Literature DB >> 6364514

Topographical distribution of the cerebral lesions in mice infected with Plasmodium berghei.

T Polder, C Jerusalem, W Eling.   

Abstract

In the mouse P. berghei malaria model systematic studies were carried out on the relationship between the type and the topographical distribution of the brain lesion in cerebral malaria. As previously stated for pernicious P. falciparum malaria in man, petechial haemorrhage was not the sole morphologic lesion. In addition to severe brain oedema, microthrombosis, sludging of mononuclear cells, arteriolar spasms, scattered disturbances of the microcirculation, and the occasional proliferation of gliocytes were the prevailing morphologic changes. Pronounced perivascular oedema with compression of capillaries and ischaemic demyelinisation were particular frequent in the nucleus caudatus putamen, while the adjacent regions (radiatio corporis callosi, claustrum, hippocampus, and fimbria hippocampi) were the sites of predilection of petechial haemorrhage. Arteriolar spasms were particularly frequent in branches of the posterior choroidal artery. The proliferation of gliocytes was practically restricted to the tubercula olfactoria and to the subependymal zone of the lateral wall of the lateral ventricle. The present results indicate a neurovascular component in the pathogenesis of cerebral malaria. The preponderance of a special histopathological lesion in a certain cerebral region may be the result of a particular sensitivity of cells of these areas to noxious events (pathoclisis), for instance hypoxia, and/or exaggeration of autoregulatory phenomena that exist between the cerebral parenchyma and the supplying vasculature.

Entities:  

Mesh:

Year:  1983        PMID: 6364514

Source DB:  PubMed          Journal:  Tropenmed Parasitol        ISSN: 0303-4208


  7 in total

Review 1.  Oxidative stress in malaria; implications for prevention and therapy.

Authors:  N S Postma; E C Mommers; W M Eling; J Zuidema
Journal:  Pharm World Sci       Date:  1996-08

2.  Prevention of murine cerebral malaria by low-dose cyclosporin A.

Authors:  G E Grau; D Gretener; P H Lambert
Journal:  Immunology       Date:  1987-08       Impact factor: 7.397

3.  CNS hypoxia is more pronounced in murine cerebral than noncerebral malaria and is reversed by erythropoietin.

Authors:  Casper Hempel; Valery Combes; Nicholas Henry Hunt; Jørgen Anders Lindholm Kurtzhals; Georges Emile Raymond Grau
Journal:  Am J Pathol       Date:  2011-08-18       Impact factor: 4.307

4.  Cytokine profile suggesting that murine cerebral malaria is an encephalitis.

Authors:  V M Jennings; J K Actor; A A Lal; R L Hunter
Journal:  Infect Immun       Date:  1997-11       Impact factor: 3.441

5.  Immunological aspects of cerebral lesions in murine malaria.

Authors:  J H Curfs; T P Schetters; C C Hermsen; C R Jerusalem; A A van Zon; W M Eling
Journal:  Clin Exp Immunol       Date:  1989-01       Impact factor: 4.330

6.  Erythropoietin treatment alleviates ultrastructural myelin changes induced by murine cerebral malaria.

Authors:  Casper Hempel; Poul Hyttel; Trine Staalsø; Jens R Nyengaard; Jørgen A L Kurtzhals
Journal:  Malar J       Date:  2012-06-28       Impact factor: 2.979

7.  Host matrix metalloproteinases in cerebral malaria: new kids on the block against blood-brain barrier integrity?

Authors:  Manuela Polimeni; Mauro Prato
Journal:  Fluids Barriers CNS       Date:  2014-01-27
  7 in total

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