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Exploring the Etiological Links behind Neurodegenerative Diseases: Inflammatory Cytokines and Bioactive Kynurenines

机译:探索神经退行性疾病背后的病因学联系:炎性细胞因子和生物活性滑膜尿素

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摘要

Alzheimer’s disease (AD) and Parkinson’s disease (PD) are the most common neurodegenerative diseases (NDs), presenting a broad range of symptoms from motor dysfunctions to psychobehavioral manifestations. A common clinical course is the proteinopathy-induced neural dysfunction leading to anatomically corresponding neuropathies. However, current diagnostic criteria based on pathology and symptomatology are of little value for the sake of disease prevention and drug development. Overviewing the pathomechanism of NDs, this review incorporates systematic reviews on inflammatory cytokines and tryptophan metabolites kynurenines (KYNs) of human samples, to present an inferential method to explore potential links behind NDs. The results revealed increases of pro-inflammatory cytokines and neurotoxic KYNs in NDs, increases of anti-inflammatory cytokines in AD, PD, Huntington’s disease (HD), Creutzfeldt–Jakob disease, and human immunodeficiency virus (HIV)-associated neurocognitive disorders, and decreases of neuromodulatory KYNs in AD, PD, and HD. The results reinforced a strong link between inflammation and neurotoxic KYNs, confirmed activation of adaptive immune response, and suggested a possible role in the decrease of neuromodulatory KYNs, all of which may contribute to the development of chronic low grade inflammation. Commonalities of multifactorial NDs were discussed to present a current limit of diagnostic criteria, a need for preclinical biomarkers, and an approach to search the initiation factors of NDs.
机译:阿尔茨海默氏病(AD)和帕金森氏病(PD)是最常见的神经退行性疾病(ND),表现出从运动功能障碍到心理行为表现的多种症状。常见的临床过程是蛋白病引起的神经功能障碍,导致解剖上相应的神经病。然而,当前基于病理和症状学的诊断标准对于疾病预防和药物开发没有什么价值。概述NDs的致病机理,该综述结合了对人类样品中炎性细胞因子和色氨酸代谢物犬尿氨酸(KYNs)的系统评价,提出了一种推断方法,以探索NDs背后的潜在联系。结果显示,NDs中的促炎细胞因子和神经毒性KYNs增加,AD,PD,亨廷顿舞蹈病(HD),Creutzfeldt–Jakob病和人类免疫缺陷病毒(HIV)相关的神经认知障碍的抗炎细胞因子增加,以及AD,PD和HD中神经调节性KYN的减少。结果加强了炎症和神经毒性KYN之间的牢固联系,证实了适应性免疫反应的激活,并暗示了在神经调节性KYN减少中的可能作用,所有这些都可能导致慢性低度炎症的发展。讨论了多因素ND的共性,以提出当前诊断标准的局限性,对临床前生物标志物的需求以及搜索ND起始因子的方法。

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