The Multixenobiotic Resistance Mechanism in Aquatic Organisms
- 1 January 1992
- journal article
- research article
- Published by Taylor & Francis in Critical Reviews in Toxicology
- Vol. 22 (1), 23-43
- https://doi.org/10.3109/10408449209145320
Abstract
Many aquatic organisms thrive and reproduce in polluted waters. This fact indicates that they are well equipped with a defense system(s) against several toxic xenobiotics simultaneously because water pollution is typically caused by a mixture of a number of pollutants. We have found that the biochemical mechanism underlying such “multixenobiotic” resistance in freshwater and marine mussel, in several marine sponges, and in freshwater fish is similar to the mechanism of multidrug resistance (MDR) found in tumor cells that became refractory to treatment with a variety of chemotherapeutic agents. All these organisms possess a verapamil-sensitive potential to bind 2-acetylaminofluorene and vincristine onto membrane vesicles. They all express mRNA formdr 1 gene, andmdr 1 protein product, the glycoprotein P170. Finally, inin vivo experiments, the accumulation of xenobiotics is enhanced in all investigated organisms in the presence of verapamil, the inhibitor of the P170 extrusion pump. The knowledge that the presence of one xenobiotic may block the pumping out, and hence accelerating accumulation, of others, may help us to understand and interprete our present and past data on different environmental parameters obtained using indicator organisms.Keywords
This publication has 65 references indexed in Scilit:
- Retention of vital dyes correlates inversely with the multidrug-resistant phenotype of adriamycin-selected murine fibrosarcoma variantsExperimental Cell Research, 1990
- Alterations inras-gene expression and intracellular distribution of protein kinase C in the spongeGeodia cydonium in response to marine pollutionMarine Biology, 1990
- Circumvention of multidrug resistance in P388 murine leukemia cells by a novel inhibitor of cyclic AMP-dependent protein kinase, H-87Cancer Letters, 1990
- Correlation of protein kinase C translocation, P-glycoprotein phosphorylation and reduced drug accumulation in multidrug resistant human KB cellsBiochemical and Biophysical Research Communications, 1990
- DNA Adducts Formed by 2‐Amino‐3,8‐dimethylimidazo[4,5‐f]quinoxaline in Rat Liver: Dose‐Response on Chronic AdministrationJapanese Journal of Cancer Research, 1990
- The Clinical Relevance of Multidrug ResistanceCancer Investigation, 1990
- Distinct glutathione-dependent enzyme activities and a verapamil-sensitive binding of xenobiotics in a fresh-water mussel Anodonta cygneaBiochemical and Biophysical Research Communications, 1989
- Role of the Glutathione Redox Cycle in Acquired and de Novo Multidrug ResistanceScience, 1988
- Transformation of rat liver epithelial cells with v-H-ras or v-raf causes expression of MDR-1, glutathione-S-transferase-P and increased resistance to cytotoxic chemicalsCarcinogenesis: Integrative Cancer Research, 1988
- The mdrl gene, responsible for multidrug-resistance, codes for P-glycoproteinBiochemical and Biophysical Research Communications, 1986