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Transport of isometamidium (Samorin) by drug-resistant and drug-sensitive Trypanosoma congolense

Published online by Cambridge University Press:  06 April 2009

I. A. Sutherland
Affiliation:
Department of Veterinary Physiology, University of Glasgow Veterinary School, Bearsden Road, Glasgow G61 1QH, Scotland
A. Mounsey
Affiliation:
Department of Veterinary Physiology, University of Glasgow Veterinary School, Bearsden Road, Glasgow G61 1QH, Scotland
P. H. Holmes
Affiliation:
Department of Veterinary Physiology, University of Glasgow Veterinary School, Bearsden Road, Glasgow G61 1QH, Scotland

Extract

The uptake kinetics of a 14C-labelled trypanocidal compound isometamidium chloride (SamorinR, RMB Animal Health Ltd, UK) was measured in drug-resistant and drug-sensitive Trypanosoma congolense. It was established that drug uptake was significantly more rapid and quantitatively greater in drug-sensitive parasites. There was clear evidence that drug uptake in both the resistant and sensitive trypanosomes was by a specific, receptor-mediated process. This specific drug transport was energy-dependent, being sensitive to metabolic inhibition with SHAM/glycerol. Significant differences in drug transport were observed which could be correlated with resistance to isometamidium. The optimal pH for drug accumulation was lowered in the resistant trypanosomes; this finding, along with an observed change in specificity for the related compound homidium bromide, suggested that the specific receptor for isometamidium is altered in the resistant trypanosomes, possibly resulting in a reduction in drug uptake. In addition to these alterations in drug uptake, efflux of isometamidium also appears to occur in the resistant trypanosomes. Both a reduction in incubation temperature and metabolic inhibition increased the level of trypanosome-associated isometamidium in the resistant parasites. This was in contrast to observations using drug-sensitive parasites. Furthermore, the addition of calcium flux-modulating agents to the incubation medium also resulted in an increase in accumulation by the resistant parasites.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1992

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References

Bitonti, A. J., Sjoerdsma, A., Mccann, P. P., Kyle, D. E., Oduola, A. M. J., Rossan, R. N., Milhous, W. K. & Davidson, D. E. Jr (1988). Reversal of chloroquine resistance in the malaria parasite Plasmodium falciparum by desipramine. Science 242, 1301–3.Google Scholar
Damper, D. & Patton, C. L. (1976). Pentamidine transport and sensitivity in brucei-group trypanosomes. Journal of Protozoology 23, 349–56.Google Scholar
Fairlamb, A. H., Opperdoes, F. R. & Borst, P. (1977). New approach to screening drugs for activity against African trypanosomes. Nature, London 265, 270–1.Google Scholar
Fitch, C. D., Chevli, R. & Gonzalez, Y. (1975). Chloroquine resistance in malaria: variations of substrate-stimulated chloroquine accumulation. Journal of Pharmacology and Experimental Therapeutics 195, 389–96.Google Scholar
Fojo, A., Akiyama, S., Gottesman, M. M. & Pastan, I. (1985). Reduced drug accumulation in multiple drug-resistant human KB carcinoma cell lines. Cancer Research 45, 3002–7.Google Scholar
Frame, I., Ross, C. A. & Luckins, A. G. (1990). Characterization of Trypanosoma congolense serodemes in stocks isolated from Chipata District, Zambia. Parasitology 101, 235–41.Google Scholar
Frommel, T. O. & Balber, A. E. (1987). Flow cytofluorimetric analysis of drug accumulation by multidrug-resistant Trypanosoma brucei brucei and T. b. rhodesiense. Molecular and Biochemical Parasitology 26, 183–92.Google Scholar
Kartner, N. & Ling, V. (1989). Multidrug resistance in cancer. Scientific American 260, 2633.CrossRefGoogle Scholar
Krogstad, D. J., Gluzman, I. Y., Kyle, D. E., Oduola, A. M. J., Martin, S. K., Milhous, W. K. & Schlesinger, P. H. (1987). Efflux of chloroquine from Plasmodium falciparum: mechanism of chloroquine resistance. Science 238, 1283–5.Google Scholar
Kupper, W. & Wolters, M. (1983). Observations on drug resistance of Trypanosoma (Nannomonas) congolense and Trypanosoma (Duttonella) vivax in cattle at a feed lot in Northern Ivory Coast. Zeitschrift für Tropenmedizin und Parasitologie 34, 203–5.Google Scholar
Lanham, S. M. & Godfrey, D. G. (1970). Isolation of salivarian trypanosomes from man and other animals using DEAE-cellulose. Experimental Parasitology 28, 521–34.CrossRefGoogle Scholar
Martin, S. K., Oduola, A. M. J. & Milhous, W. K. (1987). Reversal of chloroquine resistance in Plasmodium falciparum by verapamil. Science 235, 899901.Google Scholar
Mayombo, T. M. (1990). African animal trypanosomiasis: immunochemical studies of the trypanocide, isometamidium chloride. MVM thesis, University of Glasgow.Google Scholar
Neal, R. A., Van Beuren, J., Mccoy, N. G. & Iwobi, M. (1989). Reversal of drug resistance in Trypanosoma cruzi and Leishmania donovani by verapamil. Transactions of the Royal Society of Tropical Medicine and Hygiene 83, 197–8.Google Scholar
Opperdoes, F. R., Aarsen, P. N., Van Der Meer, C. & Borst, P. (1976). Trypanosoma brucei: An evaluation of salicylhydroxamic acid as a trypanocidal drug. Experimental Parasitology 40, 198205.Google Scholar
Pinder, M. & Authie, E. (1984). The appearance of isometamidium resistant Trypanosoma congolense in West Africa. Acta Tropica 41, 247–52.Google Scholar
Riehm, H. & Biedler, J. L. (1972). Potentiation of drug effect by Tween 80 in Chinese hamster cells resistant to actinomycin D and daunomycin. Cancer Research 32, 1195–200.Google Scholar
Ross, C. A., Gray, M. A., Taylor, A. M. & Luckins, A. G. (1985). In vitro cultivation of Trypanosoma congolense: establishment of infective mammalian forms in continuous culture after isolation from the blood of infected mice. Acta Tropica 42, 113–23.Google Scholar
Samuelson, J., Ayala, P., Orozco, E. & Wirth, D. (1990). Emetine-resistant mutants of Entamoeba histolytica overexpress mRNAs for multidrug resistance. Molecular and Biochemical Parasitology 38, 281–90.Google Scholar
Schonefeld, A. R., Rottcher, D. & Moloo, S. K. (1987). The sensitivity to trypanocidal drugs of Trypanosoma vivax isolated in Kenya and Somalia. Tropical Medicine and Parasitology 38, 177–80.Google Scholar
Sutherland, I. A., Peregrine, A. S., Lonsdale-Eccles, J. D. & Holmes, P. H. (1991). Reduced accumulation of isometamidium by drug-resistant Trypanosoma congolense. Parasitology 103, 245–51.Google Scholar
Tanabe, K., Kato, M., Izumo, A., Hagiwara, A. & Doi, S. (1990). Plasmodium chabaudi: in vivo effects of Ca2+ antagonists on chloroquine-resistant and chloroquine-sensitive parasites. Experimental Parasitology 70, 419–26.Google Scholar
Whitelaw, D. D., Bell, I. R., Holmes, P. H., Moloo, S. K., Hirumi, H., Urquhart, G. H. & Murray, M. (1986). Isometamidium chloride prophylaxis against Trypanosoma congolense challenge and the development of immune responses in Boran cattle. Veterinary Record 118, 722–6.Google Scholar