氧化应激
活性氧
抗氧化剂
椎间盘
过氧化氢
变性(医学)
医学
氧化磷酸化
细胞内
药理学
病理
化学
细胞生物学
生物化学
生物
外科
内科学
作者
Qingzheng Zhang,Zongtai Liu,Yirong Sun,Changfeng Fu,Jianxun Ding
标识
DOI:10.1002/advs.202514217
摘要
Abstract Intervertebral disc degeneration (IVDD) is a progressive degenerative disorder of the spine characterized by oxidative stress and cellular dysfunction. Current clinical treatments for IVDD include surgical procedures, such as discectomy and spinal fusion, as well as pharmacological therapies using analgesics and anti‐inflammatory agents. However, these strategies primarily offer symptomatic relief and do not address the underlying causes of IVDD. Targeting oxidative stress has emerged as a promising therapeutic approach, yet its effectiveness remains limited. To overcome this limitation, an antioxidant carbon dot of selenomethionine (Se‐Met‐CD) is developed for efficient IVDD therapy. Se‐Met‐CD effectively scavenges excess reactive oxygen species (ROS), alleviates oxidative stress, and restores intracellular redox homeostasis in nucleus pulposus cells. Se‐Met‐CD exhibits an antioxidant capacity 3.1 times that of its precursor, Se‐Met, when compared at the same concentration. In hydrogen peroxide (H 2 O 2 )‐treated nucleus pulposus cells, Se‐Met‐CD significantly reduces intracellular ROS levels to 17.7% of those in untreated control cells. In a puncture‐induced IVDD rat model, Se‐Met‐CD demonstrates remarkable therapeutic efficacy by significantly attenuating disc degeneration, reflected in lower Pfirrmann and histological scores. These results underscore the potential of Se‐Met‐CD to treat IVDD by scavenging ROS, restoring antioxidant balance, and modulating the local microenvironments.
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