论文标题
骨骼疼痛的管理,治疗和研究束缚组织工程模型
The management, treatment and study of skeletal pain harnessing tissue engineering models
论文作者
论文摘要
骨骼疼痛通常会在骨骼损伤后立即发生,而伤害感受器的机械失真或破裂。疼痛机制还与慢性疼痛状况受损有关。任何影响骨折骨骼区域的负荷都会增加骨内压力,从而刺激伤害感受反应,因此需要快速临床干预,以减轻与骨骼损伤相关的疼痛,并适当缓解与骨骼质量,肌肉,迁移率丧失相关的任何过程,以防止死亡。以下综述研究了与创新或与癌症相关的骨骼损害相关的疼痛机制,重点是开发创新治疗干预措施的新方法。特别是,当前的评论突出了组织工程方法,这些方法在应用骨和神经组织的功能性仿生制造方面提供了相当大的希望,类似于病理微环境。骨骼和神经组织工程模型的战略组合为开发一类新的体外平台提供了重要潜力,能够替换体内模型并测试旨在解决骨相关疼痛的新型药物治疗的安全性和功效。迄今为止,骨痛研究领域一直集中在动物模型上,并且在模型中伴随着差异,并且数据与人类生理反应相关的数据很少。这篇综述探讨了疼痛药物开发研究中的明显差距,并提出了线束组织工程技术方法的逐步变化,以概括受损的骨组织的复杂病理生理环境,从而评估相关的模拟疼痛机制,并最终具有重要的治疗潜力,以改善其生活质量。
Bone pain typically occurs immediately following skeletal damage with mechanical distortion or rupture of nociceptive fibres. The pain mechanism is also associated with chronic pain conditions where the healing process is impaired. Any load impacting on the area of the fractured bone will increase the intraosseous pressure, consequently stimulating the nociceptive response, necessitating rapid clinical intervention to relieve pain associated with the bone damage and appropriate mitigation of any processes involved with the loss of bone mass, muscle, mobility and, to prevent death. The following review has examined the mechanisms of pain associated with trauma or cancer-related skeletal damage focusing on new approaches for the development of innovative therapeutic interventions. In particular, the current review highlights tissue engineering approaches that offer considerable promise in the application of functional biomimetic fabrication of bone and nerve tissues, resembling the pathological micro-environment. The strategic combination of bone and nerve tissue engineered models provides significant potential to develop a new class of in vitro platforms, capable of replacing in vivo models and testing the safety and efficacy of novel drug treatments aimed at the resolution of bone-associated pain. To date, the field of bone pain research has centred on animal models, with accompanying disparity within models often noted and a paucity of data correlating to the human physiological response. This review explores the evident gap in pain drug development research and suggests a step change in approach to harness tissue engineering technologies to recapitulate the complex pathophysiological environment of the damaged bone tissue enabling evaluation of the associated pain-mimicking mechanism with, ultimately, significant therapeutic potential therein for improved patient quality of life.