口腔疾病中线粒体功能障碍的相互作用:发病机制和治疗意义的最新进展。

IF 3.9 3区 生物学 Q2 CELL BIOLOGY
Al-Hassan Soliman Wadan , Mohamed Abdelsattar Ahmed , Abdelnaser Hussein Ahmed , Doha El-Sayed Ellakwa , Nourhan Hamed Elmoghazy , Abeer Gawish
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引用次数: 0

摘要

线粒体功能障碍与各种全身性和局部性疾病有关,包括牙周炎、口腔癌和颞下颌关节疾病等口腔疾病。本文探讨了口腔病理中线粒体功能障碍的复杂机制,包括氧化应激、炎症和能量代谢受损。此外,论文还阐明了线粒体功能障碍与口腔疾病之间的双向关系,即线粒体功能受损会加剧疾病进展,而口腔病变反过来又会加剧线粒体功能障碍。了解了这些错综复杂的相互作用,就能深入了解针对线粒体功能的新型治疗策略,从而控制口腔疾病。本文涉及线粒体功能障碍的内在机制、线粒体功能障碍在各种口腔病理和炎症中的影响以及新兴的多功能治疗方法。它回顾了目前缓解线粒体功能障碍的治疗策略,包括抗氧化剂、线粒体靶向药物和代谢调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Interplay of Mitochondrial Dysfunction in Oral Diseases: Recent Updates in Pathogenesis and Therapeutic Implications

Mitochondrial dysfunction is linked to various systemic and localized diseases, including oral diseases like periodontitis, oral cancer, and temporomandibular joint disorders. This paper explores the intricate mechanisms underlying mitochondrial dysfunction in oral pathologies, encompassing oxidative stress, inflammation, and impaired energy metabolism. Furthermore, it elucidates the bidirectional relationship between mitochondrial dysfunction and oral diseases, wherein the compromised mitochondrial function exacerbates disease progression, while oral pathologies, in turn, exacerbate mitochondrial dysfunction. Understanding these intricate interactions offers insights into novel therapeutic strategies targeting mitochondrial function for managing oral diseases. This paper pertains to the mechanisms underlying mitochondrial dysfunction, its implications in various oral pathological and inflammatory conditions, and emerging versatile treatment approaches. It reviews current therapeutic strategies to mitigate mitochondrial dysfunction, including antioxidants, mitochondrial-targeted agents, and metabolic modulators.

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来源期刊
Mitochondrion
Mitochondrion 生物-细胞生物学
CiteScore
9.40
自引率
4.50%
发文量
86
审稿时长
13.6 weeks
期刊介绍: Mitochondrion is a definitive, high profile, peer-reviewed international research journal. The scope of Mitochondrion is broad, reporting on basic science of mitochondria from all organisms and from basic research to pathology and clinical aspects of mitochondrial diseases. The journal welcomes original contributions from investigators working in diverse sub-disciplines such as evolution, biophysics, biochemistry, molecular and cell biology, genetics, pharmacology, toxicology, forensic science, programmed cell death, aging, cancer and clinical features of mitochondrial diseases.
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