Literature DB >> 15261730

Acute and subchronic oral toxicity of fluoranthene in F-344 rats.

Maurice E Knuckles1, Frank Inyang, Aramandla Ramesh.   

Abstract

We have studied the acute and subchronic oral toxicity of fluoranthene (FLA) in male and female F-344 rats. Single acute FLA doses of 0, 1000, 2000, and 3000 mg/kg body weight (BW) dissolved in peanut oil were administered daily by oral gavage. Subchronic doses of 0, 150, 750, and 1500 mg FLA/kg BW/day were administered for 90 days in the rats' diet. The toxicological endpoints examined included rat body and organ weights, as well as histopathological examinations of liver, kidney, stomach, prostate, testes, and ovaries; hematological parameters including red blood cell (RBC) counts, white blood cell (WBC) counts, hemoglobin (Hgb) concentration, hematocrit (Hct) concentration, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC); blood chemistry including alanine amino transferase (ALT), aspartate amino transferase (AST), blood urea nitrogen (BUN); and urine chemistry including glucose, bilirubin, specific gravity, pH, protein, urobilinogen, nitrite, occult blood, and leukocytes. In acute toxicity studies, WBC counts were significantly decreased and MCHC was significantly increased in both males and females at all doses. In the subchronic study, several of the blood cell parameters were significantly decreased in males and females after 90 days; RBCs (< or = 10877;12%), WBCs (< or = 10877;40%), Hct (< or = 10877;9%), and Hgb (< or = 10877;12%). Only BUN in males was significantly increased in the high-dose group (1500 mg FLA/kg BW/day) at the 90-day time point. None of the other clinical chemistry parameters were affected. The histopathological examinations showed significant abnormalities (tubular casts) only in the male kidney at the two highest doses after 90 days. We propose a subchronic oral no-observed-adverse-effect level (NOAEL) of 150 mg/kg BW/day for FLA in rats, based on the hematological and renal changes. Overall, our findings indicate that FLA affects specific hematological parameters and kidneys, and has a greater effect on males than females. Copyright 2003 Elsevier Inc.

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Year:  2004        PMID: 15261730     DOI: 10.1016/S0147-6513(03)00110-6

Source DB:  PubMed          Journal:  Ecotoxicol Environ Saf        ISSN: 0147-6513            Impact factor:   6.291


  5 in total

1.  Tumor microsomal metabolism of the food toxicant, benzo(a)pyrene, in ApcMin mouse model of colon cancer.

Authors:  Deacqunita L Diggs; Kelly L Harris; Perumalla V Rekhadevi; Aramandla Ramesh
Journal:  Tumour Biol       Date:  2012-03-20

2.  Effect of benzo(a)pyrene exposure on fluoranthene metabolism by mouse adipose tissue microsomes.

Authors:  Ashley C Huderson; Deacqunita L Harris; Mohammad S Niaz; Aramandla Ramesh
Journal:  Toxicol Mech Methods       Date:  2010-02       Impact factor: 2.987

3.  Benzo(a)pyrene modulates fluoranthene-induced cellular responses in HT-29 colon cells in a dual exposure system.

Authors:  Kelly L Harris; Jeremy N Myers; Aramandla Ramesh
Journal:  Environ Toxicol Pharmacol       Date:  2013-05-10       Impact factor: 4.860

4.  Acute and subchronic toxicological evaluation of Stachys lavandulifolia aqueous extract in Wistar rats.

Authors:  M Modarresi; L Hosseinzadeh; N Nematy; Z M Siavash-Haghighi; K Ghanbari
Journal:  Res Pharm Sci       Date:  2014 May-Jun

5.  Vehicle-dependent disposition kinetics of fluoranthene in Fisher-344 rats.

Authors:  Deacqunita L Harris; Darry B Hood; Aramandla Ramesh
Journal:  Int J Environ Res Public Health       Date:  2008-03       Impact factor: 3.390

  5 in total

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