Publication: Electron microscopic features of brain edema in rodent cerebral malaria in relation to glial fibrillary acidic protein expression
Issued Date
2014-01-01
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19362625
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2-s2.0-84902449050
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Mahidol University
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SCOPUS
Bibliographic Citation
International Journal of Clinical and Experimental Pathology. Vol.7, No.5 (2014), 2056-2067
Suggested Citation
Sumate Ampawong, Urai Chaisri, Parnpen Viriyavejakul, Apichart Nontprasert, Georges E. Grau, Emsri Pongponratn Electron microscopic features of brain edema in rodent cerebral malaria in relation to glial fibrillary acidic protein expression. International Journal of Clinical and Experimental Pathology. Vol.7, No.5 (2014), 2056-2067. Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/34486
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Title
Electron microscopic features of brain edema in rodent cerebral malaria in relation to glial fibrillary acidic protein expression
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Abstract
The mechanisms leading to cerebral malaria (CM) are not completely understood. Brain edema has been suggested as having an important role in experimental CM. In this study, CBA/CaH mice were infected with Plasmodium berghei ANKA blood-stage and when typical symptoms of CM developed on day 7, brain tissues were processed for electron-microscopic and immunohistochemical studies. The study demonstrated ultrastructural hallmarks of cerebral edema by perivascular edema and astroglial dilatation confirming existing evidence of vasogenic and cytogenic edema. This correlates closely with the clinical features of CM. An adaptive response of astrocytic activity, represented by increasing glial fibrillary acidic protein (GFAP) expression in the perivascular area and increasing numbers of large astrocyte clusters were predominately found in the CM mice. The presence of multivesicular and lamellar bodies indicates the severity of cerebral damage in experimental CM. Congestion of the microvessels with occluded white blood cells (WBCs), parasitized red blood cells (PRBCs) and platelets is also a crucial covariate role for CM pathogenesis.