Lead inhibition of the zinc metalloenzyme delta-aminolevulinate dehydratase (ALAD) is one of the most sensitive indicators of blood lead levels.
ALAD is polymorphic, with about 20% of Caucasians expressing the rarer ALAD2 allele.
Previous studies indicated that this polymorphism may be a genetic factor in lead transport, metabolism, and/or distribution.
Whole blood lead, serum lead, and ALAD genotype were determined for 381 lead smelter workers, including 70 workers expressing the ALAD2 allele, whose blood lead elevations were observed for more than 20 years of employment.
The same employees demonstrated higher serum lead levels.
Using a cumulative blood lead index (CBLI) for each worker, based on individual blood lead histories, and in vivo X-ray fluorescence measurements of bone lead to estimate total lead body burden, the slopes of linear relations of bone lead to CBLI were greater for workers homoallelic for ALAD1, indicating more efficient uptake of lead from blood into bone.
This effect was most significant in calcaneus bone and for workers hired since 1977 [ALAD1.1 : 0.0528±0.0028 and ALAD1-2 or 2-2 : 0.0355±0.0031 (P Thus the ALAD genotype affected lead metabolism and potentially modified lead delivery to target organs including the brain ; however, the ALAD genotype did not significantly affect the net accumulation of lead in bone.
Thus the ALAD genotype affected lead metabolism and potentially modified lead delivery to target organs including the brain ; however, the ALAD genotype did not significantly affect the net accumulation of lead in bone.
Mots-clés Pascal : Plomb, Métal lourd, Exposition professionnelle, Médecine travail, Homme, Soudage, Industrie métallurgique, Polymorphisme, Génétique, Activité enzymatique, Porphobilinogen synthase, Hydro-lyases, Carbon-oxygen lyases, Lyases, Enzyme, Taux, Toxicocinétique, Pharmacocinétique, Génotype, Accumulation, Os, Sang
Mots-clés Pascal anglais : Lead, Heavy metal, Occupational exposure, Occupational medicine, Human, Welding, Metallurgical industry, Polymorphism, Genetics, Enzymatic activity, Porphobilinogen synthase, Hydro-lyases, Carbon-oxygen lyases, Lyases, Enzyme, Rate, Toxicokinetics, Pharmacokinetics, Genotype, Accumulation, Bone, Blood
Notice produite par :
Inist-CNRS - Institut de l'Information Scientifique et Technique
Cote : 98-0316376
Code Inist : 002B03L05. Création : 27/11/1998.