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纳米姜黄素通过影响炎症介质成为多发性硬化症的一种有潜力的新型治疗方法。

Nanocurcumin is a potential novel therapy for multiple sclerosis by influencing inflammatory mediators.

机构信息

Aging Research Institute, Tabriz University of Medical Sciences, Tabriz, Iran; Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Student's Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.

Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Department of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Pharmacol Rep. 2018 Dec;70(6):1158-1167. doi: 10.1016/j.pharep.2018.05.008. Epub 2018 May 24.

DOI:10.1016/j.pharep.2018.05.008
PMID:30340096
Abstract

BACKGROUND

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS). Inflammation has ever been thought as disadvantageous in the pathophysiology of MS. Nanocurcumin has been used as an anti-inflammatory compound. The aim of this study was to identify effects of nanocurcumin on inflammatory mediators in patients with relapsing-remitting multiple sclerosis (RRMS).

METHODS

Fifty MS patients were randomly divided into two groups. The test group received nanocurcumin capsule daily for 6 months. Simultaneously, the control group received placebo. Real-Time PCR was employed to detect the probable changes in gene expression levels of miRNAs, and miRNA-dependent targets, and also transcription factors and pro-inflammatory cytokines in blood samples. ELISA was used to determine the alterations in these cytokines secretion levels. We have also examined EDSS score in MS patients in two groups.

RESULTS

According to the results, a significant decrease in mRNA expression levels of miR-145 (p<0.0001), miR-132 (p=0.004), miR-16 (p=0.0034), STAT1 (p=0.0002), NF-κB (p<0.0001), AP-1 (p=0.0007), IL-1β (p=0.0017), IL-6 (p=0.017), IFN-γ (p<0.0001), CCL2 (p=0.0067), CCL5 (p=0.0034), TNF-α (p<0.0001) and also significant increase in expression levels of miRNAs targets; Sox2 (p=0.0001), sirtuin-1(p=0.0007), Foxp3 (p=0.0082), PDCD1 (p=0.003) was evident in nanocurcumin treated group compared with before treatment. The secretion levels of IFN-γ (p=0.0025), CCL2 (p=0.0029), and CCL5 (p=0.0003) were reduced dramatically in test group compared with placebo group.

CONCLUSION

In conclusion, nanocurcumin may be more effective on the inflammatory features of MS. According to present results, nanocurcumin may inhibit neuroinflammation in MS patients.

摘要

背景

多发性硬化症(MS)是一种中枢神经系统(CNS)的慢性炎症性疾病。炎症在 MS 的病理生理学中曾被认为是不利的。纳米姜黄素已被用作一种抗炎化合物。本研究的目的是确定纳米姜黄素对复发缓解型多发性硬化症(RRMS)患者炎症介质的影响。

方法

50 名 MS 患者被随机分为两组。实验组每天服用纳米姜黄素胶囊 6 个月。同时,对照组服用安慰剂。实时 PCR 用于检测血液样本中 miRNA、miRNA 依赖性靶标以及转录因子和促炎细胞因子的可能变化,ELISA 用于确定这些细胞因子分泌水平的变化。我们还检查了两组 MS 患者的 EDSS 评分。

结果

结果显示,miR-145(p<0.0001)、miR-132(p=0.004)、miR-16(p=0.0034)、STAT1(p=0.0002)、NF-κB(p<0.0001)、AP-1(p=0.0007)、IL-1β(p=0.0017)、IL-6(p=0.017)、IFN-γ(p<0.0001)、CCL2(p=0.0067)、CCL5(p=0.0034)、TNF-α(p<0.0001)的 mRNA 表达水平显著降低,以及 miRNA 靶标;Sox2(p=0.0001)、sirtuin-1(p=0.0007)、Foxp3(p=0.0082)、PDCD1(p=0.003)在纳米姜黄素治疗组与治疗前相比明显增加。与安慰剂组相比,实验组 IFN-γ(p=0.0025)、CCL2(p=0.0029)和 CCL5(p=0.0003)的分泌水平显著降低。

结论

总之,纳米姜黄素可能对 MS 的炎症特征更有效。根据目前的结果,纳米姜黄素可能抑制 MS 患者的神经炎症。

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