Donate Help Contact The AHA Sign In Home
American Heart Association
Hypertension
Search: search_blue_button Advanced Search
Hypertension. 2005;46:341-348
Published online before print July 18, 2005, doi: 10.1161/01.HYP.0000179216.04357.49
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
46/2/341    most recent
01.HYP.0000179216.04357.49v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gomes da Silva, A. Q.
Right arrow Articles by Peliky Fontes, M. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gomes da Silva, A. Q.
Right arrow Articles by Peliky Fontes, M. A.
Related Collections
Right arrow ACE/Angiotension receptors

(Hypertension. 2005;46:341.)
© 2005 American Heart Association, Inc.


Original Articles

Blockade of Endogenous Angiotensin-(1–7) in the Hypothalamic Paraventricular Nucleus Reduces Renal Sympathetic Tone

Ana Quênia Gomes da Silva; Robson Augusto Sousa dos Santos; Marco Antônio Peliky Fontes

From the Laboratório de Hipertensão, Departamento de Fisiologia e Biofísica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

Correspondence to Dr M.A.P. Fontes, Laboratório de Hipertensão Departamento de Fisiologia e Biofísica—ICB Universidade Federal de Minas Gerais Belo Horizonte, MG 31270 901. E-mail peliky{at}mono.icb.ufmg.br

In this study, we tested the hypothesis that angiotensin-(1–7) [Ang-(1–7)] acting in the neurons of paraventricular hypothalamic nucleus (PVN) contributes to the maintenance of sympathetic activity and blood pressure. For this purpose, the effects of microinjection of the A-779, the receptor Mas antagonist, into the PVN on mean arterial pressure (MAP), heart rate (HR), and renal sympathetic nerve activity (RSNA) were evaluated. In rats anesthetized with urethane (1.2 to 1.4 g/kg IP), bilateral microinjections of A-779 (0.1 nmol) into the PVN resulted in a selective and significant decrease in RSNA (–26±6% versus –2±3% vehicle; saline 0.9%). The magnitude of the decrease in RSNA produced by A-779 was comparable to that observed after microinjection of muscimol (1 nmol; –26±4%), a powerful neuronal inhibitor. A higher dose of A-779 (1 nmol) caused a reduction in RSNA (–21±4%) that was comparable in magnitude to the reduction observed with the lower dose. When compared with vehicle solution, no significant changes in MAP or HR were observed with both doses of A-779 tested. A decrease in RSNA was also observed after microinjections into the PVN of the angiotensin II type 2 (AT2) receptor antagonist PD123319 (1 nmol; –18±4%). Microinjections of the AT1 antagonist losartan but not CV 11974 reduced MAP without changing RSNA. These results suggest that Ang-(1–7) Mas receptors and AT2 receptors in the PVN neurons play a role in mediating the tonic maintenance of RSNA.


Key Words: angiotensin antagonist • angiotensin • rats