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2-邻苯二甲酰亚氨基乙醇和 2-邻苯二甲酰亚氨基乙基硝酸酯抑制关节炎症小鼠模型中的机械性痛觉过敏、中性粒细胞募集以及细胞因子和趋化因子的产生。

2-Phthalimidethanol and 2-phthalimidethyl nitrate inhibit mechanical allodynia, neutrophil recruitment and cytokine and chemokine production in a murine model of articular inflammation.

机构信息

Departamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

出版信息

Pharmacol Rep. 2017 Aug;69(4):691-695. doi: 10.1016/j.pharep.2017.01.033. Epub 2017 Feb 8.

DOI:10.1016/j.pharep.2017.01.033
PMID:28550800
Abstract

BACKGROUND

Phthalimide analogs have been shown to exhibit anti-inflammatory, analgesic and immunomodulatory activities in different preclinical assays. This study aimed to investigate the potential role of 2-phthalimidethanol (PTD-OH) and 2-phthalimidethyl nitrate (PTD-NO) in a murine model of antigen-induced articular inflammation.

METHODS

Articular inflammation was induced by intra-articular injection of methylated bovine serum albumin (mBSA) in the knee joint of immunized male C57BL/6J mice. The animals were pre-treated with PTD-OH or PTD-NO (500mg/kg, per os, - 1h). Nociceptive threshold was measured using an electronic von Frey apparatus. The total number of leukocytes in the synovial cavity was determined. Concentrations of tumor necrosis factor (TNF)-α and CXCL-1 and myeloperoxidase (MPO) activity were determined in periarticular tissue.

RESULTS

Both PTD-OH and PTD-NO inhibited at similar extent the mechanical allodynia, neutrophil recruitment to the synovial cavity and periarticular tissue and TNF-α and CXCL-1 production induced by intra-articular challenge with mBSA in immunized mice.

CONCLUSIONS

PTD-OH and PTD-NO exhibit a marked activity in a murine model of antigen-induced articular inflammation in immunized animals. These results reinforce the interest in the investigation of phthalimide analogs devoid of the glutarimide ring as candidates to analgesic and anti-inflammatory drugs.

摘要

背景

邻苯二甲酰亚胺类似物在不同的临床前试验中表现出抗炎、镇痛和免疫调节活性。本研究旨在探讨 2-邻苯二甲酰亚胺基乙醇(PTD-OH)和 2-邻苯二甲酰亚胺基乙基硝酸盐(PTD-NO)在抗原诱导关节炎症的小鼠模型中的潜在作用。

方法

通过向免疫雄性 C57BL/6J 小鼠膝关节内注射甲基化牛血清白蛋白(mBSA)诱导关节炎症。动物在 PTD-OH 或 PTD-NO(500mg/kg,口服,-1h)预处理。使用电子 von Frey 仪器测量痛觉阈值。测定滑膜腔中白细胞的总数。测定关节周围组织中肿瘤坏死因子(TNF)-α、CXCL-1 和髓过氧化物酶(MPO)活性的浓度。

结果

PTD-OH 和 PTD-NO 以相似的程度抑制了机械性痛觉过敏、中性粒细胞向滑膜腔和关节周围组织的募集以及 mBSA 关节内挑战诱导的 TNF-α和 CXCL-1 的产生。

结论

PTD-OH 和 PTD-NO 在免疫动物的抗原诱导关节炎症的小鼠模型中表现出显著的活性。这些结果加强了对无戊二酰亚胺环的邻苯二甲酰亚胺类似物作为镇痛和抗炎药物候选物的研究兴趣。

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