洞察骨组织氧化应激和生物材料的新挑战

G. Cerqueni, A. Scalzone, C. Licini, P. Gentile, M. Mattioli-Belmonte
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引用次数: 32

摘要

活性氧(ROS)在骨中的存在可以影响驻留细胞的行为以及细胞外基质组成和组织结构。衰老,再加上过度负荷、不平衡的饮食、吸烟、易感的遗传因素,都会导致活性氧增加,如果伴随着不适当的清除剂产生,就会促进氧化应激的产生,从而促进骨分解代谢。此外,骨损伤可由许多事件引发,如道路和运动事故或肿瘤切除。尽管骨组织具有众所周知的修复和再生能力,但这些机制在修复大尺寸缺陷时效率低下,骨移植往往是必要的。活性氧在植入物引入后的反应中起着至关重要的作用,并影响植入物的成功。本文综述了体内植入物产生氧化应激的机制及其调节方法。活性分子(如多酚)的局部传递增强了骨生物材料的整合,证明氧化应激的管理是植入物有效性的目标。由于其抗氧化和抗炎特性,多酚已广泛应用于心血管、神经退行性疾病、骨骼疾病和癌症的医学中。此外,新的智能生物材料和分子医学的观点,以可编程的方式进行氧化应激调节,通过使用ROS反应材料或通过选择性分子途径参与ROS的产生,将进行批判性的分析和讨论。
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Insights into Oxidative Stress in Bone Tissue and Novel Challenges for Biomaterials
The presence of Reactive Oxygen Species (ROS) in bone can influence resident cells behaviour as well as the extra-cellular matrix composition and the tissue architecture. Aging, in addition to excessive overloads, unbalanced diet, smoking, predisposing genetic factors, lead to an increase of ROS and, if it is accompanied with an inappropriate production of scavengers, promotes the generation of oxidative stress that encourages bone catabolism. Furthermore, bone injuries can be triggered by numerous events such as road and sports accidents or tumour resection. Although bone tissue possesses a well-known repair and regeneration capacity, these mechanisms are inefficient in repairing large size defects and bone grafts are often necessary. ROS play a fundamental role in response after the implant introduction and can influence its success. This review provides insights on the mechanisms of oxidative stress generated by an implant in vivo and suitable ways for its modulation. The local delivery of active molecules, such as polyphenols, enhanced bone biomaterial integration evidencing that the management of the oxidative stress is a target for the effectiveness of an implant. Polyphenols have been widely used in medicine for cardiovascular, neurodegenerative, bone disorders and cancer, thanks to their antioxidant and anti-inflammatory properties. In addition, the perspective of new smart biomaterials and molecular medicine for the oxidative stress modulation in a programmable way, by the use of ROS responsive materials or by the targeting of selective molecular pathways involved in ROS generation, will be analysed and discussed critically.
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