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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 320 (1982), S. 152-159 
    ISSN: 1432-1912
    Keywords: α- and β-Adrenoceptors ; Positive inotropic effect ; Acetylcholine ; Accentuated antagonism ; Rabbit papillary muscle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The influence of acetylcholine (ACh) on the positive inotropic responses to α- as well as β-adrenoceptor stimulation was investigated in the isolated electrically driven rabbit ventricular muscle. 1. Stimulation of muscarinic receptors by ACh (10−9–10−4 mol/l) reduced the positive inotropic effect evoked by isoprenaline (10−8 mol/l) via β-adrenoceptor stimulation, but enhanced the positive inotropic effect of the α-adrenoceptor stimulating agent phenylephrine (10−6 mol/l) in the presence of pindolol (3×10−8 mol/l). 2. Sodium nitroprusside (SNP) (10−6–10−3 mol/l) reduced the β-adrenoceptor-mediated positive inotropic effect but did not effect the α-adrenoceptor-mediated one. 3. The depression by ACh (10−6 mol/l) or SNP (10−4 mol/l) of the positive inotropic effects evoked by β-adrenoceptor stimulation was accompanied by a decrease of the cAMP level which has been elevated by isoprenaline. However, the enhancement of the α-adrenoceptor mediated positive inotropic effect by ACh seems to be independent of changes in cAMP- and/or cGMP-levels. 4. ACh (10−6 mol/l) diminished the shortening of the action potential duration induced by isoprenaline (10−8 mol/l) in Tyrode solution and Ca2+-dependent potential restored by β-adrenoceptor stimulation in 27 mmol/l K+ Tyrode solution. In contrast, ACh (10−6 mol/l) affected neither the prolongation of action potential duration nor the Ca2+-dependent potential caused by α-adrenoceptor stimulation. The depression by acetylcholine of the β-adrenoceptor mediated positive inotropic effect may be due to the decrease in cAMP content and to the reduction of the slow inward current while the enhancement by ACh of the α-adrenoceptor mediated positive inotropic effect is not associated with changes in cAMP- and/or cGMP-levels and in electrophysiological phenomena. It is concluded that the accentuated antagonism (Levy 1971) between sympathomimetic and parasympathomimetic agents at the postsynaptic region results mainly from the interaction between β-adrenoceptor- and muscarinic receptor-mediated responses, and that the α-adrenoceptor-mediated responses are able to counteract the accentuated antagonism.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1912
    Keywords: α-Adenoceptors ; β-Adrenoceptors ; Phenylephrine ; cAMP ; Papaverine ; Rabbit papillary muscle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The time course of changes of the level of 3′,5′-cyclic AMP (cAMP) and of the tension developed under stimulation of α- and β-adrenoceptors by phenylephrine was investigated in the isolated rabbit papillary muscle. Furthermore the doseresponse relationships for increases of cAMP and of developed tension elicited by phenylephrine were determined. 1. A submaximally effective concentration of phenylephrine (10−5 M) increased significantly the level of cAMP of the papillary muscle at 15 and 30 s by 45 and 36%, respectively; the level of cAMP returned to the control value at 60 s after the administration. The developed tension increased significantly not before 45 s and reached its maximal level at 180 s. 2. When α-adrenoceptors were blocked by phentolamine (10−6 M), the positive inotropic effect of phenylephrine was decreased significantly but the increase of cAMP induced by phenylephrine was not reduced. In the presence of phentolamine the increase of cAMP induced by phenylephrine lasted longer than in the control experiments. 3. The effects of phenylephrine (10−5 M) both on the level of cAMP and the developed tension mediated via stimulation of β-adrenoceptors in the presence of phentolamine were enhanced by the phosphodiesterase inhibitor papaverine throughout the course of responses. 4. Phenylephrine produced an increase in developed tension as well as in cAMP. The corresponding dose-response curves run parallel to each other but differed by about 1.5 log units whereby the developed tension was evoked by lower concentrations. Phentolamine (10−6 M) shifted the curve for the positive inotropic action by about 1.5 log units but did not affect that for increase in cAMP. Therefore, in the presence of the α-adrenolytic drug phentolamine the difference between both curves became smaller so that both curves were superimposed. Papaverine (10−5 M) shifted the whole curve for cAMP upwards and enhanced the maximal contractile response to phenylephrine mediated by stimulation of β-adrenoceptors. 5. The present results indicate that the positive inotropic action of phenylephrine in lower concentrations (〈10−5 M) induced by stimulation of α-adrenoceptors is independent of the level of cAMP. The positive inotropic action of the higher concentrations of phenylephrine induced via stimulation of β-adrenoceptors was preceded by an accumulation of cAMP; the inhibition of the cAMP phosphodiesterase activity by papaverine enhanced the actions of phenylephrine both on the level of cAMP and on the contractile force.
    Type of Medium: Electronic Resource
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