Rodan G A, Balena R
Department of Bone Biology and Osteoporosis Research, Merck Sharp and Dohme Research Laboratories, West Point, PA 19486.
Ann Med. 1993 Aug;25(4):373-8. doi: 10.3109/07853899309147299.
Bisphosphonates (BP) are pyrophosphate analogs, P-C-P with various carbon side-chains. The phosphate groups are responsible for the low gastrointestinal absorption (about 1%), limited penetration into cells, adsorption to bone mineral and rapid excretion in the urine. Based on the C side-chains, BPs can inhibit osteoclastic bone resorption with potencies which differ by as much as 10,000-fold among compounds. The most potent inhibitors are aminobisphosphonates. Studies of the amino-BP alendronate show preferential uptake at sites of bone resorption where they block osteoclastic activity by inhibiting ruffled border formation. BPs are the treatment of choice for hypercalcaemia of malignancy, where a single infusion with a potent BP will normalize serum calcium in 80% of the patients. Paget's disease also shows an excellent long-term response to BPs. In addition, BPs are being studied for the treatment of osteoporosis and other bone disorders which could be helped by inhibition of bone resorption.
双膦酸盐(BP)是焦磷酸盐类似物,即带有各种碳侧链的P-C-P。磷酸基团导致其胃肠道吸收率低(约1%)、细胞穿透性有限、吸附于骨矿物质并经尿液快速排泄。根据碳侧链不同,双膦酸盐抑制破骨细胞骨吸收的效力在不同化合物之间相差高达10000倍。最有效的抑制剂是氨基双膦酸盐。对氨基双膦酸盐阿仑膦酸钠的研究表明,其在骨吸收部位优先摄取,通过抑制皱褶缘形成来阻断破骨细胞活性。双膦酸盐是恶性肿瘤高钙血症的首选治疗药物,单次输注强效双膦酸盐可使80%的患者血清钙恢复正常。佩吉特病对双膦酸盐也显示出良好的长期反应。此外,正在研究双膦酸盐用于治疗骨质疏松症和其他可通过抑制骨吸收得到改善的骨疾病。