Toxicity of certain products of lipid peroxidation to the human malaria parasite Plasmodium falciparum.

Abstract:

:Aldehydes generated during radical-induced lipid peroxidation, in particular 4-hydroxynonenal, are known to inhibit growth of certain cells. To extend our arguments that free radicals might be involved in the host response against malaria parasites we tested 26 carbonyls (n-alkanals, C6-C11; 2-alkenals, C3-C9; 2,4-alkadienals, C7, C9, C10; 4-OH-2-alkenals, C6, C8, C9; 2-alkanones, C3-C9; and malonyldialdehyde) against Plasmodium falciparum in vitro. We had previously detected many of these substances in oxidant-stressed, malaria-infected erythrocytes. Three 2,4-alkadienals (C7, C9 and C10) and three 4-OH-2-alkenals (C6, C8 and C9), at 20-100 microM concentrations, markedly inhibited incorporation of [3H]-hypoxanthine by P. falciparum. Acrolein had low effect, and none of the other compounds (12 aldehydes and 7 ketones) were active at concentrations up to 100 microM. Malonyldialdehyde was without effect at concentrations up to 450 microM. The aldehydes found to be inhibitory against P. falciparum could contribute to both the non-antibody host responses against this parasite and the antimalarial effects of radical-generating compounds such as t-butyl hydroperoxide, hydrogen peroxide, alloxan, isouramil, divicine and primaquine.

journal_name

Biochem Pharmacol

journal_title

Biochemical pharmacology

authors

Clark IA,Butcher GA,Buffinton GD,Hunt NH,Cowden WB

doi

10.1016/0006-2952(87)90364-9

subject

Has Abstract

pub_date

1987-02-15 00:00:00

pages

543-6

issue

4

eissn

0006-2952

issn

1873-2968

pii

0006-2952(87)90364-9

journal_volume

36

pub_type

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