TY - JOUR
T1 - Testicular toxicity and infertility in male rats treated with 1, 3-dinitrobenzene
AU - Linder, Ralph E.
AU - Hess, Rex A.
AU - Strader, Lillian F.
PY - 1986/12
Y1 - 1986/12
N2 - Weanling male Sprague-Dawley rats were gavaged 5 d/wk with 1, 3-dinitrobenzene (m-DNB) at dosages of 0, 0.75, 1.5, 3.0, and 6.0 mg/kg • d. Males were bred to untreated females during treatment wk 10 and were killed during treatment wk 12. Although males dosed with 3 mg/kg • d inseminated the females and evidence of mating was observed in males dosed with 6 mg/kg • d, none of the males in these groups sired litters. Diminished sperm production (reduced testicular sperm head counts), decreased cauda epididymal sperm reserves, nonmotile spermatozoa, atypical sperm morphology, decreased weights of the testes and epididymides, seminiferous tubular atrophy, and incomplete spermatogenesis were also observed in these groups. Sperm production was also decreased in males dosed with 1.5 mg/kg • d. Changes in the spleen included increased weight at dosages of 1.5 mg/kg • d or higher and splenic hemosiderosis, which ranged from slight in rats treated with 0.75 mg/kg • d to moderately severe in those dosed with 6 mg/kg • d. The data indicate that m-DNB is a potent testicular toxicant in the male rat, capable of producing extensive damage to reproductive tissues and reproductive failure. Limited data on four rats that received 6 mg/kg • d and were allowed a 5-mo posttreatment recovery period suggested that the testicular effects are at least partially reversible.
AB - Weanling male Sprague-Dawley rats were gavaged 5 d/wk with 1, 3-dinitrobenzene (m-DNB) at dosages of 0, 0.75, 1.5, 3.0, and 6.0 mg/kg • d. Males were bred to untreated females during treatment wk 10 and were killed during treatment wk 12. Although males dosed with 3 mg/kg • d inseminated the females and evidence of mating was observed in males dosed with 6 mg/kg • d, none of the males in these groups sired litters. Diminished sperm production (reduced testicular sperm head counts), decreased cauda epididymal sperm reserves, nonmotile spermatozoa, atypical sperm morphology, decreased weights of the testes and epididymides, seminiferous tubular atrophy, and incomplete spermatogenesis were also observed in these groups. Sperm production was also decreased in males dosed with 1.5 mg/kg • d. Changes in the spleen included increased weight at dosages of 1.5 mg/kg • d or higher and splenic hemosiderosis, which ranged from slight in rats treated with 0.75 mg/kg • d to moderately severe in those dosed with 6 mg/kg • d. The data indicate that m-DNB is a potent testicular toxicant in the male rat, capable of producing extensive damage to reproductive tissues and reproductive failure. Limited data on four rats that received 6 mg/kg • d and were allowed a 5-mo posttreatment recovery period suggested that the testicular effects are at least partially reversible.
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U2 - 10.1080/15287398609530946
DO - 10.1080/15287398609530946
M3 - Article
C2 - 3783767
AN - SCOPUS:0022970339
SN - 0098-4108
VL - 19
SP - 477
EP - 489
JO - Journal of Toxicology and Environmental Health
JF - Journal of Toxicology and Environmental Health
IS - 4
ER -