Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine

Author:

Aronowitz Danielle I.1ORCID,Geoffrion Tracy R.1,Piel Sarah2,Morton Sarah R.2,Starr Jonathan2,Melchior Richard W.1,Gaudio Hunter A.2,Degani Rinat2ORCID,Widmann Nicholas J.2,Weeks M. Katie2,Ranieri Nicolina R.3ORCID,Benson Emilie34ORCID,Ko Tiffany S.234ORCID,Licht Daniel J.3,Hefti Marco5,Gaynor J. William1ORCID,Kilbaugh Todd J.2ORCID,Mavroudis Constantine D.1

Affiliation:

1. Division of Cardiothoracic Surgery, Children’s Hospital of Philadelphia, Philadelphia, PA 19104, USA

2. Resuscitation Science Center of Emphasis, Children’s Hospital of Philadelphia, Philadelphia, PA 19104, USA

3. Department of Neurology, Children’s Hospital of Philadelphia, Philadelphia, PA 19104, USA

4. Department of Physics & Astronomy, University of Pennsylvania, Philadelphia, PA 19104, USA

5. Department of Pathology, University of Iowa Health Care, Iowa City, IA 52242, USA

Abstract

Optimal oxygen management during pediatric cardiopulmonary bypass (CPB) is unknown. We previously demonstrated an increase in cortical mitochondrial reactive oxygen species and decreased mitochondrial function after CPB using hyperoxic oxygen management. This study investigates whether controlled oxygenation (normoxia) during CPB reduces cortical mitochondrial dysfunction and oxidative injury. Ten neonatal swine underwent three hours of continuous CPB at 34 °C (flow > 100 mL/kg/min) via cervical cannulation targeting a partial pressure of arterial oxygen (PaO2) goal < 150 mmHg (normoxia, n = 5) or >300 mmHg (hyperoxia, n = 5). The animals underwent continuous hemodynamic monitoring and serial arterial blood sampling. Cortical microdialysate was serially sampled to quantify the glycerol concentration (represents neuronal injury) and lactate-to-pyruvate ratio (represents bioenergetic dysfunction). The cortical tissue was analyzed via high-resolution respirometry to quantify mitochondrial oxygen consumption and reactive oxygen species generation, and cortical oxidized protein carbonyl concentrations were quantified to assess for oxidative damage. Serum PaO2 was higher in hyperoxia animals throughout CPB (p < 0.001). There were no differences in cortical glycerol concentration between groups (p > 0.2). The cortical lactate-to-pyruvate ratio was modestly elevated in hyperoxia animals (p < 0.03) but the values were not clinically significant (<30). There were no differences in cortical mitochondrial respiration (p = 0.48), protein carbonyls (p = 0.74), or reactive oxygen species generation (p = 0.93) between groups. Controlled oxygenation during CPB does not significantly affect cortical mitochondrial function or oxidative injury in the acute setting. Further evaluation of the short and long-term effects of oxygen level titration during pediatric CPB on cortical tissue and other at-risk brain regions are needed, especially in the presence of cyanosis.

Funder

Congenital Heart Defect Coalition

Children’s Hospital of Philadelphia Institutional Development Fund

Publisher

MDPI AG

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