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
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).