Shinoda H
Department of Pharmacology, School of Dentistry, Tohoku University, Sendai, Japan.
Nihon Yakurigaku Zasshi. 1995 May;105(5):285-94. doi: 10.1254/fpj.105.285.
Bisphosphonates have a P-C-P bond instead of the P-O-P bond of inorganic pyrophosphate that makes them resistant to enzymatic degradation and gives them a high affinity for hydroxyapatite. They are potent blockers of osteoclastic bone resorption and have been successfully used to treat metabolic bone diseases that involve increased bone resorption. It is possible to synthesize a variety of bisphosphonates by substituting the hydrogen on the carbon atom. The pharmacological characteristics and activity varies greatly from compound to compound, ranging from 1 to 10,000. Some structure-activity relationships have been found, but no clear-cut one has been established yet. There is a general consensus that the inhibition of bone resorption by bisphosphonates is not caused by the inhibition of dissolution of the hydroxyapatite crystal, but is actually caused through a cellular mechanism that is not completely understood. In the present review article, the possible mode of bisphosphonate action was discussed with special reference to: (1) whether bisphosphonates inhibit the function of mature osteoclasts directly or through osteoblasts and (2) whether bisphosphonates inhibit the proliferation or differentiation of osteoclast progenitors to osteoclasts.
双膦酸盐具有P-C-P键而非无机焦磷酸盐的P-O-P键,这使得它们对酶促降解具有抗性,并赋予它们对羟基磷灰石的高亲和力。它们是破骨细胞骨吸收的有效阻滞剂,并已成功用于治疗涉及骨吸收增加的代谢性骨病。通过取代碳原子上的氢,可以合成多种双膦酸盐。不同化合物的药理特性和活性差异很大,范围从1到10000。已经发现了一些构效关系,但尚未建立明确的构效关系。人们普遍认为,双膦酸盐对骨吸收的抑制不是由羟基磷灰石晶体溶解的抑制引起的,而是实际上通过一种尚未完全理解的细胞机制引起的。在本综述文章中,特别参考以下方面讨论了双膦酸盐作用的可能模式:(1)双膦酸盐是直接抑制成熟破骨细胞的功能还是通过成骨细胞抑制其功能;(2)双膦酸盐是否抑制破骨细胞祖细胞向破骨细胞的增殖或分化。