4.7 Article

Hemodynamic phenotyping of transgenic rats with ubiquitous expression of an angiotensin-(1-7)-producing fusion protein

Journal

CLINICAL SCIENCE
Volume 135, Issue 18, Pages 2197-2216

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/CS20210599

Keywords

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Funding

  1. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES, Brazil)
  2. German Academic Exchange Service (DAAD, Germany) [88881.198677/2018-01]
  3. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  4. Fundacao de Amparo a Pesquisa do Estado de Minas Gerais (FAPEMIG) [306962/2019-5, APQ-02724-18]
  5. German Research Foundation [DFG SFB1365]

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The new transgenic rat line TG7371 exhibits a hypotensive phenotype in the cardiovascular phenotype, characterized by widespread vasodilation and decreased peripheral resistance. This phenotype is associated with an increase in ANP levels, as well as an increase in AVP and sympathetic drive.
Activation of the angiotensin (Ang)-converting enzyme (ACE) 2/Ang-(1-7)/MAS receptor pathway of the renin-angiotensin system (RAS) induces protective mechanisms in differ-ent diseases. Herein, we describe the cardiovascular phenotype of a new transgenic rat line (TG7371) that expresses an Ang-(1-7)-producing fusion protein. The transgene-specific mRNA and the corresponding protein were shown to be present in all evaluated tissues of TG7371 with the highest expression in aorta and brain. Plasma Ang-(1-7) levels, measured by radioimmunoassay (RIA) were similar to control Sprague-Dawley (SD) rats, however high Ang-(1-7) levels were found in the hypothalamus. TG7371 showed lower baseline mean ar-terial pressure (MAP), assessed in conscious or anesthetized rats by telemetry or short-term recordings, associated with increased plasma atrial natriuretic peptide (ANP) and higher uri-nary sodium concentration. Moreover, evaluation of regional blood flow and hemodynamic parameters with fluorescent microspheres showed a significant increase in blood flow in dif-ferent tissues (kidneys, mesentery, muscle, spleen, brown fat, heart and skin), with a result-ing decrease in total peripheral resistance (TPR). TG7371 rats, on the other hand, also pre-sented increased cardiac and global sympathetic tone, increased plasma vasopressin (AVP) levels and decreased free water clearance. Altogether, our data show that expression of an Ang-(1-7)-producing fusion protein induced a hypotensive phenotype due to widespread vasodilation and consequent fall in peripheral resistance. This phenotype was associated with an increase in ANP together with an increase in AVP and sympathetic drive, which did not fully compensate the lower blood pressure (BP). Here we present the hemodynamic im-pact of long-term increase in tissue expression of an Ang-(1-7)-fusion protein and provide a new tool to investigate this peptide in different pathophysiological conditions.

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