Reproductive toxicity of di-n-butylphthalate in a continuous breeding protocol in Sprague-Dawley rats
- PMID: 9074889
- PMCID: PMC1469857
- DOI: 10.1289/ehp.97105102
Reproductive toxicity of di-n-butylphthalate in a continuous breeding protocol in Sprague-Dawley rats
Abstract
The phthalate ester di-n-butylphthalate (DBP) is used extensively in the manufacture of plastics; its reproductive toxicity was tested in rats by the National Toxicology Program's Reproductive Assessment by Continuous Breeding protocol. Levels of 0.1, 0.5, and 1.0% DBP in the diet were selected, and this dosing design yielded average daily DBP intakes of 52, 256, and 509 mg/kg for males and 80, 385, and 794 mg/kg for females, respectively. DBP consumption by F0 rats reduced the total number of live pups per litter in all treated groups by 8-17% and live pup weights in the 0.5% and 1.0% dose groups by < 13%. In tests to determine the affected sex, the number of offspring was unchanged, but the weights of pups from treated females were significantly decreased and offspring from treated males were unchanged. At necropsy, high-dose F0 females had a 14% reduction in body weight, and both sexes had approximately 10-15% increased kidney and liver to body weight ratios compared to controls. Sperm parameters and estrous cyclicity were not affected. In the F1 mating trial, indices of mating, pregnancy, and fertility in the 1.0% dose group were all sharply decreased (one live litter was delivered out of 20 cohabited pairs), concomitant with a 13% decrease in dam body weight. Live F2 pup weights were 6-8% lower in all dose groups. F1 necropsy results revealed that epididymal sperm counts and testicular spermatid head counts were significantly decreased in the 1.0% dose group. Histopathologic investigation showed that 8 of 10 F1 males consuming 1.0% DBP had degenerated seminiferous tubules and 5 of 10 had underdeveloped or otherwise defective epididymides. No ovarian or uterine lesions were observed. In conclusion, this study showed that DBP is a reproductive/developmental toxicant in Sprague-Dawley rats exposed both as adults and during development; it also indicates that the adverse reproductive/developmental effects of DBP on the second generation were greater than on the first generation.
Similar articles
-
NTP technical report on the toxicity studies of Dibutyl Phthalate (CAS No. 84-74-2) Administered in Feed to F344/N Rats and B6C3F1 Mice.Toxic Rep Ser. 1995 Apr;30:1-G5. Toxic Rep Ser. 1995. PMID: 12209194
-
Reproductive and developmental toxicity in F1 Sprague-Dawley male rats exposed to di-n-butyl phthalate in utero and during lactation and determination of its NOAEL.Reprod Toxicol. 2004 Jul;18(5):669-76. doi: 10.1016/j.reprotox.2004.04.009. Reprod Toxicol. 2004. PMID: 15219629
-
Assessment of the reproductive toxicity of a complex mixture of 25 groundwater contaminants in mice and rats.Fundam Appl Toxicol. 1995 Apr;25(1):9-19. doi: 10.1006/faat.1995.1035. Fundam Appl Toxicol. 1995. PMID: 7601330
-
Toxicology and carcinogenesis studies of milk thistle extract (CAS No. 84604-20-6) in F344/N rats and B6C3F1 mice (Feed Studies).Natl Toxicol Program Tech Rep Ser. 2011 May;(565):1-177. Natl Toxicol Program Tech Rep Ser. 2011. PMID: 21685957 Review.
-
Effects of di-n-butyl phthalate (DBP) on male reproductive development in the rat: implications for human risk assessment.Food Chem Toxicol. 2000;38(1 Suppl):S97-9. doi: 10.1016/s0278-6915(99)00128-3. Food Chem Toxicol. 2000. PMID: 10717378 Review.
Cited by
-
Phthalates in food and medical devices.J Med Toxicol. 2006 Sep;2(3):126-35. doi: 10.1007/BF03161027. J Med Toxicol. 2006. PMID: 18077888 Free PMC article.
-
Tissue-specific changes in Srebf1 and Srebf2 expression and DNA methylation with perinatal phthalate exposure.Environ Epigenet. 2019 Jun 20;5(2):dvz009. doi: 10.1093/eep/dvz009. eCollection 2019 Apr. Environ Epigenet. 2019. PMID: 31240115 Free PMC article.
-
In utero exposure to simvastatin reduces postnatal survival and permanently alters reproductive tract development in the Crl:CD(SD) male rat.Toxicol Appl Pharmacol. 2019 Feb 15;365:112-123. doi: 10.1016/j.taap.2019.01.001. Epub 2019 Jan 11. Toxicol Appl Pharmacol. 2019. PMID: 30639414 Free PMC article.
-
Fungal biodegradation of dibutyl phthalate and toxicity of its breakdown products on the basis of fungal and bacterial growth.World J Microbiol Biotechnol. 2014 Nov;30(11):2811-9. doi: 10.1007/s11274-014-1705-1. Epub 2014 Jul 26. World J Microbiol Biotechnol. 2014. PMID: 25063688
-
Dose Addition Models Based on Biologically Relevant Reductions in Fetal Testosterone Accurately Predict Postnatal Reproductive Tract Alterations by a Phthalate Mixture in Rats.Toxicol Sci. 2015 Dec;148(2):488-502. doi: 10.1093/toxsci/kfv196. Epub 2015 Sep 8. Toxicol Sci. 2015. PMID: 26350170 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous