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Oxidative Stress Evaluation in Ischemia Reperfusion Models: Characteristics, Limits and Perspectives
P. Chazelas, C. Steichen, F. Favreau, P. Trouillas, P. Hannaert, R. Thuillier, S. Giraud, T. Hauet, J. Guillard
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, přehledy
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
33673423
DOI
10.3390/ijms22052366
Knihovny.cz E-zdroje
- MeSH
- buněčné linie MeSH
- lidé MeSH
- modely nemocí na zvířatech * MeSH
- molekulární modely MeSH
- oxidační stres * MeSH
- reaktivní formy kyslíku MeSH
- reperfuzní poškození metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Ischemia reperfusion injury is a complex process consisting of a seemingly chaotic but actually organized and compartmentalized shutdown of cell function, of which oxidative stress is a key component. Studying oxidative stress, which results in an imbalance between reactive oxygen species (ROS) production and antioxidant defense activity, is a multi-faceted issue, particularly considering the double function of ROS, assuming roles as physiological intracellular signals and as mediators of cellular component damage. Herein, we propose a comprehensive overview of the tools available to explore oxidative stress, particularly in the study of ischemia reperfusion. Applying chemistry as well as biology, we present the different models currently developed to study oxidative stress, spanning the vitro and the silico, discussing the advantages and the drawbacks of each set-up, including the issues relating to the use of in vitro hypoxia as a surrogate for ischemia. Having identified the limitations of historical models, we shall study new paradigms, including the use of stem cell-derived organoids, as a bridge between the in vitro and the in vivo comprising 3D intercellular interactions in vivo and versatile pathway investigations in vitro. We shall conclude this review by distancing ourselves from "wet" biology and reviewing the in silico, computer-based, mathematical modeling, and numerical simulation options: (a) molecular modeling with quantum chemistry and molecular dynamic algorithms, which facilitates the study of molecule-to-molecule interactions, and the integration of a compound in a dynamic environment (the plasma membrane...); (b) integrative systemic models, which can include many facets of complex mechanisms such as oxidative stress or ischemia reperfusion and help to formulate integrated predictions and to enhance understanding of dynamic interaction between pathways.
Faculté de Médecine et de Pharmacie Université de Poitiers F 86000 Poitiers France
FHU SUPORT Survival Optimization in Organ Transplantation F 86000 Poitiers France
INSERM U1082 IRTOMIT F 86000 Poitiers France
INSERM U1248 IPPRITT Université de Limoges F 87000 Limoges France
Laboratoire de Biochimie et Génétique Moléculaire CHU de Limoges F 87000 Limoges France
RCPTM University Palacký of Olomouc 771 47 Olomouc Czech Republic
Service de Biochimie CHU de Poitiers F 86000 Poitiers France
UMR CNRS 7285 IC2MP Team 5 Chemistry Université de Poitiers F 86000 Poitiers France
Citace poskytuje Crossref.org
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