Protective effect of polyethylene glycol against prolonged cold ischemia and reperfusion injury: Study in the isolated perfused rat kidney

Citation
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
ISSN journal
00223565 → ACNP
Volume
297
Issue
3
Year of publication
2001
Pages
946 - 952
Database
ISI
SICI code
0022-3565(200106)297:3<946:PEOPGA>2.0.ZU;2-P
Abstract
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.