Published in:
Open Access
01-12-2011 | Research
Atorvastatin prevents Plasmodium falciparum cytoadherence and endothelial damage
Authors:
Zacharie Taoufiq, Paco Pino, Nadine N'dilimabaka, Issam Arrouss, Serge Assi, Florent Soubrier, Angelita Rebollo, Dominique Mazier
Published in:
Malaria Journal
|
Issue 1/2011
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Abstract
Background
The adhesion of Plasmodium falciparum parasitized red blood cell (PRBC) to human endothelial cells (EC) induces inflammatory processes, coagulation cascades, oxidative stress and apoptosis. These pathological processes are suspected to be responsible for the blood-brain-barrier and other organs' endothelial dysfunctions observed in fatal cases of malaria. Atorvastatin, a drug that belongs to the lowering cholesterol molecule family of statins, has been shown to ameliorate endothelial functions and is widely used in patients with cardiovascular disorders.
Methods
The effect of this compound on PRBC induced endothelial impairments was assessed using endothelial co-culture models.
Results
Atorvastatin pre-treatment of EC was found to reduce the expression of adhesion molecules and P. falciparum cytoadherence, to protect cells against PRBC-induced apoptosis and to enhance endothelial monolayer integrity during co-incubation with parasites.
Conclusions
These results might suggest a potential interest use of atorvastatin as a protective treatment to interfere with the pathophysiological cascades leading to severe malaria.