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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 279 (1973), S. 313-325 
    ISSN: 1432-1912
    Keywords: Dibutyryl-c-AMP ; Adrenaline ; Isolated Rat and Guinea-Pig Auricles ; Positive Inotropic Effect ; 45Ca Exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The positive inotropic effect of adrenaline has been assumed to result from an increase in the intracellular level of c-AMP which, in turn, might enhance the permeability of the cardiac cell membrane to Ca2+. In order to further test this hypothesis, the effects of cyclic N6-2′-O-dibutyryl-adenosine-3′,5′-monophosphate (DB-c-AMP; 10−3 M) on mechanical performance, 45Ca uptake and total tissue calcium concentration were investigated in electrically stimulated (120 beats/min) left auricles isolated from female rats weighing 180–220 g. The experiments were performed in Tyrode solution containing 0.9 mM CaCl2; the duration of 45Ca exposure was 3–60 min. In this study, DB-c-AMP markedly enhanced contractile force but the drug failed to detectably increase 45Ca exchange (Figs. 1 and 2). This finding seemed to indicate that the effects of DB-c-AMP on myocardial 45Ca exchange were completely different from those of adrenaline which previously (and in this study; Fig. 4) has been shown to accelerate 45Ca exchange in auricles obtained from guinea-pigs of “normal” size. However, under the conditions used, adrenaline (2.2–5.5×10−6 M) also failed to significantly enhance 45Ca exchange not only in rat auricles (Fig. 3) but also in small auricles isolated from very light guinea-pigs (body-weight 75–150 g; Fig. 4). From these findings it is concluded that druginduced changes in membrane calcium fluxes, which possibly occur, only might have escaped detection under the present experimental conditions. The “pool saturation phenomenon” previously described by Grossman and Furchgott (1964b; 1964c) is discussed to be the underlying mechanism. Thus, substantial conclusions on the effects of DB-c-AMP on myocardial Ca fluxes can as yet not be drawn. They must await experiments in which an adrenaline induced increase in cardiac 45Ca exchange becomes detectable.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 277 (1973), S. 107-112 
    ISSN: 1432-1912
    Keywords: Dibutyryl Cyclic AMP ; Adrenaline ; Heart ; Contractile Force ; 45Ca Uptake
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of dibutyryl cyclic AMP (DB-AMP; 10−3M) and adrenaline (2.2×10−6 M) on contractile force, 45Ca uptake, and total myocardial Ca concentration were investigated in electrically driven left auricles isolated from rat hearts. The experiments were performed at an extracellular Ca concentration of 0.45 mM and at low frequency of stimulation (15 beats/min). 45Ca exposure was 5 min. Under the conditions used, both drugs increased contractile force and enhanced 45Ca uptake (expressed as relative specific activity) by about 30% (DB-AMP) and 40% (adrenaline), respectively. Thus, the results provide evidence that the effects of adrenaline on 45Ca uptake in mammalian cardiac muscle can be mimicked by DB-AMP.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1912
    Keywords: Dibutyryl-c-AMP ; Adrenaline ; Isolated Rat Auricles ; Positive Inotropic Effect ; 45Ca Exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of adrenaline (2.2×10−6 M) and cyclic N6-2′-O-dibutyryl-adenosine-3′,5′-monophosphate (DB-c-AMP; 10−3 M) on mechanical performance, 45Ca uptake and total tissue calcium concentration were investigated in electrically stimulated left auricles isolated from female rats weighing 180–220 g. The experiments were performed at reduced [Ca]e of 0.45 mM and at various frequencies of stimulation (0–120 beats/min). In the first series of experiments 45Ca incubation time was 5 min. Under these conditions DB-c-AMP as well as adrenaline enhanced contractile force to 300–450% of the control values at all frequencies tested (Fig.1). This increase in contractile force was accompanied by a significant enhancement in 45Ca exchange (Fig.2) while the total tissue calcium concentration remained unchanged (Table 1). In resting auricles 45Ca exchange was not altered under the influence of both drugs. At long periods of 45Ca exposure (40–90 min) both drugs augmented contractile force in a way similar to that of the first series of experiments (Fig.4) but no influence of DB-c-AMP or adrenaline on 45Ca exchange could be detected (Fig.3). It is concluded that DB-c-AMP can mimic the wellknown effects of adrenaline on myocardial calcium movements. Under the assumption that DB-c-AMP is representative for c-AMP, the results thus provide experimental support for the view that the positive inotropic effect of adrenaline is mediated by primary changes in the intracellular level of c-AMP which secondarily might enhance calcium fluxes across the cardiac cell membrane.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 282 (1974), S. 143-153 
    ISSN: 1432-1912
    Keywords: DB-c-AMP ; Positive Inotropic Action ; Isometric Contraction Curve ; Isolated Ventricular and Atrial Preparations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Conflicting results exist about the influence of cyclic N6-2′-O-dibutyryl-AMP (DB-c-AMP) on myocardial contractile force. The present study was designed to examine whether the positive inotropic action of DB-c-AMP is restricted to certain model preparations or whether it can be assumed to represent a more general effect of the drug. Therefore, the effects of DB-c-AMP on myocardial force and on various parameters of the isometric contraction curve were examined in isolated electrically driven (0.5–2Hz) ventricular and atrial preparations of several mammalian species (cat, rabbit, calf, sheep, rat and guinea-pig). The following results were obtained: 1. At concentrations above 3×10−4M, DB-c-AMP exerted concentrationdependent positive inotropic effects in all ventricular preparations studied. These effects were accompanied by increases in the rates of force development and relaxation and by decreases in time to peak force and relaxation time. 2. Positive inotropic responses to DB-c-AMP were also obtained in atrial preparations of cats, rabbits, calves, sheep and rats. In guinea-pig auricles, similar effects were seen when the preparations were treated with the phosphodiesterase inhibitor papaverine. The results suggest that the positive inotropic action of DB-c-AMP is not restricted to certain model preparations and can be obtained in all cases under suitable experimental conditions.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 52 (1974), S. 701-703 
    ISSN: 1432-1440
    Keywords: Isolated human ventricular myocardium ; c-AMP ; DB-c-AMP ; Positive inotropic effect ; Isoliertes menschliches Ventrikelmyokard ; c-AMP ; DB-c-AMP ; Positiv inotroper Effekt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Am isolierten menschlichen Ventrikelmyokard hatte c-AMP (10−4–10−3 M) keinen Einfluß auf die Kontraktionskraft. Im Gegensatz dazu wirkte DB-c-AMP (10−4−5·10−3 M) konzentrationsabhängig und reversibel positiv inotrop. Dieser Effekt ging einher mit einer Verkürzung von Anstiegzeit und Erschlaffungszeit der Kontraktion und wurde durch Vorbehandlung mit Propranolol nicht beeinflußt.
    Notes: Summary The contractile responses to c-AMP and DB-c-AMP were studied in isolated electrically stimulated human papillary muscle strips. C-AMP (1×10−4 to 1×10−3 M) had no effect on contractile force in all of 6 human papillary muscle preparations studied. In contrast, DB-c-AMP (10−4 to 5×10−3 M) produced a concentration-dependent and reversible positive inotropic effect which was associated by a decrease in time to peak force and in relaxation time and which was not inhibited by 10−6 M propranolol. The possibility of a clinical applicability of DB-c-AMP is discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 333 (1972), S. 197-212 
    ISSN: 1432-2013
    Keywords: Positive Inotropic Effect ; Dibutyryl-3′,5′-AMP ; Isolated Rat ; Atria ; [Ca]e ; Adrenaline and Theophylline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. In isolated electrically driven (frequency 2 Hz) rat left atria the N6-2′-O-dibutyryl derivative of cyclic 3′,5′-AMP (DB-AMP; monosodium salt) produced a concentration-dependent and reversible positive inotropic effect. In normal Tyrode solution (1.8 mM Ca++, the threshold concentration was 5×10−5 M; the peak concentration (10−3 M) increased contractile force to 203% of control values. Negative inotropic responses were not observed in these experiments even with supramaximal DB-AMP concentrations (Fig. 1). 2. The positive inotropic effect of DB-AMP developed gradualy (Fig. 2). It began 0.3–7.7 min after addition of the drug and was maximal within 3.5–28.3 min (Tab. 2). Once established, the effect was prolonged and decreased only slightly within 60 min (Fig. 2). 3. The positive inotropic effect of DB-AMP was due to an increase in the rate of tension development. The time to peak tension and the duration of contraction remained unchanged (Tab. 3). 4. At high concentrations (10−3–5×10−3M) DB-AMP caused contractures in some experiments (Tab. 1). 5. The time course and the magnitude of the inotropic effects of DB-AMP were influenced by the [Ca]e. The increment in myocardial contractility caused by 10−3M DB-AMP developed faster at high than at low [Ca]e (Tab. 4; Fig. 5). On the other hand, the positive inotropic effect of 10−3M DB-AMP was most evident at normal (1.8 mM) and reduced (0.45; 0.9 mM) [Ca]e, less pronounced at 3.6 mM Ca++ and was insignificant at 7.2 mM Ca++ (Fig.3). 6. Sodium butyrate (10−4–10−2M) did not alter the contractile behaviour of isolated rat atria. 7. In isolated electrically driven (frequency 3 Hz) left guinea-pig atria no positive inotropic effects could be demonstrated with DB-AMP at concentrations up to 10−3M. It is concluded that the positive inotropic action of DB-AMP—at least in isolated rat atria—may resemble that of adrenaline or theophylline in some points, e.g. with regard to its dependence on the [Ca]e. But as no positive inotropic effect could be observed in guinea-pig atria and as the mechanism by which DB-AMP augments contractile force remains obscure, the results are not thought to necessarily support the view that the effects of adrenaline or theophylline on contractile behaviour of mammalian cardiac muscle occur via cyclic AMP.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 278 (1973), S. 165-178 
    ISSN: 1432-1912
    Keywords: Inotropic Effect ; Butyryl Derivatives of c-AMP ; Non-Cyclic Tributyryl-AMP ; Isolated Rat Auricles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This study was designed to further elucidate relevance and mechanism of the positive inotropic action of cyclic N6-2′-O-dibutyryl-AMP (DB-c-AMP). For this purpose the effects of cyclic N6-monobutyryl-AMP (N6-MB-c-AMP), noncyclic N6-2′-O-3′-O-tributyryl-5′-AMP (TB-AMP), c-AMP, adenosine and various adenine nucleotides (ATP, ADP, AMP) on myocardial contractile force (CF) were investigated and compared to that of DB-c-AMP. The experiments were performed on isolated, electrically driven (frequency 2 Hz) rat left auricles, i.e. on a preparation in which DB-c-AMP consistently produced positive inotropic effects. The following results were obtained: 1. N6-MB-c-AMP (2×10−4–5×10−3 M) produced a concentration-dependent positive inotropic effect (Fig. 2). This effect began 5.5 to 1.8 min after addition of the drug (Table 2), developed gradually (Fig.2), and was maximal within 44.5 to 9.5 min (Table 2). It was preceded by a transitory decrease in CF which was also concentration-dependent (Fig.2, Table 1). 2. The inotropic effects of cyclic N6-MB-AMP and cyclic DB-AMP were qualitatively similar. Quantitatively, the positive inotropic effect of N6-MB-c-AMP developed more slowly (Table 2) and was smaller in magnitude than that of DB-c-AMP (Fig.2). The initial negative inotropic effect, however, was more pronounced (Table 1) and longer in duration (Table 2) with N6-MB-c-AMP than with DB-c-AMP. 3. The time course of the reversal of the positive inotropic effects during washout in drug-free solution was practically not different with both drugs (Fig.3). Predrug levels were reached within 50–60 min. 4. No positive inotropic effects were found with the non-cyclic but butyryl substituted adenine nucleotide, TB-AMP. In contrast, this compound (10−7 to 10−3 M) produced a concentration-dependent decrease in CF (Fig.4). 5. c-AMP, ATP, ADP, AMP and adenosine depressed CF. No secondary positive inotropic effects could be detected within 60 min (Fig.5; Fig.6). From the failure of non-cyclic TB-AMP to increase contractile force it is concluded that the positive inotropic effects seen with cyclic DB-AMP and cyclic N6-MB-AMP are due to both acyl substitution and the intact cyclophosphate structure. In so far we probably have ruled out one of the objections to the view that the positive inotropic responses to acyl substituted derivatives of c-AMP are “representative” for c-AMP itself. Since the effects of cyclic DB-AMP and cyclic N6-MB-AMP were qualitatively similar and since the time course of the loss of the positive inotropic effects during washout were practically not differen with both drugs, one may further conclude that within the cell both drugs are likely to act via the same compound. This agent could be c-AMP. However, cyclic N6-MB-AMP as the active intracellular compound cannot be ruled out.
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