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人类肠道微生物群:骨质疏松症和骨生成的关键调解者。

The Human Gut Microbiota: A Key Mediator of Osteoporosis and Osteogenesis.

机构信息

College of Osteopathic Medicine, Rocky Vista University, Ivins, UT 84738, USA.

Department of Research and Scholarly Activity, Rocky Vista University, Ivins, UT 84738, USA.

出版信息

Int J Mol Sci. 2021 Aug 31;22(17):9452. doi: 10.3390/ijms22179452.

Abstract

An expanding body of research asserts that the gut microbiota has a role in bone metabolism and the pathogenesis of osteoporosis. This review considers the human gut microbiota composition and its role in osteoclastogenesis and the bone healing process, specifically in the case of osteoporosis. Although the natural physiologic processes of bone healing and the pathogenesis of osteoporosis and bone disease are now relatively well known, recent literature suggests that a healthy microbiome is tied to bone homeostasis. Nevertheless, the mechanism underlying this connection is still somewhat enigmatic. Based on the literature, a relationship between the microbiome, osteoblasts, osteoclasts, and receptor activator of nuclear factor-kappa-Β ligand (RANKL) is contemplated and explored in this review. Studies have proposed various mechanisms of gut microbiome interaction with osteoclastogenesis and bone health, including micro-RNA, insulin-like growth factor 1, and immune system mediation. However, alterations to the gut microbiome secondary to pharmaceutical and surgical interventions cannot be discounted and are discussed in the context of clinical therapeutic consideration. The literature on probiotics and their mechanisms of action is examined in the context of bone healing. The known and hypothesized interactions of common osteoporosis drugs and the human gut microbiome are examined. Since dysbiosis in the gut microbiota can function as a biomarker of bone metabolic activity, it may also be a pharmacological and nutraceutical (i.e., pre- and probiotics) therapeutic target to promote bone homeostasis.

摘要

越来越多的研究表明,肠道微生物群在骨骼代谢和骨质疏松症的发病机制中起作用。这篇综述考虑了人类肠道微生物群的组成及其在破骨细胞形成和骨愈合过程中的作用,特别是在骨质疏松症的情况下。尽管骨愈合的自然生理过程和骨质疏松症及骨疾病的发病机制现在已经相对清楚,但最近的文献表明,健康的微生物组与骨稳态有关。然而,这种联系的机制仍然有些神秘。基于文献,本文考虑并探讨了微生物组、成骨细胞、破骨细胞和核因子-κB 受体激活剂配体(RANKL)之间的关系。研究提出了肠道微生物组与破骨细胞形成和骨骼健康相互作用的各种机制,包括 micro-RNA、胰岛素样生长因子 1 和免疫系统介导。然而,不能忽视由于药物和手术干预而导致的肠道微生物组的改变,并在临床治疗考虑的背景下进行了讨论。本文还考察了益生菌及其作用机制在骨愈合中的应用。研究了常见骨质疏松症药物和人类肠道微生物群的已知和假设相互作用。由于肠道微生物群的失调可以作为骨代谢活性的生物标志物,因此它也可能是促进骨稳态的药理学和营养治疗(即益生菌和益生元)的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b74d/8431678/651538865ed4/ijms-22-09452-g001.jpg

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