评价关节内注射聚二氧环酮(PDO)作为一种新型粘剂治疗骨关节炎的疗效。

IF 5.2 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Linh Thi Thuy Le , Pham Ngoc Chien , Thuy-Tien Thi Trinh , Ji-Won Seo , Nguyen Ngan Giang , Pham Thi Nga , Xin Rui Zhang , Yong Xun Jin , Sun-Young Nam , Chan-Yeong Heo
{"title":"评价关节内注射聚二氧环酮(PDO)作为一种新型粘剂治疗骨关节炎的疗效。","authors":"Linh Thi Thuy Le ,&nbsp;Pham Ngoc Chien ,&nbsp;Thuy-Tien Thi Trinh ,&nbsp;Ji-Won Seo ,&nbsp;Nguyen Ngan Giang ,&nbsp;Pham Thi Nga ,&nbsp;Xin Rui Zhang ,&nbsp;Yong Xun Jin ,&nbsp;Sun-Young Nam ,&nbsp;Chan-Yeong Heo","doi":"10.1016/j.lfs.2024.123303","DOIUrl":null,"url":null,"abstract":"<div><h3>Aims</h3><div>Osteoarthritis (OA) is a chronic joint disorder marked by cartilage breakdown, bone alterations, and inflammation, leading to significant pain and disability. Current therapeutic strategies, ranging from lifestyle interventions to pharmacological and surgical treatments, offer limited efficacy and are often accompanied by side effects. This study investigates the potential of Polydioxanone (PDO), a biocompatible synthetic polymer, as a novel intra-articular (IA) viscosupplement in OA.</div></div><div><h3>Materials and methods</h3><div>A validated rabbit model of OA was employed to compare the therapeutic effects of IA injections of PDO against established viscosupplements like hyaluronic acid (HA) and Conjuran (CJR). Sixty rabbits with collagenase-induced OA were randomized into four groups, receiving respective treatments over 12 weeks. The effect of PDO was analyzed by histopathological examination, immunofluorescence staining (IF), immunoblotting, quantitative real-time polymerase chain reaction (qRT-PCR), and enzyme-linked immunosorbent assay (ELISA).</div></div><div><h3>Key findings</h3><div>The histopathological examination revealed substantial improvements in the PDO group's cartilage structure and matrix composition. qRT-PCR, IF staining, and Western Blot showed significant downregulation of matrix metalloproteinases (MMPs) and upregulation of type II collagen (COL II) and aggrecan (ACAN). ELISA results corroborated decreased inflammatory mediators- interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) in the PDO-treatment group.</div></div><div><h3>Significance</h3><div>Preliminary results indicate that PDO may enhance cartilage regeneration and reduce inflammation, suggesting it is a viable and superior treatment option for OA. These findings merit further investigation to translate into clinical applications.</div></div>","PeriodicalId":18122,"journal":{"name":"Life sciences","volume":"361 ","pages":"Article 123303"},"PeriodicalIF":5.2000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluating the efficacy of intra-articular polydioxanone (PDO) injections as a novel viscosupplement in osteoarthritis treatment\",\"authors\":\"Linh Thi Thuy Le ,&nbsp;Pham Ngoc Chien ,&nbsp;Thuy-Tien Thi Trinh ,&nbsp;Ji-Won Seo ,&nbsp;Nguyen Ngan Giang ,&nbsp;Pham Thi Nga ,&nbsp;Xin Rui Zhang ,&nbsp;Yong Xun Jin ,&nbsp;Sun-Young Nam ,&nbsp;Chan-Yeong Heo\",\"doi\":\"10.1016/j.lfs.2024.123303\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aims</h3><div>Osteoarthritis (OA) is a chronic joint disorder marked by cartilage breakdown, bone alterations, and inflammation, leading to significant pain and disability. Current therapeutic strategies, ranging from lifestyle interventions to pharmacological and surgical treatments, offer limited efficacy and are often accompanied by side effects. This study investigates the potential of Polydioxanone (PDO), a biocompatible synthetic polymer, as a novel intra-articular (IA) viscosupplement in OA.</div></div><div><h3>Materials and methods</h3><div>A validated rabbit model of OA was employed to compare the therapeutic effects of IA injections of PDO against established viscosupplements like hyaluronic acid (HA) and Conjuran (CJR). Sixty rabbits with collagenase-induced OA were randomized into four groups, receiving respective treatments over 12 weeks. The effect of PDO was analyzed by histopathological examination, immunofluorescence staining (IF), immunoblotting, quantitative real-time polymerase chain reaction (qRT-PCR), and enzyme-linked immunosorbent assay (ELISA).</div></div><div><h3>Key findings</h3><div>The histopathological examination revealed substantial improvements in the PDO group's cartilage structure and matrix composition. qRT-PCR, IF staining, and Western Blot showed significant downregulation of matrix metalloproteinases (MMPs) and upregulation of type II collagen (COL II) and aggrecan (ACAN). ELISA results corroborated decreased inflammatory mediators- interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) in the PDO-treatment group.</div></div><div><h3>Significance</h3><div>Preliminary results indicate that PDO may enhance cartilage regeneration and reduce inflammation, suggesting it is a viable and superior treatment option for OA. These findings merit further investigation to translate into clinical applications.</div></div>\",\"PeriodicalId\":18122,\"journal\":{\"name\":\"Life sciences\",\"volume\":\"361 \",\"pages\":\"Article 123303\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-01-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Life sciences\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0024320524008932\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Life sciences","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0024320524008932","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

摘要

目的:骨关节炎(OA)是一种慢性关节疾病,以软骨破裂、骨改变和炎症为特征,导致明显的疼痛和残疾。目前的治疗策略,从生活方式干预到药物和手术治疗,疗效有限,往往伴有副作用。本研究探讨了聚二氧环酮(PDO),一种生物相容性合成聚合物,在OA中作为一种新型关节内(IA)粘补剂的潜力。材料和方法:采用经验证的家兔OA模型,比较IA注射PDO对透明质酸(HA)和莪术兰(CJR)等已建立的黏液补充剂的治疗效果。将60只胶原酶诱导的OA兔随机分为4组,分别接受12 周的治疗。采用组织病理学检查、免疫荧光染色(IF)、免疫印迹、实时定量聚合酶链反应(qRT-PCR)和酶联免疫吸附试验(ELISA)分析PDO的作用。主要发现:组织病理学检查显示PDO组软骨结构和基质组成有实质性改善。qRT-PCR、IF染色和Western Blot均显示基质金属蛋白酶(MMPs)显著下调,II型胶原(COL II)和聚集蛋白(ACAN)显著上调。ELISA结果证实,pdo治疗组炎症介质-白细胞介素-1β (IL-1β)和肿瘤坏死因子-α (TNF-α)降低。意义:初步结果表明PDO可促进软骨再生,减轻炎症,提示PDO是OA的一种可行且优越的治疗选择。这些发现值得进一步研究以转化为临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the efficacy of intra-articular polydioxanone (PDO) injections as a novel viscosupplement in osteoarthritis treatment

Aims

Osteoarthritis (OA) is a chronic joint disorder marked by cartilage breakdown, bone alterations, and inflammation, leading to significant pain and disability. Current therapeutic strategies, ranging from lifestyle interventions to pharmacological and surgical treatments, offer limited efficacy and are often accompanied by side effects. This study investigates the potential of Polydioxanone (PDO), a biocompatible synthetic polymer, as a novel intra-articular (IA) viscosupplement in OA.

Materials and methods

A validated rabbit model of OA was employed to compare the therapeutic effects of IA injections of PDO against established viscosupplements like hyaluronic acid (HA) and Conjuran (CJR). Sixty rabbits with collagenase-induced OA were randomized into four groups, receiving respective treatments over 12 weeks. The effect of PDO was analyzed by histopathological examination, immunofluorescence staining (IF), immunoblotting, quantitative real-time polymerase chain reaction (qRT-PCR), and enzyme-linked immunosorbent assay (ELISA).

Key findings

The histopathological examination revealed substantial improvements in the PDO group's cartilage structure and matrix composition. qRT-PCR, IF staining, and Western Blot showed significant downregulation of matrix metalloproteinases (MMPs) and upregulation of type II collagen (COL II) and aggrecan (ACAN). ELISA results corroborated decreased inflammatory mediators- interleukin-1 beta (IL-1β) and tumor necrosis factor-alpha (TNF-α) in the PDO-treatment group.

Significance

Preliminary results indicate that PDO may enhance cartilage regeneration and reduce inflammation, suggesting it is a viable and superior treatment option for OA. These findings merit further investigation to translate into clinical applications.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Life sciences
Life sciences 医学-药学
CiteScore
12.20
自引率
1.60%
发文量
841
审稿时长
6 months
期刊介绍: Life Sciences is an international journal publishing articles that emphasize the molecular, cellular, and functional basis of therapy. The journal emphasizes the understanding of mechanism that is relevant to all aspects of human disease and translation to patients. All articles are rigorously reviewed. The Journal favors publication of full-length papers where modern scientific technologies are used to explain molecular, cellular and physiological mechanisms. Articles that merely report observations are rarely accepted. Recommendations from the Declaration of Helsinki or NIH guidelines for care and use of laboratory animals must be adhered to. Articles should be written at a level accessible to readers who are non-specialists in the topic of the article themselves, but who are interested in the research. The Journal welcomes reviews on topics of wide interest to investigators in the life sciences. We particularly encourage submission of brief, focused reviews containing high-quality artwork and require the use of mechanistic summary diagrams.
×
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