Abstract:
:Untreated and Aroclor 1254-pretreated male Wistar rats were given a single dose of 1.0 mg/kg body weight of randomly tritium-labelled 2-amino-1-methyl-6-phenylimidazo[4,5-b] pyridine (3H-PhIP) by oral intubation. Urine and faeces were collected at 24, 48 and 72 hours after dosing, and total radioactivity determined. At 2, 4, 6, 16, 26, 48 and 72 h, animals were killed and several organs, including liver, bladder, lungs, kidney, stomach, large and small intestines, heart, thigh muscles, spleen and blood were collected for DNA extraction and for determination of total radioactivity. Highest total radioactivity at 2 h was not unexpectedly observed in the stomach, small intestines and bladder, whereas radiolabels corresponding to approximately 2.5 nmol PhIP/g of kidney and liver showed the highest levels observed at 24 h. Several tissues, including blood, plasma, liver and muscles had a slightly bimodal time-distribution of radioactivity showing a second peak at 16-24 h. At 72 h after a single dose of PhIP, highest radioactivity was observed in the liver and the large intestine (0.4 nmol PhIP/g tissue), whereas most other organs, irrespective of pretreatment had levels at approximately 0.2 nmol/g of tissue. At earlier time points, Aroclor 1254-treated rats had lower amounts of radiolabel in all tissues. Radioactivity bound to DNA was determined by high sensitivity scintillation counting. In contrast to total radioactivity, DNA-associated radioactivity was generally higher in the Aroclor 1254-treated rats, most notably in the heart, but levels had decreased to approximately the same level in controls and in Aroclor 1254-treated rats at 72 h. DNA-binding was highest at 2-6 h after dosing, highest in the heart of Aroclor 1254-treated animals at 6 h (120 adducts/10(8) bases) followed by thigh muscle at 4-6 h (approximately 50 adducts/10(8) bases, irrespective of pretreatment). Levels were approximately 1.5-3 times lower in other organs at 2-6 h after dosing. At 72 h, radioactivity associated with DNA was again highest in the heart of Aroclor 1254-treated rats (20 adducts/10(8) bases) and 5-10 times lower in most other organs, approaching the detection limit. Total DNA was extracted from the livers of PhIP dosed rats at 4 ad 72 h. DNA was hydrolysed, affinity-concentrated, and analysed by liquid chromatography. A radiolabelled peak had identical retention time and UV-spectral characteristics as peaks isolated by affinity chromatography and HPLC of acid-hydrolysed synthetic PhIP-DNA and PhIP-deoxyguanosine adduct.(ABSTRACT TRUNCATED AT 400 WORDS)
journal_name
Carcinogenesisjournal_title
Carcinogenesisauthors
Dragsted LO,Frandsen H,Reistad R,Alexander J,Larsen JCdoi
10.1093/carcin/16.11.2785subject
Has Abstractpub_date
1995-11-01 00:00:00pages
2785-93issue
11eissn
0143-3334issn
1460-2180journal_volume
16pub_type
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