Arsenite-resistant Leishmania donovani promastigotes express an enhanced membrane P-type adenosine triphosphatase activity that is sensitive to verapamil treatment |
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Authors: | Vikram Prasad Jaspreet Kaur Chinmoy S. Dey |
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Affiliation: | (1) Department of Biotechnology, National Institute of Pharmaceutical Education and Research, Sector 67, S.A.S. Nagar, Punjab 160 062, India e-mail: niper@chd.nic.in Tel.: +91-172-673848; Fax: +91-172-677185, IN |
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Abstract: | An arsenite-resistant strain of Leishmania donovani was generated in vitro by sequential exposure to higher concentrations of sodium m-arsenite. The resistant strain displayed a low level of cross-resistance to structurally unrelated drugs such as doxorubicin and pentamidine. This cross-resistance was sensitive to the calcium-channel blocker verapamil. The membrane-associated P-type adenosine triphosphatase (ATPase) activity detected in crude membrane fractions of the resistant strain was 3-fold that found in the wild-type parasites. The enhanced ATPase activity was unaffected by the presence of verapamil in the reaction mixture. However, when cells were grown in the presence of verapamil the membrane-associated ATPase activity of the resistant strain showed significant inhibition. Received: 6 December 1999 / Accepted: 11 January 2000 |
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Keywords: | AbbreviationsMTT 3-[4,5-Dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide MDR Multiple-drug resistance EGTA Ethylene glycol bis(2-aminoethyl ether)-N,N,N′ N′ -tetraacetic acid |
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