Angiotensin 1-7 Is a Negative Modulator of Aldosterone Secretion In Vitro and In Vivo

Hypertension. 2016 Aug;68(2):378-84. doi: 10.1161/HYPERTENSIONAHA.116.07088. Epub 2016 May 31.

Abstract

Angiotensin (1-7) [Ang 1-7] is a 7 amino acid peptide generated predominantly from Ang II by the action of Ang-converting enzyme 2. We previously showed that Ang 1-7 reduced plasma aldosterone and plasma renin activity in high fructose-fed rats, and that the reduction in circulating aldosterone seemed to accord a parallel reduction in plasma renin activity. Here, we tested the possibility that Ang 1-7 affects aldosterone secretion acting directly in glomerulosa cells. First, as detected by immunofluorescence, the receptor for Ang 1-7, Mas1 is localized predominantly at the rat adrenal subcapsular region. Second, in isolated rat glomerulosa cells incubates, Ang 1-7 attenuated the aldosterone response to Ang II, with the strongest effect seen on Ang II (10(-9) M) (control 22±2.5 pg/10(5) cells; Ang II [10(-9) M] 189±11 pg/10(5) cells; Ang II [10(-9) M]+Ang 1-7 [10(-6) M] 33±3.6 pg/10(5) cells; P<0.001) and the largest effect on adrenocorticotropic hormone (10(-8) M) (control 30±3.4 pg/10(5) cells; ACTH [10(-8) M] 409±32.5 pg/10(5) cells; ACTH [10(-8) M]+Ang 1-7 [10(-6) M] 280±12.5 pg/10(5) cells; P<0.001). In contrast, Ang 1-7 did not affect the aldosterone response to potassium (K(+)). In rats subjected to a low-salt diet for 7 days, continuous infusion of Ang 1-7 (576 μg/kg per day) resulted in a lesser rise in aldosterone (salt deplete+Ang 1-7, 16.4±4.8 ng/dL) compared with rats receiving vehicle (salt deplete+vehicle, 27.6±5.3 ng/dL; P<0.01) but did not modify plasma renin activity. Taken together, these results indicate that Ang 1-7 can act as a negative modulator of aldosterone secretion in vitro and in vivo.

Keywords: aldosterone; aldosterone-system; angiotensin; angiotensins; fructose; hypertension; renin.

MeSH terms

  • Aldosterone* / blood
  • Aldosterone* / metabolism
  • Angiotensin I* / metabolism
  • Angiotensin I* / pharmacology
  • Animals
  • Antihypertensive Agents / metabolism
  • Antihypertensive Agents / pharmacology
  • Fluorescent Antibody Technique / methods
  • Humans
  • Hypertension / metabolism*
  • Peptide Fragments* / metabolism
  • Peptide Fragments* / pharmacology
  • Proto-Oncogene Mas
  • Rats
  • Renin-Angiotensin System / physiology
  • Zona Glomerulosa / metabolism*

Substances

  • Antihypertensive Agents
  • MAS1 protein, human
  • Mas1 protein, rat
  • Peptide Fragments
  • Proto-Oncogene Mas
  • Aldosterone
  • Angiotensin I
  • angiotensin I (1-7)