间歇性甲状旁腺激素(PTH)与组织蛋白酶K抑制剂或阿仑膦酸盐联合使用时的合成代谢作用,因去卵巢小鼠骨骼的重塑状态不同而有所差异。
The anabolic action of intermittent PTH in combination with cathepsin K inhibitor or alendronate differs depending on the remodeling status in bone in ovariectomized mice.
作者信息
Yamane Hirotoshi, Sakai Akinori, Mori Toshiharu, Tanaka Shinya, Moridera Kuniaki, Nakamura Toshitaka
机构信息
Department of Orthopaedic Surgery, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555, Japan.
出版信息
Bone. 2009 Jun;44(6):1055-62. doi: 10.1016/j.bone.2008.05.010. Epub 2008 May 23.
We hypothesized that the anabolic action of parathyroid hormone (PTH) with the anti-catabolic agents cathepsin K inhibitor and alendronate differs depending on the remodeling status in the bone. C57/BL/6J mice, 8 weeks of age, were subjected to ovariectomized (OVX) or sham surgery. At 6 weeks after surgery, the mice were treated with cathepsin K inhibitor, alendronate, or a vehicle (daily, for 8 weeks), with or without PTH (1-34) (5 times/week, for the last 4 weeks). We assessed the bone chemical markers of the serum and urine, bone mineral density (BMD), histomorphomery in the primary and secondary spongiosa of the proximal tibia after fluorescence labeling, primary cell culture, and mRNA expressions in bone marrow cells. Cathepsin K inhibitor and alendronate significantly increased the BMD and the bone volume of the primary and secondary spongiosa, with a reduction of the urinary C-telopeptide of type I collagen that was increased by OVX, respectively. Cathepsin K inhibitor augmented the anabolic action of PTH on the BMD and bone volume at both the primary and secondary spongiosa, while alendronate had the same effect on the BMD and bone volume only at the primary spongiosa. Cathepsin K inhibitor did not decrease serum osteocalcin with or without PTH, while alendronate did decrease it. Cathepsin K inhibitor did not decrease the values of osteoclast number or bone formation rate with or without PTH, while alendronate decreased those values and increased osteoclast apoptosis. The combination of PTH and cathepsin K inhibitor increased alkaline phosphatase-positive CFU-f formation and c-fos, osterix, and osteocalcin mRNA expressions of bone marrow cells as well as PTH alone, while the combination of PTH and alendronate decreased those values. This study demonstrated that alendronate enhances the anabolic action of PTH at the primary spongiosa, but blunts it in the remodeling trabecular bone, while cathepsin K inhibitor enhances the action at both sites in OVX mice. In conclusion, the anabolic action of intermittent PTH in combination with cathepsin K inhibitor or alendronate differs depending on the remodeling status of bone in OVX mice.
我们推测,甲状旁腺激素(PTH)与抗分解代谢剂组织蛋白酶K抑制剂和阿仑膦酸钠的合成代谢作用因骨骼的重塑状态而异。对8周龄的C57/BL/6J小鼠进行卵巢切除(OVX)或假手术。术后6周,给小鼠使用组织蛋白酶K抑制剂、阿仑膦酸钠或赋形剂(每日给药,持续8周),同时或不同时给予PTH(1-34)(每周5次,持续最后4周)。我们评估了血清和尿液中的骨化学标志物、骨矿物质密度(BMD)、荧光标记后胫骨近端初级和次级海绵骨的组织形态计量学、原代细胞培养以及骨髓细胞中的mRNA表达。组织蛋白酶K抑制剂和阿仑膦酸钠显著增加了初级和次级海绵骨的BMD和骨体积,同时分别降低了因OVX而升高的I型胶原尿C端肽水平。组织蛋白酶K抑制剂增强了PTH对初级和次级海绵骨BMD和骨体积的合成代谢作用,而阿仑膦酸钠仅对初级海绵骨的BMD和骨体积有相同作用。无论有无PTH,组织蛋白酶K抑制剂均未降低血清骨钙素水平,而阿仑膦酸钠则降低了该水平。无论有无PTH,组织蛋白酶K抑制剂均未降低破骨细胞数量或骨形成率的值,而阿仑膦酸钠降低了这些值并增加了破骨细胞凋亡。PTH与组织蛋白酶K抑制剂的组合与单独使用PTH一样,增加了骨髓细胞中碱性磷酸酶阳性CFU-f的形成以及c-fos、osterix和骨钙素mRNA的表达,而PTH与阿仑膦酸钠的组合则降低了这些值。本研究表明,阿仑膦酸钠增强了PTH在初级海绵骨的合成代谢作用,但在重塑的小梁骨中使其减弱,而组织蛋白酶K抑制剂在OVX小鼠的两个部位均增强了该作用。总之,间歇性PTH与组织蛋白酶K抑制剂或阿仑膦酸钠联合使用时的合成代谢作用因OVX小鼠骨骼的重塑状态而异。