| Autor: |
Haenen HE; Department of Toxicology, Agricultural University, Tuinlaan 5, 6703 HE Wageningen, The Netherlands., Rogmans P, Temmink JH, van Bladeren PJ |
| Jazyk: |
angličtina |
| Zdroj: |
Toxicology in vitro : an international journal published in association with BIBRA [Toxicol In Vitro] 1994 Apr; Vol. 8 (2), pp. 207-14. |
| DOI: |
10.1016/0887-2333(94)90184-8 |
| Abstrakt: |
This in vitro study describes proximal tubular toxicity of quinone thioethers after incubation of these compounds on either side of a renal proximal tubular cell (RPTC) monolayer. These cells were cultured to confluency on porous supports of tissue culture inserts, and the apically and basolaterally induced toxicity of two thioether conjugates of menadione (2-methyl-1,4-naphthoquinone) was investigated. As judged by lactate dehydrogenase (LDH) leakage, the glutathione (GSH) conjugate of menadione (MGNQ) was only toxic after basolateral challenge. However, after inhibition of gamma-glutamyl transpeptidase by acivicin, MGNQ was also toxic after apical challenge. The mercapturic acid of menadione [M(NAC)NQ] displayed cytotoxicity both after apical and basolateral challenge. From the basolateral side, MGNQ and M(NAC)NQ-induced cytotoxicity could be enhanced by inhibition of the organic anion transport system with probenecid. Inhibition of beta-lyase did not influence M(NAC)NQ-induced cytotoxicity. In addition, inhibition of intracellular N-deacetylation of M(NAC)NQ using paraoxon potentiated the observed toxic effect. Thus, it appears that the MGNQ and M(NAC)NQ-induced cytotoxicity is the result of extracellular events, presumably redox cycling. Putative uptake of the conjugates is likely to be associated with detoxification of these compounds. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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