Toxicity of lead acetate to female rabbits after chronic subcutaneous administration. 1. Biochemical and clinical effects
- 1 October 1990
- journal article
- research article
- Published by Springer Nature in Archives of Toxicology
- Vol. 64 (7) , 522-529
- https://doi.org/10.1007/bf01971830
Abstract
The effect of chronic subcutaneous administration of lead acetate was studied in female rabbits. The low-dose group (15 animals) received three times a week 0.10–0.20 μg/kg body weight and the high-dose group (15 animals) 0.80–1.20 μg/kg. The control group received the vehicle only. Concentrations of lead in blood in the low-dose group increased to ca. 400 μg/l after 70 days and in the high-dose group to ca. 900 μg/l after 110 days. After 7.5 months eight animals of each group were sacrificed. The remaining rabbits were kept for an additional 4 months without treatment. Blood lead concentrations decreased with a half-time of 60–70 days. During exposure the gain in body weight was lower in the high-dose group than in the control group and the low-dose group. The high-dose group developed slight anaemia and low MCV, MCH and MCHC, and basophilic stippling of erythrocytes. These effects disappeared during recovery. ALAD activity in erythrocytes was very low during exposure in both exposed groups and did not reach control values during recovery. During exposure the concentrations of ZPP and ALA-U increased, but only ALA-U returned to normal during recovery. No other effects of lead on the composition of the urine were observed. No effects were observed on plasma urea and creatinine concentrations. In the highdose group the concentration of ALAD in the liver decreased by 30%. During recovery this effect was no longer present. No effects were seen in cytochrome P-450 content or cytochrome P-450-dependent enzyme activities. Lead was mainly stored in bones, but some also in serveral soft tissues. After recovery the concentrations in soft tissues decreased to a variable degree. In the high-dose group the relative weights of heart and liver increased. These effects disappeared during recovery. At 400 μg lead/l blood no adverse effects were observed that did occur at the high dose level.Keywords
This publication has 21 references indexed in Scilit:
- Cellular adaptation in metal toxicology and metallothioneinToxicology, 1983
- Tissue distribution of lead in rat pups nourished by lead‐poisoned mothersJournal of Toxicology and Environmental Health, 1982
- Ultrastructural changes in the kidneys of rabbits treated with lead acetateArchives of Toxicology, 1981
- LeadPublished by Elsevier ,1981
- Amino acid analysis of physiological fluids by a single-column programme based on stepwise elution with lithium citrateJournal of Chromatography A, 1977
- Second international workshop permissible levels for occupational exposure to inorganic leadInternationales Archiv für Arbeitsmedizin, 1977
- Automated assay of N-acetyl-β-GLucosaminidase in normal and pathological human urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1975
- The Use of Animal Models for Comparative Studies of Lead PoisoningClinical Toxicology, 1973
- Determination of drug metabolizing enzymes in needle biopsies of human liverEuropean Journal of Clinical Pharmacology, 1972
- Urinary Delta-Aminolevulinic Acid (ALA) Levels in Lead PoisoningArchives of environmental health, 1967