Abstract |
We studied the differential effect of tryptophan-N-formylated gramicidin on uninfected and Plasmodium falciparum-infected erythrocytes. Trp-N-formylated gramicidin induces a much faster leakage of K+ from infected cells than from uninfected cell whereas, and at an even lower concentration, gramicidin A' causes a rapid K+ leakage from both uninfected and infected cells. We also studied the effect of Trp-N-formylated gramicidin and gramicidin A' incorporated in liposomes on the growth of Plasmodium falciparum in an in vitro culture. Incorporation of Trp-N-formylated gramicidin in the membranes of so-called 'stealth' vesicles strongly decreases the concentration needed to induce 50% inhibition of parasite growth. Moreover, no decrease in the K+ content of uninfected cells was observed when cells were exposed to liposome-incorporated Trp-N-formylated gramicidin at a concentration which causes full inhibition of parasite growth. These observations strongly suggest that Trp-N-formylated gramicidin incorporated in 'stealth' vesicles ends up specifically in the infected cell, thereby inhibiting the growth of the growth of the malaria parasite.
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Authors | G N Moll, V van den Eertwegh, H Tournois, B Roelofsen, J A Op den Kamp, L L van Deenen |
Journal | Biochimica et biophysica acta
(Biochim Biophys Acta)
Vol. 1062
Issue 2
Pg. 206-10
(Feb 25 1991)
ISSN: 0006-3002 [Print] Netherlands |
PMID | 1706202
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Drug Carriers
- Liposomes
- tryptophan-N-formylgramicidin
- Gramicidin
- Potassium
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Topics |
- Animals
- Cell Membrane Permeability
(drug effects)
- Drug Carriers
- Erythrocytes
(drug effects, metabolism, parasitology)
- Gramicidin
(administration & dosage, pharmacology)
- In Vitro Techniques
- Liposomes
- Plasmodium falciparum
(drug effects, growth & development)
- Potassium
(blood)
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