Effect of chronic administration of ostruthin on depression-like behavior in chronically stressed mice

IF 2 Q3 NEUROSCIENCES
Masayoshi Okada , Thi Thu Thuy Tran
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引用次数: 0

Abstract

We have previously shown that a single dose of a TREK-1 channel activator, ostruthin, exhibited antidepressant and anxiolytic effects in acute behavioral test models in mice. To assess the potential clinical application, it is essential to evaluate the effects of long-term administration of ostruthin in a chronically stressed mouse model, which is considered to be similar to the clinical condition of major depression in humans. Here, we tested the effects of a single and a 7-day administration of ostruthin on mice that were subjected to chronic unpredictable mild stress (CUMS). A single administration of ostruthin showed antidepressive effects in the tail suspension and forced swim tests of CUMS-treated mice. Unexpectedly, the 7-day administration exhibited only insignificant antidepressive and anxiolytic effects. The 7-day regimen did not affect food intake or body-weight gain, suggesting the absence of apparent cytotoxicity. The mice receiving the 7-day administration had significantly lower blood concentrations of ostruthin compared to those receiving a single dose, suggesting an upregulation of drug-metabolizing activities. These findings suggest that there is a need for stable TREK-1 channel activators that are not affected by drug metabolism.

长期服用奥曲肽对慢性应激小鼠抑郁样行为的影响
我们曾在小鼠急性行为测试模型中发现,单剂量 TREK-1 通道激活剂奥曲肽具有抗抑郁和抗焦虑作用。为了评估其潜在的临床应用价值,有必要评估长期服用奥曲肽对小鼠慢性应激模型的影响,这种模型被认为与人类重度抑郁症的临床症状相似。在这里,我们测试了单次和连续 7 天服用奥曲肽对慢性不可预测轻度应激(CUMS)小鼠的影响。单次服用奥曲肽后,CUMS小鼠的尾悬和强迫游泳试验均显示出抗抑郁效果。出乎意料的是,7天的给药仅表现出微弱的抗抑郁和抗焦虑作用。为期 7 天的给药方案不影响食物摄入量或体重增加,表明不存在明显的细胞毒性。与接受单次给药的小鼠相比,接受7天给药的小鼠血液中奥曲肽的浓度明显较低,这表明药物代谢活动发生了上调。这些发现表明,需要不受药物代谢影响的稳定的 TREK-1 通道激活剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
IBRO Neuroscience Reports
IBRO Neuroscience Reports Neuroscience-Neuroscience (all)
CiteScore
2.80
自引率
0.00%
发文量
99
审稿时长
14 weeks
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