Metformin preconditioning protects against myocardial stunning and preserves protein translation in a mouse model of cardiac arrest.

AMPK Cardiac arrest Metformin Myocardial stunning

Journal

Journal of molecular and cellular cardiology plus
ISSN: 2772-9761
Titre abrégé: J Mol Cell Cardiol Plus
Pays: Netherlands
ID NLM: 9918470779706676

Informations de publication

Date de publication:
Jun 2023
Historique:
medline: 10 7 2023
pubmed: 10 7 2023
entrez: 10 7 2023
Statut: ppublish

Résumé

Cardiac arrest (CA) causes high mortality due to multi-system organ damage attributable to ischemia-reperfusion injury. Recent work in our group found that among diabetic patients who experienced cardiac arrest, those taking metformin had less evidence of cardiac and renal damage after cardiac arrest when compared to those not taking metformin. Based on these observations, we hypothesized that metformin's protective effects in the heart were mediated by AMPK signaling, and that AMPK signaling could be targeted as a therapeutic strategy following resuscitation from CA. The current study investigates metformin interventions on cardiac and renal outcomes in a non-diabetic CA mouse model. We found that two weeks of metformin pretreatment protects against reduced ejection fraction and reduces kidney ischemia-reperfusion injury at 24 h post-arrest. This cardiac and renal protection depends on AMPK signaling, as demonstrated by outcomes in mice pretreated with the AMPK activator AICAR or metformin plus the AMPK inhibitor compound C. At this 24-h time point, heart gene expression analysis showed that metformin pretreatment caused changes supporting autophagy, antioxidant response, and protein translation. Further investigation found associated improvements in mitochondrial structure and markers of autophagy. Notably, Western analysis indicated that protein synthesis was preserved in arrest hearts of animals pretreated with metformin. The AMPK activation-mediated preservation of protein synthesis was also observed in a hypoxia/reoxygenation cell culture model. Despite the positive impacts of pretreatment in vivo and in vitro, metformin did not preserve ejection fraction when deployed at resuscitation. Taken together, we propose that metformin's in vivo cardiac preservation occurs through AMPK activation, requires adaptation before arrest, and is associated with preserved protein translation.

Identifiants

pubmed: 37425219
doi: 10.1016/j.jmccpl.2023.100034
pmc: PMC10327679
mid: NIHMS1911045
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : F32 HL156428
Pays : United States
Organisme : BLRD VA
ID : IK2 BX005785
Pays : United States
Organisme : NIH HHS
ID : S10 OD023684
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL129964
Pays : United States

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no conflicts of interest with the contents of this article.

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Auteurs

Cody A Rutledge (CA)

Division of Cardiology, Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Claudia Lagranha (C)

Division of Cardiology, Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Takuto Chiba (T)

Rangos Research Center, Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA, USA.
Division of Nephrology, Department of Pediatrics, University of Pittsburgh School, Pittsburgh, PA, USA.

Kevin Redding (K)

Division of Cardiology, Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Donna B Stolz (DB)

Department of Cell Biology, University of Pittsburgh, Pittsburgh, PA, USA.

Eric Goetzman (E)

Division of Genetic and Genomic Medicine, Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA, USA.

Sunder Sims-Lucas (S)

Rangos Research Center, Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA, USA.
Division of Nephrology, Department of Pediatrics, University of Pittsburgh School, Pittsburgh, PA, USA.

Brett A Kaufman (BA)

Division of Cardiology, Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

Classifications MeSH