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DNA methylation as a new frontier in treating fear-related disorders:A need for careful evaluation
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作者 Xiao-Ling Huang De-Fang Chen +4 位作者 Ying Wang Yi-Ning Zhang Ntim Michael yu-song ge Bin Wang 《World Journal of Psychiatry》 2025年第11期10-18,共9页
In the contemporary research landscape of mental illness treatment,fear-related disorders such as post-traumatic stress disorder continue to pose significant challenges.Although exposure therapy remains a fundamental ... In the contemporary research landscape of mental illness treatment,fear-related disorders such as post-traumatic stress disorder continue to pose significant challenges.Although exposure therapy remains a fundamental component of treatment,its efficacy varies considerably among individuals.DNA methylation plays a pivotal role in the extinction of fear memories,providing a promising molecular mechanism that could enhance the success of exposure-based interventions.Extensive studies have consistently demonstrated a substantial association between DNA methylation and neuronal plasticity.While DNA methylation holds potential regulatory effects on the effectiveness of exposure therapy,the bidirectional regulatory relationship between it and neuronal activity necessitates addressing several challenges before its widespread clinical application for mental disorders.First,excessive DNA methylation may suppress neural function,and non-selective enhancement of methylation could be counterproductive.Furthermore,due to potential systemic side effects,the use of methylation-modulating agents might disrupt the physiological balance and functionality of other organs and systems.Despite the dynamic interplay between DNA methylation and neuronal activity offering novel insights into the treatment of mental disorders, the strict consideration of target specificity and an appropriate dosing window requirescautious implementation in clinical practice. 展开更多
关键词 DNA methylation Fear extinction Exposure therapy Fear-related disorders Neuronal plasticity Epigenetic regulation
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TAK-242对Aβ_(25-35)诱导大鼠海马神经元损伤的作用及其机制研究 被引量:3
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作者 葛宇松 马成永 +1 位作者 徐晏雯 林永忠 《中国现代医学杂志》 CAS 2018年第4期1-5,共5页
目的探讨TAK-242对β-淀粉样蛋白25-35(Aβ_(25-35))诱导的大鼠海马神经元损伤的作用及其相关机制。方法用Aβ_(25-35)注射大鼠双侧海马复制阿尔兹海默病的动物模型,TAK-242腹腔注射进行治疗,Nissl染色观察大鼠海马CA3区神经元的形态和... 目的探讨TAK-242对β-淀粉样蛋白25-35(Aβ_(25-35))诱导的大鼠海马神经元损伤的作用及其相关机制。方法用Aβ_(25-35)注射大鼠双侧海马复制阿尔兹海默病的动物模型,TAK-242腹腔注射进行治疗,Nissl染色观察大鼠海马CA3区神经元的形态和数量,Western blot检测大鼠海马Toll样受体4(TLR4)和髓样分化因子88(My D88)蛋白的表达,酶联免疫吸附法检测大鼠海马白细胞介素1β(IL-1β)和肿瘤坏死因子α(TNF-α)表达水平。结果大鼠海马注射Aβ_(25-35)后引起大鼠海马CA3区神经元破坏和数量减少,而TAK-242可以抵抗Aβ_(25-35)所造成的神经毒性并保护海马神经元,同时TAK-242可降低Aβ_(25-35)所引起的海马组织内TLR4、My D88、IL-1β和TNF-α表达升高。结论 TAK-242可以通过抑制TLR4/My D88信号通路,降低炎症因子IL-1β和TNF-α水平,从而保护大鼠海马神经元抵抗Aβ_(25-35)诱导的神经毒性。 展开更多
关键词 阿尔茨海默病 Β-淀粉样蛋白 TAK-242 TOLL样受体4 髓样分化因子88
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Core fucosylation and its roles in gastrointestinal glycoimmunology 被引量:1
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作者 Nian-Zhu Zhang Li-Fen Zhao +5 位作者 Qian Zhang Hui Fang Wan-Li Song Wen-Zhe Li yu-song ge Peng Gao 《World Journal of Gastrointestinal Oncology》 SCIE 2023年第7期1119-1134,共16页
Glycosylation is a common post-translational modification in eukaryotic cells.It is involved in the production of many biologically active glycoproteins and the regulation of protein structure and function.Core fucosy... Glycosylation is a common post-translational modification in eukaryotic cells.It is involved in the production of many biologically active glycoproteins and the regulation of protein structure and function.Core fucosylation plays a vital role in the immune response.Most immune system molecules are core fucosylated glycoproteins such as complements,cluster differentiation antigens,immunoglobulins,cytokines,major histocompatibility complex molecules,adhesion molecules,and immune molecule synthesis-related transcription factors.These core fucosylated glycoproteins play important roles in antigen recognition and clearance,cell adhesion,lymphocyte activation,apoptosis,signal transduction,and endocytosis.Core fucosylation is dominated by fucosyltransferase 8(Fut8),which catalyzes the addition ofα-1,6-fucose to the innermost GlcNAc residue of N-glycans.Fut8 is involved in humoral,cellular,and mucosal immunity.Tumor immunology is associated with aberrant core fucosylation.Here,we summarize the roles and potential modulatory mechanisms of Fut8 in various immune processes of the gastrointestinal system. 展开更多
关键词 Fucosyltransferase 8 Core fucosylation Glycoimmunology Gastrointestinal tumor immunology T cell signal pathway
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