Contribution of angiotensin-(1-7) to blood pressure regulation in salt-depleted hypertensive rats

Citation
Sn. Iyer et al., Contribution of angiotensin-(1-7) to blood pressure regulation in salt-depleted hypertensive rats, HYPERTENSIO, 36(3), 2000, pp. 417-422
Citations number
36
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
HYPERTENSION
ISSN journal
0194911X → ACNP
Volume
36
Issue
3
Year of publication
2000
Pages
417 - 422
Database
ISI
SICI code
0194-911X(200009)36:3<417:COATBP>2.0.ZU;2-J
Abstract
We exposed 63 adult spontaneously hypertensive rats (SHR) and 10 (mRen-2)27 transgenic hypertensive rats to a 12-day regimen of either a normal diet ( 0.5%) or a low-salt diet (0.05%) to evaluate the hypothesis that the vasode pressor heptapeptide, angiotensin-(1-7) [Ang-(1-7)], buffers the presser ef fects of angiotensin II during endogenous stimulation of the renin-angioten sin system. Catheters were inserted into a carotid artery and jugular vein under Light anesthesia the day before the experiment. Separate groups of co nscious instrumented SHR were given short-term infusions of an affinity-pur ified monoclonal Ang-(1-7) antibody or the neprilysin inhibitor SCH 39370. In addition, SHR and (mRen-2)27 rats were given the Ang-(1-7) receptor anta gonist [D-Ala(7)]Ang-(1-7). Exposure to the low-salt diet increased plasma renin activity and elevated plasma levels of angiotensin I and angiotensin II in SHR by 81% and 68%, respectively, above values determined in SHR fed a normal salt diet. Concentrations of angiotensin I and angiotensin II were also higher in the kidney of salt-depleted SHR, whereas plasma and renal t issue levels of Ang-(1-7) were unchanged. Infusion of the Ang-(1-7) antibod y produced dose-dependent presser and tachycardic responses in salt-deplete d SHR but no effect in SHR maintained on a normal-salt diet. A comparable c ardiovascular response was produced in salt-depleted SHR given either SCH 3 9370 or [D-Ala(7)]Ang-(1-7). These agents had negligible effects on SHR fed a normal-salt diet. Blockade of Ang-(1-7) receptors produced a similar car diovascular response in (mRen-2)27 transgenic hypertensive rats fed a low-s alt diet. Injections of the heat-inactivated antibody or the subsequent inf usion of the antibody to rats given [D-Ala(7)]Ang-(1-7) produced no additio nal effects. The data support the hypothesis that the hemodynamic effects o f neurohormonal activation after salt restriction stimulate a tonic depress or action of Ang-(1-7).