Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the lactating rat on maternal and neonatal vitamin A status
- PMID: 3572570
- DOI: 10.1093/jn/117.3.580
Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the lactating rat on maternal and neonatal vitamin A status
Abstract
Female Sprague-Dawley rats were given a single oral dose of 10 micrograms TCDD/kg body wt after delivery. Pups were killed on postnatal day (PND) 0, 2, 4, 8, or 16. Dams and remaining weanlings were killed on PND 22 and 32, respectively. Thymus weight was lower in dams exposed to TCDD than in controls, whereas no differences in body weight or relative liver weight were found. The total amount and the concentration of vitamin A were lower in the liver but higher in the kidneys and in serum of TCDD-treated dams than in controls. TCDD-exposed weanlings showed lower weight gain, liver enlargement and thymus atrophy compared to controls. Growth reduction became more pronounced with time, liver enlargement was at its peak on PND 8 and thymus atrophy was most pronounced on PND 16, although all three effects persisted throughout the study. The total amount of vitamin A increased at a similar rate in control and TCDD-exposed weanlings throughout lactation. When the young started to eat pelleted diet there was a pronounced increase in hepatic vitamin A content. Between PND 16 and 32 controls increased their hepatic vitamin A content 21-fold, compared to 12-fold in TCDD-exposed offspring. The hepatic stores of TCDD-treated animals reached 45% of the stores of control pups on PND 32. From PND 8 renal vitamin A was significantly higher in the TCDD-exposed young than in the controls. At PND 32 TCDD-exposed weanlings had six times more renal vitamin A than controls.
Similar articles
-
Hydronephrosis in mice exposed to TCDD-contaminated breast milk: identification of the peak period of sensitivity and assessment of potential recovery.Toxicol Appl Pharmacol. 1991 Mar 1;107(3):413-28. doi: 10.1016/0041-008x(91)90305-x. Toxicol Appl Pharmacol. 1991. PMID: 2000632
-
The effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on the uptake, distribution and excretion of a single oral dose of [11,12-3H]retinyl acetate and on the vitamin A status in the rat.J Nutr. 1985 Jun;115(6):759-71. doi: 10.1093/jn/115.6.759. J Nutr. 1985. PMID: 3998869
-
Reproductive toxicity and tissue concentrations of low doses of 2,3,7,8-tetrachlorodibenzo-p-dioxin in male offspring rats exposed throughout pregnancy and lactation.Toxicol Appl Pharmacol. 1998 Jun;150(2):383-92. doi: 10.1006/taap.1998.8433. Toxicol Appl Pharmacol. 1998. PMID: 9653070
-
Effects of TCDD on vitamin A status and liver microsomal enzyme activities in a TCDD-susceptible and a TCDD-resistant rat strain.Food Chem Toxicol. 1990 Mar;28(3):197-203. doi: 10.1016/0278-6915(90)90007-a. Food Chem Toxicol. 1990. PMID: 2111793
-
2,3,7,8-tetrachlorodibenzo-p-dioxin increases serum and kidney retinoic acid levels and kidney retinol esterification in the rat.Toxicol Appl Pharmacol. 2000 Dec 1;169(2):121-31. doi: 10.1006/taap.2000.9059. Toxicol Appl Pharmacol. 2000. PMID: 11097864
Cited by
-
2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) enhances placental inflammation.J Reprod Immunol. 2013 Jun;98(1-2):10-20. doi: 10.1016/j.jri.2013.02.005. Epub 2013 May 1. J Reprod Immunol. 2013. PMID: 23642494 Free PMC article.
-
Retinoid-xenobiotic interactions: the Ying and the Yang.Hepatobiliary Surg Nutr. 2015 Aug;4(4):243-67. doi: 10.3978/j.issn.2304-3881.2015.05.05. Hepatobiliary Surg Nutr. 2015. PMID: 26311625 Free PMC article. Review.
-
Immunotoxic effects of exposure of rats to xenobiotics via maternal lactation. Part I 2,3,7,8-tetrachlorodibenzo-p-dioxin.Int J Exp Pathol. 1995 Dec;76(6):425-39. Int J Exp Pathol. 1995. PMID: 8652363 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical