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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 290 (1975), S. 69-80 
    ISSN: 1432-1912
    Keywords: Verapamil ; D 600 ; Optical Isomers ; Cardiac Muscle ; Inotropic Effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary On isotonically contracting cat papillary muscles using pattern analysis, a comparison of the effects of the optical isomers of verapamil and D 600 and the racemic drugs was periormed. 1. (-)-verapamil (0.2–0.3 μg/ml) and (-)-D-600 (0.1 μg/ml–3.0 μg/ml) leave the steady state contraction amplitudes nearly, unchanged at 6/min, but produce a strong depression at 60/min. (-)-D 600 is about 8 times as effective as (-)-verapamil. The (+)-isomers exert only a moderate negative inotropic effect (particularly at low frequencies). 2. Increase of [Ca2+]0 does not restitute the normal amplitude-frequency relationship during exposure to either the (-)-isomers or the (+)-isomers. 3. The (-)-isomers lead to typical biphasic staircases after step changes of frequency. A fast negative staircase occurs first followed by a rather slowly developing positive staircase. In contrast, the (+)-isomers have little influence on the usual staircase pattern. 4. The strength-interval relationship for single test contractions elicited after frequent conditioning stimulation indicated that the (-)-isomers probably slow the restitution of intracellular Ca-reavailability. The (+)-isomers have no such effects. 5. The effects produced by the (±)-compounds correspond qualitatively to those of the (-)-isomers. 6. The very different patterns of inotropic actions observed indicate that the (-)- and (+)-isomers of verapamil and D 600 probably interfere with cardiac excitation-contraction coupling at different sites.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 290 (1975), S. 81-97 
    ISSN: 1432-1912
    Keywords: Verapamil ; D 600 ; Optical Isomers ; Cardiac Muscle ; Transmembrane Action Potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Excitability, maximum velocity of depolarization (MVD), conduction velocity, discharge rate and the duration of transmembrane action potentials as a function of frequency of stimulation were studied in isolated cardiac tissues exposed to the optical isomers of verapamil and D 600. 1. In isolated papillary muscles depression of the MVD and the conduction velocity depend on concentration (1–8 μg/ml) of (+)-verapamil and (+)-D 600. 2. (+)-Verapamil and (+)-D 600 (1–30 μg/ml) increase frequency-dependently the threshold intensity of electrical stimuli needed to elicit conducted action potentials. 3. (-)-Verapamil and (-)-D 600 are about one order of magnitude less effective than the corresponding (+)-isomers. 4. Both (+)- and (-)-isomers slightly prolong the transmembrane action potential at 90% repolarization level, particularly at low frequencies. In addition, the (-)-isomers induce a frequency-dependent depression of the plateau phase. 5. The results indicate that, at least in ventricular myocardium, the (+)-isomers of verapamil and D 600 have a quite specific inhibitory effect on the fast Na-inward current and, therefore, may contribute to some extent to the anti-dysrhythmic potency of the racemic drugs. 6. In isolated cat SA-nodes, both (+)- and (-)-isomers of verapamil and D 600 (0.2–1.0 μg/ml) reduce the discharge rate to the point of complete suppression of automaticity; different mechanisms are responsible for the effects. 7. The (-)-isomers (0.3–0.6 μg/ml) slightly reduce the slope of the slow diastolic depolarization, while causing a more effective depression of MVD and nodal conduction velocity until partial or complete nodal conduction blocks occur. 8. The (+)-isomers (1–2μg/ml) do not affect MVD or nodal conduction, but obviously shift the threshold voltage for the fast depolarization to less negative voltages. Cessation of automaticity occurs with a stable membrane potential and the ability to generate conducted action potentials by electrical stimulation persists.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 290 (1975), S. 49-68 
    ISSN: 1432-1912
    Keywords: Verapamil ; D 600 ; Cardiac Muscle ; Amplitude-Frequency Relation ; Staircase Phenomena
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A pattern analysis of inotropic actions was carried out on isotonically shortening cat papillary muscles exposed to (±)-verapamil and (±)-D 600 and compared to other Ca-antagonistic interventions. 1. (±)-Verapamil (1–5 μg/ml) leaves contraction amplitudes nearly unchanged at 6/min, whereas at 60/min more than 90% depression (5 μ/ml) occurs. (±)-D 600 is about twice as effective as (±)-verapamil. 2. An increase of [Ca2+]0 in the presence of (±)-verapamil or (±)-D 600 does not restitute the normal amplitude-frequency relationship. There is only a shift toward higher contraction amplitudes. 3. (±)-Verapamil and (±)-D 600 lead to typical biphasic inotropic transients after step changes of the driving rhythm. First a fast and (at higher frequencies) very pronounced negative staircase occurs, followed by a rather slowly developing positive staircase. 4. These drug effects contrast to the effects of lowering [Ca2+]0 or of adding Ni2+ or La3+, which all produce a rather uniform depression of contraction amplitudes at all frequencies and do not elicit staircase phenomena such as seen under the influence of (±)-verapamil or (±)-D 600. 5. In contrast to the action of Ni2+, La3+ or low [Ca2+]0, (±)-verapamil slows down the restitution kinetics of Ca-reavailability from internal stores as determined by the amplitude of test contractions elicited after various periods of rest. 6. Drug-induced changes in the time course of the transmembrane action potential as depending on frequency may partially but not fully explain the contractile phenomena. 7. Possible interpretations as to the sites where (±)-verapamil or (±)-D 600 interferes with cardiac excitation-contraction coupling are given by the aid of a multicompartment model. This model describes excitation-contraction coupling in terms of transmembrane and intracellular Ca-movements.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 83 (1911), S. 325-328 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 274 (1893), S. 304-311 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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