the potential of β carbolin alkaloids to hinder growth and re¬verse chloroquine resistance in plasmodium falciparum
نویسندگان
چکیده
background: nowadays, scourge of malaria as a fatalistic disease has increased due to emergence of drug resistance and tolerance among different strains of plasmodium falciparum . emergence of chloroquine (cq) resistance has worsened the calamity as cq is still considered the most efficient, safe and cost effective drug among other antimalarials. this urged the scientists to search for other alternatives or sensitizers that may be able to augment cq action and reverse its resistance. method: three β-carbolin derivatives, namely, harmalin, harmol and harmalol were tested for their anti-plasmodial and cq resistance reversal effects against p. falciparum 3d7 and k1 . sybre green-1 based drug sensitivity assay and isobologram analysis were used to screen the mentioned effects respectively. results: all of them showed moderate anti-plasmodium effect and harmalin was the most effective as compared to the others in reversing cq resistance and tolerance. conclusion: the mentioned phytochemicals are not ideal to be used as conventional anti-malarials and only harmalin can be suggested to reverse cq resistance in p. falciparum k1.
منابع مشابه
The Potential of β Carbolin Alkaloids to Hinder Growth and Reverse Chloroquine Resistance in Plasmodium falciparum
BACKGROUND Nowadays, scourge of malaria as a fatalistic disease has increased due to emergence of drug resistance and tolerance among different strains of Plasmodium falciparum. Emergence of chloroquine (CQ) resistance has worsened the calamity as CQ is still considered the most efficient, safe and cost effective drug among other antimalarials. This urged the scientists to search for other alte...
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In vivo and in vitro assessments of the response of P. falciparum to chloroquine using WHO standard kits and techniques were carried out in I ran Shahr, Sistan and Baluchestan province of Iran in 1985. In the in vivo assessment, 24 malaria patients treated with chloroquine (25mg/kg over three days) were followed up for one to four weeks. The mean parasite clearance time was 4.3 days and in...
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Resistance to chloroquine of malaria strains is known to be associated with a parasite protein named PfCRT, the mutated form of which is able to reduce chloroquine accumulation in the digestive vacuole of the pathogen. Whether the protein mediates extrusion of the drug acting as a channel or as a carrier and which is the protonation state of its chloroquine substrate is the subject of a scienti...
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عنوان ژورنال:
iranian journal of parasitologyجلد ۱۰، شماره ۴، صفحات ۵۷۷-۵۸۳
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