Blood pressure-independent cardiac hypertrophy induced by locally activated renin-angiotensin system.


Autoria(s): Mazzolai L.; Nussberger J.; Aubert J.F.; Brunner D.B.; Gabbiani G.; Brunner H.R.; Pedrazzini T.
Data(s)

1998

Resumo

Cardiac hypertrophy is frequent in chronic hypertension. The renin-angiotensin system, via its effector angiotensin II (Ang II), regulates blood pressure and participates in sustaining hypertension. In addition, a growing body of evidence indicates that Ang II acts also as a growth factor. However, it is still a matter of debate whether the trophic effect of Ang II can trigger cardiac hypertrophy in the absence of elevated blood pressure. To address this question, transgenic mice overexpressing the rat angiotensinogen gene, specifically in the heart, were generated to increase the local activity of the renin-angiotensin system and therefore Ang II production. These mice develop myocardial hypertrophy without signs of fibrosis independently from the presence of hypertension, demonstrating that local Ang II production is important in mediating the hypertrophic response in vivo.

Identificador

http://serval.unil.ch/?id=serval:BIB_EA30D8FD2ECD

isbn:0194-911X

pmid:9622149

isiid:000074011100019

Idioma(s)

en

Fonte

Hypertension, vol. 31, no. 6, pp. 1324-30

Palavras-Chave #Angiotensin II; Angiotensinogen; Animals; Blood Pressure; Blotting, Northern; Blotting, Southern; Blotting, Western; Cardiomegaly; DNA; Heart Rate; Immunohistochemistry; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Transgenic; Myocardium; Polymerase Chain Reaction; RNA; Rabbits; Rats; Renin; Renin-Angiotensin System; Transgenes
Tipo

info:eu-repo/semantics/article

article