Localisation of mepacrine inPlasmodium bergheiandPlasmodium falciparumby fluorescence microscopy
- 30 November 1975
- journal article
- research article
- Published by Taylor & Francis in Pathogens and Global Health
- Vol. 69 (4), 417-420
- https://doi.org/10.1080/00034983.1975.11687029
Abstract
Mouse erythrocytes infected with P. berghei were incubated in vitro with 3 .times. 10-8 or 10-7 M mepacrine. In trophozoites the fluorescence due to the drug was detectable, after 5 min incubation, at the host cell/parasite interface and on the membranes of the digestive vacuoles. No fluorescence was detected within the digestive vacuoles although the cytoplasm rapidly became fluorescent. There was no marked nuclear localization of fluorescence. In dividing and divided schizonts, intense points of fluorescence were seen which appeared to be localized in the conoid area, possibly in the paried organellas. These observations were confirmed on P. falciparum in Aotus erythrocytes and possible explanations are discussed.This publication has 5 references indexed in Scilit:
- The chemotherapy of rodent malaria, XXIPathogens and Global Health, 1975
- The chemotherapy of rodent malaria, XX Autophagic vacuole formation inPlasmodium berghei in vitroPathogens and Global Health, 1974
- Chloroquine accumulation by erythrocytes: A latent capabilityLife Sciences, 1974
- Lysosomes, pH and the Anti-malarial Action of ChloroquineNature, 1972
- CHLOROQUINE RESISTANCE IN MALARIA: A DEFICIENCY OF CHLOROQUINE BINDINGProceedings of the National Academy of Sciences, 1969