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Am J Physiol Regul Integr Comp Physiol (April 17, 2003). doi:10.1152/ajpregu.00481.2002
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Submitted on August 14, 2002
Accepted on March 16, 2003

Maturation-Dependent Changes of Angiotensin Receptor Expression in Fowl

Hiroko Nishimura1*, Yimu Yang1, Christine Hubert2, Jean-Marie Gasc2, Karin Ruijtenbeek3, Jo De Mey3, Harry A Struijker Boudier3, and Pierre Corvol2

1 Department of Physiology, University of Tennessee Health Science Center, Memphis, TN, USA
2 INSERM Unit 36 and College de France, Paris, France
3 Departments of Pharmacology and Toxicology, and Cardiovascular Research Institute, Universiteit Maastricht, Maastricht, Netherlands

* To whom correspondence should be addressed. E-mail: nishimur{at}physio1.utmem.edu tmem.edu.

An angiotensin (Ang) receptor homologous to the type 1 receptor (AT1) has been cloned in chickens (cAT1). We investigated whether cAT1 expression in various tissues shows maturation/age-dependent changes. cAT1 mRNA levels detected in renal glomeruli (in situ hybridization) and kidney extract (RT-PCR) are significantly (P < 0.01) higher in 19-d embryos (EB) than in chicks (CH, 2-3 wk) and pullets/cockerels (PL/CK, 14-16 wk). The levels in adrenal glands (concentrated in subcapsular regions) is high in EB and further increased in CH and PL/CK. cAT1 mRNA is also detectable in smooth muscle (SM)/adventitia of EB and CH aortae, and in the adventitia, but not SM, from PL/CL aortae. The endothelia from small arteries and arterioles, but not from aorta, express cAT1 mRNA (ISH). In all age groups, Ang II induces profound endothelium-dependent relaxation of abdominal aorta, partly (37-47%) inhibitable (P < 0.01) by N{omega}-nitro arginine methyl ester (L-NAME, 10-4 M), suggesting the presence of Ang receptor in aortic endothelium. L-NAME-resistant Ang II relaxation, examined in a limited number of EB or CH aortae, was reduced by 125 mM K+ or apamin plus charybdotoxin. The results suggest that: 1) cAT1 is present in kidney, adrenal gland, and vascular endothelium (heterogeneity exists among arteries) of EB, CH, and PL/CK, and in aortic SM/adventitia of EB/CH but only in adventitia of PL/CK, 2) levels of cAT1 gene expression change during maturation in tissue-specific manner, and 3) Ang II-induced relaxation may be partly attributable to nitric oxide and potassium channel activation.




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