We have previously shown that the immature tubule is tolerant of prolo
nged anoxia. In addition, cellular ATP is maintained at 2-fold higher
levels during anoxia in the immature tubules compared with the mature
tubules. The purpose of this study was: 1) to determine whether anaero
bic glycolysis contributes to the tolerance to anoxia and preservation
of cellular ATP in immature tubules and 2) to evaluate whether the to
lerance demonstrated by immature tubules is dependent on preservation
of cellular ATP. Suspensions of proximal tubules from immature (8-10 d
) and mature (8-10 wk) rats were subjected to 15 and 45 min of anoxia
in a standard buffer and in buffers designed to inhibit glycolysis. La
ctate dehydrogenase release was used to assess plasma membrane damage,
ATP levels were determined as an index of cellular energy and total l
actate production was measured to evaluate glycolytic activity. After
45 min of anoxia, total lactate production was less in immature tubule
s (101 +/- 48 mu g of lactate/mg of DNA) compared with mature tubules
(148 +/- 36 mu g of lactate/mg of DNA). After inhibition of glycolytic
metabolism, ATP decreased to similar levels in both immature and matu
re tubules. However, immature tubules remained resistant to anoxic dam
age (lactate dehydrogenase: mature tubules 38 +/- 4%, immature tubules
29 +/- 1.0%). Therefore, enhanced glycolytic activity does not play a
dominant role in the tolerance of the developing kidney to anoxia, an
d this tolerance is not primarily dependent on preservation of cellula
r ATP.