Shevde Nirupama K, Plum Lori A, Clagett-Dame Margaret, Yamamoto Hironori, Pike J Wesley, DeLuca Hector F
Department of Biochemistry, University of Wisconsin, Madison, WI 53706, USA.
Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13487-91. doi: 10.1073/pnas.202471299. Epub 2002 Oct 8.
1,25-Dihydroxyvitamin D(3) [1,25(OH)(2)D(3)] is a principal regulator of calcium and phosphorus homeostasis through actions on intestine, kidney, and bone. 1,25(OH)(2)D(3) is not considered to play a significant role in bone formation, except for its role in supporting mineralization. We report here on the properties of 2-methylene-19-nor-(20S)-1alpha,25(OH)(2)D(3) (2MD), a highly potent analog of 1,25(OH)(2)D(3) that induces bone formation both in vitro and in vivo. Selectivity for bone was first demonstrated through the observation that 2MD is at least 30-fold more effective than 1,25(OH)(2)D(3) in stimulating osteoblast-mediated bone calcium mobilization while being only slightly more potent in supporting intestinal calcium transport. 2MD is also highly potent in promoting osteoblast-mediated osteoclast formation in vitro, a process essential to both bone resorption and formation. Most significantly, 2MD at concentrations as low as 10(-12) M causes primary cultures of osteoblasts to produce bone in vitro. This effect is not found with 1,25(OH)(2)D(3) even at 10(-8) M, suggesting that 2MD might be osteogenic in vivo. Indeed, 2MD (7 pmol/day) causes a substantial increase (9%) in total body bone mass in ovariectomized rats over a 23-week period. 1,25(OH)(2)D(3) (500 pmol three times a week) only prevented the bone loss associated with ovariectomy and did not increase bone mass. These results indicate that 2MD is a potent bone-selective analog of 1,25(OH)(2)D(3) potentially effective in treating bone loss diseases.
1,25-二羟基维生素D(3)[1,25(OH)₂D(3)]通过作用于肠道、肾脏和骨骼,是钙和磷稳态的主要调节因子。1,25(OH)₂D(3)除了在支持矿化方面发挥作用外,一般不被认为在骨形成中起重要作用。我们在此报告2-亚甲基-19-去甲-(20S)-1α,25(OH)₂D(3)(2MD)的特性,它是1,25(OH)₂D(3)的一种高效类似物,在体外和体内均能诱导骨形成。对骨骼的选择性首先通过以下观察得到证明:2MD在刺激成骨细胞介导的骨钙动员方面比1,25(OH)₂D(3)至少有效30倍,而在支持肠道钙转运方面仅略强。2MD在体外促进成骨细胞介导的破骨细胞形成方面也具有高效性,这一过程对骨吸收和形成都至关重要。最显著的是,低至10⁻¹² M的2MD就能使成骨细胞原代培养物在体外产生骨组织。即使在10⁻⁸ M的浓度下,1,25(OH)₂D(3)也未发现这种效果,这表明2MD在体内可能具有成骨作用。事实上,2MD(7 pmol/天)在23周的时间里使去卵巢大鼠的全身骨量显著增加(9%)。1,25(OH)₂D(3)(每周三次,每次500 pmol)仅能预防与去卵巢相关的骨丢失,并未增加骨量。这些结果表明,2MD是1,25(OH)₂D(3)的一种有效的骨选择性类似物,在治疗骨质流失疾病方面可能具有潜在疗效。