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Mechanisms of maturation and ageing of collagen.

机译:胶原蛋白成熟和衰老的机制。

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The deleterious age-related changes in collagen that manifest in the stiffening of the joints, the vascular system and the renal and retinal capillaries are primarily due to the intermolecular cross-linking of the collagen molecules within the tissues. The formation of cross-links was elegantly demonstrated by Verzar over 40 years ago but the nature and mechanisms are only now being unravelled. Cross-linking involves two different mechanisms, one a precise enzymically controlled cross-linking during development and maturation and the other an adventitious non-enzymic mechanism following maturation of the tissue. It is this additional non-enzymic cross-linking, known as glycation, involving reaction with glucose and subsequent oxidation products of the complex, that is the major cause of dysfunction of collagenous tissues in old age. The process is accelerated in diabetic subjects due to the higher levels of glucose. The effect of glycation on cell-matrix interactions is now being studied and may be shown to be an equally important aspect of ageing of collagen. An understanding of these mechanisms is now leading to the development of inhibitors of glycation and compounds capable of cleaving the cross-links, thus alleviating the devastating effects of ageing.
机译:胶原蛋白中与年龄相关的有害有害变化表现在关节,血管系统以及肾和视网膜毛细血管的硬化中,这主要归因于组织内胶原蛋白分子的分子间交联。 Verzar在40多年前曾优雅地演示过交叉链接的形成,但直到现在才揭示了其本质和机制。交联涉及两种不同的机制,一种是在发育和成熟过程中精确的酶控制交联,另一种是组织成熟后的不定的非酶促机制。正是这种额外的非酶交联,称为糖基化,涉及与葡萄糖的反应以及复合物的随后氧化产物的反应,这是老年胶原组织功能障碍的主要原因。由于较高的葡萄糖水平,在糖尿病受试者中该过程被加速。糖基化对细胞-基质相互作用的影响目前正在研究中,可能被证明是胶原蛋白老化的同等重要方面。现在,对这些机理的理解导致了糖基化抑制剂和能够裂解交联键的化合物的开发,从而减轻了老化的破坏性影响。

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