Mechanisms involved in the antidepressant-like action of orally administered 5-((4-methoxyphenyl)thio)benzo[c][1,2,5]thiadiazole (MTDZ) in male and female mice.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2024-11-01 Epub Date: 2024-07-15 DOI:10.1007/s00213-024-06647-0
Karline da Costa Rodrigues, Meliza da Conceição Oliveira, Beatriz Fuzinato Dos Santos, Nelson Luís de Campos Domingues, Mariana Gallio Fronza, Lucielli Savegnago, Ethel Antunes Wilhelm, Cristiane Luchese
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引用次数: 0

Abstract

Rationale: The compound 5-((4-methoxyphenyl)thio)benzo[c][1,2,5]thiadiazole (MTDZ) has recently been shown to inhibit in vitro acetylcholinesterase activity, reduce cognitive damage, and improve neuropsychic behavior in mice, making it a promising molecule to treat depression.

Objectives: This study investigated the antidepressant-like action of MTDZ in mice and its potential mechanisms of action.

Results: Molecular docking assays were performed and suggested a potential inhibition of monoamine oxidase A (MAO-A) by MTDZ. The toxicity study revealed that MTDZ displayed no signs of toxicity, changes in oxidative parameters, or alterations to biochemistry markers, even at a high dose of 300 mg/kg. In behavioral tests, MTDZ administration reduced immobility behavior during the forced swim test (FST) without adjusting the climbing parameter, suggesting it has an antidepressant effect. The antidepressant-like action of MTDZ was negated with the administration of 5-HT1A, 5-HT1A/1B, and 5-HT3 receptor antagonists, implying the involvement of serotonergic pathways. Moreover, the antidepressant-like action of MTDZ was linked to the NO system, as L-arginine pretreatment inhibited its activity. The ex vivo assays indicated that MTDZ normalized ATPase activity, potentially linking this behavior to its antidepressant-like action. MTDZ treatment restricted MAO-A activity in the cerebral cortices and hippocampi of mice, proposing a selective inhibition of MAO-A associated with the antidepressant-like effect of the compound.

Conclusions: These findings suggest that MTDZ may serve as a promising antidepressant agent due to its selective inhibition of MAO-A and the involvement of serotonergic and NO pathways.

Abstract Image

雌雄小鼠口服 5-((4-甲氧基苯基)硫)苯并[c][1,2,5]噻二唑(MTDZ)抗抑郁样作用的机制。
理论依据:化合物 5-((4-甲氧基苯基)硫)苯并[c][1,2,5]噻二唑(MTDZ)最近被证明可以抑制体外乙酰胆碱酯酶活性、减少认知损伤并改善小鼠的神经心理行为,使其成为一种治疗抑郁症的有前途的分子:本研究调查了MTDZ在小鼠体内的抗抑郁样作用及其潜在的作用机制:结果:进行了分子对接试验,结果表明MTDZ对单胺氧化酶A(MAO-A)具有潜在的抑制作用。毒性研究表明,即使在 300 毫克/千克的高剂量下,MTDZ 也未显示出毒性迹象、氧化参数变化或生化指标的改变。在行为测试中,MTDZ能减少强迫游泳测试(FST)中的不动行为,而不影响爬行参数,这表明它具有抗抑郁作用。在服用5-HT1A、5-HT1A/1B和5-HT3受体拮抗剂后,MTDZ的抗抑郁样作用被否定,这意味着5-羟色胺能通路的参与。此外,MTDZ的抗抑郁样作用与氮氧化物系统有关,因为L-精氨酸预处理抑制了其活性。体内外试验表明,MTDZ使ATP酶活性正常化,这可能与其抗抑郁样作用有关。MTDZ治疗限制了小鼠大脑皮层和海马中MAO-A的活性,这表明MAO-A的选择性抑制与该化合物的抗抑郁样作用有关:这些研究结果表明,由于MTDZ对MAO-A有选择性抑制作用,并且有5-羟色胺能和NO通路的参与,因此它可能是一种很有前途的抗抑郁剂。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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