Hahn T J, DeBartolo T F, Halstead L R
Endocr Res Commun. 1980;7(3):189-200. doi: 10.3109/07435808009065972.
Ouabain in concentrations from 20-100 micromoles produced a dose-related inhibition of in vitro stimulation of bone resorption by parathyroid hormone, 1,25-dihydroxyvitamin D3 and calcium ionophore A23187, as measured by 45Ca and [3H]-hydroxyproline release in 5-day cultures of fetal rat forelimb rudiments. The inhibitory effect on 45Ca release was completely reversed by subsequent incubation in ouabain-free medium. At a concentration of 100 micromoles ouabain virtually abolished active bone resorption; however, basal and stimulated bone cyclic AMP (cAMP) content were significantly increased above levels observed in the absence of ouabain. The increased cAMP content did not appear to be the result of phosphodiesterase inhibition. It is concluded that intact Na/K ATPase function is required for hormonally-stimulated bone resorptive processes and that the inhibitory effect of ouabain on bone resorption is produced at a point subsequent to cyclic AMP generation.
哇巴因浓度在20 - 100微摩尔时,对甲状旁腺激素、1,25 - 二羟基维生素D3和钙离子载体A23187体外刺激骨吸收产生剂量相关的抑制作用,这是通过在胎鼠前肢雏形5天培养物中45Ca和[3H] - 羟脯氨酸释放来测定的。对45Ca释放的抑制作用在随后于无哇巴因培养基中孵育时完全逆转。在100微摩尔浓度时,哇巴因几乎消除了活跃的骨吸收;然而,基础和刺激后的骨环磷酸腺苷(cAMP)含量显著高于在无哇巴因情况下观察到的水平。cAMP含量的增加似乎不是磷酸二酯酶抑制的结果。结论是,激素刺激的骨吸收过程需要完整的钠/钾ATP酶功能,并且哇巴因对骨吸收的抑制作用在环磷酸腺苷生成后的某个点产生。