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白藜芦醇通过靶向SIRT1/FOXO3a信号通路增强钙补充剂对脊髓损伤所致骨质疏松症的保护作用。

Resveratrol enhances the protective effects of calcium supplements on spinal cord injury-induced osteoporosis by targeting the SIRT1/FOXO3a pathway.

作者信息

Zhong Qiuwen

机构信息

Department of Orthopedics Guangdong Yingde People's Hospital, Yingde City, 513000, China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 Mar;398(3):2823-2832. doi: 10.1007/s00210-024-03412-0. Epub 2024 Sep 17.

Abstract

Spinal cord injury (SCI) often leads to osteoporosis due to factors like immobilization and hormonal imbalances. Calcium supplements are prescribed to help maintain bone health, but their efficacy may be limited. This study investigated whether resveratrol (RSV), a polyphenolic compound, could enhance the protective effects of calcium supplements on SCI-induced osteoporosis via the SIRT1/FOXO3a pathway, which regulates bone metabolism. Surgical cord transection induced SCI at the T9 vertebral level. An SCI mouse model was used with four groups: sham, SCI, SCI + 2% calcium, and SCI + calcium + RSV (20 mg/kg body weight). ‌‌‌‌‌‌‌‌‌‌‌‌‌‌‌‌‌‌Biomechanical testing, gene expression, and Western blots were performed. Resveratrol and calcium supplementation synergistically preserved bone mass, microarchitecture, strength, and fracture resistance compared to calcium alone after SCI. This was accompanied by upregulated osteoblast markers, downregulated osteoclast markers, and increased SIRT1/FOXO3a expression and activation. The results suggest resveratrol enhances calcium's bone-protective effects in SCI-induced osteoporosis by modulating the SIRT1/FOXO3a pathway and osteoblast/osteoclast activities. Combining resveratrol with calcium supplementation may be a promising therapeutic approach for managing SCI-induced osteoporosis.

摘要

脊髓损伤(SCI)常因制动和激素失衡等因素导致骨质疏松。通常会开钙补充剂来帮助维持骨骼健康,但其疗效可能有限。本研究调查了白藜芦醇(RSV)这种多酚类化合物是否能通过调节骨代谢的SIRT1/FOXO3a途径增强钙补充剂对SCI诱导的骨质疏松的保护作用。通过手术在T9椎体水平进行脊髓横断诱导SCI。使用SCI小鼠模型,分为四组:假手术组、SCI组、SCI + 2%钙组和SCI + 钙 + RSV组(20毫克/千克体重)。进行了生物力学测试、基因表达分析和蛋白质免疫印迹分析。与SCI后单独补钙相比,白藜芦醇和钙补充剂协同保留了骨量、微观结构、强度和抗骨折能力。同时伴有成骨细胞标志物上调、破骨细胞标志物下调以及SIRT1/FOXO3a表达和激活增加。结果表明,白藜芦醇通过调节SIRT1/FOXO3a途径和成骨细胞/破骨细胞活性,增强了钙对SCI诱导的骨质疏松的骨骼保护作用。将白藜芦醇与钙补充剂联合使用可能是治疗SCI诱导的骨质疏松的一种有前景的治疗方法。

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