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骨保护素是小鼠航天诱导骨质流失的有效对策。

Osteoprotegerin is an effective countermeasure for spaceflight-induced bone loss in mice.

作者信息

Lloyd Shane A, Morony Sean E, Ferguson Virginia L, Simske Steven J, Stodieck Louis S, Warmington Kelly S, Livingston Eric W, Lacey David L, Kostenuik Paul J, Bateman Ted A

机构信息

Department of Orthopaedics and Rehabilitation, The Pennsylvania State University College of Medicine, Hershey, PA 17033, United States.

Metabolic Disorders, Amgen Incorporated, Thousand Oaks, CA 91320, United States.

出版信息

Bone. 2015 Dec;81:562-572. doi: 10.1016/j.bone.2015.08.021. Epub 2015 Aug 28.

Abstract

Bone loss associated with microgravity exposure poses a significant barrier to long-duration spaceflight. Osteoprotegerin-Fc (OPG-Fc) is a receptor activator of nuclear factor kappa-B ligand (RANKL) inhibitor that causes sustained inhibition of bone resorption after a single subcutaneous injection. We tested the ability of OPG-Fc to preserve bone mass during 12 days of spaceflight (SF). 64-day-old female C57BL/6J mice (n=12/group) were injected subcutaneously with OPG-Fc (20mg/kg) or an inert vehicle (VEH), 24h prior to launch. Ground control (GC) mice (VEH or OPG-Fc) were maintained under environmental conditions that mimicked those in the space shuttle middeck. Age-matched baseline (BL) controls were sacrificed at launch. GC/VEH, but not SF/VEH mice, gained tibia BMD and trabecular volume fraction (BV/TV) during the mission (P<0.05 vs. BL). SF/VEH mice had lower BV/TV vs. GC/VEH mice, while SF/OPG-Fc mice had greater BV/TV than SF/VEH or GC/VEH. SF reduced femur elastic and maximum strength in VEH mice, with OPG-Fc increasing elastic strength in SF mice. Serum TRAP5b was elevated in SF/VEH mice vs. GC/VEH mice. Conversely, SF/OPG-Fc mice had lower TRAP5b levels, suggesting that OPG-Fc preserved bone during spaceflight via inhibition of osteoclast-mediated bone resorption. Decreased bone formation also contributed to the observed osteopenia, based on the reduced femur periosteal bone formation rate and serum osteocalcin level. Overall, these observations suggest that the beneficial effects of OPG-Fc during SF are primarily due to dramatic and sustained suppression of bone resorption. In growing mice, this effect appears to compensate for the SF-related inhibition of bone formation, while preventing any SF-related increase in bone resorption. We have demonstrated that the young mouse is an appropriate new model for SF-induced osteopenia, and that a single pre-flight treatment with OPG-Fc can effectively prevent the deleterious effects of SF on mouse bone.

摘要

与微重力暴露相关的骨质流失对长期太空飞行构成了重大障碍。骨保护素-Fc(OPG-Fc)是一种核因子κB受体活化因子配体(RANKL)抑制剂,单次皮下注射后可导致骨吸收的持续抑制。我们测试了OPG-Fc在12天太空飞行(SF)期间维持骨量的能力。64日龄雌性C57BL/6J小鼠(每组n = 12)在发射前24小时皮下注射OPG-Fc(20mg/kg)或惰性载体(VEH)。地面对照(GC)小鼠(VEH或OPG-Fc)维持在模拟航天飞机中舱环境的条件下。年龄匹配的基线(BL)对照在发射时处死。在任务期间,GC/VEH小鼠(而非SF/VEH小鼠)的胫骨骨密度和骨小梁体积分数(BV/TV)增加(与BL相比,P < 0.05)。与GC/VEH小鼠相比,SF/VEH小鼠的BV/TV较低,而SF/OPG-Fc小鼠的BV/TV高于SF/VEH或GC/VEH小鼠。太空飞行降低了VEH小鼠股骨的弹性和最大强度,而OPG-Fc增加了太空飞行小鼠的弹性强度。与GC/VEH小鼠相比,SF/VEH小鼠血清中的抗酒石酸酸性磷酸酶5b(TRAP5b)升高。相反,SF/OPG-Fc小鼠的TRAP5b水平较低,这表明OPG-Fc通过抑制破骨细胞介导的骨吸收在太空飞行期间保护骨骼。基于股骨骨膜骨形成率降低和血清骨钙素水平降低,骨形成减少也导致了观察到的骨质减少。总体而言,这些观察结果表明,OPG-Fc在太空飞行期间的有益作用主要归因于对骨吸收的显著且持续的抑制。在生长中的小鼠中,这种作用似乎补偿了太空飞行相关的骨形成抑制,同时防止了任何与太空飞行相关的骨吸收增加。我们已经证明,幼鼠是太空飞行诱导的骨质减少的合适新模型,并且飞行前单次使用OPG-Fc治疗可以有效预防太空飞行对小鼠骨骼的有害影响。

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