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

Journal articles  - Journal Article
Aronowitz, DI; Geoffrion, TR; Piel, S; Morton, SR; Starr, J; Melchior, RW; Gaudio, HA; Degani, R; Widmann, NJ; Weeks, MK; Ranieri, NR; Ko, TS ...
Published in: Int J Mol Sci
May 17, 2024

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.

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Published In

Int J Mol Sci

DOI

EISSN

1422-0067

Publication Date

May 17, 2024

Volume

25

Issue

10

Location

Switzerland

Related Subject Headings

  • Swine
  • Reactive Oxygen Species
  • Pyruvic Acid
  • Oxygen Consumption
  • Oxygen
  • Oxidative Stress
  • Mitochondria
  • Lactic Acid
  • Hyperoxia
  • Chemical Physics
 

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Aronowitz, D. I., Geoffrion, T. R., Piel, S., Morton, S. R., Starr, J., Melchior, R. W., … Mavroudis, C. D. (2024). Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine. Int J Mol Sci, 25(10). https://doi.org/10.3390/ijms25105466
Aronowitz, Danielle I., Tracy R. Geoffrion, Sarah Piel, Sarah R. Morton, Jonathan Starr, Richard W. Melchior, Hunter A. Gaudio, et al. “Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine.Int J Mol Sci 25, no. 10 (May 17, 2024). https://doi.org/10.3390/ijms25105466.
Aronowitz DI, Geoffrion TR, Piel S, Morton SR, Starr J, Melchior RW, et al. Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine. Int J Mol Sci. 2024 May 17;25(10).
Aronowitz, Danielle I., et al. “Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine.Int J Mol Sci, vol. 25, no. 10, May 2024. Pubmed, doi:10.3390/ijms25105466.
Aronowitz DI, Geoffrion TR, Piel S, Morton SR, Starr J, Melchior RW, Gaudio HA, Degani R, Widmann NJ, Weeks MK, Ranieri NR, Benson E, Ko TS, Licht DJ, Hefti M, Gaynor JW, Kilbaugh TJ, Mavroudis CD. Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine. Int J Mol Sci. 2024 May 17;25(10).

Published In

Int J Mol Sci

DOI

EISSN

1422-0067

Publication Date

May 17, 2024

Volume

25

Issue

10

Location

Switzerland

Related Subject Headings

  • Swine
  • Reactive Oxygen Species
  • Pyruvic Acid
  • Oxygen Consumption
  • Oxygen
  • Oxidative Stress
  • Mitochondria
  • Lactic Acid
  • Hyperoxia
  • Chemical Physics