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普通肝素和来自海鞘(脊索动物-被囊动物)的新型肝素类似物可改善大鼠结肠炎。

Unfractionated heparin and new heparin analogues from ascidians (chordate-tunicate) ameliorate colitis in rats.

作者信息

Belmiro Celso L R, Castelo-Branco Morgana T L, Melim Leandra M C, Schanaider Alberto, Elia Celeste, Madi Kalil, Pavão Mauro S G, de Souza Heitor S P

机构信息

Laboratório de Tecido Conjuntivo, Hospital Universitário Clementino Fraga Filho (HUCFF) and Instituto de Bioquímica Médica, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro 21941-913, Brazil.

出版信息

J Biol Chem. 2009 Apr 24;284(17):11267-78. doi: 10.1074/jbc.M807211200. Epub 2009 Mar 2.

Abstract

The anti-inflammatory effect of mammalian heparin analogues, named dermatan sulfate and heparin, isolated from the ascidian Styela plicata was accessed in a TNBS-induced colitis model in rats. Subcutaneous administration of the invertebrate compounds during a 7-day period drastically reduced inflammation as observed by the normalization of the macroscopic and histological characteristics of the colon. At the molecular level, a decrease in the production of TNF-alpha, TGF-beta, and VEGF was observed, as well as a reduction of NF-kappaB and MAPK kinase activation. At the cellular level, the heparin analogues attenuated lymphocyte and macrophage recruitment and epithelial cell apoptosis. A drastic reduction in collagen-mediated fibrosis was also observed. No hemorrhagic events were observed after glycan treatment. These results strongly indicate the potential therapeutic use of these compounds for the treatment of colonic inflammation with a lower risk of hemorrhage when compared with mammalian heparin.

摘要

从海鞘皱瘤海鞘中分离出的名为硫酸皮肤素和肝素的哺乳动物肝素类似物的抗炎作用,在大鼠三硝基苯磺酸诱导的结肠炎模型中进行了评估。在7天的时间内皮下注射这些无脊椎动物化合物,通过结肠宏观和组织学特征的正常化观察到炎症显著减轻。在分子水平上,观察到肿瘤坏死因子-α、转化生长因子-β和血管内皮生长因子的产生减少,以及核因子-κB和丝裂原活化蛋白激酶激酶激活的减少。在细胞水平上,肝素类似物减弱了淋巴细胞和巨噬细胞的募集以及上皮细胞凋亡。还观察到胶原介导的纤维化显著减少。聚糖治疗后未观察到出血事件。这些结果有力地表明,与哺乳动物肝素相比,这些化合物在治疗结肠炎症方面具有潜在的治疗用途,且出血风险较低。

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