De Vos Brunhildé, Kasonga Abe E, Joubert Anna M, Nyakudya Trevor T
Department of Physiology, School of Medicine, Faculty of Health Sciences, University of Pretoria, Private Bag X323, Gezina, Pretoria 0031, South Africa.
Metabolites. 2024 Dec 9;14(12):693. doi: 10.3390/metabo14120693.
Ensuring adequate bone health is crucial for preventing conditions such as osteoporosis and fractures. Zingerone, a phytonutrient isolated from cooked ginger, has gained attention for its potential benefits in bone health. This study evaluated the osteoprotective potential of zingerone and its effects on differentiation and signalling pathways using SAOS-2 osteosarcoma and RAW264.7 macrophage cell lines, aiming to elucidate its mechanism of action in bone remodelling.
SAOS-2 osteosarcoma and RAW264.7 macrophage cells were treated with zingerone at concentrations of 200 µM. Osteoblast differentiation was assessed by alkaline phosphatase (ALP) activity, bone mineralisation via Alizarin Red S stain, and gene expression markers (, runt-related transcription factor 2 (), and osteocalcin) via quantitative polymerase chain reaction (q-PCR). Osteoclast differentiation was evaluated by tartrate-resistant acid phosphatase (TRAP) staining, TRAP activity, and mitogen-activated protein kinase (MAPK) pathways.
Treatment with zingerone was non-toxic at 200 µM. Zingerone (200 µM) significantly stimulated the gene expression of and in SAOS-2 cells ( < 0.05) without statistically significantly enhancing SAOS-2 mineralisation via calcium deposits. Moreover, zingerone significantly inhibited osteoclast differentiation in RAW264.7 cells as evidenced by reduced TRAP staining and activity ( < 0.05).
Zingerone shows promise in reducing osteoclast activity and supporting early osteoblast differentiation, suggesting its potential as a dietary supplement for bone health. and clinical studies are needed to confirm its role in managing osteoporosis.
确保充足的骨骼健康对于预防骨质疏松症和骨折等病症至关重要。姜辣素是一种从熟姜中分离出的植物营养素,因其对骨骼健康的潜在益处而受到关注。本研究使用SAOS-2骨肉瘤细胞系和RAW264.7巨噬细胞系评估了姜辣素的骨保护潜力及其对分化和信号通路的影响,旨在阐明其在骨重塑中的作用机制。
用浓度为200μM的姜辣素处理SAOS-2骨肉瘤细胞和RAW264.7巨噬细胞。通过碱性磷酸酶(ALP)活性评估成骨细胞分化,通过茜素红S染色评估骨矿化,并通过定量聚合酶链反应(q-PCR)评估基因表达标志物( runt相关转录因子2 ,和骨钙素)。通过抗酒石酸酸性磷酸酶(TRAP)染色、TRAP活性和丝裂原活化蛋白激酶(MAPK)途径评估破骨细胞分化。
200μM的姜辣素处理无毒性。姜辣素(200μM)显著刺激SAOS-2细胞中 和 的基因表达(P<0.05),但通过钙沉积在统计学上未显著增强SAOS-2矿化。此外,姜辣素显著抑制RAW264.7细胞中的破骨细胞分化,TRAP染色和活性降低证明了这一点(P<0.05)。
姜辣素在降低破骨细胞活性和支持早期成骨细胞分化方面显示出前景,表明其作为骨骼健康膳食补充剂的潜力。需要进一步的体内和临床研究来证实其在管理骨质疏松症中的作用。