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嗜酸性粒细胞趋化因子和 C-C 趋化因子受体 3 在帕金森病中的作用。

Eotaxins and C-C chemokine receptor type 3 in Parkinson's disease.

机构信息

Non Communicable Diseases Research Center, Rafsanjan University of Medical Science, Rafsanjan, Iran.

Neurology Department, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

出版信息

Acta Neurol Belg. 2020 Jun;120(3):589-594. doi: 10.1007/s13760-018-01061-8. Epub 2018 Dec 13.

Abstract

Parkinson's disease (PD) is one of the most common neuroinflammatory disorders and inflammatory processes seem to play an important role in the pathogenesis of PD. Chemokines as inflammatory mediators, which are involved in the recruitment of leukocytes, can play a role in the pathogenesis of PD. The aim of this study was to examine the serum level of eotaxins (CCL11, CCL24, and CCL26) and the expression of C-C chemokine receptor type 3 (CCR3) in patients with PD compared with healthy subjects. In this study, we measured the serum levels of CCL11, CCL24, and CCL26 with ELISA. In addition, gene and protein expression of CCR3 were measured by RT-PCR and flow cytometry techniques in PD patients (n = 30) and age- and sex-matched healthy subjects (n = 30). All patients suffering from PD were assessed clinically through Unified Parkinson's Disease Rating Scale, Motor Examination (UPDRS ME). The results of this study showed that there was no significant alteration in the serum level of these chemokines and also their receptor among patients with PD and healthy subjects. No significant correlation was observed between the eotaxins serum levels and the clinical measures of PD severity. Based on the results, it can be concluded that eotaxins cannot be considered as appropriate targets for the diagnosis or treatment of PD.

摘要

帕金森病(PD)是最常见的神经炎症性疾病之一,炎症过程似乎在 PD 的发病机制中起重要作用。趋化因子作为炎症介质,参与白细胞的募集,可能在 PD 的发病机制中发挥作用。本研究旨在检查帕金森病患者与健康受试者相比,血清中嗜酸性粒细胞趋化因子(CCL11、CCL24 和 CCL26)的水平和 C-C 趋化因子受体 3(CCR3)的表达。在这项研究中,我们通过 ELISA 测量了 CCL11、CCL24 和 CCL26 的血清水平。此外,通过 RT-PCR 和流式细胞术技术测量了 PD 患者(n = 30)和年龄和性别匹配的健康受试者(n = 30)中 CCR3 的基因和蛋白表达。所有患有 PD 的患者均通过统一帕金森病评定量表、运动检查(UPDRS ME)进行临床评估。这项研究的结果表明,PD 患者和健康受试者之间,这些趋化因子及其受体的血清水平没有明显改变。趋化因子血清水平与 PD 严重程度的临床指标之间也没有观察到显著相关性。基于这些结果,可以得出结论,嗜酸性粒细胞趋化因子不能作为 PD 的诊断或治疗的合适靶点。

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