Pathogenetic Mechanisms of the Relationship Between Osteoarthritis and Intestinal Dysbiosis

Q4 Medicine
G. V. Poryadin, A. N. Zakhvatov, I. A. Zakharkin, A. Yu. Parshina, A. A. Shaev
{"title":"Pathogenetic Mechanisms of the Relationship Between Osteoarthritis and Intestinal Dysbiosis","authors":"G. V. Poryadin, A. N. Zakhvatov, I. A. Zakharkin, A. Yu. Parshina, A. A. Shaev","doi":"10.20514/2226-6704-2023-13-5-325-334","DOIUrl":null,"url":null,"abstract":"The potential association between dysbiosis of the gut microbiota and osteoarthritis is confirming by a growing number of studies. Given the social significance, the high prevalence of osteoarthritis, and evidences that quantitative and qualitative modification of the gut microbiota affects its progression, it seems important to clarify the underlying mechanisms of this association. Osteoarthritis is a multifactorial joint disease, which is based primarily on the progressive degeneration of articular cartilage. Impaired metabolic activity of chondrocytes, consisting in an imbalance in the extracellular matrix synthesis and degradation processes, causes the persistent release of molecular patterns associated with damage. This leads to the activation of a wide range of innate immune cells receptors and is the basis for the development of an inflammatory reaction in the joint. The involvement of macrophages in the synovial membrane and their activation leads to the production of pro-inflammatory cytokines, leading to the development of chronic low-grade inflammation in the joint, supporting the synthesis of catabolic enzymes by chondrocytes and escalating the cartilage degeneration. Microbial dysbiosis, defined as an adverse modification in the diversity, structure, or metabolic activity of the gut microbiota, is a hidden risk factor, accompanied by metabolic endotoxemia and, consequently, by increased production of pro-inflammatory cytokines, that support the systematic low-grade inflammation and pathophysiological mechanisms of osteoarthritis. It has been shown that dysbiosis of the gut microbiota intestinal takes part in the formation of other osteoarthritis risk factors for, for example, obesity and metabolic disorders. The identification of important interrelated pathophysiological mechanisms of these pathologies will contribute to the development of new pathogenetic treatment methods with their subsequent active introduction into clinical practice.","PeriodicalId":31058,"journal":{"name":"Arhiv\" Vnutrennej Mediciny","volume":"20 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arhiv\" Vnutrennej Mediciny","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20514/2226-6704-2023-13-5-325-334","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

The potential association between dysbiosis of the gut microbiota and osteoarthritis is confirming by a growing number of studies. Given the social significance, the high prevalence of osteoarthritis, and evidences that quantitative and qualitative modification of the gut microbiota affects its progression, it seems important to clarify the underlying mechanisms of this association. Osteoarthritis is a multifactorial joint disease, which is based primarily on the progressive degeneration of articular cartilage. Impaired metabolic activity of chondrocytes, consisting in an imbalance in the extracellular matrix synthesis and degradation processes, causes the persistent release of molecular patterns associated with damage. This leads to the activation of a wide range of innate immune cells receptors and is the basis for the development of an inflammatory reaction in the joint. The involvement of macrophages in the synovial membrane and their activation leads to the production of pro-inflammatory cytokines, leading to the development of chronic low-grade inflammation in the joint, supporting the synthesis of catabolic enzymes by chondrocytes and escalating the cartilage degeneration. Microbial dysbiosis, defined as an adverse modification in the diversity, structure, or metabolic activity of the gut microbiota, is a hidden risk factor, accompanied by metabolic endotoxemia and, consequently, by increased production of pro-inflammatory cytokines, that support the systematic low-grade inflammation and pathophysiological mechanisms of osteoarthritis. It has been shown that dysbiosis of the gut microbiota intestinal takes part in the formation of other osteoarthritis risk factors for, for example, obesity and metabolic disorders. The identification of important interrelated pathophysiological mechanisms of these pathologies will contribute to the development of new pathogenetic treatment methods with their subsequent active introduction into clinical practice.
骨关节炎与肠道生态失调关系的发病机制
越来越多的研究证实了肠道菌群失调与骨关节炎之间的潜在联系。鉴于骨关节炎的社会意义、高患病率以及肠道微生物群定量和定性改变影响其进展的证据,阐明这种关联的潜在机制似乎很重要。骨关节炎是一种多因素的关节疾病,主要是基于关节软骨的进行性变性。软骨细胞的代谢活动受损,包括细胞外基质合成和降解过程的不平衡,导致与损伤相关的分子模式的持续释放。这导致广泛的先天免疫细胞受体的激活,是关节炎症反应发展的基础。巨噬细胞参与滑膜及其激活导致促炎细胞因子的产生,导致关节慢性低度炎症的发展,支持软骨细胞合成分解代谢酶,加剧软骨退变。微生物生态失调,被定义为肠道微生物群多样性、结构或代谢活性的不良改变,是一个潜在的危险因素,伴随着代谢性内毒素血症,因此,促炎细胞因子的产生增加,支持系统性低级别炎症和骨关节炎的病理生理机制。研究表明,肠道菌群失调参与了其他骨关节炎风险因素的形成,例如肥胖和代谢紊乱。识别这些病理的重要的相互关联的病理生理机制将有助于新的病理治疗方法的发展,并将其随后积极地引入临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Arhiv" Vnutrennej Mediciny
Arhiv" Vnutrennej Mediciny Medicine-General Medicine
CiteScore
0.50
自引率
0.00%
发文量
43
审稿时长
8 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信