氧化应激在II型糖尿病骨修复损伤中的作用:抗氧化治疗干预的范围?

IF 1.5 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Frontiers in dental medicine Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.3389/fdmed.2024.1464009
Pui Li, Kuraym Khalid Kuraym Alenazi, Jordanna Dally, Emma Louise Woods, Rachel Jane Waddington, Ryan Moseley
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引用次数: 0

摘要

骨愈合受损是2型糖尿病(T2DM)患者的一个重要并发症,导致恢复时间延长、并发症风险增加、生活质量下降和患者发病率增加。氧化应激,由活性氧(ROS)的产生和细胞/组织抗氧化防御机制之间的不平衡引起,已被确定为T2DM骨愈合受损的发病机制的关键因素。抗氧化剂在减轻氧化应激和促进骨修复方面显示出希望,尤其是非酶抗氧化剂。本文旨在探讨氧化应激、骨愈合受损和2型糖尿病之间的潜在机制和复杂关系,并特别关注当前的临床前和临床证据,这些证据支持抗氧化治疗干预在改善2型糖尿病患者骨愈合结果方面的潜力。从不断涌现的现有证据来看,外源性补充抗氧化剂,特别是非酶抗氧化剂,显然可以改善氧化应激、炎症和细胞功能受损对未控制的高血糖期间骨愈合过程的有害影响;因此,作为一种新型有效的治疗实体,具有相当大的前景。然而,尽管有这样的结论,我们的知识中仍有几个重要的空白有待解决,包括涉及更复杂的基于酶的抗氧化剂递送系统的研究,进一步的机制研究这些抗氧化剂如何发挥其理想的修复作用;以及更广泛的临床试验研究,以优化抗氧化治疗的剂量、频率、持续时间及其随后的生物分布和生物利用度。通过加强我们对这些关键问题的理解,我们可以充分利用这些抗氧化剂的氧化应激中和特性来开发有效的抗氧化干预措施,以减轻这些T2DM患者群体的骨愈合受损并减少相关并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of oxidative stress in impaired type II diabetic bone repair: scope for antioxidant therapy intervention?

Impaired bone healing is a significant complication observed in individuals with type 2 diabetes mellitus (T2DM), leading to prolonged recovery, increased risk of complications, impaired quality of life, and increased risk of patient morbidity. Oxidative stress, resulting from an imbalance between the generation of reactive oxygen species (ROS) and cellular/tissue antioxidant defence mechanisms, has been identified as a critical contributor to the pathogenesis of impaired bone healing in T2DM. Antioxidants have shown promise in mitigating oxidative stress and promoting bone repair, particularly non-enzymic antioxidant entities. This comprehensive narrative review aims to explore the underlying mechanisms and intricate relationship between oxidative stress, impaired bone healing and T2DM, with a specific focus on the current preclinical and clinical evidence advocating the potential of antioxidant therapeutic interventions in improving bone healing outcomes in individuals with T2DM. From the ever-emerging evidence available, it is apparent that exogenously supplemented antioxidants, especially non-enzymic antioxidants, can ameliorate the detrimental effects of oxidative stress, inflammation, and impaired cellular function on bone healing processes during uncontrolled hyperglycaemia; and therefore, hold considerable promise as novel efficacious therapeutic entities. However, despite such conclusions, several important gaps in our knowledge remain to be addressed, including studies involving more sophisticated enzymic antioxidant-based delivery systems, further mechanistic studies into how these antioxidants exert their desirable reparative effects; and more extensive clinical trial studies into the optimisation of antioxidant therapy dosing, frequency, duration and their subsequent biodistribution and bioavailability. By enhancing our understanding of such crucial issues, we can fully exploit the oxidative stress-neutralising properties of these antioxidants to develop effective antioxidant interventions to mitigate impaired bone healing and reduce the associated complications in such T2DM patient populations.

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