J. Llamas et al., INCREASE IN THE RENAL DAMAGE-INDUCED BY PARACETAMOL IN RATS EXPOSED TO ETHANOL TRANSLACTATIONALLY, Biology of the neonate, 74(5), 1998, pp. 385-392
Administration of ethanol (8%) or acetone (1%) to nursing dams in the
drinking water, for 10 days, increased the nephrotoxicity of paracetam
ol (APAP) in the 14-day-old lactating offspring. The percentage of pro
ximal tubular cells with evidence of necrotic damage in male rats was
higher in those animals that received APAP (500 mg/kg, i.p.) and whose
nursing rats were exposed to ethanol (25.0 +/- 8.4%) or acetone (17.2
+/- 1.2%), than in the group treated with APAP alone (10.6 +/- 1.6%).
The activity of urinary N-acetylglucuronidase was also significantly
higher in the rats exposed translactationally to ethanol or acetone th
an in animals treated with the APAP alone. Nephrotoxicity showed a sex
ual dimorphic pattern with a higher toxicity in male than in female ra
ts. The percentage of necrotic tubules in the male rats not exposed to
inductor was 10.6 +/- 1.6%, and in female rats 5.0 +/- 1.4% (p < 0.05
). Animals exposed to ethanol or acetone and treated with APAP showed
less weight gain than the group treated only with APAP. Our results su
ggest that renal toxicity is enhanced in the nursing animals that were
exposed, via maternal milk, to ethanol or acetone (inductors of cytoc
hrome P(450)2E1), than in the control animals, This circumstance may b
e relevant in alcoholic women while they are lactating.