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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 32 (1976), S. 613-614 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The absorption of3H-digitoxin from perfused rat small intestine was inhibited by probenecid (1.0×10−2 M), ethacrynic acid (0.5×10−3 M), and mersalyl (8.0×10−3 M) indicating that digitoxin absorption is at least partly an active process.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 291 (1975), S. 371-383 
    ISSN: 1432-1912
    Keywords: Digitoxin ; Plasma binding ; Tissue uptake ; Species differences
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The content of cardiac glycosides in plasma and several organs of rats and mice was investigated 30 min and 12 hrs after i.p. administration of 160 μg/kg b.w. 3H-digitoxin. In rat plasma a glycoside concentration of 124.8 and 44.7 ng/ml resp. was found. The corresponding values in the liver were 834.7 and 579.7 ng/g w.w. An opposite liver/plasma distribution was obtained in mice: while in plasma 772.5 and 571.8 ng/ml were recovered, the glycoside concentration in liver was relatively small (284.8 and 235.6 ng/g w.w.). In order to find out the reason for such species differences observed in vivo, liver slices of rats and mice were incubated with 3H-digitoxin in a medium with and without various plasma proteins. The uptake of 3H-digitoxin into liver slices was drastically reduced by adding mouse plasma or albumin to the medium, while rat plasma lowered the uptake far less. These differences are well reflected by binding studies on agargel electrophoresis: only in mouse plasma a binding of 3H-digitoxin could be demonstrated. The binding rate and binding constant analyzed by equilibrium dialysis were higher in mouse than in rat plasma. It is concluded that the lower tissue accumulation in mice compared to rats must be due to the affinity of 3H-digitoxin to mouse plasma albumin. Moreover digitoxin has a higher affinity to the rat than to the mouse liver in the presence of mouse or rat plasma as well as of bovine serum albumin.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 289 (1975), S. 217-227 
    ISSN: 1432-1912
    Keywords: Digitoxin ; Intestinal Transport ; Dose Dependence ; Functional Asymmetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary On everted jejunal segments of mice the transfer and tissue uptake of 3H-digitoxin, over a concentration range from 2×10−10–1×10−4M, was investigated from the mucosal (“m”) to the serosal (“s”) side as well as in the opposite direction. 1. The time course of the absorption of 3H-digitoxin and some other compounds investigated (glucose, urea, p-aminohippurate) gave evidence of functional integrity throughout the 75 min-periods of the experiments. 2. When 3H-digitoxin was applied to the mucosal side the permeability coeffcient showed a dose-dependent increase but returned to lower values at higher concentrations. When 3H-digitoxin was administered to the serosal side the permeability coefficient showed a dose-dependent decrease at high concentrations. The ratio of both coefficients “m” → “s”/“s” → “m” increased dose-dependently from 0.4–2.6. 3. The uptake of 3H-digitoxin — applied on the serosal side — into the tissue was independent of dose. However, having administered 3H-digitoxin on the mucosal side the tissue accumulation was 2–5 fold higher and the tissue/medium (T/M) ratio increased within the concentration range from 3.0–9.0. 4. Under DNP (1 mM) the asymmetry and dose dependence of the permeability and tissue uptake of 3H-digitoxin observed in controls were almost abolished. Therefore it is likely that the transfer of 3H-digitoxin in the intestine involves a mechanism more complex than simple diffusion. The existence of more than a two compartment system and/or the contribution of an active transport mechanism is suggested.
    Type of Medium: Electronic Resource
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