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Acute lead exposure induces renal haeme oxygenase-1 and decreases urinary Na excretionDepartment of Molecular Biomedicine, Centro de Investigació n y de Estudios Avanzados del IPN, Avenida Instituto Politécnico Nacional 2508, México, D.F., CP 07300, México; bescalan{at}mail.cinvestav.mx; Escuela Superior de Medicina Instituto Politécnico Nacional México D.F., México
Escuela Superior de Medicina Instituto Politécnico Nacional México D.F., México
Department of Pharmacology, Centro de Investigación y de Estudios Avanzados del IPN, México
Department of Molecular Biomedicine, Centro de Investigación y de Estudios Avanzados del IPN. México The effects of acute lead exposure on renal function, lipid peroxidation and the expression of haeme oxygenase (HO) in rat kidney were determined. A single injection of lead acetate (50 mg Pb/kg) was given to rats. Changes in renal function, characterized by a significant reduction in the Na excretion was observed six hours after Pb exposure; this effect persisted for 24 hours. TBARS levels increased in kidney cortex 24 hours after Pb administration. In kidney cortex, Pb exposure affected the expression of HO-1, a renal protein associated with oxidative stress. HO-1 mRNA increased 2.3-fold, three hours after Pb administration and remained increased for six, 12 and 24 hours. HO enzymatic activity and HO-1 protein increased six and three hours after Pb administration, respectively, and remained increased at 24 hours. HO inhibition by tin-protoporphyrin, potentiated Pb-induced increase in TBARS and prevented the Pb-induced reduction in Na excretion. Our data suggest that Pb may be acting through the generation of oxidant products and induction of HO.
Key Words: haeme oxygenase-1 lead acetate lipid peroxidation
Human & Experimental Toxicology, Vol. 22, No. 5,
237-244 (2003) This article has been cited by other articles:
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