Cannabidiol and Cannabigerol, Nonpsychotropic Cannabinoids, as Analgesics that Effectively Manage Bone Fracture Pain and Promote Healing in Mice

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Bone and Mineral Research Pub Date : 2023-08-19 DOI:10.1002/jbmr.4902
Deepak Kumar Khajuria, Vengadeshprabhu Karuppagounder, Irena Nowak, Diana E. Sepulveda, Gregory S. Lewis, Christopher C. Norbury, Wesley M. Raup-Konsavage, Kent E. Vrana, Fadia Kamal, Reyad A. Elbarbary
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引用次数: 2

Abstract

Bone fractures are among the most prevalent musculoskeletal injuries, and pain management is an essential part of fracture treatment. Fractures heal through an early inflammatory phase, followed by repair and remodeling. Nonsteroidal anti-inflammatory drugs (NSAIDs) are not recommended for fracture pain control as they potently inhibit the inflammatory phase and, thus, impair the healing. Opioids do not provide a better alternative for several reasons, including abuse potential. Accordingly, there is an unmet clinical need for analgesics that effectively ameliorate postfracture pain without impeding the healing. Here, we investigated the analgesic efficacy of two nonpsychotropic cannabinoids, cannabidiol (CBD) and cannabigerol (CBG), in a mouse model for tibial fracture. Mice with fractured tibiae exhibited increased sensitivity to mechanical, cold, and hot stimuli. Both CBD and CBG normalized pain sensitivity to all tested stimuli, and their analgesic effects were comparable to those of the NSAIDs. Interestingly, CBD and CBG promoted bone healing via multiple mechanisms during the early and late phases. During the early inflammatory phase, both cannabinoids increased the abundance of periosteal bone progenitors in the healing hematoma and promoted the osteogenic commitment of these progenitors. During the later phases of healing, CBD and CBG accelerated the fibrocartilaginous callus mineralization and enhanced the viability and proliferation of bone and bone-marrow cells. These effects culminated in higher bone volume fraction, higher bone mineral density, and improved mechanical quality of the newly formed bone. Together, our data suggest CBD and CBG as therapeutic agents that can replace NSAIDs in managing postfracture pain as both cannabinoids exert potent analgesic effects and, at the same time, promote bone healing. © 2023 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

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大麻二酚和大麻二酚,非精神性大麻酚类药物,作为有效治疗小鼠骨折疼痛和促进愈合的镇痛药。
骨折是最常见的肌肉骨骼损伤之一,疼痛管理是骨折治疗的重要组成部分。骨折通过早期炎症阶段愈合,随后进行修复和重塑。不建议使用非甾体抗炎药(NSAIDs)来控制骨折疼痛,因为它们能有效抑制炎症阶段,从而损害愈合。阿片类药物不能提供更好的替代品,原因有几个,包括滥用的可能性。因此,临床上对镇痛药的需求没有得到满足,这种镇痛药可以有效地减轻骨折后的疼痛,而不会阻碍愈合。在此,我们在小鼠胫骨骨折模型中研究了两种非精神性大麻素,大麻二酚(CBD)和大麻酚(CBG)的镇痛效果。胫骨骨折的小鼠表现出对机械、冷和热刺激的敏感性增加。CBD和CBG对所有测试刺激的疼痛敏感性均正常化,其镇痛效果与非甾体抗炎药相当。有趣的是,CBD和CBG在早期和晚期通过多种机制促进骨愈合。在早期炎症阶段,两种大麻素都增加了愈合血肿中骨膜骨祖细胞的丰度,并促进了这些祖细胞的成骨承诺。在愈合的后期,CBD和CBG加速了纤维软骨骨痂的矿化,增强了骨和骨髓细胞的活力和增殖。这些效应最终导致更高的骨体积分数、更高的骨骼矿物质密度和改善新形成的骨骼的机械质量。总之,我们的数据表明,CBD和CBG是可以取代非甾体抗炎药治疗骨折后疼痛的治疗剂,因为这两种大麻素都具有强大的镇痛作用,同时促进骨愈合。©2023作者。由Wiley Periodicals LLC代表美国骨与矿物研究学会(ASBMR)出版的《骨与矿产研究杂志》。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
期刊最新文献
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