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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Disintegration of collagen fibrils by Glucono-delta-lactone: An implied lead for disintegration of fibrosis
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Disintegration of collagen fibrils by Glucono-delta-lactone: An implied lead for disintegration of fibrosis

机译:Glucono-Delta-内酯的胶原蛋白原纤维的解体:纤维化崩解的隐含铅

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摘要

Excess accumulation of collagen (fibrosis) undergoes self-aggregation, which leads to fibrillar collagen, on the extracellular matrix is the hallmark of a number of diseases such as keloids, hypertrophic scars, and systemic scleroderma. Direct inhibition or disintegration of collagen fibrils by small molecules offer a therapeutic approach to prevent or treat the diseases related to fibrosis. Herein, the anti-fibrotic property of Glucono-delta-lactone (GdL), known as acidifier, on the fibrillation and its disintegration of collagen was investigated. As collagen fibrillation is pH dependent, the pH modulation property of GdL is attractive to inhibit self-association of collagen. Optical density and microscopic data indicate that GdL elicits concentration-dependent fibril inhibition and also disintegrates pre-formed collagen fibrils. The simultaneous pH analysis showed that the modulation(lowering) of pH by GdL is the primary cause for its anti-fibrotic activity. The intact triple helical structure of collagen upon treatment of GdL suggests that collagen fibril disintegration can be achieved without affecting the native structure of collagen which is essential for any anti-fibrotic agents. Saturation transfer difference (STD) NMR result reveals that GdL is in proximity to collagen. The present results thus suggest that GdL provides a lead to design novel anti-fibrotic agents for the pathologies related to collagen deposition. (C) 2017 Elsevier B.V. All rights reserved.
机译:胶原蛋白(纤维化)的过度积累经历自聚集,这导致纤维状胶原蛋白,细胞外基质是瘢痕疙瘩,肥厚疤痕和全身疾病等疾病的标志。小分子直接抑制或崩解胶原型原纤维提供治疗方法,以预防或治疗与纤维化有关的疾病。在此,研究了葡萄糖醇 - δ-内酯(GDL)的抗纤维化特性,称为酸化剂,胶原蛋白的崩解剂。随着胶原蛋白的原纤化依赖于pH,GDL的pH调节性能是抑制胶原的自我关联的吸引力。光学密度和微观数据表明GDL引发浓度依赖性原纤维抑制,并且还崩解预形成的胶原纤维。同时pH分析表明,GDL的pH调节(降低)是其抗纤维化活性的主要原因。在治疗GDL时胶原的完整三重螺旋结构表明,可以实现胶原型原纤维崩解,而不影响对于任何抗纤维化剂至关重要的胶原的天然结构。饱和转移差(STD)NMR结果表明,GDL邻近胶原蛋白。因此,目前的结果表明GDL提供了用于设计与胶原沉积有关的病理的新型抗纤维化剂的导致。 (c)2017年Elsevier B.V.保留所有权利。

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