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双膦酸盐的作用。阿仑膦酸钠在大鼠骨骼中的定位及其对破骨细胞超微结构的影响。

Bisphosphonate action. Alendronate localization in rat bone and effects on osteoclast ultrastructure.

作者信息

Sato M, Grasser W, Endo N, Akins R, Simmons H, Thompson D D, Golub E, Rodan G A

机构信息

Department of Bone Biology and Osteoporosis Research, Merck Sharp & Dohme Research Laboratories, West Point, Pennsylvania 19486.

出版信息

J Clin Invest. 1991 Dec;88(6):2095-105. doi: 10.1172/JCI115539.

Abstract

Studies of the mode of action of the bisphosphonate alendronate showed that 1 d after the injection of 0.4 mg/kg [3H]alendronate to newborn rats, 72% of the osteoclastic surface, 2% of the bone forming, and 13% of all other surfaces were densely labeled. Silver grains were seen above the osteoclasts and no other cells. 6 d later the label was 600-1,000 microns away from the epiphyseal plate and buried inside the bone, indicating normal growth and matrix deposition on top of alendronate-containing bone. Osteoclasts from adult animals, infused with parathyroid hormone-related peptide (1-34) and treated with 0.4 mg/kg alendronate subcutaneously for 2 d, all lacked ruffled border but not clear zone. In vitro alendronate bound to bone particles with a Kd of approximately 1 mM and a capacity of 100 nmol/mg at pH 7. At pH 3.5 binding was reduced by 50%. Alendronate inhibited bone resorption by isolated chicken or rat osteoclasts when the amount on the bone surface was around 1.3 x 10(-3) fmol/microns 2, which would produce a concentration of 0.1-1 mM in the resorption space if 50% were released. At these concentrations membrane leakiness to calcium was observed. These findings suggest that alendronate binds to resorption surfaces, is locally released during acidification, the rise in concentration stops resorption and membrane ruffling, without destroying the osteoclasts.

摘要

对双膦酸盐阿仑膦酸钠作用模式的研究表明,给新生大鼠注射0.4mg/kg[3H]阿仑膦酸钠1天后,72%的破骨细胞表面、2%的成骨表面和13%的所有其他表面被密集标记。在破骨细胞上方可见银颗粒,未见其他细胞。6天后,标记物距离骺板600 - 1000微米并埋于骨内,表明在含阿仑膦酸钠的骨上方正常生长和基质沉积。成年动物的破骨细胞,注入甲状旁腺激素相关肽(1 - 34)并皮下注射0.4mg/kg阿仑膦酸钠2天,均缺乏皱襞缘但透明区正常。在体外,阿仑膦酸钠在pH 7时与骨颗粒结合,解离常数(Kd)约为1mM,结合容量为100nmol/mg。在pH 3.5时,结合减少50%。当骨表面阿仑膦酸钠量约为1.3×10(-3) fmol/微米2时,阿仑膦酸钠抑制分离的鸡或大鼠破骨细胞的骨吸收,如果50%释放,在吸收空间中会产生0.1 - 1mM的浓度。在这些浓度下观察到细胞膜对钙的通透性增加。这些发现表明阿仑膦酸钠与吸收表面结合,在酸化过程中局部释放,浓度升高停止吸收和膜皱襞形成,而不破坏破骨细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8dc/295810/63d86e5b44cb/jcinvest00065-0332-a.jpg

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