Mechanism of action and new developments in the study of curcumin in the treatment of osteoarthritis: a narrative review.

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Inflammopharmacology Pub Date : 2025-03-01 Epub Date: 2025-02-26 DOI:10.1007/s10787-025-01665-6
Yong-Ze Yang, Ji-Dong Li, Jing-Guo Zhang, Kai Zhang, An-Ren Zhang, Peng-Peng Li, Qing-Jun Li, Hong-Zhang Guo
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引用次数: 0

Abstract

Osteoarthritis is a degenerative joint disease that affects the aging population worldwide. It has an underlying inflammatory cause that leads to loss of chondrocytes, reducing the cartilage layer at the affected joints. Compounds with anti-inflammatory properties are potential therapeutic agents for osteoarthritis. Curcumin, derived from species of the Curcuma, is an anti-inflammatory compound. The purpose of this review is to summarize the anti-osteoarthritic effects of curcumin from clinical and preclinical studies. Many clinical trials have been conducted to determine curcumin's effectiveness in osteoarthritis patients. Available studies have shown that curcumin prevents chondrocyte apoptosis and inhibits the release of proteoglycans and metalloproteinases as well as the expression of cyclooxygenase, prostaglandin E-2, and inflammatory cytokines in chondrocytes. The mechanism of action of curcumin also involves multiple cell signaling pathways, including Nuclear factor kappa-B(NF-κB), Mitogen-activated protein kinase (MAPK), Wnt/β-catenin pathway (Wnt/β-catenin), The Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3), Nuclear factor erythroid 2-related factor 2/antioxidant response elements/heme oxygenase-1(Nrf2/ARE/HO-1), and Phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (PI3K/AKT/mTOR) signaling pathways. Curcumin further reduced the release of inflammatory factors and apoptosis by inhibiting the activation of NF-κB. In addition, curcumin modulates the MAPK, Nrf2/ARE/HO-1, and PI3K/Akt/mTOR signaling pathways and affects cell proliferation and apoptosis processes, a series of effects that together promote the healthy state of chondrocytes. In conclusion, curcumin, as a natural plant compound, exhibits significant anti-inflammatory potential by modulating inflammatory factors associated with articular osteoarthritis through multiple mechanisms. Its protective effects on articular cartilage and synovium make it a promising candidate for the treatment of OA. Future studies should further explore the mechanism of action of curcumin and its optimal dosage and therapeutic regimen in clinical applications, to provide more effective therapeutic options for osteoarthritis patients.

姜黄素治疗骨关节炎的作用机制及研究进展综述。
骨关节炎是一种影响全球老年人口的退行性关节疾病。它有一个潜在的炎症原因,导致软骨细胞的损失,减少受影响关节的软骨层。具有抗炎特性的化合物是骨关节炎的潜在治疗剂。姜黄素是从姜黄属植物中提取的,是一种抗炎化合物。本文就姜黄素抗骨关节炎的临床及临床前研究作一综述。许多临床试验已经进行,以确定姜黄素对骨关节炎患者的有效性。已有研究表明,姜黄素可阻止软骨细胞凋亡,抑制蛋白聚糖和金属蛋白酶的释放,抑制软骨细胞中环氧合酶、前列腺素E-2和炎性细胞因子的表达。姜黄素的作用机制还涉及多种细胞信号通路,包括核因子κ b (NF-κB)、丝裂原活化蛋白激酶(MAPK)、Wnt/β-catenin通路(Wnt/β-catenin)、Janus激酶2/信号转导和转录激活因子3 (JAK2/STAT3)、核因子红系2相关因子2/抗氧化反应元件/血红素加氧酶-1(Nrf2/ARE/HO-1)、磷酸肌肽3激酶(PI3K)/蛋白激酶B (AKT)/哺乳动物雷帕霉素靶蛋白(PI3K/AKT/mTOR)信号通路。姜黄素通过抑制NF-κB的活化进一步减少炎症因子的释放和细胞凋亡。此外,姜黄素调节MAPK、Nrf2/ARE/HO-1、PI3K/Akt/mTOR信号通路,影响细胞增殖和凋亡过程,共同促进软骨细胞的健康状态。综上所述,姜黄素作为一种天然植物化合物,通过多种机制调节与关节骨关节炎相关的炎症因子,显示出显著的抗炎潜力。其对关节软骨和滑膜的保护作用使其成为治疗OA的有希望的候选药物。未来的研究应进一步探讨姜黄素的作用机制及临床应用中的最佳剂量和治疗方案,为骨关节炎患者提供更有效的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Inflammopharmacology
Inflammopharmacology IMMUNOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
8.00
自引率
3.40%
发文量
200
期刊介绍: Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas: -Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states -Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs -Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents -Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain -Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs -Muscle-immune interactions during inflammation [...]
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