Changes in hemodynamic and neurohumoral control cause cardiac damage in one-kidney, one-clip hypertensive mice


Autoria(s): BORGES, Giulianna R.; SALGADO, Helio C.; SILVA, Carlos Alberto A.; ROSSI, Marcos A.; PRADO, Cibele M.; FAZAN JR., Rubens
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Borges GR, Salgado HC, Silva CA, Rossi MA, Prado CM, Fazan R Jr. Changes in hemodynamic and neurohumoral control cause cardiac damage in one-kidney, one-clip hypertensive mice. Am J Physiol Regul Integr Comp Physiol 295: R1904-R1913, 2008. First published October 1, 2008; doi:10.1152/ajpregu.00107.2008.-Sympathovagal balance and baroreflex control of heart rate (HR) were evaluated during the development (1 and 4 wk) of one-kidney, one-clip (1K1C) hypertension in conscious mice. The development of cardiac hypertrophy and fibrosis was also examined. Overall variability of systolic arterial pressure (AP) and HR in the time domain and baroreflex sensitivity were calculated from basal recordings. Methyl atropine and propranolol allowed the evaluation of the sympathovagal balance to the heart and the intrinsic HR. Staining of renal ANG II in the kidney and plasma renin activity (PRA) were also evaluated. One and four weeks after clipping, the mice were hypertensive and tachycardic, and they exhibited elevated sympathetic and reduced vagal tone. The intrinsic HR was elevated only 1 wk after clipping. Systolic AP variability was elevated, while HR variability and baroreflex sensitivity were reduced 1 and 4 wk after clipping. Renal ANG II staining and PRA were elevated only 1 wk after clipping. Concentric cardiac hypertrophy was observed at 1 and 4 wk, while cardiac fibrosis was observed only at 4 wk after clipping. In conclusion, these data further support previous findings in the literature and provide new features of neurohumoral changes during the development of 1K1C hypertension in mice. In addition, the 1K1C hypertensive model in mice can be an important tool for studies evaluating the role of specific genes relating to dependent and nondependent ANG II hypertension in transgenic mice.

CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

CAPES Coordenadoria de Aperfeicoamento de Pessoal de Nivel Superior

Fundacao de Apoio ao Ensino (FAEPA)

Pesquisa e Assistencia do Hospital das Clinicas da Faculdade de Medicina de Ribeirao Preto (FAEPA)

Identificador

AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, v.295, n.6, p.R1904-R1913, 2008

0363-6119

http://producao.usp.br/handle/BDPI/24431

10.1152/ajpregu.00107.2008

http://dx.doi.org/10.1152/ajpregu.00107.2008

Idioma(s)

eng

Publicador

AMER PHYSIOLOGICAL SOC

Relação

American Journal of Physiology-regulatory Integrative and Comparative Physiology

Direitos

restrictedAccess

Copyright AMER PHYSIOLOGICAL SOC

Palavras-Chave #renovascular hypertension #sympathetic tone #vagal tone #intrinsic heart rate #baroreflex #BLOOD-PRESSURE VARIABILITY #HEART-RATE-VARIABILITY #ROSTRAL VENTROLATERAL MEDULLA #ANGIOTENSIN-II #RENAL-HYPERTENSION #BAROREFLEX CONTROL #ORGAN DAMAGE #CHRONOTROPIC ACTION #TIME COURSE #RATS #Physiology
Tipo

article

original article

publishedVersion