Literature DB >> 8323956

Hemozoin production by Plasmodium falciparum: variation with strain and exposure to chloroquine.

A U Orjih1, C D Fitch.   

Abstract

Synchronized Plasmodium falciparum parasites were grown in erythrocytic culture for measurement of malaria pigment (hemozoin) production using a simple method based on the insolubility of beta-hematin, the principal pigment of hemozoin. In the last 44 h of the life cycle, one strain (chloroquine-susceptible) incorporated an average of 960 pmol of ferriprotoporphyrin IX (FP) from hemoglobin into beta-hematin per 10(6) parasitized erythrocytes. By comparison, another strain (chloroquine-resistant) incorporated 515 pmol of FP into beta-hematin. When exposed to 25 ng of chloroquine per ml of culture medium, chloroquine-susceptible P. falciparum incorporated 240 pmol of FP into beta-hematin per 10(6) parasitized erythrocytes in one intraerythrocytic life cycle. In contrast chloroquine-resistant P. falciparum exposed to 100 ng of chloroquine per ml incorporated 630 pmol of FP into beta-hematin. Thus, chloroquine inhibits hemozoin production in chloroquine-susceptible P. falciparum but not in chloroquine-resistant P. falciparum. On the contrary, sublethal concentrations of chloroquine partially reverse a deficiency of hemozoin production in chloroquine-resistant P. falciparum. These results indicate that the adaptation responsible for chloroquine resistance in P. falciparum prevents the accumulation of toxic FP by preventing chloroquine from uncoupling the processes of hemoglobin degradation and hemozoin production.

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Year:  1993        PMID: 8323956     DOI: 10.1016/0304-4165(93)90109-l

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  22 in total

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Authors:  Godfrey Lisk; Margaret Pain; Ilya Y Gluzman; Shivkumar Kambhampati; Tetsuya Furuya; Xin-Zhuan Su; Michael P Fay; Daniel E Goldberg; Sanjay A Desai
Journal:  Antimicrob Agents Chemother       Date:  2008-04-28       Impact factor: 5.191

4.  Hemoglobin catabolism and the killing of intraerythrocytic Plasmodium falciparum by chloroquine.

Authors:  A U Orjih; J S Ryerse; C D Fitch
Journal:  Experientia       Date:  1994-01-15

5.  High-resolution three-dimensional imaging of red blood cells parasitized by Plasmodium falciparum and in situ hemozoin crystals using optical diffraction tomography.

Authors:  Kyoohyun Kim; HyeOk Yoon; Monica Diez-Silva; Ming Dao; Ramachandra R Dasari; YongKeun Park
Journal:  J Biomed Opt       Date:  2014-01       Impact factor: 3.170

6.  Photoacoustic spectroscopy of β-hematin.

Authors:  Edward B Samson; Benjamin S Goldschmidt; Paul J D Whiteside; Amanda S M Sudduth; John R Custer; Brenda Beerntsen; John A Viator
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7.  Stage independent chloroquine resistance and chloroquine toxicity revealed via spinning disk confocal microscopy.

Authors:  Bojana Gligorijevic; Kyle Purdy; David A Elliott; Roland A Cooper; Paul D Roepe
Journal:  Mol Biochem Parasitol       Date:  2008-01-09       Impact factor: 1.759

8.  Fatal Plasmodium falciparum, Clostridium perfringens, and Candida spp. Coinfections in a Traveler to Haiti.

Authors:  Gillian L Genrich; Julu Bhatnagar; Christopher D Paddock; Sherif R Zaki
Journal:  J Trop Med       Date:  2009-05-05

9.  Inhibiting Plasmodium falciparum growth and heme detoxification pathway using heme-binding DNA aptamers.

Authors:  Jacquin C Niles; Joseph L Derisi; Michael A Marletta
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-24       Impact factor: 11.205

10.  Hemoglobin degradation in malaria-infected erythrocytes determined from live cell magnetophoresis.

Authors:  Lee R Moore; Hisashi Fujioka; P Stephen Williams; Jeffrey J Chalmers; Brian Grimberg; Peter A Zimmerman; Maciej Zborowski
Journal:  FASEB J       Date:  2006-02-06       Impact factor: 5.191

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