Neuroprotective Effect of Morin Against Chemical-Induced Neurotoxicities and Neurodegenerative Disease Models

IF 2.5 4区 医学 Q3 NEUROSCIENCES
Bidemi Emmanuel Ekundayo, Motunrayo Comfort Ekundayo, Sunday Ayodele Alonge, Blessing Ariyo Obafemi, Tajudeen Olabisi Obafemi, Sogolo Lucky Lebelo, Monde McMillan Ntwasa
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引用次数: 0

Abstract

Morin (3,5,7,2′,4′-pentahydroxyflavone) is a dietary flavonol with broad neuroprotective, anti-inflammatory, and antioxidant actions across central and peripheral nervous system models. This synthesis consolidates evidence from in vitro and rodent studies—covering neurodegenerative proteinopathies (Alzheimer's, Parkinson's, and Huntington's), neuropathic pain, epilepsy, stress- and schizophrenia-like phenotypes, and chemo-/toxicant-induced neurotoxicity—to evaluate morin's consistent benefits on survival, motor/cognitive performance, and biochemical normalization. Morin mitigated neurotoxicity induced by doxorubicin, ifosfamide, vincristine, acrylamide, heavy metals, and endocrine disruptors. Context-specific effects included modulation of disease-defining pathways (GSK3β/CDK5, mTORC1, PARP, and AMPK–ULK1–TFEB), microglial polarization, and normalization of neurotransmission (dopamine, GABA, 5-HT, and reduced AChE). Core mechanisms included the following: restoration of redox and mitochondrial homeostasis via Nrf2/HO-1 activation; replenishment of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), and glutathione (GSH); decreased reactive oxygen species (ROS), malondialdehyde (MDA), and nitric oxide (NO); and preserved mitochondrial potential/fusion; suppression of innate immune and inflammasome signaling through downregulation of TLR4/NF-κB and ERK–p65, reduced TNF-α, IL-1β/IL-6, iNOS/COX-2; inhibition of NLRP3/caspase-1; and rebalancing of cell-death programs (↓Bax/caspase-3, ↑Bcl-2; attenuation of RIPK1/RIPK3/MLKL-mediated necroptosis). Formulation strategies (intranasal microemulsions, pluronic micelles, and more soluble derivatives) have enhanced brain exposure and efficacy, but translation now warrants optimized delivery, pharmacokinetic–pharmacodynamic mapping, target engagement biomarkers, and rigorously controlled trials to define dose, route, and indications as adjunctive to standard care in neurodegeneration, neuropathic pain, and toxicant-related brain injury. Collectively, morin emerges as a multitarget neuroprotective scaffold with reproducible functional and mechanistic benefits.

桑辣素对化学诱导的神经毒性和神经退行性疾病模型的神经保护作用。
桑辣素(3,5,7,2',4'-pentahydroxyflavone)是一种膳食黄酮醇,在中枢和周围神经系统模型中具有广泛的神经保护、抗炎和抗氧化作用。这一综合综合了来自体外和啮齿动物研究的证据,包括神经退行性蛋白质病变(阿尔茨海默氏症、帕金森症和亨廷顿氏症)、神经性疼痛、癫痫、应激和精神分裂症样表型,以及化学/毒物诱导的神经毒性,以评估莫宁在生存、运动/认知表现和生化正常化方面的一致益处。桑辣素减轻由阿霉素、异环磷酰胺、长春新碱、丙烯酰胺、重金属和内分泌干扰物引起的神经毒性。背景特异性作用包括疾病定义途径(GSK3β/CDK5, mTORC1, PARP和AMPK-ULK1-TFEB),小胶质细胞极化和神经传递正常化(多巴胺,GABA, 5-HT和乙酰胆碱酯酶降低)的调节。核心机制包括:通过Nrf2/HO-1激活恢复氧化还原和线粒体稳态;补充超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)和谷胱甘肽(GSH);活性氧(ROS)、丙二醛(MDA)和一氧化氮(NO)降低;保存了线粒体的潜能/融合;通过下调TLR4/NF-κB和ERK-p65,降低TNF-α、IL-1β/IL-6、iNOS/COX-2抑制先天免疫和炎性小体信号传导;抑制NLRP3/caspase-1;以及细胞死亡程序的再平衡(↓Bax/caspase-3,↑Bcl-2; RIPK1/RIPK3/ mlkl介导的坏死坏死的衰减)。配方策略(鼻内微乳、多克隆胶束和更多可溶性衍生物)提高了脑暴露和疗效,但翻译现在需要优化递送、药代动力学-药效学作图、目标接触生物标志物和严格的对照试验,以确定剂量、途径和适应症,作为神经退行性疾病、神经性疼痛和毒性相关脑损伤的标准护理的辅助。总的来说,桑酸作为一种多靶点神经保护支架,具有可重复的功能和机制益处。
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
European Journal of Neuroscience
European Journal of Neuroscience 医学-神经科学
CiteScore
7.10
自引率
5.90%
发文量
305
审稿时长
3.5 months
期刊介绍: EJN is the journal of FENS and supports the international neuroscientific community by publishing original high quality research articles and reviews in all fields of neuroscience. In addition, to engage with issues that are of interest to the science community, we also publish Editorials, Meetings Reports and Neuro-Opinions on topics that are of current interest in the fields of neuroscience research and training in science. We have recently established a series of ‘Profiles of Women in Neuroscience’. Our goal is to provide a vehicle for publications that further the understanding of the structure and function of the nervous system in both health and disease and to provide a vehicle to engage the neuroscience community. As the official journal of FENS, profits from the journal are re-invested in the neuroscientific community through the activities of FENS.
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