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Author Spotlight: Real-Time Monitoring of Parasite Burden and Host Response
Published on: May 31, 2024
Antagonistic effect of atorvastatin on high fat diet induced survival during acute Chagas disease
Dazhi Zhao1, Kezia Lizardo2, Min Hui Cui3
1Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Insights
Statins like atorvastatin may worsen Chagas disease outcomes. This study found atorvastatin increased parasite load, inflammation, and mortality in mice with Trypanosoma cruzi infection, suggesting adverse effects during acute Chagas disease.
Area of Science:
- Parasitology
- Cardiology
- Metabolic Diseases
Background:
- Chagasic cardiomyopathy, a severe manifestation of Trypanosoma cruzi infection, is influenced by lipid metabolism.
- Hyperlipidemia is common in Chagas disease endemic regions, often treated with statins like atorvastatin.
Purpose of the Study:
- To investigate the effects of atorvastatin on Trypanosoma cruzi infection-induced myocarditis in mice.
- To evaluate atorvastatin's impact on adipose tissue and cardiac pathology during infection.
Main Methods:
- Mice were fed either a regular or high-fat diet and treated with atorvastatin during acute T. cruzi infection.
- Assessed effects on lipolysis, cardiac lipidopathy, parasite load, LDL levels, inflammation, and mortality.
Main Results:
- Atorvastatin regulated lipolysis and cardiac lipidopathy but enhanced parasite load, cardiac LDL, inflammation, and mortality.
- These effects were observed in mice on both regular and high-fat diets during acute infection.
Conclusions:
- Statins, exemplified by atorvastatin, may have deleterious effects during the acute phase of Chagas disease.
- Further research is needed to understand the complex interactions between statins, lipid metabolism, and T. cruzi infection.
Abstract:
Chagasic cardiomyopathy, which is seen in Chagas disease, is the most severe and life-threatening manifestation of infection by the kinetoplastid Trypanosoma cruzi. Adipose tissue and diet play a major role in maintaining lipid homeostasis and regulating cardiac pathogenesis during the development of Chagas cardiomyopathy. We have previously reported that T. cruzi has a high affinity for lipoproteins and that the invasion rate of this parasite increases in the presence of cholesterol, suggesting that drugs that inhibit cholesterol synthesis, such as statins, could affect infection and the development of Chagasic cardiomyopathy. The dual epidemic of diabetes and obesity in Latin America, the endemic regions for Chagas disease, has led to many patients in the endemic region of infection having hyperlipidemia that is being treated with statins such as atorvastatin. The current study was performed to examine mice fed on either regular or high fat diet for effects of atorvastatin on T. cruzi infection-induced myocarditis and to evaluate the effect of this treatment during infection on adipose tissue physiology and cardiac pathology. Atorvastatin was found to regulate lipolysis and cardiac lipidopathy during acute T. cruzi infection in mice and to enhance tissue parasite load, cardiac LDL levels, inflammation, and mortality in during acute infection. Overall, these data suggest that statins, such as atorvastatin, have deleterious effects during acute Chagas disease.
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