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氧化应激在II型糖尿病性骨修复受损中的作用:抗氧化治疗干预的空间?

Role of oxidative stress in impaired type II diabetic bone repair: scope for antioxidant therapy intervention?

作者信息

Li Pui, Alenazi Kuraym Khalid Kuraym, Dally Jordanna, Woods Emma Louise, Waddington Rachel Jane, Moseley Ryan

机构信息

Disease Mechanisms Group, School of Dentistry, College of Biomedical and Life Sciences, Cardiff University, Cardiff, United Kingdom.

Biomaterials Group, School of Dentistry, College of Biomedical and Life Sciences, Cardiff University, Cardiff, United Kingdom.

出版信息

Front Dent Med. 2024 Oct 14;5:1464009. doi: 10.3389/fdmed.2024.1464009. eCollection 2024.

Abstract

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.

摘要

骨愈合受损是2型糖尿病(T2DM)患者中观察到的一种重要并发症,会导致恢复时间延长、并发症风险增加、生活质量受损以及患者发病风险增加。氧化应激是由活性氧(ROS)生成与细胞/组织抗氧化防御机制之间的失衡引起的,已被确定为T2DM骨愈合受损发病机制的关键因素。抗氧化剂,尤其是非酶抗氧化实体,在减轻氧化应激和促进骨修复方面显示出前景。本全面的叙述性综述旨在探讨氧化应激、骨愈合受损和T2DM之间的潜在机制和复杂关系,特别关注目前支持抗氧化治疗干预对改善T2DM患者骨愈合结果潜力的临床前和临床证据。从现有的不断涌现的证据来看,显然外源性补充的抗氧化剂,尤其是非酶抗氧化剂,可以改善氧化应激、炎症和细胞功能受损对血糖控制不佳时骨愈合过程的有害影响;因此,作为新型有效的治疗实体具有很大的前景。然而,尽管有这些结论,我们的知识仍存在几个重要空白有待解决,包括涉及更复杂的基于酶的抗氧化剂递送系统的研究、对这些抗氧化剂如何发挥其理想修复作用的进一步机制研究;以及对抗氧化剂治疗剂量、频率、持续时间及其随后的生物分布和生物利用度优化的更广泛临床试验研究。通过加强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,开发有效的抗氧化干预措施,以减轻骨愈合受损并减少此类T2DM患者群体中的相关并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbe9/11797775/dd3ebf0a7b54/fdmed-05-1464009-g001.jpg

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