Neuropharmacological characteristics of antidepressant action of a new 3-substituted thietane-1,1-dioxide derivative

Q3 Pharmacology, Toxicology and Pharmaceutics
I. Nikitina, G. G. Gaisina
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引用次数: 4

Abstract

Introduction: Due to severe burden of depressive disorders and a low rate of remission in patients receiving antidepressant therapy, there is an urgent need for developing novel agents with antidepressant action and a fundamentally new mechanism of action. 3-ethoxythietane-1,1-dioxide (N-199/1) is a new molecule that showed significant antidepressant properties when administered intraperitoneally once or repeatedly. The aim of the present study was to investigate the mechanism of action of N-199/1, using reserpine test. Materials and methods: N-199/1 (2 mg/kg and 4.86 mg/kg) and the reference drugs (imipramine and fluoxetine) were administered once intraperitoneally to outbred male mice 4 h (Experiment 1) and 18 h (Experiment 2) after a single intraperitoneal injection of reserpine (2.5 mg/kg). The severity of reserpine-induced symptoms (hypothermia, ptosis and akinesia) was assessed. Results and discussion: N-199/1 potentiated reserpine-induced hypothermia at both doses and reduced ptosis at a dose of 2 mg/kg when administered 4 h after reserpine. N-199/1 increased the duration of reserpine akinesia at a dose of 2 mg/kg when administered 18 h after reserpine and at a dose of 4.86 mg/kg when administered 4 h after reserpine. The effect of N-199/1 resembled the effect of fluoxetine and was dose-dependent. Conclusion: Based on the results obtained, it can be assumed that the antidepressant action of N-199/1 is due to its serotonin-positive properties, and probably the blockade of serotonin 5HT2A/2C receptors and/or α2-adrenergic receptors. The effect of N-199/1 is dose-dependent and resembles the effect of fluoxetine. Graphical abstract:
一种新的3-取代噻吩并-1,1-二氧化物衍生物抗抑郁作用的神经药理学特征
导论:由于抑郁症负担严重,且接受抗抑郁治疗的患者缓解率低,迫切需要开发具有抗抑郁作用的新型药物和一种全新的作用机制。3-乙氧基乙烷-1,1-二氧化物(N-199/1)是一种新的抗抑郁分子,当腹腔注射一次或多次时显示出显著的抗抑郁作用。本研究采用利血平试验探讨N-199/1的作用机制。材料与方法:异交雄性小鼠单次腹腔注射利血平(2.5 mg/kg)后4 h(实验1)和18 h(实验2)分别腹腔注射N-199/1 (2 mg/kg和4.86 mg/kg)和对照药物丙咪嗪和氟西汀一次。评估利血平引起的症状(体温过低、上睑下垂和肌无力)的严重程度。结果和讨论:N-199/1增强了两种剂量的利血平诱导的低温,并在利血平后4小时给药时,以2mg /kg的剂量减少了上睑下垂。N-199/1在利血平后18小时以2mg /kg剂量给药,在利血平后4小时以4.86 mg/kg剂量给药,可延长利血平肌动障碍持续时间。N-199/1的作用与氟西汀相似,且呈剂量依赖性。结论:基于上述结果,可以推测N-199/1的抗抑郁作用可能与血清素阳性有关,可能与血清素5HT2A/2C受体和α2-肾上腺素能受体的阻断作用有关。N-199/1的作用是剂量依赖性的,类似于氟西汀的作用。图形化的简介:
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
Research Results in Pharmacology
Research Results in Pharmacology Medicine-Pharmacology (medical)
CiteScore
1.50
自引率
0.00%
发文量
32
审稿时长
12 weeks
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