Abstract
1. 1. In rat papillary muscle, stimulation of α 1-adrenoceptors results in a biphasic inotropic response: a transient negative inotropic phase and a subsequent sustained positive inotropic phase. This study was designed to determine whether the positive and negative inotropic effects in this tissue are mediated by different α 1-adrenoceptor subtypes. 2. 2. After treatment with the tumor-promoting compound, phorbol 12,13-dibutyrate, phenylephrine (in the presence of propranolol) produced only a positive inotropic effect. The selective α 1A-adrenoceptor antagonist, WB4101, significantly inhibited the positive inotropic effect. In contrast, inactivation of α 1B-adrenoceptors with chloroethylclonidine (CEC) did not alter the positive effect. 3. 3. In the presence of the Ca 2+ channel antagonist, nifedipine, phenylephrine induced only a sustained negative inotropic effect. The negative inotropic effect was significantly attenuated by WB4101, but was not affected by CEC. 4. 4. We conclude that both the positive and negative inotropic responses of rat papillary muscle to phenylephrine are mediated exclusively by the WB4101-sensitive but CEC-resistant α 1-adrenoceptor subtype. The α 1-adrenoceptor subtype with such a property may correspond to the α 1A-subtype.
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