Lever R, Page C
Sackler Institute of Pulmonary Pharmacology, GKT School of Biomedical Sciences, 5th Floor Hodgkin Building, Guy's Campus, London SE1 9RT, UK.
Pulm Pharmacol Ther. 2001;14(3):249-54. doi: 10.1006/pupt.2001.0296.
Glycosaminoglycans (GAGs) are large, polyanionic molecules expressed throughout the body. The GAG heparin, co-released with histamine, is synthesised by and stored exclusively in mast cells, whereas the closely related molecule heparan sulphate is expressed, as part of a proteoglycan, on cell surfaces and throughout tissue matrices. These molecules are increasingly thought to play a role in regulation of the inflammatory response and heparin, for many years, has been considered to hold potential in the treatment of diseases such as asthma. Heparin and related molecules have been found to exert antiinflammatory effects in a wide range of in vitro assays, animal models and, indeed, human patients. Moreover, the results of studies carried out to date indicate that the antiinflammatory activities of heparin are dissociable from its well-established anticoagulant nature, suggesting that the separation of these characteristics could yield novel antiinflammatory drugs which may be useful in the future treatment of diseases such as asthma
糖胺聚糖(GAGs)是一类在全身表达的大型多阴离子分子。与组胺共同释放的GAG肝素,由肥大细胞合成并仅存储于肥大细胞中,而与之密切相关的分子硫酸乙酰肝素则作为蛋白聚糖的一部分,表达于细胞表面和整个组织基质中。这些分子越来越被认为在炎症反应调节中发挥作用,多年来,肝素一直被认为在治疗哮喘等疾病方面具有潜力。在广泛的体外试验、动物模型乃至人类患者中,已发现肝素及相关分子具有抗炎作用。此外,迄今为止的研究结果表明,肝素的抗炎活性与其已确立的抗凝特性可分离,这表明分离这些特性可能会产生新型抗炎药物,有望用于未来哮喘等疾病的治疗。