Solgaard Marie, Jørgensen Niklas Rye
H:S Hvidovre Hospital, Forskningsenheden for osteoporose og metaboliske knoglesygdomme, Klinisk Biokemisk Afdeling.
Ugeskr Laeger. 2005 Aug 22;167(34):3152-6.
Osteoporosis is a disabling disease, and despite the progress in treating this disease in recent years, it is still necessary to develop new treatment options. A potential target for new pharmacological agents with the ability to regulate bone metabolism is the purinergic receptors, also called P2 receptors. Nucleotides activate these receptors, and recent studies have shown a possible role for these in bone turnover and metabolism. P2 receptors can be further divided into P2X and P2Y subtypes, which have strikingly different mechanisms of action. They are expressed both by osteoblasts and by osteoclasts, and agonist binding affects cell proliferation, differentiation, activity and apoptosis. With increasing knowledge of the function and role of these receptors in bone biology, they will undoubtedly be a future target for the design of new drugs which can be used for treatment of metabolic bone diseases, including osteoporosis.
骨质疏松症是一种致残性疾病,尽管近年来在治疗该疾病方面取得了进展,但仍有必要开发新的治疗方案。具有调节骨代谢能力的新型药物的一个潜在靶点是嘌呤能受体,也称为P2受体。核苷酸激活这些受体,最近的研究表明它们在骨转换和代谢中可能发挥作用。P2受体可进一步分为P2X和P2Y亚型,其作用机制截然不同。它们在成骨细胞和破骨细胞中均有表达,激动剂结合会影响细胞增殖、分化、活性和凋亡。随着对这些受体在骨生物学中的功能和作用的了解不断增加,它们无疑将成为未来设计可用于治疗包括骨质疏松症在内的代谢性骨疾病的新药的靶点。