Effects of lysosomotropic detergents on the human malarial parasite Plasmodium falciparum in in vitro culture.

Various lysosomotropic detergents were tested in this work on in vitro cultures of Plasmodium falciparum and are shown to be potent antimalarial agents. The order of antimalarial potency was similar to that of cell toxicity on mammalian cells in culture (Miller DK et al., J Cell Biol 97, 1841-51 (1983]. The most efficient agents, N-dodecyl-imidazole (NDI) and N-dodecyl morpholine (NDM) displayed IC50 values of 6.7 +/- 0.7 microM and 23 +/- 5 microM. The mechanism of action of NDI measured at IC50 concentrations displayed the following features: irreversible antimalarial effect after 15 min exposure of cells to drug; alkalinization of the parasite food vacuole; inhibition of protein synthesis; inhibition of host cell protein digestion by the parasite; lack of vacuolar membrane disruption; lack of effect on the rate of constitutive autoproteolysis. No biochemical or ultrastructural indications were found to support a detergent-like action of NDI and its structural congeners on the major acidic compartment of the parasite, the food vacuole. Rather, alkalinization of that compartment by weak-base accumulation properties of the amphiphilic drugs and ensuing protonophoric effect are likely to play a major role in the various parasite-associated properties affected by these drugs.

Bioflavonoid effects on in vitro cultures of Plasmodium falciparum. Inhibition of permeation pathways induced in the host cell membrane by the intraerythrocytic parasite.

A series of polyhydroxyphenol glycosides including bioflavonoid-glycosides structurally-related to phlorizin (phloretin-2-beta-glucoside) have been tested for their capacity to inhibit permeation pathways induced in red cell membranes by intraerythrocytic Plasmodium falciparum parasites. The permeation through these pathways has been assessed on trophozoites by sorbitol-mediated hemolysis based on a novel technique of high sensitivity and time resolution which has been adapted for handling relatively large number of samples in microtitration plates. Changes in the number of phenolic groups and to a lesser extent changes in the relative position of these groups had a substantial effect on the inhibitory efficacy of the phlorizin derivatives. Diglycoside derivatives were completely ineffective while various monoglycoside derivatives had comparable effects. Structure-activity relationship (SAR) studies of 3-monosubstituted phlorizin derivatives indicate that the inhibitory potency varied considerably with the chemical nature of the group substituted in the 3 position. Inhibition correlated best (r = 0.90) with Hammett's constant, underscoring the role of the electron withdrawing capacity of the chemical groups substituted on the hydroxydihydrochalcone moiety. On the other hand, substitution with lipophilic groups had either minimal effects or reduced the inhibitory power of the derivatives. Inhibition of transport correlated with the inhibition of intraerythrocytic parasite growth and provides a basis for new therapeutic approaches of malaria. Based on the SAR studies, a 3-isothiocyano analog of phlorizin was synthesized and shown to block irreversibly the above permeation pathways (20 microM, 10 min reaction at ambient temperature) as well as the intraerythrocytic growth of the parasite. The present study provides proof for the involvement of amino groups in red cell membrane components as controlling elements of the permeation pathways induced by the intraerythrocytic parasite. The putative groups could serve as targets for affinity labeling of the membrane components associated with the permeation function.

Relative affinities of bilirubin for serum albumins from different species.

Relative equilibrium constants ("affinity ratios") of complexes of bilirubin with a molar excess of charcoal-treated serum albumins from different species (human, bovine, rabbit and chicken) in aqueous solution, were estimated by circular dichroism measurements in the visible region at 26-27 degrees C, pH 7.4, and in the presence of 0.1 M NaCl. By variation of the mol ratios of the components of pairs of different bilirubin-serum albumin complexes showing circular dichroic bands of opposite sign, the apparent association constants of complexes of bilirubin with either human or chicken albumin were found to be greater by factors between 6 and 17 than those of bovine or rabbit albumins. The usefulness in the determination of affinity ratios is illustrated by the evaluation of single equilibrium constants of systems of high-ligand affinity from those of relatively lower affinity, the latter of which are more readily amendable to direct experimental measurement.