Sex differences in angiotensin II- induced hypertension

Sex differences in the development of hypertension and cardiovascular disease have been described in humans and in animal models. In this paper we will review some of our studies which have as their emphasis the examination of the role of sex differences and sex steroids in modulating the central ac...

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Main Authors: B. Xue, A.K. Johnson, M. Hay
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2007-05-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2007000500018
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spelling doaj-9af14f3b68d844089f89d0776315e4a12020-11-24T22:38:44ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X2007-05-0140572773410.1590/S0100-879X2007000500018Sex differences in angiotensin II- induced hypertensionB. XueA.K. JohnsonM. HaySex differences in the development of hypertension and cardiovascular disease have been described in humans and in animal models. In this paper we will review some of our studies which have as their emphasis the examination of the role of sex differences and sex steroids in modulating the central actions of angiotensin II (ANG II) via interactions with free radicals and nitric oxide, generating pathways within brain circumventricular organs and in central sympathomodulatory systems. Our studies indicate that low-dose infusions of ANG II result in hypertension in wild-type male mice but not in intact wild-type females. Furthermore, we have demonstrated that ANG II-induced hypertension in males is blocked by central infusions of the androgen receptor antagonist, flutamide, and by central infusions of the superoxide dismutase mimetic, tempol. We have also found that, in comparison to females, males show greater levels of intracellular reactive oxygen species in circumventricular organ neurons following long-term ANG II infusions. In female mice, ovariectomy, central blockade of estrogen receptors or total knockout of estrogen a receptors augments the pressor effects of ANG II. Finally, in females but not in males, central blockade of nitric oxide synthase increases the pressor effects of ANG II. Taken together, these results suggest that sex differences and estrogen and testosterone play important roles in the development of ANG II-induced hypertension.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2007000500018Angiotensin IIEstrogenEstrogen a and ß receptorsNitric oxideReactive oxygen speciesTestosterone
collection DOAJ
language English
format Article
sources DOAJ
author B. Xue
A.K. Johnson
M. Hay
spellingShingle B. Xue
A.K. Johnson
M. Hay
Sex differences in angiotensin II- induced hypertension
Brazilian Journal of Medical and Biological Research
Angiotensin II
Estrogen
Estrogen a and ß receptors
Nitric oxide
Reactive oxygen species
Testosterone
author_facet B. Xue
A.K. Johnson
M. Hay
author_sort B. Xue
title Sex differences in angiotensin II- induced hypertension
title_short Sex differences in angiotensin II- induced hypertension
title_full Sex differences in angiotensin II- induced hypertension
title_fullStr Sex differences in angiotensin II- induced hypertension
title_full_unstemmed Sex differences in angiotensin II- induced hypertension
title_sort sex differences in angiotensin ii- induced hypertension
publisher Associação Brasileira de Divulgação Científica
series Brazilian Journal of Medical and Biological Research
issn 0100-879X
1414-431X
publishDate 2007-05-01
description Sex differences in the development of hypertension and cardiovascular disease have been described in humans and in animal models. In this paper we will review some of our studies which have as their emphasis the examination of the role of sex differences and sex steroids in modulating the central actions of angiotensin II (ANG II) via interactions with free radicals and nitric oxide, generating pathways within brain circumventricular organs and in central sympathomodulatory systems. Our studies indicate that low-dose infusions of ANG II result in hypertension in wild-type male mice but not in intact wild-type females. Furthermore, we have demonstrated that ANG II-induced hypertension in males is blocked by central infusions of the androgen receptor antagonist, flutamide, and by central infusions of the superoxide dismutase mimetic, tempol. We have also found that, in comparison to females, males show greater levels of intracellular reactive oxygen species in circumventricular organ neurons following long-term ANG II infusions. In female mice, ovariectomy, central blockade of estrogen receptors or total knockout of estrogen a receptors augments the pressor effects of ANG II. Finally, in females but not in males, central blockade of nitric oxide synthase increases the pressor effects of ANG II. Taken together, these results suggest that sex differences and estrogen and testosterone play important roles in the development of ANG II-induced hypertension.
topic Angiotensin II
Estrogen
Estrogen a and ß receptors
Nitric oxide
Reactive oxygen species
Testosterone
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2007000500018
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