Paraoxonase-1 genetic polymorphisms and susceptibility to DNA damage in workers occupationally exposed to organophosphate pesticides

• Published in: Toxicology and applied pharmacology 2011-04, Vol.252 (2), p.130-137
• Main Authors: Singh, Satyender, Kumar, Vivek, Thakur, Sachin, Banerjee, Basu Dev, Rautela, Rajender Singh, Grover, Shyam Sunder, Rawat, Devendra Singh, Pasha, Syed Tazeen, Jain, Sudhir Kumar, Ichhpujani, Rattan Lal, Rai, Arvind
• Format: Article
• Language: English
• Subjects: 60 APPLIED LIFE SCIENCES; Acetylcholinesterase; Adult; Aryldialkylphosphatase - blood; Aryldialkylphosphatase - genetics; Arylesterase; Biological and medical sciences; CONTROL; Cross-Sectional Studies; DETOXIFICATION; DISTRIBUTION; DNA damage; DNA Damage - drug effects; DNA Damage - physiology; DNA DAMAGES; ENZYME ACTIVITY; ENZYMES; GENES; GENOTYPE; HAZARDS; Humans; LIPIDS; LIPOPROTEINS; Male; Medical sciences; Middle Aged; Occupational Exposure - adverse effects; ORGANIC COMPOUNDS; Organophosphate pesticides; Organophosphorus Compounds - blood; Organophosphorus Compounds - toxicity; Paraoxonase; PERSONNEL; PESTICIDES; Pesticides - blood; Pesticides - toxicity; Pesticides, fertilizers and other agrochemicals toxicology; PHENOTYPE; Polymorphism, Genetic - genetics; PON1 polymorphism; PROTEINS; TOXICITY; Toxicology
• ISSN: 0041-008X; 1096-0333
• DOI: 10.1016/j.taap.2011.01.014

Human paraoxonase 1 (PON1) is a lipoprotein-associated enzyme involved in the detoxification of organophosphate pesticides (OPs) by hydrolyzing the bioactive oxons. Polymorphisms of the PON1 gene are responsible for variation in the expression and catalytic activity of PON1 enzyme. In the present study, we have determined (a) the prevalence of two common PON1 polymorphisms, (b) the activity of PON1 and acetylcholinesterase enzymes, and (c) the influence of PON1 genotypes and phenotypes variation on DNA damage in workers exposed to OPs. We examined 230 subjects including 115 workers exposed to OPs and an equal number of normal healthy controls. The results revealed that PON1 activity toward paraoxon (179.19 ± 39.36 vs. 241.52 ± 42.32 nmol/min/ml in controls) and phenylacetate (112.74 ± 17.37 vs. 134.28 ± 25.49 μmol/min/ml in controls) was significantly lower in workers than in control subjects ( p < 0.001). No significant difference was observed in the distribution of genotypes and allelic frequencies of PON1 192QR (Gln/Arg) and PON1 55LM (Leu/Met) in workers and control subjects ( p > 0.05). The PON1 activity toward paraoxonase was found to be significantly higher in the R/R (Arg/Arg) genotypes than Q/R (Gln/Arg) and lowest in Q/Q (Gln/Gln) genotypes in both workers and control subjects ( p < 0.001). For PON1 55LM (Leu/Met), PON1 activity toward paraoxonase was observed to be higher in individuals with L/L (Leu/Leu) genotypes and lowest in individuals with M/M (Met/Met) genotypes in both groups ( p < 0.001). No influence of PON1 genotypes and phenotypes was seen on the activity of acetylcholinesterase and arylesterase. The DNA damage was observed to be significantly higher in workers than in control subjects ( p < 0.05). Further, the individuals who showed least paraoxonase activity i.e., those with (Q/Q [Gln/Gln] and M/M [Met/Met]) genotypes showed significantly higher DNA damage compared to other isoforms in workers exposed to OPs ( p < 0.05). The results indicate that the individuals with PON1 Q/Q and M/M genotypes are more susceptible toward genotoxicity. In conclusion, the study suggests wide variation in enzyme activities and DNA damage due to polymorphisms in PON1 gene, which might have an important role in the identification of individual risk factors in workers occupationally exposed to OPs.