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β-D-甘露糖醛酸(M2000)作为一种新型 NSAID,对强直性脊柱炎患者和小鼠单核细胞/巨噬细胞 J774 细胞系中 COX1 和 COX2 活性和基因表达的影响。

The effects of β-D-mannuronic acid (M2000), as a novel NSAID, on COX1 and COX2 activities and gene expression in ankylosing spondylitis patients and the murine monocyte/macrophage, J774 cell line.

机构信息

Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Box: 14155-6446, Tehran, Iran.

Department of Immunology, International Campus, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

出版信息

Inflammopharmacology. 2018 Apr;26(2):375-384. doi: 10.1007/s10787-017-0386-4. Epub 2017 Aug 17.

Abstract

Ankylosing spondylitis (AS) is a debilitating chronic inflammatory disease with genetic predisposition, which is characterized by the involvement of spine and sacroiliac joints. Due to the relatively unsuccessful treatments, we designed β-D-mannuronic (M2000) with the beneficial effects in various experimental models as a novel non-steroidal anti-inflammatory drug (NSAID). The aims of our present study were: first, to compare the therapeutic effects of M2000, as a novel designed NSAID, with naproxen and placebo in Iranian patients with AS during 12 weeks; second, to evaluate the effect of M2000 on gene expression of cyclooxygenase enzyme (COX-1/COX-2), a key enzyme in the initiation of inflammatory pathways in AS patients; and third, to assess the activity of COX-1 and COX-2 enzymes in the presence/absence of M2000 at the different doses in the murine macrophage, J774 cell line. This was a sub-study of phase II, randomized, placebo-controlled trial with three treatment arms: M2000, naproxen, and placebo. The outcome measures were the mean changes from baseline to week 12. The gene expression was assessed by real-time PCR. The COX-1 and COX-2 activities were evaluated by ELISA in J774 cell line induced by LPS and arachidonic acid (AA). Our findings demonstrated that M2000 had beneficial therapeutic effects on pain, stiffness, and inflammation, whereas no adverse effects were observed following the use of M2000 after 12 weeks. The analysis of gene expression showed that M2000 could effectively reduce the expression levels of COX-1 and COX-2 in comparison with untreated patients. In addition, the enzymatic activities in the presence of M2000 were significantly less than LPS- and AA-treated groups. Our results indicate that M2000, as a novel designed NSAID with immunosuppressive properties, can be considered as one of the therapeutic options for the treatment of inflammatory diseases without adverse events. Clinical trial identifier IRCT2013062213739N1/ http://www.IRCT.ir .

摘要

强直性脊柱炎(AS)是一种具有遗传易感性的致残性慢性炎症性疾病,其特征是脊柱和骶髂关节受累。由于治疗效果相对不理想,我们设计了β-D-甘露糖醛酸(M2000),它在各种实验模型中具有有益的作用,是一种新型的非甾体抗炎药(NSAID)。本研究的目的是:首先,比较新型 NSAID M2000 与萘普生和安慰剂在 12 周内对伊朗 AS 患者的治疗效果;其次,评估 M2000 对 AS 患者中炎症途径起始的关键酶环氧化酶酶(COX-1/COX-2)基因表达的影响;第三,评估在不同剂量下 M2000 对鼠巨噬细胞 J774 细胞系中 COX-1 和 COX-2 酶活性的影响。这是一项 II 期、随机、安慰剂对照试验的亚研究,分为三个治疗组:M2000、萘普生和安慰剂。主要观察指标为从基线到第 12 周的平均变化。通过实时 PCR 评估基因表达。通过 LPS 和花生四烯酸(AA)诱导的 J774 细胞系评估 COX-1 和 COX-2 活性的 ELISA。我们的研究结果表明,M2000 对疼痛、僵硬和炎症具有有益的治疗作用,而在 12 周后使用 M2000 没有观察到不良反应。基因表达分析表明,与未经治疗的患者相比,M2000 能有效降低 COX-1 和 COX-2 的表达水平。此外,在存在 M2000 的情况下,酶活性明显低于 LPS 和 AA 处理组。我们的研究结果表明,M2000 作为一种具有免疫抑制特性的新型 NSAID,可以作为治疗炎症性疾病的一种治疗选择,而无不良反应。临床试验标识符 IRCT2013062213739N1/[临床试验注册网站名称]。

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