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Bencaosome [16:0 Lyso PA+XLGB28-sRNA] 通过同时促进成骨和抑制破骨细胞生成来改善小鼠的骨质疏松症。

Bencaosome [16:0 Lyso PA+XLGB28-sRNA] improves osteoporosis by simultaneously promoting osteogenesis and inhibiting osteoclastogenesis in mice.

机构信息

State Key Laboratory of Common Mechanism Research for Major Diseases, Department of Biochemistry, Institute of Basic Medical Sciences Chinese Academy of Medical Sciences, School of Basic Medicine Peking Union Medical College, Beijing, China.

Department of Orthopaedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC), Beijing, China.

出版信息

IUBMB Life. 2024 Oct;76(10):832-844. doi: 10.1002/iub.2857. Epub 2024 Jul 16.

Abstract

Osteoporosis (OP) is a systemic metabolic bone disease resulting in reduced bone strength and increased susceptibility to fractures, making it a significant public health and economic problem worldwide. The clinical use of anti-osteoporosis agents is limited because of their serious side effects or the high cost of long-term use. The Xianlinggubao (XLGB) formula is an effective traditional Chinese herbal medicine commonly used in orthopedics to treat osteoporosis; however, its mechanism of action remains unclear. In this study, we screened 40 small RNAs derived from XLGB capsules and found that XLGB28-sRNA targeting TNFSF11 exerted a significant anti-osteoporosis effect in vitro and in vivo by simultaneously promoting osteogenesis and inhibiting osteoclastogenesis. Oral administration of bencaosome [16:0 Lyso PA+XLGB28-sRNA] effectively improved bone mineral density and reduced the damage to the bone microstructure in mice. These results suggest that XLGB28-sRNA may be a novel oligonucleotide drug that promotes osteogenesis and inhibits osteoclastogenesis in mice.

摘要

骨质疏松症(OP)是一种全身性代谢性骨病,导致骨强度降低和骨折易感性增加,成为全球重大的公共卫生和经济问题。由于抗骨质疏松药物存在严重的副作用或长期使用成本高,其临床应用受到限制。仙灵骨葆(XLGB)配方是一种常用于骨科治疗骨质疏松症的有效中药,但作用机制尚不清楚。本研究从 XLGB 胶囊中筛选出 40 种小 RNA,发现靶向 TNFSF11 的 XLGB28-sRNA 通过同时促进成骨和抑制破骨细胞生成,在体外和体内均具有显著的抗骨质疏松作用。口服 bencaosome [16:0 Lyso PA+XLGB28-sRNA] 可有效改善小鼠的骨矿物质密度并减少对骨微结构的损害。这些结果表明,XLGB28-sRNA 可能是一种新型的促进成骨和抑制破骨细胞生成的寡核苷酸药物。

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