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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 334 (1986), S. 56-62 
    ISSN: 1432-1912
    Schlagwort(e): β-Adrenoceptor antagonists ; β-Adrenoceptor subtypes ; Cardiac sarcolemma ; Cardiomyocytes ; Coronary endothelial cells
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary In mammalian heart tissue β2 are known to coexist with β1. In the present study, evidence that β2 in guinea-pig and rat ventricles are primarily localized on the coronary endothelium is provided by competition binding studies with the subtype-selective β-adrenoceptor antagonists ICI 89.406 (β1) and ICI 118.551 (β2) on four different plasma membrane preparations. (1) Following density gradient centrifugation of cardiac ventricular microsomes from rats or guinea-pigs, endothelial plasma membranes migrated at slightly higher density than the sarcolemmal membranes, as verified by endothelial (angiotensin converting enzyme) and sarcolemmal markers (adenylate cyclase, [3H] ouabain binding). At the activity peak of angiotensin converting enzyme, the relative amount of β2 in guinea-pigs and rats was 25% and 65%, respectively. (2) On sarcolemmal membranes corresponding to the activity peak of adenylate, cyclase, β-adrenoceptors consisted of the β1 exclusively (guinea-pig), or to at least 90% (rat). (3) Cultures of coronary endothelial cells derived from guinea-pigs revealed only β2. (4) Isolated guinea-pig cardiomyocytes contained only β1, a finding recently established in rat myocytes as well.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 340 (1989), S. 87-92 
    ISSN: 1432-1912
    Schlagwort(e): A1-Adenosine receptors ; [3H]8-cyclopentyl-1,3-dipropylxanthine ; Guanine nucleotides ; G-Protein ; Solubilization
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary Using [3H]8-cyclopentyl-1,3-dipropylxanthine (DPCPX), a 3H-labeled A1-selective adenosine antagonist with high affinity and extremely low non-specific binding, it was possible to quantitatively evaluate the effect of GTP on agonist binding. Competition experiments on [3H]DPCPX binding to guinea-pig cerebral cortical membranes in the absence of GTP showed a high- and a low-affinity state for adenosine receptor agonists (82/18% for N6-cyclopentyladenosine). Addition of 1 mmol/l GTP only partially converted the high-affinity state of the A1-adenosine receptor into a low-affinity state. This failure of complete conversion from high- to low-affinity state was also seen in membranes from rat testes under the same experimental conditions and, moreover, in guinea-pig brain membranes under different experimental conditions, such as in the presence of Na+ or when free Mg2+ has been reduced by EDTA. The only difference was that in the absence of Mg2+ the high-affinity state of the A1-receptor was markedly smaller than in the presence of Mg2+ (36% vs. 82%). By contrast, in the solubilized state of the receptor total conversion of all receptors into the low-affinity state was obtained upon addition of 1 mmol/l GTP. Reduction of binding of the agonist radioligand [125]iodo-N6-(4-hydroxyphenylisopropyl)-adenosine with increasing concentrations of GTP and Gpp(NH)p demonstrated that the guanine nucleotide affinity to the solubilized A1-receptor was more than 100-fold higher than to the membrane-bound receptor. Hence, the incomplete transition of the high-affinity into the low-affinity state of the membrane-bound A1-receptor upon addition of GTP may be attributable to the low affinity of the membrane-bound receptor-G-protein complex for GTP.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 336 (1987), S. 519-525 
    ISSN: 1432-1912
    Schlagwort(e): β-Adrenoceptor antagonists ; β-Adrenoceptor subtypes ; Competition binding studies ; [3H]CGP-12177 ; Subtype selectivity
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary On the basis of saturation binding studies on rat cardiac microsomes, which contained a mixed population of β-adrenoceptor subtypes, [3H]CGP-12177 is presumed to be a non-selective β-adrenergic radioligand. However, saturation binding studies carried out in the presence of subtype-saturating concentrations of the β2-selective antagonist ICI 118,551 and the β1-selective antagonist ICI 89,406, respectively, revealed a K D for β1-adrenoceptors of 0.33 ± 0.02 nmol/l and a K D for β2-adrenoceptors of 0.90 ± 0.14 nmol/l. Competition experiments with the highly selective antagonists revealed greatly different competition binding curves in the presence of either [3H]CGP-12177 or (−)[125I]iodocyanopindolol (ICYP), a β-adrenergic radioligand considered to be as non-selective as [3H]CGP-12177. The following results are further suggestive for a selectivity of [3H]CGP-12177 for β1-adrenoceptors: (1) Using non-linear regression analysis, a significantly lower selectivity (expressed as the ratio of the IC50 for β2-adrenoceptors to the IC50 for β1-adrenoceptors) as well as a larger proportion of β1-adrenoceptors were calculated by competition of the β1-selective antagonist ICI 89,406 with [3H]CGP-12177 binding than by competition of ICI 89,406 with ICYP binding; (2) reducing the [3H]CGP-12177 concentration from 2 to 0.4 nmol/l, competition experiments with ICI 89,406 led to an increase in the estimated selectivity of the competitor and in the estimated proportion of β1-adrenoceptors; (3) reverse findings were obtained with ICI 118,551, a β2-selective antagonist. Theoretical competition data assuming a varying selectivity of the radioligand were generated using an equation which describes inhibition of the binding of a selective radioligand by a selective competing ligand. Analysis of these data by the model which assumes that the radioligand is entirely non-selective revealed a logarithmic relationship between the distortion of the true selectivity of the competing ligand and the degree of selectivity of the radioligand. For instance, the selectivity of ICI 89,406, estimated against [3H]CGP-12177 binding, was 23% of its selectivity estimated against ICYP binding. Hence, non-linear fits of competition curves with subtype-selective unlabeled ligands will result in serious distortion in the estimates of affinity of the competing ligands and in the size of subtype populations if [3H]CGP-12177 is considered entirely non-selective.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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