Skip to content
2000
image of Geniposide Attenuates Post-Myocardial Infarction Cardiac Remodeling via Parkin-Dependent Suppression of Hyperactivated Mitophagy

Abstract

Background

Cardiac remodeling Post-Myocardial Infarction (MI) drives heart failure. Geniposide (GP), a traditional Chinese medicine-derived compound, exhibits cardioprotective potential, yet its mechanisms remain unclear. This study explored the GP’s role in post-MI remodeling Parkin-dependent mitophagy.

Methods

Murine MI and cardiomyocyte Chronic Hypoxia (CH) models were established. MI mice received GP; cardiac function, histopathology, apoptosis, fibrosis/autophagy markers, and mitochondrial clearance were assessed. , Parkin-silenced hypoxic cardiomyocytes were used to evaluate GP’s effects on viability, oxidative stress, mitochondrial function, autophagy proteins, and autophagosome formation.

Results

, GP improved cardiac function, reduced fibrosis/apoptosis, and suppressed fibrosis-related genes (Col1a1, Col3a1, Tgfb1, Mmp9). GP enhanced clearance of damaged mitochondria autophagy, mitigating oxidative stress. GP’s protection against hypoxia required Parkin: it preserved mitochondrial homeostasis, inhibited ROS-mediated apoptosis, and reduced autophagosome accumulation. Mechanistically, GP attenuated excessive mitophagy by modulating Parkin, thereby maintaining mitochondrial quality and reducing oxidative injury.

Discussion

The mechanism by which GP regulates Parkin-dependent mitophagy identified in this study addresses the limitations of existing standard therapies that lack targeted regulation of mitochondrial quality. However, the upstream and downstream molecular regulatory mechanisms of the GP-Parkin pathway, as well as GP’s long-term safety and pharmacokinetic interactions with standard drugs, remain to be further elucidated. Future studies may explore the synergistic efficacy and optimal dose ratio of GP combined with first-line drugs liver microsome experiments and animal models, and conduct chronic toxicity studies to support its clinical translation.

Conclusion

GP alleviates post-MI remodeling by suppressing Parkin-dependent hyperactivated mitophagy, reducing cardiomyocyte loss and fibrosis. Parkin is central to GP’s therapeutic effects, highlighting its potential as a target for MI-related heart failure. This study elucidates GP’s cardioprotective mechanism and proposes Parkin pathway modulation as a novel strategy to counteract pathological cardiac remodeling.

Loading

Article metrics loading...

/content/journals/cmc/10.2174/0109298673402330251125051751
2026-01-13
2026-03-02
Loading full text...

Full text loading...

References

  1. Ferrero L. In-hospital mortality of acute myocardial infarction. Epidemic Preparedness and Control United Kingdom IntechOpen 2023 10.5772/intechopen.1001453
    [Google Scholar]
  2. The top 10 causes of death. 2024 Available from: https://www.who.int/news-room/fact-sheets/detail/the-top-10-causes-of-death
  3. Jenča D. Melenovský V. Stehlik J. Staněk V. Kettner J. Kautzner J. Adámková V. Wohlfahrt P. Heart failure after myocardial infarction: Incidence and predictors. ESC Heart Fail. 2021 8 1 222 237 10.1002/ehf2.13144 33319509
    [Google Scholar]
  4. Prabhu S.D. The cardiosplenic axis is essential for the pathogenesis of ischemic heart failure. Trans. Am. Clin. Climatol. Assoc. 2018 129 202 214
    [Google Scholar]
  5. Kehat I. Molkentin J.D. Molecular pathways underlying cardiac remodeling during pathophysiological stimulation. Circulation 2010 122 25 2727 2735 10.1161/CIRCULATIONAHA.110.942268 21173361
    [Google Scholar]
  6. Leancă S.A. Crișu D. Petriș A.O. Afrăsânie I. Genes A. Costache A.D. Tesloianu D.N. Costache I.I. Left ventricular remodeling after myocardial infarction: From physiopathology to treatment. Life 2022 12 8 1111 10.3390/life12081111 35892913
    [Google Scholar]
  7. Ghafoor M. Kamal M. Nadeem U. Husain A.N. Educational case: Myocardial infarction: Histopathology and timing of changes. Acad. Pathol. 2020 7 2374289520976639 10.1177/2374289520976639 33415186
    [Google Scholar]
  8. Muhlestein J.B. Adverse left ventricular remodelling after acute myocardial infarction: Is there a simple treatment that really works? Eur. Heart J. 2014 35 3 144 146 10.1093/eurheartj/eht505 24344189
    [Google Scholar]
  9. Xu X. Pang Y. Fan X. Mitochondria in oxidative stress, inflammation and aging: From mechanisms to therapeutic advances. Signal Transduct. Target. Ther. 2025 10 1 190 10.1038/s41392‑025‑02253‑4 40500258
    [Google Scholar]
  10. Marek-Iannucci S. Ozdemir A.B. Moreira D. Gomez A.C. Lane M. Porritt R.A. Lee Y. Shimada K. Abe M. Stotland A. Zemmour D. Parker S. Sanchez-Lopez E. Van Eyk J. Gottlieb R.A. Fishbein M.C. Karin M. Crother T.R. Rivas M.N. Arditi M. Autophagy-mitophagy induction attenuates cardiovascular inflammation in a murine model of Kawasaki disease vasculitis. JCI. Insight 2021 6 18 151981 10.1172/jci.insight.151981 34403365
    [Google Scholar]
  11. Li Y. Liang P. Jiang B. Tang Y. Liu X. Liu M. Sun H. Chen C. Hao H. Liu Z. Xiao X. CARD9 promotes autophagy in cardiomyocytes in myocardial ischemia/reperfusion injury via interacting with Rubicon directly. Basic Res. Cardiol. 2020 115 3 29 10.1007/s00395‑020‑0790‑6 32248306
    [Google Scholar]
  12. Shires S.E. Gustafsson Å.B. Mitophagy and heart failure. J. Mol. Med. 2015 93 3 253 262 10.1007/s00109‑015‑1254‑6 25609139
    [Google Scholar]
  13. Guo C. Chen M.J. Zhao J.R. Wu R.Y. Zhang Y. Li Q.Q. Zhao H. Dou J.H. Song S.F. Wei J. Exercise training improves cardiac function and regulates myocardial mitophagy differently in ischaemic and pressure-overload heart failure mice. Exp. Physiol. 2022 107 6 562 574 10.1113/EP090374 35365954
    [Google Scholar]
  14. Dorn G.W. II Central parkin: The evolving role of Parkin in the heart. Biochim. Biophys. Acta Bioenerg. 2016 1857 8 1307 1312 10.1016/j.bbabio.2016.03.014 26992930
    [Google Scholar]
  15. Li H. Qin S. Liang Q. Xi Y. Bo W. Cai M. Tian Z. Exercise training enhances myocardial mitophagy and improves cardiac function via Irisin/FNDC5-PINK1/Parkin pathway in MI mice. Biomedicines 2021 9 6 701 10.3390/biomedicines9060701 34205641
    [Google Scholar]
  16. Dong Y. Hu M. Tan K. Dai R. ZNF143 inhibits hepatocyte mitophagy and promotes non-alcoholic fatty liver disease by targeting increased lncRNA NEAT1 expression to activate ROCK2 pathway. Epigenetics 2023 18 1 2239592 10.1080/15592294.2023.2239592 37566742
    [Google Scholar]
  17. Ivankovic D. Chau K.Y. Schapira A.H.V. Gegg M.E. Mitochondrial and lysosomal biogenesis are activated following PINK 1/parkin-mediated mitophagy. J. Neurochem. 2016 136 2 388 402 10.1111/jnc.13412 26509433
    [Google Scholar]
  18. Ge P. Dawson V.L. Dawson T.M. PINK1 and Parkin mitochondrial quality control: A source of regional vulnerability in Parkinson’s disease. Mol. Neurodegener. 2020 15 1 20 10.1186/s13024‑020‑00367‑7 32169097
    [Google Scholar]
  19. Jin S.M. Youle R.J. The accumulation of misfolded proteins in the mitochondrial matrix is sensed by PINK1 to induce PARK2/Parkin-mediated mitophagy of polarized mitochondria. Autophagy 2013 9 11 1750 1757 10.4161/auto.26122 24149988
    [Google Scholar]
  20. Wauer T. Simicek M. Schubert A. Komander D. Mechanism of phospho-ubiquitin-induced PARKIN activation. Nature 2015 524 7565 370 374 10.1038/nature14879 26161729
    [Google Scholar]
  21. Chen Y. Dorn G.W. II PINK1-phosphorylated mitofusin 2 is a Parkin receptor for culling damaged mitochondria. Science 2013 340 6131 471 475 10.1126/science.1231031 23620051
    [Google Scholar]
  22. Ma K. Chen G. Li W. Kepp O. Zhu Y. Chen Q. Mitophagy, mitochondrial homeostasis, and cell fate. Front. Cell Dev. Biol. 2020 8 467 10.3389/fcell.2020.00467 32671064
    [Google Scholar]
  23. Marek-Iannucci S. Thomas A. Hou J. Crupi A. Sin J. Taylor D.J. Czer L.S. Esmailian F. Mentzer R.M. Jr Andres A.M. Gottlieb R.A. Myocardial hypothermia increases autophagic flux, mitochondrial mass and myocardial function after ischemia-reperfusion injury. Sci. Rep. 2019 9 1 10001 10.1038/s41598‑019‑46452‑w 31292486
    [Google Scholar]
  24. Yong J. Tao J. Wang K. Li X. Yang Y. Post-myocardial infarction cardiac remodeling: Multidimensional mechanisms and clinical prospects of stem cell therapy. Stem Cell Rev. Rep. 2025 21 5 1369 1427 10.1007/s12015‑025‑10888‑7 40323498
    [Google Scholar]
  25. Mortensen R.M. Immune cell modulation of cardiac remodeling. Circulation 2012 125 13 1597 1600 10.1161/CIRCULATIONAHA.112.097832 22388322
    [Google Scholar]
  26. Poncelas M. Inserte J. Aluja D. Hernando V. Vilardosa U. Garcia-Dorado D. Delayed, oral pharmacological inhibition of calpains attenuates adverse post-infarction remodelling. Cardiovasc. Res. 2017 113 8 950 961 10.1093/cvr/cvx073 28460013
    [Google Scholar]
  27. Tarone G. Balligand J.L. Bauersachs J. Clerk A. De Windt L. Heymans S. Hilfiker-Kleiner D. Hirsch E. Iaccarino G. Knöll R. Leite-Moreira A.F. Lourenço A.P. Mayr M. Thum T. Tocchetti C.G. Targeting myocardial remodelling to develop novel therapies for heart failure. Eur. J. Heart Fail. 2014 16 5 494 508 10.1002/ejhf.62 24639064
    [Google Scholar]
  28. Singh K.D. Karnik S.S. Angiotensin type 1 receptor blockers in heart failure. Curr. Drug Targets 2020 21 2 125 131 10.2174/1389450120666190821152000 31433752
    [Google Scholar]
  29. Agostini L.C. Silva N.N.T. Belo V.A. Luizon M.R. Lima A.A. da Silva G.N. Pharmacogenetics of angiotensin-converting enzyme inhibitors (ACEI) and angiotensin II receptor blockers (ARB) in cardiovascular diseases. Eur. J. Pharmacol. 2024 981 176907 10.1016/j.ejphar.2024.176907 39154825
    [Google Scholar]
  30. Mustafa N.H. Jalil J. Zainalabidin S. Saleh M.S.M. Asmadi A.Y. Kamisah Y. Molecular mechanisms of sacubitril/valsartan in cardiac remodeling. Front. Pharmacol. 2022 13 892460 10.3389/fphar.2022.892460 36003518
    [Google Scholar]
  31. Verma S. Pandey A. Pandey A.K. Butler J. Lee J.S. Teoh H. Mazer C.D. Kosiborod M.N. Cosentino F. Anker S.D. Connelly K.A. Bhatt D.L. Aldosterone and aldosterone synthase inhibitors in cardiorenal disease. Am. J. Physiol. Heart Circ. Physiol. 2024 326 3 H670 H688 10.1152/ajpheart.00419.2023 38133623
    [Google Scholar]
  32. Seara F.A.C. Olivares E.L. Nascimento J.H.M. Anabolic steroid excess and myocardial infarction: From ischemia to reperfusion injury. Steroids 2020 161 108660 10.1016/j.steroids.2020.108660
    [Google Scholar]
  33. Moady G. Ben Gal T. Atar S. Sodium-glucose co-transporter 2 inhibitors in heart failure—current evidence in special populations. Life 2023 13 6 1256 10.3390/life13061256 37374037
    [Google Scholar]
  34. Liao P. Liu L. Wang B. Li W. Fang X. Guan S. Baicalin and geniposide attenuate atherosclerosis involving lipids regulation and immunoregulation in ApoE−/− mice. Eur. J. Pharmacol. 2014 740 488 495 10.1016/j.ejphar.2014.06.039 24991786
    [Google Scholar]
  35. Wu S. Wang G. Liu Z. Rao J. Lü L. Xu W. Wu S. Zhang J. Effect of geniposide, a hypoglycemic glucoside, on hepatic regulating enzymes in diabetic mice induced by a high-fat diet and streptozotocin. Acta Pharmacol. Sin. 2009 30 2 202 208 10.1038/aps.2008.17 19122671
    [Google Scholar]
  36. Wang J. Zhang Y. Liu R. Li X. Cui Y. Qu L. Geniposide protects against acute alcohol-induced liver injury in mice via up-regulating the expression of the main antioxidant enzymes. Can. J. Physiol. Pharmacol. 2015 93 4 261 267 10.1139/cjpp‑2014‑0536 25730420
    [Google Scholar]
  37. Liu J. Yin F. Zheng X. Jing J. Hu Y. Geniposide, a novel agonist for GLP-1 receptor, prevents PC12 cells from oxidative damage via MAP kinase pathway. Neurochem. Int. 2007 51 6-7 361 369 10.1016/j.neuint.2007.04.021 17629357
    [Google Scholar]
  38. Germano J.F. Huang C. Sin J. Song Y. Tucker K.C. Taylor D.J.R. Saadaeijahromi H. Stotland A. Piplani H. Gottlieb R.A. Mentzer R.M. Jr Andres A.M. Intermittent use of a short-course glucagon-like peptide-1 receptor agonist therapy limits adverse cardiac remodeling via parkin-dependent mitochondrial turnover. Sci. Rep. 2020 10 1 8284 10.1038/s41598‑020‑64924‑2 32427925
    [Google Scholar]
  39. Jiang YQ Chang GL Wang Y Geniposide prevents hypoxia/reoxygenation-induced apoptosis in H9c2 cells: Improvement of mitochondrial dysfunction and activation of GLP-1R and the PI3K/AKT signaling pathway. Cell Physiol Biochem. 2016 39 1 407 421 10.1159/000445634
    [Google Scholar]
  40. Luo X. Wu S. Jiang Y. Wang L. Li G. Qing Y. Liu J. Zhang D. Inhibition of autophagy by geniposide protects against myocardial ischemia/reperfusion injury. Int. Immunopharmacol. 2020 85 106609 10.1016/j.intimp.2020.106609 32446199
    [Google Scholar]
  41. Jiang H. Fang T. Cheng Z. Mechanism of heart failure after myocardial infarction. J. Int. Med. Res. 2023 51 10 03000605231202573 10.1177/03000605231202573 37818767
    [Google Scholar]
  42. Zhao W. Zhao J. Rong J. Pharmacological modulation of cardiac remodeling after myocardial infarction. Oxid. Med. Cell. Longev. 2020 2020 1 11 10.1155/2020/8815349 33488934
    [Google Scholar]
  43. Chiao Y.A. Ramirez T.A. Zamilpa R. Okoronkwo S.M. Dai Q. Zhang J. Jin Y.F. Lindsey M.L. Matrix metalloproteinase-9 deletion attenuates myocardial fibrosis and diastolic dysfunction in ageing mice. Cardiovasc. Res. 2012 96 3 444 455 10.1093/cvr/cvs275 22918978
    [Google Scholar]
  44. Cowling R.T. Kupsky D. Kahn A.M. Daniels L.B. Greenberg B.H. Mechanisms of cardiac collagen deposition in experimental models and human disease. Transl. Res. 2019 209 138 155 10.1016/j.trsl.2019.03.004 30986384
    [Google Scholar]
  45. Zhou Y. Zhao X. Hua Y. Chen H. Yang H. Zhang T. Huang G. Fan H. Tan Z. Huang X. Liu B. Aldehyde dehydrogenase-2 protects against myocardial infarction-related cardiac fibrosis through modulation of the Wnt/β-catenin signaling pathway. Ther. Clin. Risk Manag. 2015 11 1371 1381 10.2147/TCRM.S88297 26392772
    [Google Scholar]
  46. Jia J. Zhao X. Tao S. Wang J. Zhang R. Dai H. Zhang X. Han M. Yang B. Li Y. Li J. Icariin improves cardiac function and remodeling via the TGF-β1/Smad signaling pathway in rats following myocardial infarction. Eur. J. Med. Res. 2023 28 1 607 10.1186/s40001‑023‑01588‑4 38115154
    [Google Scholar]
  47. Suryono S. Rohman M.S. Widjajanto E. Prayitnaningsih S. Wihastuti T.A. Oktaviono Y.H. Effect of Colchicine in reducing MMP-9, NOX2, and TGF- β1 after myocardial infarction. BMC Cardiovasc. Disord. 2023 23 1 449 10.1186/s12872‑023‑03464‑9 37697278
    [Google Scholar]
  48. Ji W. Wei S. Hao P. Xing J. Yuan Q. Wang J. Xu F. Chen Y. Aldehyde dehydrogenase 2 has cardioprotective effects on myocardial ischaemia/reperfusion injury via suppressing mitophagy. Front. Pharmacol. 2016 7 101 10.3389/fphar.2016.00101 27148058
    [Google Scholar]
  49. Wu C. Zhang X.C. Chen L.R. Huang H.Z. Wu W.Y. Wang Y. Li G. Pyroptosis and mitochondrial function participated in miR-654-3p-protected against myocardial infarction. Cell Death Dis. 2024 15 6 393 10.1038/s41419‑024‑06786‑4 38834627
    [Google Scholar]
  50. Kleefeld F. Horvath R. Pinal-Fernandez I. Mammen A.L. Casal-Dominguez M. Hathazi D. Melchert S. Hahn K. Sickmann A. Muselmann-Genschow C. Hentschel A. Preuße C. Roos A. Schoser B. Stenzel W. Multi-level profiling unravels mitochondrial dysfunction in myotonic dystrophy type 2. Acta Neuropathol. 2024 147 1 19 10.1007/s00401‑023‑02673‑y 38240888
    [Google Scholar]
  51. Quiles J.M. Gustafsson Å.B. The role of mitochondrial fission in cardiovascular health and disease. Nat. Rev. Cardiol. 2022 19 11 723 736 10.1038/s41569‑022‑00703‑y 35523864
    [Google Scholar]
  52. Matsuda N. Sato S. Shiba K. Okatsu K. Saisho K. Gautier C.A. Sou Y. Saiki S. Kawajiri S. Sato F. Kimura M. Komatsu M. Hattori N. Tanaka K. PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy. J. Cell Biol. 2010 189 2 211 221 10.1083/jcb.200910140 20404107
    [Google Scholar]
  53. Jin J. Wei X. Zhi X. Wang X. Meng D. Drp1-dependent mitochondrial fission in cardiovascular disease. Acta Pharmacol. Sin. 2021 42 5 655 664 10.1038/s41401‑020‑00518‑y 32913266
    [Google Scholar]
  54. Mao S. Chen P. Li T. Guo L. Zhang M. Tongguan capsule mitigates post-myocardial infarction remodeling by promoting autophagy and inhibiting apoptosis: Role of sirt1. Front. Physiol. 2018 9 589 10.3389/fphys.2018.00589 29872406
    [Google Scholar]
  55. Tang S. Geng Y. Lin Q. The role of mitophagy in metabolic diseases and its exercise intervention. Front. Physiol. 2024 15 1339128 10.3389/fphys.2024.1339128 38348222
    [Google Scholar]
  56. Chen J. Zhu T. Yang J. Shen M. Wang D. Gu B. Xu J. Zhang M. Hao X. Tang Z. Tong J. Du Y. Zhang B. Li H. Xu M. Geniposide protects against myocardial infarction injury via the restoration in gut microbiota and gut–brain axis. J. Cell. Mol. Med. 2025 29 3 70406 10.1111/jcmm.70406 39910683
    [Google Scholar]
  57. Turkieh A. El Masri Y. Pinet F. Dubois-Deruy E. Mitophagy regulation following myocardial infarction. Cells 2022 11 2 199 10.3390/cells11020199 35053316
    [Google Scholar]
  58. Narendra D.P. Jin S.M. Tanaka A. Suen D.F. Gautier C.A. Shen J. Cookson M.R. Youle R.J. PINK1 is selectively stabilized on impaired mitochondria to activate Parkin. PLoS Biol. 2010 8 1 1000298 10.1371/journal.pbio.1000298 20126261
    [Google Scholar]
  59. Tang J. Lu X. Zhang T. Feng Y. Xu Q. Li J. Lan Y. Luo H. Zeng L. Xiang Y. Zhang Y. Li Q. Mao X. Tang B. Zeng D. Shiga toxin 2 A-subunit induces mitochondrial damage, mitophagy and apoptosis via the interaction of Tom20 in Caco-2 cells. Heliyon 2023 9 9 20012 10.1016/j.heliyon.2023.e20012 37809632
    [Google Scholar]
  60. Rugarli E.I. Langer T. Mitochondrial quality control: A matter of life and death for neurons. EMBO J. 2012 31 6 1336 1349 10.1038/emboj.2012.38 22354038
    [Google Scholar]
  61. Lin L. Wei J. Zhu C. Hao G. Xue J. Zhu Y. Wu R. Sema3A alleviates viral myocarditis by modulating SIRT1 to regulate cardiomyocyte mitophagy. Environ. Toxicol. 2023 38 6 1305 1317 10.1002/tox.23765 36880403
    [Google Scholar]
  62. Saito T. Sadoshima J. Molecular mechanisms of mitochondrial autophagy/mitophagy in the heart. Circ. Res. 2015 116 8 1477 1490 10.1161/CIRCRESAHA.116.303790 25858070
    [Google Scholar]
  63. Liu L. Wu Q. Chen Y. Gu G. Gao R. Peng B. Wang Y. Li A. Guo J. Xu X. Shao X. Li L. Shen Y. Sun J. Updated pharmacological effects, molecular mechanisms, and therapeutic potential of natural product geniposide. Molecules 2022 27 10 3319 10.3390/molecules27103319 35630796
    [Google Scholar]
  64. Li H. Yang D.H. Zhang Y. Zheng F. Gao F. Sun J. Shi G. Geniposide suppresses NLRP3 inflammasome-mediated pyroptosis via the AMPK signaling pathway to mitigate myocardial ischemia/reperfusion injury. Chin. Med. 2022 17 1 73 10.1186/s13020‑022‑00616‑5 35715805
    [Google Scholar]
  65. Yao Y. Lin L. Tang W. Shen Y. Chen F. Li N. Geniposide alleviates pressure overload in cardiac fibrosis with suppressed TGF-β1 pathway. Acta Histochem. 2023 125 4 152044 10.1016/j.acthis.2023.152044 37196380
    [Google Scholar]
  66. Sun T. Ding W. Xu T. Ao X. Yu T. Li M. Liu Y. Zhang X. Hou L. Wang J. Parkin regulates programmed necrosis and myocardial ischemia/reperfusion injury by targeting cyclophilin-D. Antioxid. Redox Signal. 2019 31 16 1177 1193 10.1089/ars.2019.7734 31456416
    [Google Scholar]
  67. Wal P. Aziz N. Singh Y.K. Wal A. Kosey S. Rai A.K. Myocardial infarction as a consequence of mitochondrial dysfunction. Curr. Cardiol. Rev. 2023 19 6 080523216642 10.2174/1573403X19666230508114311 37157208
    [Google Scholar]
  68. Chang X. Liu R. Li R. Peng Y. Zhu P. Zhou H. Molecular mechanisms of mitochondrial quality control in ischemic cardiomyopathy. Int. J. Biol. Sci. 2023 19 2 426 448 10.7150/ijbs.76223 36632466
    [Google Scholar]
  69. Kitada T. Asakawa S. Hattori N. Matsumine H. Yamamura Y. Minoshima S. Yokochi M. Mizuno Y. Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998 392 6676 605 608 10.1038/33416 9560156
    [Google Scholar]
  70. Woodall B.P. Orogo A.M. Najor R.H. Cortez M.Q. Moreno E.R. Wang H. Divakaruni A.S. Murphy A.N. Gustafsson Å.B. Parkin does not prevent accelerated cardiac aging in mitochondrial DNA mutator mice. JCI Insight 2019 4 10 127713 10.1172/jci.insight.127713 30990467
    [Google Scholar]
  71. Wang S. Zhao Z. Feng X. Cheng Z. Xiong Z. Wang T. Lin J. Zhang M. Hu J. Fan Y. Reiter R.J. Wang H. Sun D. Melatonin activates Parkin translocation and rescues the impaired mitophagy activity of diabetic cardiomyopathy through Mst1 inhibition. J. Cell. Mol. Med. 2018 22 10 5132 5144 10.1111/jcmm.13802 30063115
    [Google Scholar]
  72. Wu Y. Jiang T. Hua J. Xiong Z. Dai K. Chen H. Li L. Peng J. Peng X. Zheng Z. Xiong W. PINK1/Parkin-mediated mitophagy in cardiovascular disease: From pathogenesis to novel therapy. Int. J. Cardiol. 2022 361 61 69 10.1016/j.ijcard.2022.05.025 35594994
    [Google Scholar]
  73. Shen Y. Wang X. Shen X. Wang Y. Wang S. Zhang Y. Yao X. Xu Y. Sang M. Pan J. Qin Y. Zhou Q. Shen J. Geniposide possesses the protective effect on myocardial injury by inhibiting oxidative stress and ferroptosis via activation of the Grsf1/GPx4 axis. Front. Pharmacol. 2022 13 879870 10.3389/fphar.2022.879870 35600863
    [Google Scholar]
  74. Zhou S. Sun Y. Zhao K. Gao Y. Cui J. Qi L. Huang L. miR-21/PTEN pathway mediates the cardioprotection of geniposide against oxidized low-density lipoprotein-induced endothelial injury via suppressing oxidative stress and inflammatory response. Int. J. Mol. Med. 2020 45 5 1305 1316 10.3892/ijmm.2020.4520 32323738
    [Google Scholar]
  75. Wang F. Cao J. Hao J. Liu K. Pharmacokinetics, bioavailability and tissue distribution of geniposide following intravenous and peroral administration to rats. Biopharm. Drug Dispos. 2014 35 2 97 103 10.1002/bdd.1869 24122743
    [Google Scholar]
/content/journals/cmc/10.2174/0109298673402330251125051751
Loading
/content/journals/cmc/10.2174/0109298673402330251125051751
Loading

Data & Media loading...


  • Article Type:
    Research Article
Keywords: myocardial infarction ; Parkin ; cardiac remodeling ; mitophagy ; cardiac fibrosis ; Geniposide
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test