Literature DB >> 3118052

Metabolism and distribution of [14C]glucose in rats treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD).

L W Weber1, H Greim, K K Rozman.   

Abstract

Male Sprague-Dawley rats were given a single, usually lethal, dose of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, 125 micrograms/kg ip in corn oil), or vehicle alone. Twenty-four hours after ip administration of TCDD the animals received an ip injection of 14C-labeled glucose, and the time course and amount of exhalation of 14CO2 were monitored for 8 h continuously and once daily for 20 min for the subsequent 5 d. TCDD treatment reduced the amount of 14CO2 exhaled within 8 h after the injection of [14C]glucose by 33%, as compared to pair-fed controls. Blood levels of radioactivity were affected by TCDD accordingly. No particular organ appeared to act as a sink for the radioactivity not exhaled during these 8 h by the treated animals. TCDD (125 micrograms/kg) induced significant changes in the disposition of radioactivity in heart and brown adipose tissue between 25 and 125 min after the iv injection of [14C]glucose. The areas under the curve of [14C]glucose-derived radioactivity were the same after either iv or ip injection in the blood of TCDD-treated rats, allowing a direct comparison of experiments with iv or ip injection of [14C]glucose. The half-lives of radioactivity in the exhaled air and in feces of treated animals were greatly elevated during the 5 d following administration of [14C]glucose. These results indicate that TCDD induces in rats, within 24 h after dosing, alterations in the metabolism of glucose that preceded changes in insulin homeostasis, because hypoglycemia and hypoinsulinemia in rats do not occur until about a week after TCDD treatment. Since overt signs of acute toxicity (reduced feed intake and body weight loss) are also not noticeable until several days after a lethal dose of TCDD, it is probable that this earlier disturbance of glucose metabolism is part of the biological changes that result in wasting away and eventually in death.

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Year:  1987        PMID: 3118052     DOI: 10.1080/15287398709531063

Source DB:  PubMed          Journal:  J Toxicol Environ Health        ISSN: 0098-4108


  7 in total

1.  Key enzymes of gluconeogenesis are dose-dependently reduced in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-treated rats.

Authors:  L W Weber; M Lebofsky; H Greim; K Rozman
Journal:  Arch Toxicol       Date:  1991       Impact factor: 5.153

2.  Tissue-specific alterations of de novo fatty acid synthesis in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-treated rats.

Authors:  J R Gorski; L W Weber; K Rozman
Journal:  Arch Toxicol       Date:  1988       Impact factor: 5.153

3.  Comparative toxicity of four chlorinated dibenzo-p-dioxins (CDDs) and their mixture. Part II: Structure-activity relationships with inhibition of hepatic phosphoenolpyruvate carboxykinase, pyruvate carboxylase, and gamma-glutamyl transpeptidase activities.

Authors:  L W Weber; M Lebofsky; B U Stahl; A Kettrup; K Rozman
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

4.  Composition of diet modifies toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in cold-adapted rats.

Authors:  G Muzi; J R Gorski; K Rozman
Journal:  Arch Toxicol       Date:  1987       Impact factor: 5.153

5.  Reduced gluconeogenesis in 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-treated rats.

Authors:  J R Gorski; L W Weber; K Rozman
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

Review 6.  Endocrine disrupting chemicals: Friend or foe to brown and beige adipose tissue?

Authors:  Cynthia E Francis; Logan Allee; Helen Nguyen; Rachel D Grindstaff; Colette N Miller; Srujana Rayalam
Journal:  Toxicology       Date:  2021-10-02       Impact factor: 4.571

7.  The mechanism of dioxin toxicity: relationship to risk assessment.

Authors:  L S Birnbaum
Journal:  Environ Health Perspect       Date:  1994-11       Impact factor: 9.031

  7 in total

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