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Patterns of haemozoin accumulation in tissue.

Abstract
A sensitive fluorometric method for assaying malarial pigment, haemozoin, has been developed and used to determine the haemozoin content of blood and tissue samples. Plasmodium falciparum rings and trophozoites were found to contain 23 and 339 ng haemozoin/10(6) parasitized red blood cells (PRBCs), respectively. Unsynchronized Plasmodium berghei NK65 or ANKA parasites from infected mice contained 27 and 61 ng haemozoin/10(6) PRBCs, respectively. An exponential accumulation of haemozoin within 18 days after infection was demonstrated in liver and spleen tissue, representing up to 0.2% of the tissue by wet weight by day 18. Histology indicated that the accumulation occurred predominantly in the tissue monocytes. In the brain, the levels of haemozoin after 8 days of infection were considerably lower than they were in the liver or spleen, and most of the pigment appeared to be that present inside parasitized red blood cells. CBA/Ca mice infected with P. berghei ANKA (a cerebral malaria model) had significantly higher amounts of haemozoin in the brain than did ICR mice infected with P. berghei NK65. Thus, haemozoin levels in tissue increase with the duration of infection, and its presence may be associated with cerebral pathology.
AuthorsA D Sullivan, I Ittarat, S R Meshnick
JournalParasitology (Parasitology) Vol. 112 ( Pt 3) Pg. 285-94 (Mar 1996) ISSN: 0031-1820 [Print] England
PMID8728992 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Hemeproteins
  • Pigments, Biological
  • hemozoin
Topics
  • Anemia
  • Animals
  • Brain (parasitology, pathology)
  • Erythrocytes (parasitology)
  • Hemeproteins (analysis, biosynthesis)
  • Liver (parasitology)
  • Malaria, Falciparum (blood, pathology, physiopathology)
  • Mice
  • Mice, Inbred DBA
  • Mice, Inbred ICR
  • Organ Specificity
  • Parasitemia (blood, pathology, physiopathology)
  • Pigments, Biological (biosynthesis)
  • Plasmodium falciparum (growth & development, isolation & purification)
  • Regression Analysis
  • Sensitivity and Specificity
  • Species Specificity
  • Spectrometry, Fluorescence (methods)
  • Spleen (parasitology)
  • Time Factors

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