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β-石竹烯与他汀类药物在骨折愈合中的作用——一篇叙述性综述

β-Caryophyllene and Statins in Bone Fracture Healing - A Narrative Review.

作者信息

Marom Hilik, Khan Mansoor A, Darvish Nissim, Tornetta Iii Paul, Khoury Amal, Weil Yoram A, Skelley Nathan W M, Allison Daniel C, Meiron Sahar, Ehrmann Barr Tami

机构信息

R&D, OrthoTreat Ltd, Tel Aviv-Jaffa, Israel.

Corporate Office, OrthoTreat Ltd, Tel Aviv-Jaffa, Israel.

出版信息

Orthop Res Rev. 2025 Jan 23;17:31-42. doi: 10.2147/ORR.S506427. eCollection 2025.

Abstract

Bone fractures are a leading cause of morbidity and healthcare expenditure globally. The complex healing process involves inflammation, cartilage formation, mineralization, and bone remodeling. Current treatments like immobilization, surgery, and bone grafting, though effective, pose significant challenges, such as prolonged recovery and high costs. Emerging therapies such as biological agents, pharmacological treatments, and physical stimulation techniques are also associated with high costs, side effects, and practical applicability limitations. There is a critical need for alternative therapies that are cost-effective, safe, and easy to use. Recent studies suggest the potential of β-caryophyllene (BCP) and statins in promoting bone healing. BCP, a naturally occurring anti-inflammatory and antioxidant compound found in essential oils, enhances osteoblast activity and inhibits osteoclastogenesis. Statins, known for their cholesterol-lowering effects, also promote bone formation and reduce bone resorption through multiple biochemical pathways. Both BCP and statins have shown promising results in preclinical studies, enhancing bone density and promoting fracture healing. This review explores the individual and potential synergistic effects of BCP and statins on bone fracture healing. It highlights the complementary mechanisms of these agents: BCP's anti-inflammatory and osteogenic properties and statins' ability to inhibit osteoclast activity and promote angiogenesis. Combining BCP and statins could offer a multifaceted approach to enhance fracture healing, reduce complications, and improve patient outcomes. While individual effects are supported preclinically, further studies investigating synergies, formulations, and clinical translation are needed to develop this promising novel therapeutic approach for improving fracture repair outcomes.

摘要

骨折是全球发病和医疗支出的主要原因。复杂的愈合过程包括炎症、软骨形成、矿化和骨重塑。目前的治疗方法,如固定、手术和骨移植,虽然有效,但也带来了重大挑战,如恢复时间长和成本高。新兴疗法,如生物制剂、药物治疗和物理刺激技术,也存在成本高、副作用和实际应用局限性等问题。迫切需要具有成本效益、安全且易于使用的替代疗法。最近的研究表明,β-石竹烯(BCP)和他汀类药物在促进骨愈合方面具有潜力。BCP是一种天然存在于精油中的抗炎和抗氧化化合物,可增强成骨细胞活性并抑制破骨细胞生成。他汀类药物以其降胆固醇作用而闻名,还通过多种生化途径促进骨形成并减少骨吸收。BCP和他汀类药物在临床前研究中均显示出有希望的结果,可提高骨密度并促进骨折愈合。本综述探讨了BCP和他汀类药物对骨折愈合的个体及潜在协同作用。它强调了这些药物的互补机制:BCP的抗炎和成骨特性以及他汀类药物抑制破骨细胞活性和促进血管生成的能力。联合使用BCP和他汀类药物可能提供一种多方面的方法来增强骨折愈合、减少并发症并改善患者预后。虽然临床前研究支持个体作用,但需要进一步研究协同作用、制剂和临床转化,以开发这种有前景的新型治疗方法来改善骨折修复结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6177/11771162/561cb5bcebde/ORR-17-31-g0001.jpg

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