YKL-40作为帕金森病生物标志物和治疗靶点的早期研究

IF 2.3 Q3 CLINICAL NEUROLOGY Neurodegenerative disease management Pub Date : 2023-04-01 DOI:10.2217/nmt-2022-0010
Mai M Anwar, Mohamed H Fathi
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引用次数: 4

摘要

目的:探讨脑脊液(CSF)和脑YKL-40水平的测定是否可作为帕金森病(PD)的有效生物标志物。方法:将脂多糖(LPS)注入右侧黑质致密部(SNpc)。将大鼠分为:对照组、早期lps诱导PD组(14 d)和晚期lps诱导PD组(28 d)。脑脊液及脑组织中检测YKL-40等相关因子。结果:pd诱导大鼠脑组织和脑脊液中YKL-40的表达升高,与触发炎性细胞因子释放有关。结论:目前的研究仅限于检测脑和脑脊液中的YKL-40等炎症因子。YKL-40可能被认为是PD的早期生物标志物和治疗靶点。
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Early approaches of YKL-40 as a biomarker and therapeutic target for Parkinson's disease.

Aim: To investigate whether the estimation of cerebrospinal fluid (CSF) and brain YKL-40 levels may be used as an efficient biomarker for Parkinson's disease (PD). Methods: Lipopolysaccharides (LPS) was injected into the right substantia nigra pars compacta (SNpc). Rats were divided into: control group, early LPS-induced PD group (14 days), and advanced LPS-induced PD group (28 days). YKL-40 and other related factors were detected in CSF and brain tissue. Results: Increased expression of YKL-40 was observed in brain tissue and CSF of PD-induced rats associated with triggered inflammatory cytokine release. Conclusion: The current study was limited to detecting YKL-40 and other inflammatory factors in brain and CSF. YKL-40 may be considered as an early biomarker and therapeutic target for PD.

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CiteScore
4.30
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0.00%
发文量
35
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