JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] --
 QUICK SEARCH:   [advanced]


     


Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on December 22, 2004; DOI: 10.1124/jpet.104.078725


This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jpet.104.078725v1
313/1/359    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Miquel, R.
Right arrow Articles by D'Ocon, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Miquel, R.
Right arrow Articles by D'Ocon, P.


Received for publication October 6, 2004.
Revised December 16, 2004.
Accepted for publication December 16, 2004.

Acute and chronic Captopril, but not Prazosin nor Nifedipine, normalize alterations in adrenergic intracellular Ca2+ handling observed in the mesenteric arterial tree of spontaneously hypertensive rats

Raquel Miquel 1, Regina Gisbert 1, Eva Serna 1, Francisco Perez-Vizcaino 2, Elsa Anselmi 1, Maria-Antonia Noguera 1, Maria-Dolores Ivorra 1, Pilar D'Ocon 1*

1 Departamento de Farmacologia. Facultad de Farmacia. Universidad de Valencia. 2 Departamento de Farmacologia. Facultad de Medicina. Universidad Complutense de Madrid.

* Address correspondence to: E-mail: m.pilar.docon{at}uv.es

Abstract

The effect of hypertension and acute (36h) or chronic (from age 6 to 16 weeks) antihypertensive treatment with prazosin (2 mg kg-1 per day), nifedipine (50 mg kg-1 per day) or captopril (50 mg kg-1 per day) on Ca2+ mobilization due to {alpha}1-adrenoceptor activation was analyzed in functional studies using arterial rings (four conductance/distributing vessels: aorta, main mesenteric, iliac and tail arteries and two resistance vessels: first and second small mesenteric branches (SMA) obtained from spontaneously hypertensive rats (SHR, 6 and 16 weeks old) and age-matched Wistar Kyoto (WKY) rats. Maximal response to noradrenaline in the presence of extracellular Ca2+ is not affected by hypertension nor by the antihypertensive treatment. The extracellular Ca2+ independent contractile responses increased with age in iliac, tail and SMA and were further increased in SMA from both young and adult SHR and in the main mesenteric artery of adult SHR. In main mesenteric artery from SHR, this increased contraction was associated with a higher increase in cytosolic [Ca2+] mobilized by noradrenaline without changes in the total stored Ca2+. Acute or chronic treatment with captopril abolished the differences observed between WKY and SHR in the NA-induced contraction in mesenteric arteries loaded in Ca2+-free medium. In contrast, animals acutely treated with prazosin or chronically treated with either prazosin or nifedipine exhibit the same differences in Ca2+ handling than untreated rats. In conclusion, these differences are not a consequence of increased blood pressure but precede it and can only be normalized by inhibition of the renin-angiotensin system.


Key words: adrenoceptors, captopril, hypertension, intracellular calcium, noradrenaline, rat mesenteric arteries





Home Help [Feedback] [For Subscribers] [Archive] [Search] --
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 2004 by the American Society for Pharmacology and Experimental Therapeutics.