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  • 1
    Online-Ressource
    Online-Ressource
    SAGE Publications ; 1996
    In:  Alternatives to Laboratory Animals Vol. 24, No. 2 ( 1996-03), p. 161-172
    In: Alternatives to Laboratory Animals, SAGE Publications, Vol. 24, No. 2 ( 1996-03), p. 161-172
    Kurzfassung: The effects of a widely used antitumour drug, cisplatin, on freshly isolated porcine proximal tubular cells (PPTC) in suspension were investigated. Incubation of the PPTC with 5-500μM cisplatin resulted in a decrease in mitochondrial membrane potential (MMP) and in cell death. In addition, the formation of reactive oxygen species (ROS) was observed within 20 minutes. Prevention of ROS formation with the antioxidants diphenyl- p-phenylene-diamine (DPPD) or desferrioxamine had no effect on the cisplatin-induced effects on MMP and cell death, implying that cisplatin-induced ROS formation is not a cause of cell death. In order to investigate whether the ROS formation was related to mitochondrial damage, we determined the effects of cisplatin on the enzymatic activities of NADP:ubiquinone reductase (Complex I) and succinate:ubiquinone reductase (Complex II) of the respiratory chain. Exposure of the PPTC to cisplatin resulted in a time-dependent and dose-dependent inhibition of the activities of both Complex I and Complex II. The inhibition of these activities and the depletion of ATP could not be prevented by the antioxidants, indicating that these effects are not a consequence of ROS formation. We propose that damage to the mitochondria could be a key event in cisplatin-induced cell death.
    Materialart: Online-Ressource
    ISSN: 0261-1929 , 2632-3559
    Sprache: Englisch
    Verlag: SAGE Publications
    Publikationsdatum: 1996
    ZDB Id: 2390905-5
    SSG: 12,22
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    In: Human & Experimental Toxicology, SAGE Publications, Vol. 22, No. 10 ( 2003-10), p. 535-540
    Kurzfassung: Nephrotoxicity is the most important dose-limiting factor in cisplatin based anti-neoplastic treatment. Pretreatment with bismuth salts, used as pharmaceuticals to treat gastric disorders, has been demonstrated to reduce cisplatin-induced renal cell death in clinical settings and during in vivo and in vitro animal experiments. To investigate the genomic basis of this renoprotective effect, we exposed NRK-52E cells, a cell line of rat proximal tubular epithelial origin, to 33 mM Bi 3 for 12 hours, which made them resistant to cisplatin-induced apoptosis. Differentially expressed genes in treated and untreated NRK-52E cells were detected by subtraction PCR and microarray techniques. Genes found to be down regulated (0.17 / 0.31-times) were cytochrome c oxidase subunit I, BAR (an apoptosis regulator), heat-shock protein 70-like protein, and three proteins belonging to the translation machinery (ribosomal proteins S7 and L17, and S1, a member of the elongation factor 1-alpha family). The only up-regulated gene was glutathione Stransferase subunit 3A (1.89-times). Guided by the expression levels of these genes, it may be possible to improve renoprotective treatments during anti-neoplastic therapies.
    Materialart: Online-Ressource
    ISSN: 0960-3271 , 1477-0903
    Sprache: Englisch
    Verlag: SAGE Publications
    Publikationsdatum: 2003
    ZDB Id: 1483723-7
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
    Online-Ressource
    SAGE Publications ; 1994
    In:  Alternatives to Laboratory Animals Vol. 22, No. 6 ( 1994-11), p. 462-473
    In: Alternatives to Laboratory Animals, SAGE Publications, Vol. 22, No. 6 ( 1994-11), p. 462-473
    Kurzfassung: The susceptibility to nephrotoxins of freshly isolated porcine proximal tubular cells (PPTC) and cultured PPTC in suspension were compared, with a view to using PPTC as in vitro models for studying nephrotoxicity. In a previous paper, we described how, in freshly isolated PPTC, well-known nephrotoxins such as mercury (II) chloride, cisplatin, p-aminophenol and halogenated hydrocarbons caused a dose-dependent decrease in the viability and mitochondrial membrane potential of the PPTC. In this paper, we show that suspensions of cultured PPTC, harvested by trypsinisation, are less susceptible to nephrotoxins, possibly due to the synthesis of extracellular matrix components. PPTC in primary culture are suitable for relatively long-term nephrotoxicity studies. This was demonstrated by incubation with mercury (II) chloride for 24 hours, resulting in a dose-dependent loss of viability. Freshly isolated PPTC can be cryopreserved by computer-controlled freezing. The cryopreserved PPTC displayed an increased susceptibility to mercury (II) chloride and a decreased susceptibility to cisplatin and 1,1-dichloro-2,2-difluoroethylene-cysteine, the toxicity of the latter indicating that the renal enzyme β-lyase remains active during cryopreservation.
    Materialart: Online-Ressource
    ISSN: 0261-1929 , 2632-3559
    Sprache: Englisch
    Verlag: SAGE Publications
    Publikationsdatum: 1994
    ZDB Id: 2390905-5
    SSG: 12,22
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Online-Ressource
    Online-Ressource
    SAGE Publications ; 1993
    In:  Alternatives to Laboratory Animals Vol. 21, No. 4 ( 1993-10), p. 457-465
    In: Alternatives to Laboratory Animals, SAGE Publications, Vol. 21, No. 4 ( 1993-10), p. 457-465
    Kurzfassung: Porcine proximal tubular cells (PPTC) were isolated from kidneys obtained from slaughterhouse pigs. After disruption of the connective tissue by collagenase, purification was achieved by filtration and centrifugation on a discontinuous density gradient. Single cells and clusters of 10–40 cells were obtained, having a viability of 93–99%. More than 81% of the single cells showed γ-glutamyltranspeptidase (GGT) activity and more than 95% showed non-specific esterase (NE) activity, marker enzymes for proximal tubule cells. One kidney yielded 1 x 10 7 single cells and 3x10 7 cells in clusters. Cells were kept in primary culture on plastic or collagen-coated dishes. In the presence of 10% serum, confluency was reached within four days. The monolayers could be kept in culture for four days after confluency, in serum-free conditions. When seeded in serum-free conditions, PPTC did not reach confluency, but the cells could be kept in culture for at least 16 days. The cells displayed epithelial morphology, i.e. cobblestone shape, dome formation, microvilli, basal infoldings and abundant mitochondria. PPTC in primary culture still displayed NE activity, while 80% of the cells showed GGT activity. In conclusion, the isolated cells are of proximal tubular origin, reach confluency in 3–4 days in the presence of 10% serum, and can be kept as monolayers in serum-free conditions for four additional days and may provide a suitable in vitro model for long-term nephrotoxicity studies.
    Materialart: Online-Ressource
    ISSN: 0261-1929 , 2632-3559
    Sprache: Englisch
    Verlag: SAGE Publications
    Publikationsdatum: 1993
    ZDB Id: 2390905-5
    SSG: 12,22
    Standort Signatur Einschränkungen Verfügbarkeit
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