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Vol. 297, Issue 3, 946-952, June 2001
Unité de Transplantation Expérimentale,
Département de Génétique Animale, Institut National
de Recherche Agronomique, Domaine du Magneraud, Surgères (M.C.),
and Faculté de Médecine, Poitiers and Centre Hospitalier et
Universitaire, Poitiers, France (T.H., D.M., J.-M.G., M.E.)
The purpose of this study was to evaluate an intracellular solution
with polyethylene glycol (PEG, molecular weight 20,000) as an
impermeant, compared with University of Wisconsin (UW) and Euro-Collins
(EC) solutions, after a 48-h cold storage (CS). The normothermic
isolated perfused rat kidney (IPK) technique was used to assess renal
function after CS. Five groups were studied: a control group
(immediately reperfused, n = 10); one that received EC (n = 16); one that received UW
(n = 16); and two that each received an
intracellular (IC) solution, one with PEG (ICPEG, n = 16) and one without PEG (IC, n = 16). The
perfusion flow rate was significantly greater in the PEG group and
correlated with less significant cellular and interstitial edema and
lower renal vascular resistance than in the IC, EC, and UW groups.
Glomerular filtration rate was significantly higher in the PEG group
during reperfusion than in the IC, EC, and UW groups. Proximal tubular functions were more efficient with PEG: fractional sodium reabsorption and total sodium reabsorption were significantly greater during reperfusion in the PEG group than in the IC, EC, and UW groups. Of
greater interest is the protective effect of PEG on lipid peroxidation, which reflects ischemia/reperfusion damage. The second major effect is
the dramatic ATP restoration during reperfusion, which outlines the
preservation of oxidative phosphorylation after preservation by ICPEG.
These results are supported by histological studies, particularly
concerning brush border and mitochondrial preservation. Our results
indicate that PEG is promising for cold ischemia and reperfusion injury protection.
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