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褪黑素通过抗炎和抗氧化应激作用预防丙戊酸治疗骨质疏松大鼠的骨丢失。

Melatonin prevents bone loss in osteoporotic rats with valproic acid treatment by anti-inflammatory and anti-oxidative stress.

机构信息

Department of Orthopedics, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, No. 2, Zhe Shan Xi Road, Wuhu 241001, Anhui, PR China; Anhui Province Key Laboratory of Non-coding RNA Basic and Clinical Transformation, No. 2, Zhe Shan Xi Road, Wuhu 241001, Anhui, PR China.

Department of Orthopedics, The First Affiliated Hospital of Wannan Medical College, Yijishan Hospital, No. 2, Zhe Shan Xi Road, Wuhu 241001, Anhui, PR China.

出版信息

Int Immunopharmacol. 2024 Nov 15;141:112932. doi: 10.1016/j.intimp.2024.112932. Epub 2024 Aug 17.

Abstract

Melatonin (MEL) has shown positive effects in anti-inflammatory and anti-oxidative stress research. This study investigates whether MEL can positively impact bone loss induced by valproic acid (VPA) in rats. The study examines changes in MC3T3-E1 cell viability and osteogenic potential, along with osteoclast differentiation in RAW264.7 cells in the presence of VPA using CCK-8, ALP staining, AR staining, and TRAP staining. In vitro experiments reveal that VPA-induced inhibition of osteogenic differentiation and promotion of osteoclastic differentiation are linked to increased inflammation and oxidative stress. Furthermore, MEL has demonstrated the ability to reduce oxidative stress and inflammation, boost osteogenic differentiation, and inhibit osteoclast differentiation. Animal experiments confirm that MEL significantly increases SOD2 expression and decreases TNF-α expression, leading to the restoration of impaired bone metabolism, enhanced bone strength, and higher bone mineral density. The combined experimental results strongly suggest that MEL can enhance osteogenic activity in the presence of VPA by reducing inflammation and oxidative stress, impeding osteoclast differentiation, and alleviating bone loss in VPA-treated rat models.

摘要

褪黑素(MEL)在抗炎和抗氧化应激研究中表现出积极的效果。本研究旨在探讨褪黑素是否能对丙戊酸(VPA)诱导的大鼠骨丢失产生积极影响。该研究通过 CCK-8、ALP 染色、AR 染色和 TRAP 染色,检测了 VPA 存在时 MC3T3-E1 细胞活力和成骨潜能以及 RAW264.7 细胞破骨细胞分化的变化。体外实验表明,VPA 诱导的成骨分化抑制和破骨细胞分化促进与炎症和氧化应激增加有关。此外,褪黑素已被证明具有减轻氧化应激和炎症、促进成骨分化和抑制破骨细胞分化的能力。动物实验证实,褪黑素可显著增加 SOD2 表达并降低 TNF-α 表达,从而恢复受损的骨代谢,增强骨强度和提高骨密度。综合实验结果强烈表明,褪黑素可通过减少炎症和氧化应激、阻碍破骨细胞分化以及减轻 VPA 处理大鼠模型中的骨丢失,在 VPA 存在的情况下增强成骨活性。

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