Induction of mitochondrial dysfunction in patients under cardiopulmonary by-pass: preliminary results.
Aged
Cardiac Surgical Procedures
/ methods
Cardiopulmonary Bypass
Cell Respiration
Cells, Cultured
Electron Transport Chain Complex Proteins
/ metabolism
Female
Fibroblasts
/ metabolism
Humans
Male
Membrane Potential, Mitochondrial
Middle Aged
Mitochondria
/ metabolism
Oxidative Phosphorylation
Oxygen Consumption
Reactive Oxygen Species
/ metabolism
Spectrometry, Fluorescence
Systemic Inflammatory Response Syndrome
/ metabolism
Journal
European review for medical and pharmacological sciences
ISSN: 2284-0729
Titre abrégé: Eur Rev Med Pharmacol Sci
Pays: Italy
ID NLM: 9717360
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
entrez:
11
10
2019
pubmed:
11
10
2019
medline:
7
10
2020
Statut:
ppublish
Résumé
Cardiac surgery is often performed by cardiopulmonary by-pass (CPB), generally associated with organ dysfunction. The aim of this work was to determine if and how this phenomenon is related to mitochondrial damage. To this purpose, the effect of the addition of serum from CPB patients to human fibroblasts cultures on mitochondrial respiratory chain and oxidative phosphorylation (OXPHOS) activities was investigated. Serum samples of five patients were obtained before (pre-CPB) and after 6 h CPB weaning (CPB). Mitochondrial OXPHOS activities were examined by polarographic and spectrophotometric assays, and reactive oxygen species (ROS) production was measured by a spectrofluorimeter. Addition of CPB serum to fibroblasts determined a decrease of mitochondrial oxygen consumption due to an inhibition of mitochondrial respiratory chain and some OXPHOS enzymes activities. This inhibition seems to be mainly related to a reduced activity of complex I. Our data represent the first translational research evidence showing that CPB determines mitochondrial dysfunction which leads to impairment of OXPHOX activities and to an increase in ROS production, compromising tissue bioenergetic efficiency.
Identifiants
pubmed: 31599439
doi: 10.26355/eurrev_201909_19030
pii:
doi:
Substances chimiques
Electron Transport Chain Complex Proteins
0
Reactive Oxygen Species
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM