Biochemical changes in the kidneys after perinatal intoxication with lead and/or cadmium and their antagonistic effects when coadministered

被引:30
作者
Garcia, TA [1 ]
Corredor, L [1 ]
机构
[1] Univ Complutense, Dept Anim Biol 2, Fac Biol, E-28040 Madrid, Spain
关键词
lead; cadmium; alkaline phosphatase; acid phosphatase; Na (+) /K (+) ATPase; nephrotoxicity;
D O I
10.1016/S0147-6513(03)00063-0
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Lead acetate (300 mg/L) and/or cadmium acetate (10 mg/L) were administered as drinking water to pregnant Wistar rats from day 1 of pregnancy to parturition (day 0) or until weaning (day 21) to investigate the possible nephrotoxic effects of these metals. We also studied the possibility of toxicological interactions between both metals. Kidneys were used to determine the activity of several enzymes considered key to correct renal function: alkaline and acid phosphatases, Mg2+/Ca2+-dependent ATPase, and Na+/K+ dependent ATPase. The results showed a general decrease in the activity of these enzymes after treatment with the heavy metals; this fact suggests that lead and cadmium are able to impair renal function due to biochemical alterations, since ATPases are essential for reabsorption and secretion processes and phosphatases are involved in the differentation of the proximal tubules. On the other hand, simultaneous perinatal administration of both metals seems to protect against the toxicity produced by cadmium or lead separately. It is not clear whether this is due to decreased absorption or increased sequestration or excretion. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:184 / 189
页数:6
相关论文
共 28 条
[1]   Cadmium binding and sodium-dependent solute transport in renal brush-border membrane vesicles [J].
Ahn, DW ;
Kim, YM ;
Kim, KR ;
Park, YS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1999, 154 (03) :212-218
[2]   Occupational lead exposure and amino acid profiles and liver function tests in industrial workers [J].
Al-Neamy, FRM ;
Almehdi, AM ;
Alwash, R ;
Pasha, MAH ;
Ibrahim, A ;
Bener, A .
INTERNATIONAL JOURNAL OF ENVIRONMENTAL HEALTH RESEARCH, 2001, 11 (02) :181-188
[4]   Time course of chronic oral cadmium nephrotoxicity in Wistar rats: Excretion of urinary enzymes [J].
Bombard, EM ;
Maruhn, D ;
Rinke, M .
DRUG AND CHEMICAL TOXICOLOGY, 1999, 22 (04) :679-703
[5]   Inhibition of ATPase activity in rat synaptic plasma membranes by simultaneous exposure to metals [J].
Carfagna, MA ;
Ponsler, GD ;
Muhoberac, BB .
CHEMICO-BIOLOGICAL INTERACTIONS, 1996, 100 (01) :53-65
[6]   Gestational and lactational lead intoxication produces alterations in the hepatic system of rat pups [J].
Corpas, I ;
Benito, MJ ;
Marquina, D ;
Castillo, M ;
Lopez, N ;
Antonio, T .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2002, 51 (01) :35-43
[7]   Biomarkers assessment in juvenile Cyprinus carpio exposed to waterborne cadmium [J].
de la Torre, FR ;
Salibián, A ;
Ferrari, L .
ENVIRONMENTAL POLLUTION, 2000, 109 (02) :277-282
[8]  
DEGUEVARA JL, 1995, TOXICOLOGIA MED CLIN
[9]   HUMAN FETAL LEAD-EXPOSURE - INTRAUTERINE GROWTH, MATURATION, AND POSTNATAL NEUROBEHAVIORAL DEVELOPMENT [J].
DIETRICH, KN .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1991, 16 (01) :17-19
[10]  
GUPTA A, 1993, B ENVIRON CONTAM TOX, V51, P12