Affiliations: Department of Cardiothoracic Surgery, Isala Clinics, Zwolle, The Netherlands | Heart Lung Center, Utrecht, The Netherlands | CardioNMR Laboratory, University Medical Center, Utrecht, The Netherlands
Note: [] Corresponding author: G.J. Brandon Bravo Bruinsma, MD, PhD, Cardiothoracic Surgeon, Department of Cardiothoracic Surgery, Isala Klinieken, Locatie Weezenlanden, Groot Wezenland 20, 8011 JW Zwolle, The Netherlands. Tel.: +31 38 424 2866/865; Fax: +31 38 424 3163; E‐mail: g.j.bbb@planet.nl.
Abstract: Hemodynamic instability of the brain dead potential heart donor is an exclusion criterion for heart donation for transplantation. Based on the results of myocardial biopsies it has been reported that brain death‐related catecholamine induced damage of the heart causes depletion of high‐energy phosphates which could explain contractile dysfunction. Our group has shown in a series of 31P MRS experiments in cats that neither the onset of brain death, nor the hemodynamic deterioration which follows, nor its treatment with high dosages of dopamine affect the heart energetically as expressed by PCr/ATP ratios. However, after cardioplegic arrest and explantation, an initial and prolonged lower ATP content and an anomalous higher PCr/ATP ratio in the brain death group was found when compared with controls during long‐term unperfused cold storage of the hearts. During subsequent reperfusion of the hearts, ATP and PCr levels in the brain death group were lower than in controls but equal partial recovery of PCr/ATP ratios was observed in both groups. It was concluded that PCr/ATP ratios need to be interpreted with great caution. Secondly, brain death‐related hemodynamic instability is not related to significant changes of myocardial energy metabolism. Thirdly, brain death does affect the myocardial energy metabolism but the impact became apparent only during hypothermic storage and subsequent reperfusion of the donor heart.
Journal: Spectroscopy, vol. 17, no. 2-3, pp. 503-510, 2003
