Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/32657
Title: Flavonoid dimers as bivalent modulators for pentamidine and sodium stiboglucanate resistance in Leishmania
Authors: Wong, ILK
Chan, KF
Burkett, BA
Zhao, Y
Chai, Y
Sun, H
Chan, TH
Chow, LMC 
Issue Date: 2007
Publisher: American Society for Microbiology
Source: Antimicrobial agents and chemotherapy, 2007, v. 51, no. 3, p. 930-940 How to cite?
Journal: Antimicrobial agents and chemotherapy 
Abstract: Drug resistance by overexpression of ATP-binding cassette (ABC) transporters is an impediment in the treatment of leishmaniasis. Flavonoids are known to reverse multidrug resistance (MDR) in Leishmania and mammalian cancers by inhibiting ABC transporters. Here, we found that synthetic flavonoid dimers with three (compound 9c) or four (compound 9d) ethylene glycol units exhibited a significantly higher reversing activity than other shorter or longer ethylene glycol-ligated dimers, with ∼3-fold sensitization of pentamidine and sodium stibogluconate (SSG) resistance in Leishmania, respectively. This modulatory effect was dosage dependent and not observed in apigenin monomers with the linker, suggesting that the modulatory effect is due to its bivalent nature. The mechanism of reversal activity was due to increased intracellular accumulation of pentamidine and total antimony in Leishmania. Compared to other MDR modulators such as verapamil, reserpine, quinine, quinacrine, and quinidine, compounds 9c and 9d were the only agents that can reverse SSG resistance. In terms of reversing pentamidine resistance, 9c and 9d have activities comparable to those of reserpine and quinacrine. Modulators 9c and 9d exhibited reversal activity on pentamidine resistance among LeMDR1 -/-, LeMDR1 +/+, and LeMDR1-overexpressed mutants, suggesting that these modulators are specific to a non-LeMDR1 pentamidine transporter. The LeMDR1 copy number is inversely related to pentamidine resistance, suggesting that it might be involved in importing pentamidine into the mitochondria. In summary, bivalency could be a useful strategy for the development of more potent ABC transporter modulators and flavonoid dimers represent a promising reversal agent for overcoming pentamidine and SSG resistance in parasite Leishmania.
URI: http://hdl.handle.net/10397/32657
ISSN: 0066-4804
EISSN: 1098-6596
DOI: 10.1128/AAC.00998-06
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