T. Stedeford et al., Organ-specific differences in 8-oxoguanosine glycosylase (OGG1) repair following acute treatment with Benzo[a]pyrene., RES COM M P, 109(1-2), 2001, pp. 73-85
Citations number
38
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
RESEARCH COMMUNICATIONS IN MOLECULAR PATHOLOGY AND PHARMACOLOGY
The lung has been shown to be a target organ for the deleterious effects of
Benzo[a]pyrene (B[a]P), regardless of the route of exposure. 8-hydroxy-2'-
deoxyguanosine (oxo(8)dG) is a mutagenic lesion formed in DNA following exp
osure to B[a]P. The objective of this study was to determine the capacity o
f different organs to repair oxo(8)dG following intraperitoneal (i.p.) trea
tment with B[a]P. Male Sprague-Dawley rats were administered 20 mg/kg B[a]P
i.p., 2 times/day for 5 days. A 26% decrease in the capacity to remove oxo
(8)dG was observed in lung tissue at 72 hours and recovered 20% above contr
ol values at 120 hours. The capacity of the liver and kidney remained at ba
seline for all time points analyzed. A 7-fold increase in oxo(8)dG was obse
rved in the lung at 72 hours. This study demonstrates that organ-specific d
ifferences exist in the capacity to remove oxo(8)dG and further demonstrate
s the susceptibility of lung tissue to the effects of B[a]P.