Sub-Chronic Exposure to Methylmercury at Low Levels Decreases Butyrylcholinesterase Activity in Rats


Autoria(s): VALENTINI, Juliana; VICENTINI, Juliana; GROTTO, Denise; TONELLO, Raquel; GARCIA, Solange C.; BARBOSA JR., Fernando
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

In this study, we examined the effects of low levels and sub-chronic exposure to methylmercury (MeHg) on butyrylcholinesterase (BuChE) activity in rats. Moreover, we examined the relationship between BuChE activity and oxidative stress biomarkers [delta-aminolevulinic acid dehydratase (delta-ALA-D) and malondialdehyde levels (MDA)] in the same animals. Rats were separated into three groups (eight animals per group): (Group I) received water by gavage; (Group II) received MeHg (30 mu g/kg/day) by gavage; (Group III) received MeHg (100 mu g/kg/day). The time of exposure was 90 days. BuChE and ALA-D activities were measured in serum and blood, respectively; whereas MDA levels were measured in plasma. We found BuChE and ALA-D activities decreased in groups II and III compared to the control group. Moreover, we found an interesting negative correlation between plasmatic BuChE activity and MDA (r = -0.85; p < 0.01) and a positive correlation between plasmatic BuChE activity and ALA-D activities (r = 0.78; p < 0.01), thus suggesting a possible relationship between oxidative damage promoted by MeHg exposure and the decrease of BuChE activity. In conclusion, long-term exposure to low doses of MeHg decreases plasmatic BuChE activity. Moreover, the decrease in the enzyme is strongly correlated with the oxidative stress promoted by the metal exposure. This preliminary finding highlights a possible mechanism for MeHg to reduce BuChE activity in plasma. Additionally, this enzyme could be an auxiliary biomarker on the evaluation of MeHg exposure.

Sao Paulo State Foundation for Scientific Research (FAPESP, Brazil)

Brazilian National Council for Scientific and Technologic Development (CNPq)

International Development Research Centre (IDRC)

Identificador

BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, v.106, n.2, p.95-99, 2010

1742-7835

http://producao.usp.br/handle/BDPI/20213

10.1111/j.1742-7843.2009.00475.x

http://dx.doi.org/10.1111/j.1742-7843.2009.00475.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL PUBLISHING, INC

Relação

Basic & Clinical Pharmacology & Toxicology

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL PUBLISHING, INC

Palavras-Chave #DELTA-AMINOLEVULINIC-ACID #OXIDATIVE STRESS #HOPLIAS-MALABARICUS #METHYL MERCURY #ACETYLCHOLINESTERASE ACTIVITY #MYOCARDIAL-INFARCTION #INORGANIC MERCURY #INHIBITION #RISK #HOMOCYSTEINE #Pharmacology & Pharmacy #Toxicology
Tipo

article

original article

publishedVersion