Article(id=1317125441496924939, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317125400581485316, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2026.03.019, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1791956776260, onlineDateStr=2026-10-14, pubDate=1773072000000, pubDateStr=2026-03-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1791956776260, onlineIssueDateStr=2026-10-14, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1791956776260, creator=13701087609, updateTime=1791956776260, updator=13701087609, issue=Issue{id=1317125400581485316, tenantId=1146029695717560320, journalId=1255847919539208197, year='2026', volume='44', issue='3', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1773072000000', pubDateStr='2026-03-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1791956766504, creator='13701087609', updateTime=1791958763799, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1317133777898418844, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317125400581485316, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1317133777898418845, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1317125400581485316, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=99, endPage=104, ext={EN=ArticleExt(id=1317125441773749004, articleId=1317125441496924939, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Investigating Protective Effect of Serum Containing Bushen Zhuanggu Prescription(补肾壮骨方)on IL-1β-Induced Chondrocyte Degeneration via Wnt/β-catenin Pathway, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Objective To explore the protective effect of Bushen Zhuanggu Prescription(补肾壮骨方)on chondrocyte degeneration in rats and its mechanism of action.
Methods Primary chondrocytes from rats were isolated and stimulated with various concentrations of interleukin-1β(IL-1β)to identify the optimal concentration for inducing an osteoarthritis(OA)cell model. Concurrently, the serum containing Bushen Zhuanggu Formula at high, medium and low concentration gradients, or serum containing hydrochloric aminoglucose capsules, was prepared as a cellular intervention. The expressions of mRNA and proteins related to cartilage degeneration and the Wnt/β-catenin signaling pathway were measured, and the transmission electron microscopy was used to evaluate the changes in cellular ultrastructure.
Results After stimulation with IL-1β, the expressions of proteins related to cartilage degeneration and the Wnt/β-catenin pathway in chondrocytes was significantly abnormal, and the severe cellular damage was observed under ultrastructural examination. However, Bushen Zhuanggu Formula, by inhibiting the activation of the Wnt/β-catenin signaling pathway, reduced the expressions of inflammatory factors and MMPs induced by IL-1β and promoted the expressions of Collagen Ⅱ and Aggrecan, thereby protecting the chondrocytes.
Conclusion Serum containing Bushen Zhuanggu Formula can reduce the abnormal expression of degeneration-related proteins by inhibiting the Wnt/β-catenin pathway, thus exerting a protective effect.
, authors=Liao ZHANG, Keshang FU, Yanhong SHI, Yong JIN, Quan WU, authorsList=Liao ZHANG, Keshang FU, Yanhong SHI, Yong JIN, Quan WU, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1317125442033795853, articleId=1317125441496924939, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=基于Wnt/β-catenin通路探究补肾壮骨方含药血清对IL-1β诱导软骨细胞退变的保护作用, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
目的 探究补肾壮骨方对大鼠软骨细胞退变的保护作用及其作用机制。
方法 分离大鼠原代软骨细胞并给予不同浓度白细胞介素-1β(IL-1β)刺激,探索IL-1β诱导骨关节炎(OA)细胞模型的最佳浓度,同时制备高中低浓度梯度的补肾壮骨方含药血清或盐酸氨基葡萄糖胶囊血清,作为细胞干预手段。检测软骨退化相关蛋白以及Wnt/β-catenin信号通路相关蛋白的mRNA及蛋白质表达,并使用透射电镜评价细胞超微结构变化。
结果 经过IL-1β刺激后,软骨细胞的软骨退化相关蛋白以及Wnt/β-catenin通路相关蛋白表达明显异常,超微结构也可观察到细胞严重损伤。而补肾壮骨方通过抑制Wnt/β-catenin信号通路的激活,改善降低IL-1β诱导的炎症因子和基质金属蛋白酶(MMP)的表达,并促进了Collagen Ⅱ和Aggrecan的表达,从而保护软骨细胞。
结论 补肾壮骨方含药血清能够通过抑制Wnt/β-catenin通路减少退变相关蛋白的异常表达,从而发挥保护作用。
, authors=张辽, 傅科上, 史燕红, 金甬, 吴权, authorsList=张辽, 傅科上, 史燕红, 金甬, 吴权, authorCompany=null, correspAuthors=null, authorNote=
张辽(1985 -),男,浙江宁波人,副主任中医师,硕士,研究方向:骨与关节疾病的基础与临床。
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张辽(1985 -),男,浙江宁波人,副主任中医师,硕士,研究方向:骨与关节疾病的基础与临床。
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张辽(1985 -),男,浙江宁波人,副主任中医师,硕士,研究方向:骨与关节疾病的基础与临床。
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