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  • 1
    ISSN: 1432-1238
    Keywords: Key words Hemofiltration ; Hemodiafiltration ; Folic acid ; Vitamin B6 ; Clearances ; Micronutrient
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Objective: To determine to what extent hydrosoluble vitamins are removed by continuous renal replacement therapy (CRRT); to evaluate clearances, removal rates, and evolution of serum concentrations of folic acid and pyridoxal-5′-phosphate (P-5′-P), the active moiety of vitamin B6 during CRRT. Design: A prospective, non-interventional, descriptive study on vitamin losses induced by CRRT. Setting: Medical and surgical intensive care units in a tertiary university-affiliated hospital. Patients: A total of ten critically ill patients in oligoanuric acute renal failure (five treated by continuous venovenous hemofiltration and five by continuous venovenous hemodiafiltration) with a mean effluent rate of 1801 ± 468 ml/h. Nutritional support was not modified and additional vitamin supplements were not provided during study periods. Measurements and results: Concentrations of folic acid and P-5′-P were determined daily during CRRT. Samples for folic acid, P-5′-P, urea, and creatinine were taken simultaneously from the blood at the dialyzer inlet and from the effluent, at CRRT initiation, and daily thereafter over an average of 3.4 ± 1.2 days. Samples were processed by immunochemiluminescence for folic acid and by radioenzymatic assay for P-5′-P determinations with normal ranges above 6.8 nmol/l and from 11.5 to 179.3 nmol/l, respectively. Marked decreases in serum folic acid and P-5′-P concentrations were noticed over time with mean daily reductions of 12.6 and 13.7 %. Serum folic acid concentrations decreased from 42.7 to 16.0 nmol/l and serum P-5′-P decreased from 14.4 to 5.0 nmol/l in the blood coming in to the dialyzer over the study period. Clearances and removal rates were determined from the effluent side. During CRRT, mean (± SEM) folic acid and P-5′-P clearances were 20.5 ± 6.3 ml/min (n = 34) and 13.2 ± 10.6 ml/min (n = 22), whereas mean urea clearance was 27.1 ± 5.1 ml/min (n = 26). Folic acid and P-5′-P removal rates were 27.0 ± 34.2 and 3.4 ± 2.0 nmol/h, corresponding to mean daily losses of nearly 650 and 80 nmol/day respectively. Conclusion: Significant losses of folic acid and P-5′-P (and most likely of other hydrosoluble vitamins) occur during CRRT. Considering that stores of most hydrosoluble vitamins are relatively low in critically ill patients, supplementation should be provided to patients treated similarly.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 89 (1994), S. 583-589 
    ISSN: 1432-2242
    Keywords: Coat protein ; Disease resistance ; Molecular markers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Presence of the dominant Tu gene in Lactuca sativa is sufficient to confer resistance to infection by turnip mosaic virus (TuMV). In order to obtain an immunological assay for the presence of TuMV in inoculated plants, the TuMV coat protein (CP) gene was cloned by amplification of a cDNA corresponding to the viral genome using degenerate primers designed from conserved potyvirus CP sequences. The TuMV CP was overexpressed in Escherichia coli, and polyclonal antibodies were produced. To locate Tu on the L. sativa genetic map, F3 families from a cross between cvs “Cobbham Green” (resistant to TuMV) and “Calmar” (susceptible) were genotyped for Tu. Families known to be recombinant in the region containing Tu were infected with TuMV and tested by the indirect enzyme-linked immunosorbent assay (ELISA) using the anti-CP serum. This assay placed Tu between two random amplified polymorphic DNA (RAPD) markers and 3.2 cM from Dm5/8 (which confers resistance to Bremia lactucae). Also, bulked segregant analysis was used to screen for additional RAPD markers tightly linked to the Tu locus. Five new markers linked to Tu were identified in this region, and their location on the genetic map was determined using informative recombinants in the region. Six markers were identified as being linked within 2.5 cM of Tu.
    Type of Medium: Electronic Resource
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