Literature DB >> 26612503

The mechanisms associated with the development of hypertension after exposure to lead, mercury species or their mixtures differs with the metal and the mixture ratio.

Tanja M Wildemann1, Steven D Siciliano2, Lynn P Weber3.   

Abstract

Hypertension is considered to be the most important risk factor for the development of cardiovascular diseases. Beside life-style risk factors, exposure to lead and mercury species are increasingly discussed as potential risk factors. Although there are a few previous studies, the underlying mechanism by which exposure to lead and mercury disturb blood pressure regulation is not currently understood. Potential mechanisms are oxidative stress production, kidney damage and activation of the renin-angiotensin system (RAS), all of which can interact to cause dysregulation of blood pressure. Male rats (Wistar) were exposed to lead, inorganic mercury, methylmercury or two mixtures of all three metals for four weeks through the drinking water. The two mixture ratios were based on ratios of known reference values or environmental exposure from the literature. To investigate the potential mechanism of actions, blood pressure was measured after four weeks and compared to plasma nitrotyrosine or reduced/oxidized glutathione levels in liver as markers for oxidative stress. Plasma renin and angiotensin II levels were used as markers for RAS activation. Finally, kidney function and injury were assessed via urinary and plasma creatinine levels, creatinine clearance and urinary kidney-injury molecule (KIM-1). While exposure to lead by itself increased oxidative stress and kidney damage along with blood pressure, inorganic mercury did not affect blood pressure or any end-point examined. Conversely, methylmercury instead increased RAS activation along with blood pressure. Surprisingly, when administered as mixtures, lead no longer increased oxidative stress or altered kidney function. Moreover, the mixture based on an environmental ratio no longer had an effect on blood pressure, while the reference value ratio still retained an increase in blood pressure. Based on our results, the prominent mechanism of action associated with the development of hypertension seems to be oxidative stress and kidney damage for lead, while increased RAS activation links methylmercury to hypertension, but these mechanisms along with hypertension disappear when metals are present in some mixtures.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Blood pressure; Kidney; Lead acetate; Mechanism of action; Mercury chloride; Mono-methylmercury chloride; Oxidative stress; Renin–angiotensin

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Year:  2015        PMID: 26612503     DOI: 10.1016/j.tox.2015.11.004

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  5 in total

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2.  Alterations Resulting From Exposure to Mercury in Normotensive and Hypertensive Rats.

Authors:  Luana Urbano Pagan; Marcelo Diarcadia Mariano Cezar; Ricardo Luiz Damatto
Journal:  Arq Bras Cardiol       Date:  2019-04       Impact factor: 2.000

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Authors:  Liana Shvachiy; Ângela Amaro-Leal; Tiago F Outeiro; Isabel Rocha; Vera Geraldes
Journal:  Biology (Basel)       Date:  2022-08-03

4.  Association between levels of blood trace minerals and periodontitis among United States adults.

Authors:  Handan Huang; Jingjing Yao; Nan Yang; Liuqing Yang; Lu Tao; Jinling Yu; Ying Gao; Zhihui Liu
Journal:  Front Nutr       Date:  2022-09-07

5.  The Prevalence of Inorganic Mercury in Human Kidneys Suggests a Role for Toxic Metals in Essential Hypertension.

Authors:  Roger Pamphlett; Philip A Doble; David P Bishop
Journal:  Toxics       Date:  2021-03-21
  5 in total

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