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  • 1
    ISSN: 1437-7799
    Keywords: Key words Desferrioxamine ; Cadmium ; Metallothionein ; Nephrotoxicity ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background. Desferrioxamine (DFO) a chelating agent, is used to treat metal toxicity caused by iron and aluminum in patients on hemodialysis. We hypothesized that DFO could also be used to treat cadrium-induced nephropathy. Animal experiments were therefore performed to explore whether DFO removed cadmium (Cd) from the kidneys of rats with a Cd burden. Methods. Rats received subcutaneous injections of Cd chloride (3 mg Cd/kg per day, days 0–7) followed by DFO (50 mg/kg per day, days 8–14). Levels of Cd were determined in liver, kidneys, and plasma. Enzymes assays and histopathological examination were performed in kidneys. Results. In liver, Cd injections elevated Cd levels; subsequent injections of DFO lowered the Cd levels compared with levels after injections of Cd alone. In kidneys, Cd injections increased levels of total Cd and Cd bound to cellular membranes (Mem-Cd), and decreased leucine aminopeptidase (LAP) activity (a marker of renal injury); subsequent injections of DFO elevated levels of total Cd and Mem-Cd, and lowered LAP activity compared with fundings after the injection of Cd alone. After the injections of Cd alone and DFO following Cd the renal levels of Cd were below the critical concentration required to cause renal injury, since no histopathological changes were observed in the kidney. Conclusion. DFO administration to Cd-burdened rats removed Cd from the liver, but led to accumulation of Cd in the kidneys, particularly in the cellular membranes. These results suggest that if DFO is given long-term to Cd-burdened patients, the Cd level in kidneys, particularly in renal cellular membranes, could reach concentrations that could cause manifest renal injury.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 4 (1970), S. 13-23 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Commercially available collagen membrance was evaluated as a hemodialysis membrane in the Kolff quad-coil artificial kidney. The inherent physical weakness of the membrane was strengthened by a double-screen support substracture in a coil. Greater metabolite clearance and ultrafiltration (over four times) were demonstrated with the double-screen-supported collagen coil than with either cellophane or cuprophane membrane supported by the same double-screen support substructure.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 4 (1970), S. 469-485 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: For patients performing hemodialysis at home the assembly of the artificial kidney must be simple. To achieve this, a disposable envelope, consisting of two membranes bonded to a supporting substructure, was developed for the Kiil artificial kidney. This envelope was tested in vitro for metabolite clearance, pressure-flow relationship, ultrafiltration, and priming volume. The clearance of this envelope for different metabolites proved to be higher than that achieved with conventional assembly of the Kiil with wet Cuprophan membranes. Analysis of the resistance to mass transfer indicated that the disposable envelope has decreased the blood- and dialyzate-side resistances and provides an increase in effective membrane area, thereby enhancing overall mass transfer. The envelope also showed higher resistance to blood flow and a lower priming volume. In vitro testing of this envelope has shown the feasibility of practical clinical application.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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