reduced conditioned anxiety in the contextual fear-conditioning and fear-potentiated startle models. At the tested doses, neither compound had significant anxiolytic effects on unconditioned anxiety in the elevated plus maze and open-field test models. These observations suggest that loop diuretics elicit significant anxiolytic effects in rat models of conditioned anxiety. Since loop diuretics are antagonists of the NKCC1 and KCC2 cotransporters, these results implicate the cation-chloride cotransport system as possible molecular mechanism involved in anxiety, and as novel pharmacological target for the development of anxiolytics. In view of these findings, and since furosemide and bumetanide are safe and well tolerated drugs, the clinical potential of loop diuretics for treating some types of anxiety disorders deserves further investigation.

摘要

许多调节 GABA(A) 介导的突触传递的抗癫痫药物具有抗焦虑作用。噻嗪类利尿剂呋塞米(Lasix)和布美他尼(Bumex)被认为具有抗癫痫特性。这些药物还通过拮抗阳离子-氯离子共转运体来调节 GABA(A) 介导的信号转导。鉴于噻嗪类利尿剂可能作为调节 GABA 能信号转导的抗癫痫药物,我们试图研究它们是否也介导抗焦虑作用。在这里,我们报告了这些药物在焦虑症大鼠模型中抗焦虑作用的首次研究。在成年大鼠中,我们使用四种标准焦虑模型测试了呋塞米和布美他尼的抗焦虑作用:1)情境性恐惧条件反射;2)恐惧增强性惊跳;3)高架十字迷宫;4)旷场试验。呋塞米和布美他尼显著降低了情境性恐惧条件反射和恐惧增强性惊跳模型中的条件性焦虑。在测试剂量下,这两种化合物在高架十字迷宫和旷场试验模型中对未条件化的焦虑均无明显的抗焦虑作用。这些观察结果表明,噻嗪类利尿剂在大鼠条件性焦虑模型中产生显著的抗焦虑作用。由于噻嗪类利尿剂是 NKCC1 和 KCC2 共转运体的拮抗剂,这些结果表明阳离子-氯离子共转运系统可能是焦虑相关的分子机制,并且是开发抗焦虑药物的新的药理学靶点。鉴于这些发现,并且由于呋塞米和布美他尼是安全且耐受良好的药物,噻嗪类利尿剂治疗某些类型焦虑症的临床潜力值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b7/3325958/f10d837cf9fb/pone.0035417.g001.jpg

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