Article(id=1304414799161483937, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414798482010221, articleNumber=null, orderNo=null, doi=10.7501/j.issn.0253-2670.2026.05.011, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1766851200000, receivedDateStr=2025-12-28, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1788926322975, onlineDateStr=2026-09-09, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1788926322975, onlineIssueDateStr=2026-09-09, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1788926322975, creator=13701087609, updateTime=1788926322975, updator=13701087609, issue=Issue{id=1304414798482010221, tenantId=1146029695717560320, journalId=1302319053441957962, year='2026', volume='57', issue='5', pageStart='1597', pageEnd='2008', issueExtLink='null', onlineDate='null', pubDate='1773244800000', pubDateStr='2026-03-12', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1788926322813, creator='13701087609', updateTime=1788926625459, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1304416067925864795, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414798482010221, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1304416067925864796, tenantId=1146029695717560320, journalId=1302319053441957962, issueId=1304414798482010221, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=1703, endPage=1714, ext={EN=ArticleExt(id=1304414799480251043, articleId=1304414799161483937, tenantId=1146029695717560320, journalId=1302319053441957962, language=EN, title=Mechanism of Compound Danshen Dropping Pills in improving myocardial ischemia-reperfusion injury in mice based on single-cell spatial transcriptomics, columnId=null, journalTitle=Chinese Traditional and Herbal Drugs, columnName=null, runingTitle=null, highlight=null, articleAbstract=Objective To investigate the mechanisms by which Compound Danshen Dropping Pills (复方丹参滴丸) ameliorate myocardial ischemia-reperfusion injury (MIRI) in mice using single-cell and spatial transcriptomics. Methods C57BL/6 mice were randomly divided into sham group, model group, Compound Danshen Dropping Pills low-, medium-, and high-dose (61.43, 122.85, 245.70 mg/kg) groups, with 15 mice in each group. Mice were continuously given drug intervention for 7 d, and a MIRI model was constructed using left anterior descending artery ligation reperfusion method 30 min after the last administration. Cardiac function was assessed by echocardiography 24 h after surgery, and myocardial histopathology was evaluated by hematoxylin-eosin (HE) and Masson staining. Hearts from sham group, model group, and Compound Danshen Dropping Pills medium-dose group were subjected to single-cell and spatial transcriptomic analyses. Single cell transcriptomics was used for cell type identification, cardiomyocyte subpopulation typing, differential gene expression analysis, pseudo temporal analysis, differential gene expression analysis and enrichment analysis. Spatial transcriptomics analysis was used to identify the spatial transcriptomic features of MIRI and the characteristic genes of injury boundary region. Western blotting was performed to detect the expression levels of nuclear receptor subfamily 3 group C member 1 (NR3C1), pyruvate dehydrogenase kinase 4 (PDK4), acyl-CoA synthetase long-chain family member 4 (ACSL4) and glutathione peroxidase 4 (GPX4) in myocardial tissue of mice. Results Compared with sham group, the left ventricular ejection fraction (LVEF) of mice in model group was decreased (P < 0.05), pathology showed significant necrosis of myocardial cells and increased collagen fibers. Compared with model group, Compound Danshen Dropping Pills significantly improved the cardiac function of MIRI mice (P < 0.05), reduced myocardial injury and decreased collagen fibers. The results of single-cell transcriptomics indicated that Compound Danshen Dropping Pills could increase the proportion of myocardial cells and reduce the proportion of fibroblasts and inflammatory cells. Spatial transcriptomics revealed key genes involved in the spatial transcriptomic characteristics and damage boundary regions of MIRI. Western blotting results showed that compared with sham group, the expression levels of NR3C1, PDK4 and ACSL4 proteins in myocardial tissue of mice in model group mice were significantly increased (P < 0.05), while the expression level of GPX4 protein was significantly decreased (P < 0.05). Compared with model group, the expression levels of NR3C1, PDK4 and ACSL4 proteins in myocardial tissue of mice in Compound Danshen Dropping Pills group were significantly reduced (P < 0.05), while the expression level of GPX4 protein was significantly increased (P < 0.05). Conclusion Compound Danshen Dropping Pills may alleviate MIRI in mice by modulating myocardial metabolism and attenuating ferroptosis., authors=ZHU Siyue, WANG Dongyuan, QIANG Tingting, LI Lin, LU Ruixia, LIN Wenyong, JIN Qipeng, GAO Junjie, WANG Xiaolong, authorsList=ZHU Siyue, WANG Dongyuan, QIANG Tingting, LI Lin, LU Ruixia, LIN Wenyong, JIN Qipeng, GAO Junjie, WANG Xiaolong, 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=1304414799396364962, articleId=1304414799161483937, tenantId=1146029695717560320, journalId=1302319053441957962, language=CN, title=基于单细胞-空间转录组学探究复方丹参滴丸改善小鼠心肌缺血再灌注损伤的机制, columnId=1304140191707456168, journalTitle=中草药, columnName=药理与临床, runingTitle=null, highlight=null, articleAbstract=目的 基于单细胞与空间转录组学探究复方丹参滴丸改善小鼠心肌缺血再灌注损伤(myocardial ischemia-reperfusion injury,MIRI)的作用及其潜在机制。方法 C57BL/6小鼠随机分为假手术组、模型组和复方丹参滴丸低、中、高剂量(61.43、122.85、245.70 mg/kg)组,每组15只。给药干预7 d,于末次给药30 min后采用左前降支结扎-再灌流方法构建小鼠MIRI模型。术后24 h应用超声心动图评估心功能变化;苏木素-伊红(hematoxylin-eosin,HE)及Masson染色观察心肌组织病理学改变。对假手术组、模型组及复方丹参滴丸中剂量组小鼠心脏组织进行单细胞与空间转录组学测序。单细胞转录组学进行细胞类型鉴定、心肌细胞亚群分型、差异基因表达分析、拟时序分析、差异表达基因分析及富集分析。空间转录组学分析识别MIRI空间转录组学特征与损伤边界区的特征基因。采用Western blotting检测小鼠心肌组织中核受体亚家族3C组成员1(nuclear receptor subfamily 3 group C member 1,NR3C1)、丙酮酸脱氢酶激酶 4(pyruvate dehydrogenase kinase 4,PDK4)、长链脂酰辅酶A合成酶4(acyl-CoA synthetase long-chain family member 4,ACSL4)和谷胱甘肽过氧化物酶4(glutathione peroxidase 4,GPX4)的蛋白表达。结果 与假手术组比较,模型组小鼠左室射血分数(left ventricular ejection fraction,LVEF)下降(P<0.05),病理提示心肌细胞大量坏死,胶原纤维增多。与模型组比较,复方丹参滴丸显著改善MIRI小鼠心功能(P<0.05),心肌损伤减轻,胶原纤维减少。单细胞转录组学结果表明,复方丹参滴丸可增加心肌细胞比例,减少成纤维细胞及炎症细胞比例。空间转录组学揭示了MIRI空间转录组学特质和损伤边界区的关键基因。Western blotting结果显示,与假手术组比较,模型组小鼠心肌组织NR3C1、PDK4和ACSL4蛋白表达水平显著升高(P<0.05),GPX4蛋白表达水平显著降低(P<0.05);与模型组比较,复方丹参滴丸组心肌组织NR3C1、PDK4和ACSL4蛋白表达水平显著降低(P<0.05),GPX4蛋白表达水平显著升高(P<0.05)。结论 复方丹参滴丸可能通过减轻铁死亡,调节心肌代谢,减轻小鼠MIRI。, authors=朱思越1,2, 王栋元1,2, 强婷婷1,2, 李琳1,2, 芦瑞霞1,2, 林文勇1,2, 靳琪鹏1,2, 高俊杰1,2, 王肖龙1,2, authorsList=朱思越, 王栋元, 强婷婷, 李琳, 芦瑞霞, 林文勇, 靳琪鹏, 高俊杰, 王肖龙, authorCompany=1 上海中医药大学附属曙光医院 国家中医心血管病临床医学研究中心分中心, 上海 201203;
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Circulation, 2025, 151(8): e41-e660.
国家心血管病中心, 中国心血管健康与疾病报告编写组, 胡盛寿. 中国心血管健康与疾病报告2023概要[J]. 中国循环杂志, 2024, 39(7): 625-660.
Zhang Y, Li H, Chu J H, et al. Trends and projections of burden of ischemic heart disease in China versus other G20 countries: A comparative study based on the 2021 global burden of disease database[J]. Glob Heart, 2025, 20(1): 37.
Zhang S, Yan F, Luan F, et al. The pathological mechanisms and potential therapeutic drugs for myocardial ischemia reperfusion injury[J]. Phytomedicine, 2024, 129: 155649.
程碧伟, 易雨萌, 刘强, 等. 复方丹参滴丸联合化学药治疗冠心病经皮冠状动脉介入术后的Meta分析[J]. 药物评价研究, 2024, 47(3): 617-631.
《复方丹参滴丸临床应用专家共识》编写项目组. 复方丹参滴丸临床应用专家共识[J]. 中国中西医结合杂志, 2025, 45(5): 517-525.
曹博雅, 陈家黎, 石晓溪, 等. 复方丹参滴丸调控LOX-NF-κB炎症途径治疗心肌缺血的机制研究[J]. 中草药, 2023, 54(1): 151-159.
Lu R X, Sun W H, Lin W Y, et al. Fufang Danshen Pill improves mitochondrial homeostasis by regulating the S100a9/TLR4 axis to alleviate myocardial ischemia-reperfusion injury[J]. Phytomedicine, 2025, 148: 157433.
Xu X S, Wang X X, Li Y, et al. Research progress of ankyrin repeat domain 1 protein: An updated review[J]. Cell Mol Biol Lett, 2024, 29(1): 131.
van Duijvenboden K, de Bakker D E M, Man J C K, et al. Conserved NPPB+ border zone switches from MEF2- to AP-1-driven gene program[J]. Circulation, 2019, 140(10): 864-879.
Zuurbier C J, Bertrand L, Beauloye C R, et al. Cardiac metabolism as a driver and therapeutic target of myocardial infarction[J]. J Cell Mol Med, 2020, 24(11): 5937-5954.
Wang X X, Shen X Y, Yan Y T, et al. Pyruvate dehydrogenase kinases (PDKs): An overview toward clinical applications[J]. Biosci Rep, 2021, 41(4): BSR20204402.
Li T T, Xu J, Qin X H, et al. Glucose oxidation positively regulates glucose uptake and improves cardiac function recovery after myocardial reperfusion[J]. Am J Physiol Endocrinol Metab, 2017, 313(5): E577-E585.
Connaughton S, Chowdhury F, Attia R R, et al. Regulation of pyruvate dehydrogenase kinase isoform 4(PDK4) gene expression by glucocorticoids and insulin[J]. Mol Cell Endocrinol, 2010, 315(1/2): 159-167.
She H, Hu Y, Zhao G Z, et al. Dexmedetomidine ameliorates myocardial ischemia-reperfusion injury by inhibiting MDH2 lactylation via regulating metabolic reprogramming[J]. Adv Sci, 2024, 11(48): 2409499.
Zhang T T, Han Y, Wang Y C, et al. The interaction between ferroptosis and myocardial ischemia-reperfusion injury: Molecular mechanisms and potential therapeutic targets[J]. Eur J Med Res, 2025, 30(1): 643.
Stockwell B R, Friedmann Angeli J P, Bayir H, et al. Ferroptosis: A regulated cell death nexus linking metabolism, redox biology, and disease[J]. Cell, 2017, 171(2): 273-285.
Tang L J, Luo X J, Tu H, et al. Ferroptosis occurs in phase of reperfusion but not ischemia in rat heart following ischemia or ischemia/reperfusion[J]. Naunyn Schmiedeberg Arch Pharmacol, 2021, 394(2): 401-410.
Zhao W K, Zhou Y, Xu T T, et al. Ferroptosis: Opportunities and challenges in myocardial ischemia-reperfusion injury[J]. Oxid Med Cell Longev, 2021, 2021: 9929687.
Doll S, Proneth B, Tyurina Y Y, et al. ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition[J]. Nat Chem Biol, 2017, 13(1): 91-98.
Yao L Y, He F N, Zhao Q Y, et al. Spatial multiplexed protein profiling of cardiac ischemia-reperfusion injury[J]. Circ Res, 2023, 133(1): 86-103.
Wu X X, Liu L, Zheng Q L, et al. Dihydrotanshinone I preconditions myocardium against ischemic injury via PKM2 glutathionylation sensitive to ROS[J]. Acta Pharm Sin B, 2023, 13(1): 113-127.
Liu H Q, Liu W, Qiu H L, et al. Salvianolic acid B protects against myocardial ischaemia-reperfusion injury in rats via inhibiting high mobility group box 1 protein expression through the PI3K/Akt signalling pathway[J]. Naunyn Schmiedebergs Arch Pharmacol, 2020, 393(8): 1527-1539.)
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基于单细胞-空间转录组学探究复方丹参滴丸改善小鼠心肌缺血再灌注损伤的机制
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中草药 |药理与临床 2026 , 57 (5) : 1703 -1714
基于单细胞-空间转录组学探究复方丹参滴丸改善小鼠心肌缺血再灌注损伤的机制
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朱思越1,2, 王栋元1,2, 强婷婷1,2, 李琳1,2, 芦瑞霞1,2, 林文勇1,2, 靳琪鹏1,2, 高俊杰1,2, 王肖龙1,2
作者信息
    1 上海中医药大学附属曙光医院 国家中医心血管病临床医学研究中心分中心, 上海 201203;
    2 上海中医药大学附属曙光医院 心血管病研究所, 上海 201203
通讯作者:
王肖龙
作者简介:
朱思越: 朱思越(2000—),女,硕士研究生,研究方向为中西医结合治疗心血管疾病。E-mail:sue_zhu@163.com
Mechanism of Compound Danshen Dropping Pills in improving myocardial ischemia-reperfusion injury in mice based on single-cell spatial transcriptomics
  • ZHU Siyue, WANG Dongyuan, QIANG Tingting, LI Lin, LU Ruixia, LIN Wenyong, JIN Qipeng, GAO Junjie, WANG Xiaolong
  • Affiliations
    doi: 10.7501/j.issn.0253-2670.2026.05.011
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    目的 基于单细胞与空间转录组学探究复方丹参滴丸改善小鼠心肌缺血再灌注损伤(myocardial ischemia-reperfusion injury,MIRI)的作用及其潜在机制。方法 C57BL/6小鼠随机分为假手术组、模型组和复方丹参滴丸低、中、高剂量(61.43、122.85、245.70 mg/kg)组,每组15只。给药干预7 d,于末次给药30 min后采用左前降支结扎-再灌流方法构建小鼠MIRI模型。术后24 h应用超声心动图评估心功能变化;苏木素-伊红(hematoxylin-eosin,HE)及Masson染色观察心肌组织病理学改变。对假手术组、模型组及复方丹参滴丸中剂量组小鼠心脏组织进行单细胞与空间转录组学测序。单细胞转录组学进行细胞类型鉴定、心肌细胞亚群分型、差异基因表达分析、拟时序分析、差异表达基因分析及富集分析。空间转录组学分析识别MIRI空间转录组学特征与损伤边界区的特征基因。采用Western blotting检测小鼠心肌组织中核受体亚家族3C组成员1(nuclear receptor subfamily 3 group C member 1,NR3C1)、丙酮酸脱氢酶激酶 4(pyruvate dehydrogenase kinase 4,PDK4)、长链脂酰辅酶A合成酶4(acyl-CoA synthetase long-chain family member 4,ACSL4)和谷胱甘肽过氧化物酶4(glutathione peroxidase 4,GPX4)的蛋白表达。结果 与假手术组比较,模型组小鼠左室射血分数(left ventricular ejection fraction,LVEF)下降(P<0.05),病理提示心肌细胞大量坏死,胶原纤维增多。与模型组比较,复方丹参滴丸显著改善MIRI小鼠心功能(P<0.05),心肌损伤减轻,胶原纤维减少。单细胞转录组学结果表明,复方丹参滴丸可增加心肌细胞比例,减少成纤维细胞及炎症细胞比例。空间转录组学揭示了MIRI空间转录组学特质和损伤边界区的关键基因。Western blotting结果显示,与假手术组比较,模型组小鼠心肌组织NR3C1、PDK4和ACSL4蛋白表达水平显著升高(P<0.05),GPX4蛋白表达水平显著降低(P<0.05);与模型组比较,复方丹参滴丸组心肌组织NR3C1、PDK4和ACSL4蛋白表达水平显著降低(P<0.05),GPX4蛋白表达水平显著升高(P<0.05)。结论 复方丹参滴丸可能通过减轻铁死亡,调节心肌代谢,减轻小鼠MIRI。
    复方丹参滴丸  /  单细胞转录组学  /  空间转录组学  /  心肌缺血再灌注损伤  /  铁死亡
    Objective To investigate the mechanisms by which Compound Danshen Dropping Pills (复方丹参滴丸) ameliorate myocardial ischemia-reperfusion injury (MIRI) in mice using single-cell and spatial transcriptomics. Methods C57BL/6 mice were randomly divided into sham group, model group, Compound Danshen Dropping Pills low-, medium-, and high-dose (61.43, 122.85, 245.70 mg/kg) groups, with 15 mice in each group. Mice were continuously given drug intervention for 7 d, and a MIRI model was constructed using left anterior descending artery ligation reperfusion method 30 min after the last administration. Cardiac function was assessed by echocardiography 24 h after surgery, and myocardial histopathology was evaluated by hematoxylin-eosin (HE) and Masson staining. Hearts from sham group, model group, and Compound Danshen Dropping Pills medium-dose group were subjected to single-cell and spatial transcriptomic analyses. Single cell transcriptomics was used for cell type identification, cardiomyocyte subpopulation typing, differential gene expression analysis, pseudo temporal analysis, differential gene expression analysis and enrichment analysis. Spatial transcriptomics analysis was used to identify the spatial transcriptomic features of MIRI and the characteristic genes of injury boundary region. Western blotting was performed to detect the expression levels of nuclear receptor subfamily 3 group C member 1 (NR3C1), pyruvate dehydrogenase kinase 4 (PDK4), acyl-CoA synthetase long-chain family member 4 (ACSL4) and glutathione peroxidase 4 (GPX4) in myocardial tissue of mice. Results Compared with sham group, the left ventricular ejection fraction (LVEF) of mice in model group was decreased (P < 0.05), pathology showed significant necrosis of myocardial cells and increased collagen fibers. Compared with model group, Compound Danshen Dropping Pills significantly improved the cardiac function of MIRI mice (P < 0.05), reduced myocardial injury and decreased collagen fibers. The results of single-cell transcriptomics indicated that Compound Danshen Dropping Pills could increase the proportion of myocardial cells and reduce the proportion of fibroblasts and inflammatory cells. Spatial transcriptomics revealed key genes involved in the spatial transcriptomic characteristics and damage boundary regions of MIRI. Western blotting results showed that compared with sham group, the expression levels of NR3C1, PDK4 and ACSL4 proteins in myocardial tissue of mice in model group mice were significantly increased (P < 0.05), while the expression level of GPX4 protein was significantly decreased (P < 0.05). Compared with model group, the expression levels of NR3C1, PDK4 and ACSL4 proteins in myocardial tissue of mice in Compound Danshen Dropping Pills group were significantly reduced (P < 0.05), while the expression level of GPX4 protein was significantly increased (P < 0.05). Conclusion Compound Danshen Dropping Pills may alleviate MIRI in mice by modulating myocardial metabolism and attenuating ferroptosis.
    Compound Danshen Dropping Pills  /  single-cell transcriptomics  /  spatial transcriptomics  /  myocardial ischemia-reperfusion injury  /  ferroptosis
    朱思越, 王栋元, 强婷婷, 李琳, 芦瑞霞, 林文勇, 靳琪鹏, 高俊杰, 王肖龙. 基于单细胞-空间转录组学探究复方丹参滴丸改善小鼠心肌缺血再灌注损伤的机制. 中草药, 2026 , 57 (5) : 1703 -1714 . DOI: 10.7501/j.issn.0253-2670.2026.05.011
    ZHU Siyue, WANG Dongyuan, QIANG Tingting, LI Lin, LU Ruixia, LIN Wenyong, JIN Qipeng, GAO Junjie, WANG Xiaolong. Mechanism of Compound Danshen Dropping Pills in improving myocardial ischemia-reperfusion injury in mice based on single-cell spatial transcriptomics[J]. Chinese Traditional and Herbal Drugs, 2026 , 57 (5) : 1703 -1714 . DOI: 10.7501/j.issn.0253-2670.2026.05.011

      国家自然科学基金面上项目 (82074222); 国家自然科学基金面上项目 (82374252); 上海市医学创新研究专项-重大专项 (23Y31920200); 上海市中医临床重点实验室项目 (20DZ2272200); 苏州工业园区东方华夏心血管健康研究院力心中药科研创新基金2024 (2024-CCATCM-052)

    参考文献 引证文献
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    Martin S S, Aday A W, Allen N B, et al. 2025 heart disease and stroke statistics: A report of US and global data from the American heart association[J]. Circulation, 2025, 151(8): e41-e660.
    国家心血管病中心, 中国心血管健康与疾病报告编写组, 胡盛寿. 中国心血管健康与疾病报告2023概要[J]. 中国循环杂志, 2024, 39(7): 625-660.
    Zhang Y, Li H, Chu J H, et al. Trends and projections of burden of ischemic heart disease in China versus other G20 countries: A comparative study based on the 2021 global burden of disease database[J]. Glob Heart, 2025, 20(1): 37.
    Zhang S, Yan F, Luan F, et al. The pathological mechanisms and potential therapeutic drugs for myocardial ischemia reperfusion injury[J]. Phytomedicine, 2024, 129: 155649.
    程碧伟, 易雨萌, 刘强, 等. 复方丹参滴丸联合化学药治疗冠心病经皮冠状动脉介入术后的Meta分析[J]. 药物评价研究, 2024, 47(3): 617-631.
    《复方丹参滴丸临床应用专家共识》编写项目组. 复方丹参滴丸临床应用专家共识[J]. 中国中西医结合杂志, 2025, 45(5): 517-525.
    曹博雅, 陈家黎, 石晓溪, 等. 复方丹参滴丸调控LOX-NF-κB炎症途径治疗心肌缺血的机制研究[J]. 中草药, 2023, 54(1): 151-159.
    Lu R X, Sun W H, Lin W Y, et al. Fufang Danshen Pill improves mitochondrial homeostasis by regulating the S100a9/TLR4 axis to alleviate myocardial ischemia-reperfusion injury[J]. Phytomedicine, 2025, 148: 157433.
    Xu X S, Wang X X, Li Y, et al. Research progress of ankyrin repeat domain 1 protein: An updated review[J]. Cell Mol Biol Lett, 2024, 29(1): 131.
    van Duijvenboden K, de Bakker D E M, Man J C K, et al. Conserved NPPB+ border zone switches from MEF2- to AP-1-driven gene program[J]. Circulation, 2019, 140(10): 864-879.
    Zuurbier C J, Bertrand L, Beauloye C R, et al. Cardiac metabolism as a driver and therapeutic target of myocardial infarction[J]. J Cell Mol Med, 2020, 24(11): 5937-5954.
    Wang X X, Shen X Y, Yan Y T, et al. Pyruvate dehydrogenase kinases (PDKs): An overview toward clinical applications[J]. Biosci Rep, 2021, 41(4): BSR20204402.
    Li T T, Xu J, Qin X H, et al. Glucose oxidation positively regulates glucose uptake and improves cardiac function recovery after myocardial reperfusion[J]. Am J Physiol Endocrinol Metab, 2017, 313(5): E577-E585.
    Connaughton S, Chowdhury F, Attia R R, et al. Regulation of pyruvate dehydrogenase kinase isoform 4(PDK4) gene expression by glucocorticoids and insulin[J]. Mol Cell Endocrinol, 2010, 315(1/2): 159-167.
    She H, Hu Y, Zhao G Z, et al. Dexmedetomidine ameliorates myocardial ischemia-reperfusion injury by inhibiting MDH2 lactylation via regulating metabolic reprogramming[J]. Adv Sci, 2024, 11(48): 2409499.
    Zhang T T, Han Y, Wang Y C, et al. The interaction between ferroptosis and myocardial ischemia-reperfusion injury: Molecular mechanisms and potential therapeutic targets[J]. Eur J Med Res, 2025, 30(1): 643.
    Stockwell B R, Friedmann Angeli J P, Bayir H, et al. Ferroptosis: A regulated cell death nexus linking metabolism, redox biology, and disease[J]. Cell, 2017, 171(2): 273-285.
    Tang L J, Luo X J, Tu H, et al. Ferroptosis occurs in phase of reperfusion but not ischemia in rat heart following ischemia or ischemia/reperfusion[J]. Naunyn Schmiedeberg Arch Pharmacol, 2021, 394(2): 401-410.
    Zhao W K, Zhou Y, Xu T T, et al. Ferroptosis: Opportunities and challenges in myocardial ischemia-reperfusion injury[J]. Oxid Med Cell Longev, 2021, 2021: 9929687.
    Doll S, Proneth B, Tyurina Y Y, et al. ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition[J]. Nat Chem Biol, 2017, 13(1): 91-98.
    Yao L Y, He F N, Zhao Q Y, et al. Spatial multiplexed protein profiling of cardiac ischemia-reperfusion injury[J]. Circ Res, 2023, 133(1): 86-103.
    Wu X X, Liu L, Zheng Q L, et al. Dihydrotanshinone I preconditions myocardium against ischemic injury via PKM2 glutathionylation sensitive to ROS[J]. Acta Pharm Sin B, 2023, 13(1): 113-127.
    Liu H Q, Liu W, Qiu H L, et al. Salvianolic acid B protects against myocardial ischaemia-reperfusion injury in rats via inhibiting high mobility group box 1 protein expression through the PI3K/Akt signalling pathway[J]. Naunyn Schmiedebergs Arch Pharmacol, 2020, 393(8): 1527-1539.
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