INVESTIGADORES
PERAL Maria De Los Angeles
artículos
Título:
LOSARTAN REDUCES VASORELAXANT EFFECT OF ATRIAL NATRIURETIC PEPTIDE IN AORTA BASAL TONE
Autor/es:
ROMANO, LILIANA; COVIELLO, ALFREDO; MARIA DE LOS ANGELES PERAL
Revista:
CLINICAL AND EXPERIMENTAL HYPERTENSION
Editorial:
Editorial Marcel Dekker Inc
Referencias:
Lugar: Nueva York , USA; Año: 1999 vol. 21 p. 1257 - 1271
ISSN:
1064-1963
Resumen:
LOSARTAN REDUCES VASORELAXANT EFFECT OF ATRIAL NATRIURETIC PEPTIDE IN AORTA BASAL TONE
ASBTRACT
Atrial natriuretic peptide (ANP) has a vasorelaxant effect on non-contracted rings of rabbit aorta previously sensitized with angiotensin II (Ang II). We investigated whether this Ang II-sensitization induces a calcium-dependent basal tone in non-contracted smooth muscle and the rol in this response of antagonists of Ang II type 1 (AT1) and Ang II type (AT2 ) receptors. Calcium-free Krebs, significantly lowered basal tone in thoracic rabbit aorta after complete recovery from a previous challenge with Ang II; this change was partially reversed by reexposure to calcium-containing media. The reduction in basal tone elicited by calcium-free Krebs was similar to that previously obtained with ANP and lower to that obtained by treatment with calcium-free Krebs+ EGTA+sodium nitroprusside (SNP). No one of these treatments had effect on basal tension in rings from rabbit aorta unpreviously exposed to Ang II. The vasorelaxant effect of ANP or calcium-free Krebs + EGTA + SNP on basal tone of rabbit aorta could not be obtained when the calcium was previously removed. The AT1 receptor antagonist (losartan) did not alter isometric tension in either basal or sensitized Ang II aorta, however it reduced the Ang II-contractile response. On the other hand, the reduction in basal tone elicited by ANP was significantly atenuated when the rings were pretreated with losartan. This inhibition could not be obtained with the AT2 receptor antagonist PD 123319. The effect of ANP is due to Ang II contribution to the development of an increased calcium-dependent basal tone in aortic rings through the stimulation of AT1 receptors.