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Journal of Zhejiang University SCIENCE B
ISSN 1673-1581(Print), 1862-1783(Online), Monthly
2025 Vol.26 No.12 P.1137-1155
Emerging roles of the metabolite succinate in bone-related diseases
Abstract: Bone-related diseases, including osteoporosis (OP), osteoarthritis (OA), rheumatoid arthritis (RA), fracture, and periodontitis, significantly impact human health. Succinate, primarily known as a metabolic intermediate in the tricarboxylic acid (TCA) cycle, has emerged as a regulator of cellular functions beyond its metabolic role. Under stress, succinate accumulates in mitochondria and acts as a signaling molecule, modulating cellular processes. Notably, succinate activates angiogenesis and inflammation by stabilizing hypoxia-inducible factor-1α (HIF-1α). Moreover, it influences various pathophysiological processes by interacting with the succinate receptor 1 (SUCNR1), thereby impacting immune response, inflammation, cancer metastasis, and bone homeostasis. The multifaceted roles of succinate as a signaling molecule vary depending on its cellular location and concentration. Recent metabolomic analyses have revealed elevated succinate levels in bone-related diseases, indicating its potential association with these conditions. The objective of this review is to elucidate the impacts of succinate on different bone-related diseases and to discuss potential therapeutic targets and drug molecules based on its mechanisms of action.
Key words: Succinate; Osteoarthritis; Rheumatoid arthritis; Osteoporosis; Fracture; Periodontitis
1浙江大学医学院附属口腔医院, 浙江大学口腔医学院, 浙江省口腔疾病临床医研究中心, 浙江省口腔生物医学研究重点实验室, 浙江大学癌症研究院, 中国杭州市, 310006
2广西口腔颌面修复与重建研究重点实验室, 中国南宁市, 530021
摘要:包括骨质疏松症、骨关节炎、类风湿性关节炎、骨折和牙周炎在内的骨相关疾病,显著影响了人类健康。琥珀酸作为三羧酸循环中的一种代谢中间产物,已被发现不仅在代谢中起作用,还能作为细胞功能的调节因子发挥作用。应激状态下,琥珀酸在线粒体中积累,作为信号分子调节细胞功能。值得注意的是,琥珀酸可通过稳定缺氧诱导因子1α(HIF-1α)促进血管生成和炎症发展。此外,琥珀酸还可通过与琥珀酸受体1(SUCNR1)作用介导多种病理生理过程,如免疫反应、炎症、癌症转移和骨稳态等。琥珀酸作为信号分子的多重作用取决于其在细胞中的位置和浓度。近期的代谢组学分析发现,骨相关疾病中琥珀酸水平升高,提示其可能与这些疾病相关。本综述旨在阐明琥珀酸对不同骨相关疾病的影响,并基于其作用机制探讨潜在的治疗靶点和相关药物分子。
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DOI:
10.1631/jzus.B2400406
CLC number:
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On-line Access:
2025-12-31
Received:
2024-08-08
Revision Accepted:
2024-11-19
Crosschecked:
2025-12-31