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脉冲电磁场增强骨愈合不良——从机制到临床结果

Augmentation of Deficient Bone Healing by Pulsed Electromagnetic Fields-From Mechanisms to Clinical Outcomes.

作者信息

Kaadan Amr, Salati Simona, Setti Stefania, Aaron Roy

机构信息

Department of Orthopedic Surgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.

Medical Division, Igea S.p.A, 41012 Carpi, Italy.

出版信息

Bioengineering (Basel). 2024 Dec 3;11(12):1223. doi: 10.3390/bioengineering11121223.

Abstract

Pulsed Electromagnetic Fields (PEMF) are widely used, with excellent clinical outcomes. However, their mechanism of action has not yet been completely understood. The purpose of this review is to describe current observations on the mechanisms of PEMF, together with its clinical efficacy. Osteoblast responsiveness to PEMF is described on several scales, from the cell membrane to clinically relevant bone formation. PEMF has been shown to activate membrane adenosine receptors. The role of adenosine receptors in activating intracellular second messenger pathways, such as the canonical Wnt/β-catenin pathway and the mitogen-activated protein kinases (MAPK) pathway, is described. The responsiveness of osteoblasts and the synthesis of structural and signaling proteins constitute the role of PEMFs in promoting osteogenesis and bone matrix synthesis, and they are described. Multiple studies, ranging from observational and randomized to meta-analyses that investigate the clinical efficacy of PEMF, are described. This review presents a favorable conclusion on the clinical effects of PEMF while unlocking the "black box" of PEMF's mechanism of action, thus improving confidence in the clinical utility of PEMF in bone repair.

摘要

脉冲电磁场(PEMF)被广泛应用,临床效果良好。然而,其作用机制尚未完全明确。本综述旨在描述目前关于PEMF作用机制的观察结果及其临床疗效。从细胞膜到临床相关的骨形成,在多个层面描述了成骨细胞对PEMF的反应。已证明PEMF可激活膜腺苷受体。描述了腺苷受体在激活细胞内第二信使途径(如经典的Wnt/β-连环蛋白途径和丝裂原活化蛋白激酶(MAPK)途径)中的作用。阐述了成骨细胞的反应性以及结构和信号蛋白的合成在PEMF促进成骨和骨基质合成中的作用。描述了多项研究,包括观察性研究、随机研究以及调查PEMF临床疗效的荟萃分析。本综述在揭示PEMF作用机制“黑箱”的同时,对PEMF的临床效果给出了肯定结论,从而提高了对PEMF在骨修复中临床应用的信心。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e2b/11672986/4ed11594a200/bioengineering-11-01223-g001.jpg

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