Literature DB >> 10383848

Enhancement of hypothermic heart preservation with fructose 1, 6-diphosphate.

W Niu1, F Zhang, W Ehringer, M Tseng, L Gray, S Chien.   

Abstract

BACKGROUND: We hypothesized that the addition of fructose 1, 6-diphosphate (FDP) to a hypothermic heart preservation solution could improve metabolic recovery because it has several beneficial effects.
MATERIALS AND METHODS: Twenty adult Sprague-Dawley rats were used to study hypothermic heart preservation. The hearts were removed under general anesthesia and preserved at 4 degrees C in Euro-Collins solution (30 ml/kg) for 8 h. In the study group (N = 10), FDP (5 mM) was added to the Euro-Collins solution. In the control group (N = 10), no FDP was added. Heart function was studied after preservation using a working heart model. The ability of various concentrations of fructose 1,6-phosphate to passively diffuse through an egg phosphatidylcholine multilamellar vesicle (MLV) membrane bilayer was examined.
RESULTS: Cardiac output ranged from 17.0 +/- 1.9 to 24.9 +/- 1.6 ml/min in the study group vs 2.0 +/- 1.0-12.3 +/- 1.7 ml/min for controls, average aortic flow was 10. 8 +/- 1.4 ml/min in the study group vs -1.3 +/- 1.6 ml/min for controls, and maximum LV generated power was 22.8 +/- 1.7 J/min vs 10.1 +/- 1.6 J/min for controls. Coronary flow, left ventricular stroke volume and stroke work, and myocardial oxygen consumption were much higher in the study group than in the control group. Coronary vascular resistance was lower in the study group than in the control group. Electron microscopic study indicated that many myocytes displayed patches of swollen mitochondria in the control group, but was rarely observed in the study group. The addition of 50 mM FDP caused substantial changes in MLV permeability. No dose of sucrose buffers outside the vesicles resulted in a significant changes of MLV permeability.
CONCLUSIONS: Our results indicate that the addition of FDP to Euro-Collins solution significantly improves hypothermic rat heart preservation, and FDP appeared to cross the membrane bilayer. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10383848     DOI: 10.1006/jsre.1999.5658

Source DB:  PubMed          Journal:  J Surg Res        ISSN: 0022-4804            Impact factor:   2.192


  5 in total

1.  Characterization of the high-affinity uptake of fructose-1,6-bisphosphate by cardiac myocytes.

Authors:  Thomas J Wheeler; Sufan Chien
Journal:  Mol Cell Biochem       Date:  2012-03-18       Impact factor: 3.396

2.  The uptake and metabolism of fructose-1,6-diphosphate in rat cardiomyocytes.

Authors:  W D Ehringer; B Chiang; S Chien
Journal:  Mol Cell Biochem       Date:  2001-05       Impact factor: 3.396

3.  Destabilizing effects of fructose-1,6-bisphosphate on membrane bilayers.

Authors:  William D Ehringer; Susan Su; Benjamin Chiangb; William Stillwell; Sufan Chien
Journal:  Lipids       Date:  2002-09       Impact factor: 1.880

4.  Permeability of fructose-1,6-bisphosphate in liposomes and cardiac myocytes.

Authors:  Thomas J Wheeler; John M McCurdy; Aaron denDekker; Sufan Chien
Journal:  Mol Cell Biochem       Date:  2004-04       Impact factor: 3.396

5.  Protection of rat cardiac myocytes by fructose-1,6-bisphosphate and 2,3-butanedione.

Authors:  Thomas J Wheeler; Sufan Chien
Journal:  PLoS One       Date:  2012-04-27       Impact factor: 3.240

  5 in total

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