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  • (−)[3H]-Dihydroalprenolol  (1)
  • Accentuated antagonism  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 308 (1979), S. 191-198 
    ISSN: 1432-1912
    Keywords: Cardiac α- and β-adrenoceptors ; Radioligand binding ; Rabbit heart ; [3H]-Dihydroergocryptine ; (−)[3H]-Dihydroalprenolol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary For direct identification of α-adrenoceptors in a membrane fraction of the rabbit heart the potent α-adrenoceptor antagonist [3H]-dihydroergocryptine ([3H]-DHE) was used. 1. The binding of [3H]-DHE was saturable with 80 fmol of [3H]-DHE bound/mg protein and of high affinity with an equilibrium dissociation constant (K D) of 11.5 nM. Binding of [3H]-DHE (6 nM) was rapid (t 1/2=2 min) and readily reversible. From the ratio of the rate constants for forward (K 1=1.97×107 M−1 min−1) and reverse (K 2=0.206 min−1) reactions a K D-value of 10 nM was calculated, which is in good agreement with that obtained by equilibrium studies. 2. Adrenergic agonists compete for [3H]-DHE binding in an order of potency: (−)adrenaline 〉 (−)phenylephrine≫ (−)isoprenaline and adrenergic antagonists in the order: phentolamine 〉 yohimbine≫ (−)propranolol. Binding is stereospecific as indicated by the greater potency of (−)adrenaline than (±)adrenaline in displacing [3H]-DHE from the binding sites. 3. For comparison the binding of the potent β-adrenoceptor antagonist (−)[3H]-dihydroalprenolol ((−)[3H]-DHA) was measured in the same membrane fraction. The number and affinity of β-adrenoceptors amounted to 115 fmol of (−)[3H]-DHA bound/mg protein at saturation and K D=7.9 nM. Adrenergic agonists compete for (−)[3H]-DHA binding in an order of potency: (−)isoprenaline 〉 (−)adrenaline 〉 (−)phenylephrine; and adrenergic antagonists in the order: (−)propranolol≫ phentolamine. 4. It is concluded that in a membrane fraction of the rabbit heart there exist binding sites for [3H]-DHE which have characteristics indistinguishable from α-adrenoceptors. Thus the present results are in agreement with previously reported data on the existence of cardiac α-adrenoceptors in the rabbit heart (Schümann et al., 1974; Endoh et al., 1976b).
    Type of Medium: Electronic Resource
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  • 2
    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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