Pharmaceutical treatment of bone loss: From animal models and drug development to future treatment strategies

被引:18
作者
Brent, Mikkel Bo [1 ]
机构
[1] Aarhus Univ, Dept Biomed, Wilhelm Meyers Alle 3, DK-8000 Aarhus C, Denmark
关键词
Animal models; Osteoporosis; Bone biology; Drug repurposing; Combination therapy; GLUCOCORTICOID-INDUCED OSTEOPOROSIS; OSTEOBLAST-LIKE CELLS; SCLEROSTIN-ANTIBODY TREATMENT; ACTIVATED PROTEIN-KINASE; OVARIECTOMIZED RAT MODEL; HORMONE-RELATED PROTEIN; MESENCHYMAL STEM-CELLS; ILIAC TRABECULAR BONE; GROWTH-FACTOR-I; PARATHYROID-HORMONE;
D O I
10.1016/j.pharmthera.2023.108383
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Animal models are fundamental to advance our knowledge of the underlying pathophysiology of bone loss and to study pharmaceutical countermeasures against it. The animal model of post-menopausal osteoporosis from ovariectomy is the most widely used preclinical approach to study skeletal deterioration. However, several other animal models exist, each with unique characteristics such as bone loss from disuse, lactation, glucocorti-coid excess, or exposure to hypobaric hypoxia. The present review aimed to provide a comprehensive overview of these animal models to emphasize the importance and significance of investigating bone loss and pharmaceu-tical countermeasures from perspectives other than post-menopausal osteoporosis only. Hence, the pathophys-iology and underlying cellular mechanisms involved in the various types of bone loss are different, and this might influence which prevention and treatment strategies are the most effective. In addition, the review sought to map the current landscape of pharmaceutical countermeasures against osteoporosis with an emphasis on how drug development has changed from being driven by clinical observations and enhancement or repurposing of existing drugs to today's use of targeted anti-bodies that are the result of advanced insights into the underlying molecular mechanisms of bone formation and resorption. Moreover, new treatment combinations or repurposing opportunities of already approved drugs with a focus on dabigatran, parathyroid hormone and abaloparatide, growth hormone, inhibitors of the activin signaling pathway, acetazolamide, zoledronate, and romosozumab are discussed. Despite the considerable progress in drug development, there is still a clear need to improve treatment strategies and develop new pharmaceuticals against various types of osteoporosis. The review also highlights that new treatment indications should be explored using multiple animal models of bone loss in order to ensure a broad representation of different types of skeletal deterioration instead of mainly focusing on primary osteoporosis from post-menopausal estrogen deficiency.(c) 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
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页数:32
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