Pharmacological preconditioning protects from ischemia/reperfusion‐induced apoptosis by modulating Bcl‐xL expression through a ROS‐dependent mechanism. (4th January 2021)
- Record Type:
- Journal Article
- Title:
- Pharmacological preconditioning protects from ischemia/reperfusion‐induced apoptosis by modulating Bcl‐xL expression through a ROS‐dependent mechanism. (4th January 2021)
- Main Title:
- Pharmacological preconditioning protects from ischemia/reperfusion‐induced apoptosis by modulating Bcl‐xL expression through a ROS‐dependent mechanism
- Authors:
- Rozier, Romain
Paul, Rachel
Madji Hounoum, Blandine
Villa, Elodie
Mhaidly, Rana
Chiche, Johanna
Verhoeyen, Els
Marchetti, Sandrine
Vandenberghe, Ashaina
Raucoules, Marc
Carles, Michel
Ricci, Jean‐Ehrland - Abstract:
- Abstract : Myocardial ischemia/reperfusion (I/R) injury is a frequent perioperative threat, with numerous strategies developed to limit and/or prevent it. One interesting axis of research is the anesthetic preconditioning (APc) agent's hypothesis (such as sevoflurane, SEV). However, APc's mode of action is still poorly understood and volatile anesthetics used as preconditioning agents are often not well suited in clinical practice. Here, in vitro using H9C2 cells lines (in myeloblast state or differentiated toward cardiomyocytes) and in vivo in mice, we identified that SEV‐induced APc is mediated by a mild induction of reactive oxygen species (ROS) that activates Akt and induces the expression of the anti‐apoptotic protein B‐cell lymphoma‐extra large (Bcl‐xL), therefore protecting cardiomyocytes from I/R‐induced death. Furthermore, we extended these results to human cardiomyocytes (derived from induced pluripotent stem ‐ IPS ‐ cells). Importantly, we demonstrated that this protective signaling pathway induced by SEV could be stimulated using the antidiabetic agent metformin (MET), suggesting the preconditioning properties of MET. Altogether, our study identified a signaling pathway allowing APc of cardiac injuries as well as a rational for the use of MET as a pharmacological preconditioning agent to prevent I/R injuries. Abstract : Myocardial ischemia/reperfusion (I/R) injury contributes to patient condition's worsening in numerous clinical settings. PreconditioningAbstract : Myocardial ischemia/reperfusion (I/R) injury is a frequent perioperative threat, with numerous strategies developed to limit and/or prevent it. One interesting axis of research is the anesthetic preconditioning (APc) agent's hypothesis (such as sevoflurane, SEV). However, APc's mode of action is still poorly understood and volatile anesthetics used as preconditioning agents are often not well suited in clinical practice. Here, in vitro using H9C2 cells lines (in myeloblast state or differentiated toward cardiomyocytes) and in vivo in mice, we identified that SEV‐induced APc is mediated by a mild induction of reactive oxygen species (ROS) that activates Akt and induces the expression of the anti‐apoptotic protein B‐cell lymphoma‐extra large (Bcl‐xL), therefore protecting cardiomyocytes from I/R‐induced death. Furthermore, we extended these results to human cardiomyocytes (derived from induced pluripotent stem ‐ IPS ‐ cells). Importantly, we demonstrated that this protective signaling pathway induced by SEV could be stimulated using the antidiabetic agent metformin (MET), suggesting the preconditioning properties of MET. Altogether, our study identified a signaling pathway allowing APc of cardiac injuries as well as a rational for the use of MET as a pharmacological preconditioning agent to prevent I/R injuries. Abstract : Myocardial ischemia/reperfusion (I/R) injury contributes to patient condition's worsening in numerous clinical settings. Preconditioning interventions are developed to reduce myocardial suffering. Here, Rozier and coll . demonstrated in cell lines, in iPS‐derived human cardiomyocytes, and in mice that the anesthetic agent sevoflurane can protect cells from I/R‐induced injuries. They also demonstrated that metformin can protect cardiomyocytes through the same signaling pathway involving ROS‐dependent activation of Akt resulting in B‐cell lymphoma‐extra large (Bcl‐xL)‐increased expression. … (more)
- Is Part Of:
- FEBS journal. Volume 288:Number 11(2021)
- Journal:
- FEBS journal
- Issue:
- Volume 288:Number 11(2021)
- Issue Display:
- Volume 288, Issue 11 (2021)
- Year:
- 2021
- Volume:
- 288
- Issue:
- 11
- Issue Sort Value:
- 2021-0288-0011-0000
- Page Start:
- 3547
- Page End:
- 3569
- Publication Date:
- 2021-01-04
- Subjects:
- Akt -- anesthetic preconditioning -- Bcl‐xL -- cell death -- IPS -- metformin -- myocardial ischemic -- reperfusion -- ROS
Biochemistry -- Periodicals
Molecular biology -- Periodicals
Pathology, Molecular -- Periodicals
572 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=01038983-000000000-00000 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗ - DOI:
- 10.1111/febs.15675 ↗
- Languages:
- English
- ISSNs:
- 1742-464X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3901.578500
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