Cf. Jacobson et Mg. Miller, 1,3-DINITROBENZENE METABOLISM AND TOXICITY IN SEMINIFEROUS TUBULES ISOLATED FROM RATS OF DIFFERENT AGES, Toxicology, 123(1-2), 1997, pp. 15-26
Previous in vivo studies in rats have shown that susceptibility to 1,3
-dinitrobenzene (DNB)-induced testicular damage increases with age. Th
e present study has used an in vitro approach to investigate the possi
bility that differences in testicular metabolism contribute to the age
-related differences in toxicity. Seminiferous tubules were isolated f
rom Sprague-Dawley rats (30, 75 and 120 days old) and incubated with 1
00 mu M DNB for 22 h. Formation of metabolites and tubular levels of A
TP and glutathione (GSH) were monitored over time. There was no differ
ence in seminiferous tubule metabolic capacity among the three ages of
rats examined. After 22 h of incubation with DNB, ATP levels were 20-
30% of control and GSH levels were 70-90% of control, but neither para
meter showed an age-related difference in decline. Based on these bioc
hemical indicators of cell health, this study would suggest that the l
ack of testicular toxicity in young animals in vivo may be due to the
previously described shorter half-life with consequent reduced exposur
e of the testis to DNB and that the age-related increase in severity o
f lesion between 75 and 120 days of age cannot be explained by differe
nces in tubular metabolism of DNB or whole-animal toxicokinetics. (C)
1997 Elsevier Science Ireland Ltd.