Intron 4 polymorphism of the endothelial nitric oxide synthase (eNOS) gene is associated with decreased NO production in a mercury-exposed population


Autoria(s): Marco, Kátia Cristina de; Greggi Antunes, Lusania Maria; Tanus-Santos, Jose Eduardo; Barbosa Jr., Fernando
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

07/08/2013

07/08/2013

2012

Resumo

Nitric oxide (NO), produced by endothelial nitric oxide synthase (eNOS), is a potent vasodilator and plays a prominent role in regulating the cardiovascular system. Decreased basal NO release may predispose to cardiovascular diseases. Evidence suggests that the 27 nt repeat polymorphism of the intron 4 in the eNOS gene may regulate eNOS expression. On the other hand, some recent reports strongly suggest an association between methylmercury (MeHg) exposures and altered NO synthesis. In the present study, we investigate the contribution of the 27-pb tandem repeat polymorphism on nitric oxide production, which could enhance susceptibility to cardiovascular disease in the MeHg-exposed study population. Two-hundred-two participants (98 men and 104 women), all chronically exposed to MeHg through fish consumption were examined. Mean blood Hg concentration and nitrite plasma concentration were 50.5 +/- 35.4 mu g/L and 251.4 +/- 106.3 nM, respectively. Mean systolic and diastolic blood pressure were 120.1 +/- 19.4 mm Hg and 72.0 +/- 10.6 mm Hg, respectively. Mean body mass index was 24.5 +/- 4.3 kg/m(2) and the mean heart rate was 69.8 +/- 11.8 bpm. There were no significant differences in age, arterial blood pressure, body mass index or cardiac frequency between genotype groups (all P>0.05). However, we observed different nitrite concentrations in the genotypes groups, with lower nitrite levels for the 4a4a genotype carriers. Age, gender and the presence of intron 4 polymorphism contributed to nitrite reduction as a result of blood Hg concentration. Taken together, our results show that the 27 nt repeat polymorphism of the intron 4 in the eNOS gene increases susceptibility to cardiovascular diseases after MeHg exposure by modulating nitric oxide levels. (C) 2011 Elsevier B.V. All rights reserved.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Identificador

SCIENCE OF THE TOTAL ENVIRONMENT, AMSTERDAM, v. 414, n. 2, supl. 1, Part 2, pp. 708-712, 36892, 2012

0048-9697

http://www.producao.usp.br/handle/BDPI/32516

10.1016/j.scitotenv.2011.11.010

http://dx.doi.org/10.1016/j.scitotenv.2011.11.010

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

AMSTERDAM

Relação

SCIENCE OF THE TOTAL ENVIRONMENT

Direitos

closedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #GENETIC POLYMORPHISMS #NITRIC OXIDE #MERCURY EXPOSURE #CARDIOVASCULAR DISEASES #27-BP REPEAT POLYMORPHISM #CORONARY-ARTERY-DISEASE #MYOCARDIAL-INFARCTION #CARDIOVASCULAR-DISEASE #RISK-FACTOR #EASTERN FINLAND #HEART-DISEASE #ECNOS GENE #FISH OILS #SMALL RNA #ENVIRONMENTAL SCIENCES
Tipo

article

original article

publishedVersion