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Chronic immunoneutralization of brain angiotensin-(1-12) lowers blood pressure in transgenic (mRen2)27 hypertensive rats.

Authors :
Isa, Katsunori
Garcia-Espinosa, Maria Antonia
Arnold, Amy C.
Pirro, Nancy T.
Tommasi, Ellen N.
Ganten, Detlev
Chappell, Mark C.
Ferrario, Carlos M.
Diz, Debra I.
Source :
American Journal of Physiology: Regulatory, Integrative & Comparative Physiology. Jul2009, Vol. 297, pR111-R115. 5p.
Publication Year :
2009

Abstract

Isa K, Garcia-Espinosa MA, Arnold AC, Pirro NT, Tommasi EN, Ganten D, Chappell MC, Ferrario CM, Diz DI. Chronic immunoneutralization of brain angiotensin-(1-l2) lowers blood pressure in transgenic (mRen2)27 hypertensive rats. Am J Physiol Regul Integr Comp Physiol 297: RI 11-RI 15, 2009. First published April 29, 2009; doi: 10.1152/ajpregu.90588.2008.-Angiotensin-(1-12) [ANG(1-12)] is a newly identified peptide detected in a variety of rat tissues, including the brain. To determine whether brain ANG-(1-12) participates in blood pressure regulation, we treated male adult (mRen2)27 hypertensive rats (24-28 wk of age) with Anti-ANG-(1-12) IgG or Preimmune IgG via an intracerebroventricular cannula for 14 days. Immunoneutralization of brain ANG-(1-12) lowered systolic blood pressure (-43 ± 8 mmHg on day 3 and -26 ± 7 mmHg on day 10 from baseline, P < 0.05). Water intake was lower on intracereroventricular day 6 in the Anti-ANG-(1-12) IgG group, accompanied by higher plasma osmolality on day 13, but there were no differences in urine volume, food intake, or body weight during the 2-wk treatment. In Preimmune IgG-treated animals, there were no significant changes in these variables over the 2-wk period. The antihypertensive effects produced by endogenous neutralization of brain ANG-(1-12) suggest that ANG-(1-12) is functionally active in brain pathways regulating blood pressure. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03636119
Volume :
297
Database :
Academic Search Index
Journal :
American Journal of Physiology: Regulatory, Integrative & Comparative Physiology
Publication Type :
Academic Journal
Accession number :
43441945
Full Text :
https://doi.org/10.1152/ajpregu.90588.2008