T. Hauet et al., Protective effect of polyethylene glycol against prolonged cold ischemia and reperfusion injury: Study in the isolated perfused rat kidney, J PHARM EXP, 297(3), 2001, pp. 946-952
Citations number
36
Categorie Soggetti
Pharmacology & Toxicology
Journal title
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
The purpose of this study was to evaluate an intracellular solution with po
lyethylene 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 st
udied: 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 i
ntracellular (IC) solution, one with PEG (ICPEG, n = 16) and one without PE
G (IC, n = 16). The perfusion flow rate was significantly greater in the PE
G group and correlated with less significant cellular and interstitial edem
a and lower renal vascular resistance than in the IC, EC, and UW groups. Gl
omerular filtration rate was significantly higher in the PEG group during r
eperfusion than in the IC, EC, and UW groups. Proximal tubular functions we
re more efficient with PEG: fractional sodium reabsorption and total sodium
reabsorption were significantly greater during reperfusion in the PEG grou
p than in the IC, EC, and UW groups. Of greater interest is the protective
effect of PEG on lipid peroxidation, which reflects ischemia/reperfusion da
mage. The second major effect is the dramatic ATP restoration during reperf
usion, which outlines the preservation of oxidative phosphorylation after p
reservation by ICPEG. These results are supported by histological studies,
particularly concerning brush border and mitochondrial preservation. Our re
sults indicate that PEG is promising for cold ischemia and reperfusion inju
ry protection.