There is mounting evidence that the release of haemozoin (β-haematin), which is produced in large amounts during malaria infection and is released into the circulation during schizont rupture, is associated with damage to cell membranes through an oxidative mechanism. The red blood cell membrane is thus oxidised, causing rigidity of the cell. This can contribute to the pathophysiology of severe malaria, since red blood cells will have to deform considerably in order to squeeze through the microcirculation, the patency of which is disturbed by sequestered red blood cells containing the mature forms of the parasite. Rigidity of red blood cells forms a new target for intervention. Since this seems to be caused by oxidative damage to the red blood cell membrane, the anti-oxidant N-acetylcysteine is a promising candidate for adjunctive treatment in severe malaria, which still has a mortality rate as high as 20%.
Forradee Nuchsongsin, Kesinee Chotivanich, Prakaykaew Charunwatthana, Omodeo-Salè Fausta, Donatella Taramelli, Nicholas Day, Sir Nicholas White, Arjen M. Dondorp
Prakaykaew Charunwatthana, Maryam Faiz, Ronnatrai Ruangveerayut, Richard J. Maude, Mushfiqur Rahman, L. Jackson Roberts, Kevin Moore, Emran Bin Yunus, M. Gofranul Hoque, Mahatab Uddin Hasan, Sue J. Lee, Sasithon Pukrittayakamee, Paul N. Newton, Sir Nicholas White, Nicholas Day, Arjen M. Dondorp
Katherine Plewes, Hugh W. F. Kingston, Aniruddha Ghose, Richard J. Maude, Michael Herdman, Stije J. Leopold, Haruhiko Ishioka, Md Mahtab Uddin Hasan, Md Shafiul Haider, Shamsul Alam, Kim A. Piera, Prakaykaew Charunwatthana, Kamolrat Silamut, Tsin Wen Yeo, Md Abul Faiz, Sue J. Lee, Mavuto Mukaka, Gareth D. H. Turner, Nicholas M. Anstey, L. Jackson Roberts, Sir Nicholas White,
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