Cardioprotective strategies preserve the stability of respiratory chain supercomplexes and reduce oxidative stress in reperfused ischemic hearts

• Published in: Free radical biology & medicine Vol. 129; pp. 407 - 417
• Main Authors: Ramírez-Camacho, I., Correa, F., El Hafidi, M., Silva-Palacios, A., Ostolga-Chavarría, M., Esparza-Perusquía, M., Olvera-Sánchez, S., Flores-Herrera, O., Zazueta, C.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-12-2018
• Subjects: Mitochondrial respiratory chain; N-acetylcysteine; Postconditioning; Reactive oxygen species; Supercomplexes; TTC; Reactive oxygen species; O2; SCAFI; IR; HR; H2O2; Mitochondrial respiratory chain; Postconditioning; N-acetylcysteine; NAC; Supercomplexes; NADH; LVDP; ROS; PostC; SC's
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2018.09.047

Electron leakage from dysfunctional respiratory chain and consequent superoxide formation leads to mitochondrial and cell injury during ischemia and reperfusion (IR). In this work we evaluate if the supramolecular assembly of the respiratory complexes into supercomplexes (SCs) is associated with preserved energy efficiency and diminished oxidative stress in post-ischemic hearts treated with the antioxidant N-acetylcysteine (NAC) and the cardioprotective maneuver of Postconditioning (PostC). Hemodynamic variables, infarct size, oxidative stress markers, oxygen consumption and the activity/stability of SCs were compared between groups. We found that mitochondrial oxygen consumption and the activity of respiratory complexes are preserved in mitochondria from reperfused hearts treated with both NAC and PostC. Both treatments contribute to recover the activity of individual complexes. NAC reduced oxidative stress and maintained SCs assemblies containing Complex I, Complex III, Complex IV and the adapter protein SCAFI more effectively than PostC. On the other hand, the activities of CI, CIII and CIV associated to SCs assemblies were preserved by this maneuver, suggesting that the activation of other cardioprotective mechanisms besides oxidative stress contention might participate in maintaining the activity of the mitochondrial respiratory complexes in such superstructures.
We conclude that both the monomeric and the SCs assembly of the respiratory chain contribute to the in vivo functionality of the mitochondria. However, although the ROS-induced damage and the consequent increased production of ROS affect the assembly of SCs, other levels of regulation as those induced by PostC, might participate in maintaining the activity of the respiratory complexes in such superstructures.
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•Cardioprotective strategies protect mitochondrial function and stabilize SCs (79).•N-acetylcysteine reduces oxidative stress, preserving SCs assemblies (72).•Postconditioning maintains the enzymatic activities of CI, CIII, CIV in SCs (79).