Synthesis and biological evaluation of potential modulators of malarial glutathione-S-transferase(s)

Abstract

Glutathione-S-transferase(s) (E.C.2.5.1.18, GSTs) have been investigated in parasitic protozoans with respect to their biochemistry and they have been identified as potential vaccine candidates in protozoan parasites and as a target in the synthesis of new antiparasitic agents. In a search towards the identification of novel biochemical targets for antimalarial drug design, the area of Plasmodium glutathione metabolism provides a number of promising chemotherapeutic targets. GST activity was determined in various subcellular fractions of malarial parasites Plasmodium yoelii and was found to be localized mainly in the cytosolic fraction (specific activity, c. 0.058 ± 0.016 μmol/min/mg protein). Hemin, a known inhibitor of mammalian GST(s), maximally inhibited this enzyme from P. yoelii to nearly 86%. In a search towards synthetic modulators of malarial GST(s), 575 compounds belonging to various chemical classes were screened for their effect on crude GST from P. yoelii and 92 compounds belonging to various chemical classes were studied on recombinant GST from P. falciparum. Among all the compounds screened, 83 compounds inhibited/stimulated the enzyme from P. yoelii/P. falciparum to the extent of 40% or more.

Keywords::

• Glutathione-S-transferase(s)
• inhibition
• hemin
• Plasmodium yoelii
• Plasmodium falciparum
• malaria

Acknowledgements

This investigation received financial support from Volkswagen Stiftung, Germany. We are also grateful to Dr S.K. Puri, Head, Parasitology Division, CDRI, Lucknow for providing the P. yoelii nigeriensis infected albino mice for the maintenance of infection in the present work.