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薯蓣皂苷 VI 通过调节微生物失调改变 5-HT 通路来防止骨骼生长期小鼠下肢去负荷引起的骨丢失。

Asperosaponin VI Protects Against Bone Loss Due to Hindlimb Unloading in Skeletally Growing Mice Through Regulating Microbial Dysbiosis Altering the 5-HT Pathway.

机构信息

Key Laboratory for Space Bioscience and Biotechnology, School of Life Sciences, Northwestern Polytechnical University, Xi'an, 710072, Shaanxi, People's Republic of China.

State Key Laboratory of Solidification Processing, School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an, 710072, Shaanxi, People's Republic of China.

出版信息

Calcif Tissue Int. 2023 Mar;112(3):389-402. doi: 10.1007/s00223-022-01057-w. Epub 2023 Jan 3.

Abstract

Osteoporosis is a complex multifactorial disease that can lead to an increased risk of fracture. However, selective and effective osteoporosis drugs are still lacking. We showed that Asperosaponin VI (AVI) has the implications to be further developed as an alternative supplement for the prevention and treatment of bone loss. AVI has been found to have beneficial effects on metabolic diseases such as bone loss, obesity, and atherosclerosis. Our study was designed to determine the effect and mechanism of action of AVI against bone loss through regulating microbial dysbiosis. A hindlimb unloading mouse model was established to determine the effect of AVI on bone microarchitecture, gut microbiota, and serum metabolites. Eighteen female C57BL/6 J mice were divided into three groups: control, hindlimb unloading with vehicle (HLU), and hindlimb unloading treated with AVI (HLU-AVI, 200 mg/kg/day). AVI was administrated orally for 4 weeks. The results demonstrated that AVI improved the bone microstructure by reversing the decrease in bone volume fraction and trabecular number, and the increase in trabecular separation and structure model index of cancellous bone in hindlimb suspension mice. The results of 16sRNA gene sequencing suggested that the therapeutic effect of AVI on bone loss may be achieved through it regulating the gut microbiota, especially certain specific microorganisms. Combined with the analysis of ELISA, immunohistochemistry, and serum metabolome results, it could be speculated that AVI played an important role in adjusting the balance of bone metabolism by influencing specific flora such as Clostridium and its metabolites to regulate the 5-hydroxytryptophan pathway. The study explored the novel mechanism of AVI against osteoporosis, and has implications for the further development of AVI as an alternative supplement for the prevention and treatment of bone loss.

摘要

骨质疏松症是一种复杂的多因素疾病,可导致骨折风险增加。然而,目前仍缺乏有选择性和疗效确切的抗骨质疏松症药物。我们发现,重楼皂苷 VI(AVI)具有进一步开发为预防和治疗骨质流失的替代补充剂的潜力。AVI 已被发现对代谢疾病如骨质流失、肥胖和动脉粥样硬化具有有益作用。我们的研究旨在通过调节微生物失调来确定 AVI 对骨质流失的作用和作用机制。建立了后肢去负荷小鼠模型,以确定 AVI 对骨微结构、肠道微生物群和血清代谢物的影响。将 18 只雌性 C57BL/6J 小鼠分为三组:对照组、后肢去负荷加载体组(HLU)和后肢去负荷加 AVI 组(HLU-AVI,200mg/kg/天)。AVI 经口给药 4 周。结果表明,AVI 通过逆转后肢悬吊小鼠骨体积分数和小梁数的减少,以及松质骨小梁分离和结构模型指数的增加,改善了骨微结构。16sRNA 基因测序结果表明,AVI 对骨丢失的治疗作用可能是通过调节肠道微生物群来实现的,特别是某些特定的微生物。结合 ELISA、免疫组织化学和血清代谢组学结果分析,可以推测 AVI 通过影响特定菌群如梭菌及其代谢物来调节 5-羟色氨酸途径,在调节骨代谢平衡方面发挥着重要作用。该研究探索了 AVI 防治骨质疏松症的新机制,为进一步开发 AVI 作为预防和治疗骨质流失的替代补充剂提供了依据。

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