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硫酸软骨素通过调节脂质代谢减轻钙缺乏引起的骨质疏松症。

Chondroitin sulfate alleviates osteoporosis caused by calcium deficiency by regulating lipid metabolism.

作者信息

Liu Tianshu, Yu Hai, Wang Shuai, Li Huimin, Du Xinyiran, He Xiaodong

机构信息

Department of Epidemiology, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.

Institute for Medical Dataology, Shandong University, National Institute of Health Data Science of China, Jinan, 250012, Shandong, China.

出版信息

Nutr Metab (Lond). 2023 Feb 6;20(1):6. doi: 10.1186/s12986-023-00726-3.

Abstract

The use of non-drug intervention for calcium deficiency has attracted attention in recent years. Although calcium carbonate is the preferred raw material for calcium supplementation, there are few reports on the mechanism of the combined action of chondroitin sulfate and calcium to alleviate osteoporosis from the perspective of gut microbiota and metabolomics. In this study, a rat model of osteoporosis was established by feeding a low-calcium diet. The intestinal microbiota abundance, fecal and plasma metabolite expression levels of rats fed a basal diet, a low-calcium diet, a low-calcium diet plus calcium carbonate, and a low-calcium diet plus chondroitin sulfate were compared. The results showed that compared with the low calcium group, the calcium content and bone mineral density of femur were significantly increased in the calcium carbonate and chondroitin sulfate groups. 16 S rRNA sequencing and metabolomics analysis showed that chondroitin sulfate intervention could reduce short-chain fatty acid synthesis of intestinal flora, slow down inflammatory response, inhibit osteoclast differentiation, promote calcium absorption and antioxidant mechanism, and alleviate osteoporosis in low-calcium feeding rats. Correlation analysis showed that the selected intestinal flora was significantly correlated with metabolites enriched in feces and plasma. This study provides scientific evidence of the potential impact of chondroitin sulfate as a dietary supplement for patients with osteoporosis.

摘要

近年来,非药物干预治疗钙缺乏症受到关注。虽然碳酸钙是补钙的首选原料,但从肠道微生物群和代谢组学角度,关于硫酸软骨素与钙联合作用缓解骨质疏松症机制的报道较少。本研究通过低钙饮食建立大鼠骨质疏松模型,比较了基础饮食组、低钙饮食组、低钙饮食加碳酸钙组和低钙饮食加硫酸软骨素组大鼠的肠道微生物群丰度、粪便和血浆代谢物表达水平。结果表明,与低钙组相比,碳酸钙组和硫酸软骨素组股骨钙含量和骨密度显著增加。16S rRNA测序和代谢组学分析表明,硫酸软骨素干预可减少肠道菌群短链脂肪酸合成,减缓炎症反应,抑制破骨细胞分化,促进钙吸收和抗氧化机制,减轻低钙喂养大鼠的骨质疏松症。相关性分析表明,所选肠道菌群与粪便和血浆中富集的代谢物显著相关。本研究为硫酸软骨素作为骨质疏松症患者膳食补充剂的潜在影响提供了科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1060/9901125/8d7ca943a2f8/12986_2023_726_Fig1_HTML.jpg

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