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   <subfield code="a">Contribution of both α- and β-adrenoceptors to the inotropic effects of catecholamines in the rabbit heart</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ulrich Jahnel, Barbara Kaufmann, Martin Rombusch, Hermann Nawrath]</subfield>
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   <subfield code="a">Summary: The functional role of α-adrenoceptors was investigated in different parts of the rabbit heart. Phenylephrine (PE) caused a marked increase in force of contraction (Fc) and a prolongation of the action potential (AP) in preparations from the left atrium and the right ventricle. The response was less pronounced in the right atrium and in the left ventricle, whereas APs of spontaneously beating sinoatrial preparations remained completely unchanged. Phentolamine as well as the diesters phorbol 12,13 dibutyrate (PDBu) or 12-O-tetradecanoylphorbol-13-acetate (TPA) eliminated the effects of PE. The contribution of a-adrenoceptors to the effects of adrenaline (Adr) and noradrenaline (NA) on Fc was determined in preparations from the right ventricle. Phentolamine and the phorbol diesters reduced the effects of Adr and NA by about 30 to 60%; the remaining response was abolished by propranolol. It can be derived from our experiments that, in some parts of the rabbit heart, a considerable amount of the effects of Adr and NA is due to the stimulation of a-adrenoceptors. The present findings therefore support the view that, in the rabbit heart, the maximally effective drive of the heart requires the stimulation of both α- and β-adrenoceptors. The inhibitory effects of phorbol diesters on the α-adrenoceptor-mediated response indicate that the activation of protein kinase C (PKC) specifically uncouples α-adrenoceptors from the effector system, whereas the response to β-adrenoceptor stimulation remains unchanged.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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