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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 303 (1978), S. 1-6 
    ISSN: 1432-1912
    Keywords: Cardiac ventricular muscle ; Muscle geometry ; Catecholamine uptake ; Inotropic noradrenaline effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The influence of a saturable drug uptake on the drug concentration near the receptor sites was shown theoretically to depend on the geometry of the preparation; increases in the volume/surface ratio (V/S) of the preparation decrease the sensitivity of the preparation to an agonist inactivated in the tissue. 2. The positive inotropic effect of (-)-noradrenaline was found to depend on the ratio V/S of the preparation; papillary muscles with larger V/S were less sensitive to the drug and showed steeper noradrenaline concentration-effect curves. 3. An algorithm for the statistical estimation of the parameters of the saturable uptake process was derived. It was applied to the positive inotropic noradrenaline effect in relation to muscle geometry. As an analysis of variance showed, the model explained a significant proportion of the shift of (-)-noradrenaline concentration-effect curves associated with variation in size of the preparation.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 307 (1979), S. 99-104 
    ISSN: 1432-1912
    Keywords: Guinea-pig ventricular muscle ; Propranolol ; Dihydro-ouabain ; Inotropic effect ; Bathmotropic effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The effect of dihydro-ouabain on the force of contraction and electrical excitability of the isolated guinea-pig papillary muscle was studied under the influence of (+)- and (±)-propranolol. 2. 10−5 and 4×10−5 mol/l of (+)- or (±)-propranolol had a negative inotropic effect. Both the racemate and the dextro isomer reduced the inotropic effectiveness of the glycoside to the same extent. These actions were not influenced by catecholamine depletion. Even at high concentrations of dihydro-ouabain, which cannot be investigated in the absence of propranolol due to a glycoside-induced automaticity of the muscles, endogenous catecholamines were not involved in the inotropic effect. 3. Dihydro-ouabain had a concentration-dependent negative bathmotropic effect; 8×10−5 mol/l increased the stimulation threshold by about eight percent. The negative bathmotropic action of dihydro-ouabain was enhanced by (+)- or (±)-propranolol, in addition to their own depressant effect on electrical excitability. 4. Due to the combined negative bathmotropic effects, an increasing number of muscles became in-excitable at high concentrations of the glycoside in the presence of 4×10−5 mol/l (±)-propranolol but not in the presence of the same concentration of (+)-propranolol. This difference suggests that dihydro-ouabain in high concentrations releases endogenous noradrenaline which increases excitability via β-adrenoceptors.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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