PT  - JOURNAL ARTICLE
AU  - R. Miquel
AU  - R. Gisbert
AU  - E. Serna
AU  - F. Perez-Vizcaino
AU  - E. Anselmi
AU  - M. A. Noguera
AU  - M. D. Ivorra
AU  - M. P. D'Ocon
TI  - Acute and Chronic Captopril, but Not Prazosin or Nifedipine, Normalize Alterations in Adrenergic Intracellular Ca<sup>2+</sup> Handling Observed in the Mesenteric Arterial Tree of Spontaneously Hypertensive Rats
AID  - 10.1124/jpet.104.078725
DP  - 2005 Apr 01
TA  - Journal of Pharmacology and Experimental Therapeutics
PG  - 359--367
VI  - 313
IP  - 1
4099  - http://jpet.aspetjournals.org/content/313/1/359.short
4100  - http://jpet.aspetjournals.org/content/313/1/359.full
SO  - J Pharmacol Exp Ther2005 Apr 01; 313
AB  - The effect of hypertension and acute (36-h) 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 α1-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 artery branches obtained from spontaneously hypertensive rats (SHR, 6 and 16 weeks old) and age-matched Wistar Kyoto rats (WKY)]. Maximal response to noradrenaline in the presence of extracellular Ca2+ is not affected by hypertension or by the antihypertensive treatment. The extracellular Ca2+-independent contractile responses increased with age in iliac, tail, and small mesenteric arteries (SMA) and were further increased in SHR in SMA from both young and adult animals and in the main mesenteric artery of adult SHR. In main mesenteric artery, this increased contraction in SHR 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 noradrenaline-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 rennin-angiotensin system. The American Society for Pharmacology and Experimental Therapeutics