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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
    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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  • 4
    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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