Article(id=1291404570492653844, tenantId=1146029695717560320, journalId=1246415772164075586, issueId=1291404554201985968, articleNumber=null, orderNo=null, doi=10.13699/j.cnki.1001-6821.2025.06.010, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1729353600000, receivedDateStr=2024-10-20, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1785824442742, onlineDateStr=2026-08-04, pubDate=1743091200000, pubDateStr=2025-03-28, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1785824442742, onlineIssueDateStr=2026-08-04, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1785824442742, creator=13701087609, updateTime=1785824442742, updator=13701087609, issue=Issue{id=1291404554201985968, tenantId=1146029695717560320, journalId=1246415772164075586, year='2025', volume='41', issue='6', pageStart='751', pageEnd='900', issueExtLink='null', onlineDate='null', pubDate='1743091200000', pubDateStr='2025-03-28', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1785824438858, creator='13701087609', updateTime=1785824438858, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext=null, issueFiles=null, downloadFileDto=null}, startPage=800, endPage=804, ext={EN=ArticleExt(id=1291404572338147605, articleId=1291404570492653844, tenantId=1146029695717560320, journalId=1246415772164075586, language=EN, title=Research of quercetin promote muscle regeneration in acute skeletal muscle injury, columnId=1246531407326105792, journalTitle=Chinese Journal of Clinical Pharmacology, columnName=Clinical and Basic Bridging Research, runingTitle=null, highlight=null, articleAbstract=
Objective To investigate the mechanism of quercetin in promoting muscle regeneration in acute skeletal muscle injury.
Methods Satellite cells were randomly divided into blank group (conventional culture), hydrogen peroxide (H2O2) group (100 μmol·L-1 H2O2 treated cells for 24 h), quercetin group (10 μmol·L-1 quercetin treated cells for 24 h), H2O2+quercetin group (100 μmol·L-1 H2O2+10 μmol·L-1 quercetin treated cells for 24 h). Cell proliferation was detected by cell counting kit-8 (CCK-8) method; protein expression was detected by Western blot assay; mitochondrial reactive oxygen species (ROS) levels and related indicators of mitochondrial respiration were detected by kit.
Results The 24 h proliferation rates of cells in blank group, quercetin group, H2O2 group and H2O2+quercetin group were (100.00±4.27)%, (148.79±13.17)%, (81.70±3.19)% and (120.83±8.81)%, respectively; the relative expression levels of superoxide dismutase 1 (SOD1) protein were 0.64±0.09, 0.76±0.09, 0.24±0.03 and 0.43±0.06, respectively; the relative expression levels of myosin heavy chain (MyHC) protein were 0.61±0.05, 0.67±0.06, 0.32±0.03 and 0.47±0.06, respectively; the fluorescence intensities of mitochondrial ROS were (52.56±1.97), (48.46±4.05), (119.53±13.06) and (102.91±8.93) a.u., respectively; the catalase (CAT) levels were (28.66±2.18), (35.62±3.89), (18.13±1.78) and (23.97±2.72) μmol·mg protein-1, respectively; mitochondrial respiratory chain (MRC) complex Ⅰ levels were (19.77±1.01), (23.28±2.48), (9.87±1.01) and (14.19±0.75) μmol·mg protein-1, respectively. The above indexes in quercetin group and H2O2 group were compared with blank group, the above indexes in H2O2+quercetin group were compared with H2O2 group, the difference was statistically significant (P<0.05, P<0.01, P<0.001).
Conclusion Quercetin can promote mitochondrial respiration by clearing mitochondrial ROS levels, improve oxidative damage, and then promote satellite cell proliferation, which can promote muscle regeneration in acute skeletal muscle injury.
, authors=Yu-peng YUAN
1, 2, Ya JIANG
3, authorsList=Yu-peng YUAN, Ya JIANG, authorCompany=null, correspAuthors=Ya JIANG, 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=1291404572736606486, articleId=1291404570492653844, tenantId=1146029695717560320, journalId=1246415772164075586, language=CN, title=槲皮素在急性骨骼肌损伤中促进肌肉再生的研究, columnId=1246531407485489349, journalTitle=中国临床药理学杂志, columnName=临床与基础桥接研究, runingTitle=null, highlight=null, articleAbstract=
目的 探讨槲皮素在急性骨骼肌损伤中促进肌肉再生的作用机制。
方法 将卫星细胞随机分为空白组（常规培养）、过氧化氢（H2O2）组（100 μmol·L-1 H2O2处理细胞24 h）、槲皮素组（10 μmoL·L-1的槲皮素处理细胞24 h）和H2O2+槲皮素组（100 μmol·L-1 H2O2+10 μmoL·L-1的槲皮素处理细胞24 h）。用细胞计数试剂盒-8（CCK-8）法检测细胞增殖率，用蛋白质印迹法检测相关蛋白表达情况，用试剂盒检测线粒体活性氧（ROS）水平及线粒体呼吸相关指标。
结果 空白组、槲皮素组、H2O2组和H2O2+槲皮素组的细胞24 h增殖率分别为（100.00±4.27）%、（148.79±13.17）%、（81.70±3.19）%和（120.83±8.81）%，超氧化物歧化酶1（SOD1）蛋白相对表达水平分别为0.64±0.09、0.76±0.09、0.24±0.03和0.43±0.06，肌球蛋白重链（MyHC）蛋白相对表达水平分别为0.61±0.05、0.67±0.06、0.32±0.03和0.47±0.06，线粒体ROS荧光强度分别为（52.56±1.97）、（48.46±4.05）、（119.53±13.06）和（102.91±8.93）a.u.，过氧化氢酶（CAT）水平分别为（28.66±2.18）、（35.62±3.89）、（18.13±1.78）和（23.97±2.72）μmol·mg protein-1，线粒体呼吸链（MRC）complex Ⅰ水平分别为（19.77±1.01）、（23.28±2.48）、（9.87±1.01）和（14.19±0.75）μmol·mg protein-1。槲皮素组和H2O2组的上述指标与空白组比较，H2O2+槲皮素组上述指标与H2O2组比较，在统计学上差异均有统计学意义（P<0.05，P<0.01，P<0.001）。
结论 槲皮素可通过清除线粒体ROS水平，改善氧化损伤，促进卫星细胞增殖，进而可在急性骨骼肌损伤中促进肌肉再生。
, authors=袁玉鹏
1, 2, 江亚
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袁玉鹏（1984-），男，副教授，主要从事运动医学、体育教学与训练方面的相关研究
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