Targeting Toll-like Receptor 4/Nuclear Factor-κB and Nrf2/Heme Oxygenase-1 Crosstalk via Trimetazidine Alleviates Lipopolysaccharide-Induced Depressive-like Behaviors in Mice.

IF 6.2
Sarah S Mohamed, Nora O Abdel Rasheed, Weam W Ibrahim, Nesma A Shiha
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Abstract

Depression is a global psychiatric illness that imposes a substantial economic burden. Unfortunately, traditional antidepressants induce many side effects which limit patient compliance thus, exploring alternative therapies with fewer adverse effects became urgent. This study aimed to investigate the effect of trimetazidine (TMZ); a well-known anti-ischemic drug in lipopolysaccharide (LPS) mouse model of depression focusing on its ability to regulate toll-like receptor 4 (TLR4)/nuclear factor-κB (NF-κB) as well as nuclear factor erythroid 2 related factor 2 (Nrf2)/ heme oxygenase-1 (HO-1) signaling pathways. Male Swiss albino mice were injected with LPS (500 µg/kg, i.p) every other day alone or parallel with oral doses of either escitalopram (Esc) (10 mg/kg/day) or TMZ (20 mg/kg/day) for 14 days. Treatment with TMZ attenuated LPS-induced animals' despair with reduced immobility time inforced swimming test. TMZ also diminished LPS- induced neuro-inflammation via inhibition of TLR4/NF-κB pathway contrary to Nrf2/HO-1 cascade activation with consequent increase in reduced glutathione (GSH) and HO-1 levels whereas the pro-inflammatory cytokines; tumor necrosis factor-α (TNF-α) and interleukin (IL)-1β were evidently reduced. Besides, TMZ replenished brain serotonin levels via serotonin transporter (SERT) inhibition. Thus, TMZ hindered LPS-induced neuro-inflammation, oxidative stress, serotonin deficiency besides its anti-apoptotic effect which was reflected by decreased caspase-3 level. Neuroprotective effects of TMZ were confirmed by the histological photomicrographs which showed prominent neuronal survival. Here we showed that TMZ is an affluent nominee for depression management via targeting TLR4/NF-κB and Nrf2/HO-1 pathways. Future research addressing TMZ-antidepressant activity in humans is mandatory to enroll it as a novel therapeutic strategy for depression.

通过曲美他嗪靶向 Toll-like Receptor 4/Nuclear Factor-κB 和 Nrf2/Heme Oxygenase-1 Crosstalk 减轻脂多糖诱导的小鼠抑郁样行为
抑郁症是一种全球性的精神疾病,给人们带来了沉重的经济负担。遗憾的是,传统的抗抑郁药物会产生许多副作用,从而限制了患者的依从性,因此,探索不良反应较少的替代疗法已成为当务之急。本研究旨在探讨曲美他嗪这种著名的抗缺血药物对脂多糖(LPS)抑郁症小鼠模型的影响,重点研究其调节类收费受体4(TLR4)/核因子κB(NF-κB)以及核因子红细胞2相关因子2(Nrf2)/血红素加氧酶1(HO-1)信号通路的能力。雄性瑞士白化小鼠每隔一天单独或同时口服埃西酞普兰(Esc)(10毫克/千克/天)或TMZ(20毫克/千克/天),注射LPS(500微克/千克,i.p.),共14天。TMZ可减轻LPS诱导的动物绝望情绪,减少游泳试验中的不动时间。TMZ还通过抑制TLR4/NF-κB通路减轻了LPS诱导的神经炎症,这与Nrf2/HO-1级联激活相反,还原型谷胱甘肽(GSH)和HO-1水平随之增加,而促炎细胞因子、肿瘤坏死因子-α(TNF-α)和白细胞介素(IL)-1β则明显减少。此外,TMZ 通过抑制血清素转运体(SERT)补充脑血清素水平。因此,TMZ除了具有抗细胞凋亡的作用外,还能抑制LPS诱导的神经炎症、氧化应激和血清素缺乏。组织学显微照片证实了 TMZ 的神经保护作用,显微照片显示神经元存活率很高。我们在此表明,TMZ 是一种通过靶向 TLR4/NF-κB 和 Nrf2/HO-1 通路治疗抑郁症的有效药物。未来的研究必须解决TMZ在人体中的抗抑郁活性问题,以便将其作为一种新型的抑郁症治疗策略。
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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