Calcium‐dependence and antagonism of responses to α1‐ and α2‐adrenoceptor agonists in vascular tissues from hypertensive and normotensive rats

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Abstract
1 Inhibition by D600 (methoxyverapamil) of responses to an α2-adrenoceptor selective agonist, B-HT 920, (6-allyl-2-amino-5, 6, 7, 8-tetrahydro-4H-thiazolo [4, 5-d] azepin dihydrochloride), an α1-adrenoceptor selective agonist, phenylephrine (PE), and a nonselective agonist, noradrenaline (NA), was studied in isolated preparations of the aortae and carotid arteries obtained from young (5–7 weeks) and old (15–17 weeks) hypertensive (SHR) and normotensive (WKY) rats. 2 Maximum responses of WKY tissues to B-HT 920 were the most sensitive, PE-induced responses the least sensitive and maximum responses to NA were intermediate in their sensitivity to inhibition by D600. 3 Sub-maximal responses to NA and PE were not different in their sensitivity to inhibition by D600, but were less sensitive than the responses to B-HT 20. Sub-maximal responses to PE were significantly more sensitive to D600 inhibition than were the maximal responses to this agonist. 4 NA-induced responses of tissues from older SHR were less sensitive to inhibition by D600 when compared to responses in WKY rats. 5 Responses to B-HT 920, in tissues suspended in calcium-free solutions, showed the largest decline compared to NA- and PE-induced responses. 6 We conclude that responses to B-HT 920 largely utilize extracellular calcium. PE- and NA-induced responses mobilize extracellular calcium to varying degrees depending upon the concentration of the agonist employed to elicit the response.