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
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.