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  • Electronic Resource  (4)
  • Liver  (3)
  • 24-^1^3C-labelled internal standard  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Clinica Chimica Acta 162 (1987), S. 45-51 
    ISSN: 0009-8981
    Keywords: 24-^1^3C-labelled internal standard ; Gas chromatographymass spectrometry ; Serum bile acid
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 277 (1973), S. 297-304 
    ISSN: 1432-1912
    Keywords: Liver ; Perfusion ; BSP ; Bile Salts ; Bile Flow
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Excretory function of a perfused rat liver preparation has been quantified by determination of the BSP-transport maximum (BSP-Tm). An in situ liver perfusion system employing a semisynthetic perfusion medium containing Krebs-Ringer-bicarbonate solution, bovine erythrocytes and bovine albumin was used. Taurocholate was continuously infused throughout the perfusion to provide the liver with a physiologic load of bile salts. After 3 h of perfusion the BSP-Tm was 33.8±SD 4.7 nmoles/min/g liver. In spite of a 33% reduction of bile flow due to a decrease of the bile salt independent fraction, the BSP-Tm was not significantly different from that found in bile fistula rats of the same strain (36.5±SD 9.6 nmoles/min/g liver). It is concluded that the BSP-Tm of this perfused rat liver preparation, provided with a physiologic load of bile salts, may be maintained at in vivo values. This perfusion model may therefore be particularly useful for quantitative studies of the hepatic excretory processes.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 285 (1974), S. 165-174 
    ISSN: 1432-1912
    Keywords: Liver ; Perfusion ; Bile Salts ; Biliary Excretion ; Bile Flow
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The excretory transport maximum (Tm) for taurocholate was determined in the perfused rat liver and compared to that obtained in the intact rat. An in situ liver perfusion system employing a semisynthetic perfusion medium containing Krebs-Ringer-bicarbonate solution, bovine erythrocytes and bovine albumin was used. In contrast to the bromosulfophthalein (BSP)-Tm reported previously, the taurocholate-Tm was 45% smaller in vitro (196±17 nmol/min per g liver) than in vivo (357±10 nmol/min per g liver), indicating that bile salt transport is more susceptible to alterations induced by the conditions of the perfusion than BSP transport. These findings add to the differences observed previously between the hepatic handling of anionic dyes and bile salts. At a low taurocholate infusion rat (57 nmol/min per g liver) the normal relationship between bile salt excretion and bile flow observed in vivo was maintained in the perfused liver. At higher taurocholate infusion rates, however, bile flow, for a given bile salt excretion rate, was smaller than in vivo. These findings should be taken into account when the isolated perfused rat liver is employed for studies of bile formation.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 270 (1971), S. 98-101 
    ISSN: 1432-1912
    Keywords: Bile Flow ; Bile Acids ; Liver ; Phenobarbital
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Treatment of rats with phenobarbital for 3 or 7 days increases bile flow to 150% or 151% of controls. This choleresis is not due to an increase of total bile acid output nor to a change of the bile acid pattern in bile.
    Type of Medium: Electronic Resource
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