Effect of hypertension on angiotensin-(1-7) levels in rats with different angiotensin-I converting enzyme polymorphism

María Paz Ocaranza, Cristián Palomera, Maritza Román, Jorge Bargetto, Sergio Lavandero, Jorge E. Jalil

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12 Citations (Scopus)

Abstract

To determine circulating angiotensin-(1-7) [Ang-(1,7)] levels in rats with different angiotensin converting enzyme (ACE) genotypes and to evaluate the effect of hypertension on levels of this heptapeptide, plasma levels of angiotensin II (Ang II) and Ang-(1-7) were determined by HPLC and radioimmunoassay in (a) normotensive F0 and F2 homozygous Brown Norway (BN; with high ACE) or Lewis (with low ACE) rats and (b) in hypertensive F2 homozygous male rats (Goldblatt model). Genotypes were characterized by PCR and plasma ACE activity measured by fluorimetry. Plasma ACE activity was 2-fold higher (p < 0.05) in homozygous BN compared to homozygous Lewis groups. In the Goldblatt groups, a similar degree of hypertension and left ventricular hypertrophy was observed in rats with both genotypes. Plasma Ang II levels were between 300-400% higher (p < 0.05) in the BN than in the Lewis rats, without increment in the hypertensive animals. Plasma Ang-(1-7) levels were 75-87% lower in the BN rats (p < 0.05) and they were significantly higher (p < 0.05) in the hypertensive rats from both genotypes. Plasma levels of Ang II and Ang-(1-7) levels were inversely correlated in the normotensive rats (r = - 0.64; p < 0.001), but not in the hypertensive animals. We conclude that there is an inverse relationship between circulating levels of Ang II and Ang-(1-7) in rats determined by the ACE gene polymorphism. This inverse relation is due to genetically determined higher ACE activity. Besides, plasma levels of Ang-(1-7) increase in renovascular hypertension.

Original languageEnglish
Pages (from-to)1535-1542
Number of pages8
JournalLife Sciences
Volume78
Issue number14
DOIs
Publication statusPublished - Feb 28 2006

Bibliographical note

Funding Information:
This work was partially supported by FONDECYT grant 1000576.

Funding

This work was partially supported by FONDECYT grant 1000576.

FundersFunder number
Fondo Nacional de Desarrollo Científico y Tecnológico1000576

    ASJC Scopus Subject Areas

    • General Pharmacology, Toxicology and Pharmaceutics
    • General Biochemistry,Genetics and Molecular Biology

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