Total parenteral nutrition in ex vivo lung perfusion: Addressing metabolism improves both inflammation and oxygenation

Am J Transplant. 2019 Dec;19(12):3390-3397. doi: 10.1111/ajt.15572. Epub 2019 Sep 11.

Abstract

Ex vivo lung perfusion (EVLP) protocols generally limit metabolic supplementation to insulin and glucose. We sought to determine whether the addition of total parenteral nutrition (TPN) would improve lung function in EVLP. Ten porcine lungs were perfused using EVLP for 24 hours and supplemented with insulin and glucose. In the treatment group (n = 5), the perfusate was also supplemented with a continuous infusion of TPN containing lipids, amino acids, essential vitamins, and cofactors. Physiologic parameters and perfusate electrolytes were continuously evaluated. Perfusate lactate, lipid and branch chain amino acid (BCAA) concentrations were also analyzed to elucidate how substrates were being utilized over time. Lungs in the TPN group exhibited significantly better oxygenation. Perfusate sodium was more stable in the TPN group. In the control group, free fatty acids (FFA) were quickly depleted, reaching negligible levels early in the perfusion. Alternatively, BCAA in the control group rose continually over the perfusion demonstrating a shift toward proteolysis for energy substrate. In the TPN group, both FFA and BCAA concentrations remained stable at in vivo levels after initial stabilization. TNF-α concentrations were lower in the TPN group. The addition of TPN in EVLP allows for better electrolyte composition, decreased inflammation, and improved graft performance.

Keywords: lung transplantation/pulmonology; metabolism/metabolite; organ perfusion and preservation; organ procurement and allocation; translational research/science.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Extracorporeal Circulation / methods*
  • Female
  • Inflammation / metabolism
  • Inflammation / prevention & control*
  • Lung Transplantation / methods*
  • Organ Preservation / methods*
  • Organ Preservation Solutions / pharmacology*
  • Oxygen / metabolism
  • Parenteral Nutrition, Total / methods*
  • Perfusion / methods*
  • Swine

Substances

  • Organ Preservation Solutions
  • Oxygen