EVALUATION OF METHODS INDICATING HIGHER SUSCEPTIBILITY OF IMMATURE RATS TO RENAL ISCHEMIA

Citation
C. Fleck et al., EVALUATION OF METHODS INDICATING HIGHER SUSCEPTIBILITY OF IMMATURE RATS TO RENAL ISCHEMIA, Experimental and toxicologic pathology, 45(2-3), 1993, pp. 155-160
Citations number
29
Categorie Soggetti
Pathology,Toxicology
ISSN journal
09402993
Volume
45
Issue
2-3
Year of publication
1993
Pages
155 - 160
Database
ISI
SICI code
0940-2993(1993)45:2-3<155:EOMIHS>2.0.ZU;2-A
Abstract
After 45-min bilateral warm renal ischemia lethality amounted to 45 % and 82 % in 55- and 20-day-old rats, respectively (n = 176). Lethality rates were not significantly different after 20-min unilateral ischem ia followed by contralateral nephrectomy after 24 hours (34 vs. 48 % i n young vs. adult rats; n = 168). The latter experimental approach was used to characterize age dependent differences in the susceptibility to ischemia. The degree of postischemic renal damage was the highest a t the 1st and 2nd days after ischemia; at this time, lethality rates w ere similar in young and adult rats. However, urea concentration in se rum was significantly more enhanced in young animals whereas that of c reatinine was increased to the same extent in both age groups. The inc rease in protein excretion into urine was similar in young and adult r ats, too. Furthermore, urine flow rates and GFR were significantly dim inished after ischemia, independent of age. However, excretion of Naand K+ was distinctly more depressed in immature individuals. Finally, the glutathione content in kidney tissue of both age groups was reduc ed and lipid peroxidation was significantly higher after ligation of t he renal arteries. The relative changes were similar in both age group s although the glutathione content was significantly lower in 20-day-o ld control rats. 4-5 days after ischemia, most parameters returned to baseline values. In 55-day-old rats, 45-min ischemia has more severe c onsequences on renal function compared to 20-min ischemia. Obviously l ethality after ischemia is caused by various mechanisms and the pathog enetic importance of a single event can not explain the higher lethali ty in young rats after 45-min bilateral renal ischemia.