Anxiolytic and Antidepressant Effects of Organic Polysulfide, Dimethyl Trisulfide Are Partly Mediated by the Transient Receptor Potential Ankyrin 1 Ion Channel in Mice.

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Kitti Göntér, Viktória Kormos, Erika Pintér, Gábor Pozsgai
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引用次数: 0

Abstract

Background/Objectives: Dimethyl trisulfide (DMTS) is a naturally occurring polysulfide with known antioxidant and neuroprotective properties. DMTS is a lipophilic transient receptor potential ankyrin 1 (TRPA1) ligand that reaches the central nervous system (CNS). Its role in the CNS, particularly regarding depression-like behaviour, has yet to be explored. This study investigates the influence of DMTS on stress responses and whether this effect is mediated through the TRPA1 ion channel, known for its role in stress adaptation. Using a mouse model involving three-week exposure, we examined the impact of DMTS on depression-like behaviour and anxiety and identified the involved brain regions. Methods: Our methods involved testing both Trpa1-wild-type and gene-knockout mice under CUMS conditions and DMTS treatment. DMTS was administered intraperitoneally at a dose of 30 mg/kg on days 16 and 20 of the 21-day CUMS protocol-in hourly injections seven times to ensure sustained exposure. Various behavioural assessments-including the open field, marble burying, tail suspension, forced swim, and sucrose preference tests-were performed to evaluate anxiety and depression-like behaviour. Additionally, we measured body weight changes and the relative weights of the thymus and adrenal glands, while serum levels of corticosterone and adrenocorticotropic hormone were quantified via ELISA. FOSB (FBJ murine osteosarcoma viral oncogene homolog B) immunohistochemistry was utilised to assess chronic neuronal activation in stress-relevant brain areas. Results: Results showed that CUMS induces depression-like behaviour, with the response being modulated by the TRPA1 status and that DMTS treatment significantly reduced these effects when TRPA1 channels were functional. DMTS also mitigated thymus involution due to hypothalamic-pituitary-adrenal (HPA) axis dysregulation. Conclusions: Overall, DMTS appears to relieve depressive and anxiety symptoms through TRPA1-mediated pathways, suggesting its potential as a dietary supplement or adjunct therapy for depression and anxiety.

有机多硫化物、二甲基三硫化物的抗焦虑和抗抑郁作用部分由瞬时受体电位锚蛋白1离子通道介导。
背景/目的:二甲基三硫化物(DMTS)是一种天然多硫化物,具有已知的抗氧化和神经保护特性。DMTS是一种可到达中枢神经系统(CNS)的亲脂性瞬时受体电位锚蛋白1 (TRPA1)配体。它在中枢神经系统中的作用,特别是与抑郁行为有关的作用,还有待探索。本研究探讨了DMTS对应激反应的影响,以及这种影响是否通过TRPA1离子通道介导,TRPA1离子通道以其在应激适应中的作用而闻名。我们使用小鼠模型进行了为期三周的暴露,研究了DMTS对抑郁样行为和焦虑的影响,并确定了相关的大脑区域。方法:我们的方法包括在CUMS条件和DMTS治疗下测试trpa1野生型和基因敲除小鼠。在21天CUMS方案的第16天和第20天,以30 mg/kg的剂量腹腔注射DMTS,每小时注射7次,以确保持续暴露。各种行为评估——包括空地、弹珠掩埋、悬尾、强迫游泳和蔗糖偏好测试——被用来评估焦虑和抑郁样行为。此外,我们测量了体重变化以及胸腺和肾上腺的相对重量,同时通过ELISA定量测定了血清皮质酮和促肾上腺皮质激素水平。FBJ小鼠骨肉瘤病毒癌基因同源物B (FOSB)免疫组化用于评估应激相关脑区慢性神经元激活。结果:结果表明,CUMS诱导抑郁样行为,其反应由TRPA1状态调节,当TRPA1通道功能正常时,DMTS治疗显著降低了这些影响。DMTS还减轻了由于下丘脑-垂体-肾上腺(HPA)轴失调引起的胸腺内翻。结论:总体而言,DMTS似乎通过trpa1介导的途径缓解抑郁和焦虑症状,这表明它有可能作为抑郁和焦虑的膳食补充剂或辅助疗法。
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
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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