Effects of chronic exposure to Mercury on angiotensin-converting enzyme activity and oxidative stress in normotensive and hypertensive rats
Entity
UAM. Departamento de FarmacologíaPublisher
Sociedade Brasileira de Cardiologia (SBC)Date
2019Citation
10.5935/abc.20180271
Arq Bras Cardiol 112.4 (2019): 374-380
ISSN
0066-782X (print); 1678-4170 (online)DOI
10.5935/abc.20180271Funded by
This study was funded by FAPES, CAPES, CNPq, Ministério da Economia e Competitividade (SAF 2016-80305-P)Project
Gobierno de España. SAF 2016-80305-PEditor's Version
https://doi.org/10.5935/abc.20180271Subjects
Mercury Poisoning; Oxidative Stress/radiation effects; Peptidyl-Dipeptidase A; Hypertension; Rats; MedicinaAbstract
Mercury’s deleterious effects are associated with increased cardiovascular risk.
Objective: To determine whether chronic exposure to inorganic mercury increases the activity of angiotensin-converting
enzyme and its relationship with oxidative stress in several organs and tissues.
Methods: We studied male Wistar and spontaneously hypertensive rats (SHR) (3-month-old) exposed or not to HgCl2
for 30 days. At the end of treatment, we investigated the following: changes in body weight, hemodynamic parameters,
angiotensin‑converting enzyme (ACE) activity and oxidative stress in the heart, aorta, lung, brain and kidney in hypertensive
compared to normotensive animals. A value of p < 0.05 was considered significant.
Results: Chronic exposure to HgCl2 did not affect weight gain in either group. Systolic blood pressure, measured weekly,
did not increase in Wistar rats but showed a small increase in SHR rats. We also observed increases in left ventricular
end-diastolic pressure and ACE activity in the plasma and hearts of normotensive rats. In the SHR+Hg group, ACE activity
increased in plasma but decreased in kidney, lung, heart, brain and aorta. Oxidative stress was assessed indirectly by
malondialdehyde (MDA) production, which increased in Hg-treated rats in both plasma and heart. In the SHR+Hg group,
MDA increased in heart and aorta and decreased in lungs and brain.
Conclusion: These results suggest that chronic exposure to inorganic mercury aggravates hypertension and produces more
expressive changes in ACE activity and oxidative stress in SHRs. Such exposure affects the cardiovascular system, representing
a risk factor for the development of cardiovascular disorders in normotensive rats and worsening of pre-existing risks for
hypertension. (Arq Bras Cardiol. 2019; 112(4):374-380)
Files in this item
Google Scholar:Vassallo, Dalton Valentim
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Simões, Maylla Ronacher
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Giuberti, Karina
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Azevedo, Bruna Fernandes
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Ribeiro Junior, Rogerio Faustino
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Salaices Sánchez, Mercedes
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Stefanon, Ivanita
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