Cuff-induced vascular intima thickening is influenced by titration of the Ace gene in mice


Autoria(s): LACCHINI, Silvia; HEIMANN, Andrea S.; EVANGELISTA, Fabiana S.; CARDOSO, Leandro; SILVA, Gustavo J. J.; KRIEGER, Jose E.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/10/2012

18/10/2012

2009

Resumo

Lacchini S, Heimann AS, Evangelista FS, Cardoso L, Silva GJ, Krieger JE. Cuff-induced vascular intima thickening is influenced by titration of the Ace gene in mice. Physiol Genomics 37: 225-230, 2009. First published March 3, 2009; doi:10.1152/physiolgenomics.90288.2008.-We tested the hypothesis that small changes in angiotensin I-converting enzyme (ACE) expression can alter the vascular response to injury. Male mice containing one, two, three, and four copies of the Ace gene with no detectable vascular abnormality or changes in blood pressure were submitted to cuff-induced femoral artery injury. Femoral thickening was higher in 3- and 4-copy mice (42.4 +/- 4.3% and 45.7 +/- 6.5%, respectively) compared with 1- and 2-copy mice (8.3 +/- 1.3% and 8.5 +/- 0.9%, respectively). Femoral ACE levels from control and injured vessels were assessed in 1- and 3-copy Ace mice, which represent the extremes of the observed response. ACE vascular activity was higher in 3- vs. 1-copy Ace mice (2.4-fold, P < 0.05) in the control uninjured vessel. Upon injury, ACE activity significantly increased in both groups [2.41-fold and 2.14-fold (P < 0.05) for 1- and 3-copy groups, respectively] but reached higher levels in 3- vs. 1-copy Ace mice (P < 0.05). Pharmacological interventions were then used as a counterproof and to indirectly assess the role of angiotensin II (ANG II) on this response. Interestingly, ACE inhibition (enalapril) and ANG II AT(1) receptor blocker (losartan) reduced intima thickening in 3-copy mice to 1-copy mouse values (P < 0.05) while ANG II treatment significantly increased intima thickening in 1-copy mice to 3-copy mouse levels (P < 0.05). Together, these data indicate that small physiologically relevant changes in ACE, not associated with basal vascular abnormalities or blood pressure levels, do influence the magnitude of cuff-induced neointima thickening in mice.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[01/00009-0]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[99/11908-4]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[01/11478-1]

Conselho Nacional de Pesquisa e Desenvolvimento (CNPq)[471219/01-0]

Identificador

PHYSIOLOGICAL GENOMICS, v.37, n.3, p.225-230, 2009

1094-8341

http://producao.usp.br/handle/BDPI/17213

10.1152/physiolgenomics.90288.2008

http://dx.doi.org/10.1152/physiolgenomics.90288.2008

Idioma(s)

eng

Publicador

AMER PHYSIOLOGICAL SOC

Relação

Physiological Genomics

Direitos

restrictedAccess

Copyright AMER PHYSIOLOGICAL SOC

Palavras-Chave #vascular injury #angiotensin I-converting enzyme #gene titration #transgenic mice #ANGIOTENSIN-CONVERTING ENZYME #INDUCED CARDIAC-HYPERTROPHY #COPY NUMBER POLYMORPHISM #RABBIT CAROTID-ARTERY #ATHEROSCLEROTIC LESIONS #INJURY #RECEPTOR #RESTENOSIS #INFLAMMATION #METAANALYSIS #Cell Biology #Genetics & Heredity #Physiology
Tipo

article

original article

publishedVersion