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Journal ArticleDOI

A thiazole derivative of artemisinin moderately reduces Toxoplasma gondii cyst burden in infected mice.

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TLDR
Findings suggest that artemisinin derivatives are partially effective in treating experimental T. gondii infections, with modest efficacy dependent upon the compound dose and the solvent vehicle.
Abstract
Toxoplasmosis continues to be a public health problem, causing significant morbidity worldwide. Currently available medications, effective for acute toxoplasmosis, are nonetheless problematic due to adverse side effects in many patients. In addition, no medication is able to completely eradicate the parasite cysts, rendering infected individuals at risk for reactivation upon becoming immunocompromised. We examined the anti–T. gondii activity of 2 derivatives of artemisinin. In vitro metabolic stability tests revealed that both derivatives are stable in mouse plasma but only the thiazole CPH4-136 is stable in the presence of mouse microsomes. When tested in a mouse model of acute toxoplasmosis, both derivatives showed modest efficacy dependent upon the compound dose and the solvent vehicle. Finally, in a mouse model of chronic T. gondii infection, CPH4-136 at 3 mg/kg once per day for 32 days moderately but significantly decreased mouse brain cyst burden. Collectively, our findings suggest that ar...

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Journal ArticleDOI

Treatment of Toxoplasmosis: Historical Perspective, Animal Models, and Current Clinical Practice.

TL;DR: An overview of toxoplasmosis treatment in humans and in animal models is presented and there is a strong impetus to develop novel therapeutics for both the acute and latent forms of the infection.
Journal ArticleDOI

Drugs in development for toxoplasmosis: advances, challenges, and current status.

TL;DR: The facets of toxoplasmosis that are pertinent to drug design and the advances, challenges, and current status of preclinical drug research for toxoplasmsosis are discussed.
Journal ArticleDOI

Drug Resistance in Toxoplasma gondii

TL;DR: Recent experimental studies in clinical cases have clearly shown that drug resistance in Toxoplasma is ongoing, and establishing a more effective therapeutic scheme in the treatment of toxoplasmosis is critically needed to improve the therapeutic outcome in patients.
Journal ArticleDOI

Human toxoplasmosis-Searching for novel chemotherapeutics.

TL;DR: There is urgent need to develop new drugs and establish "gold standard" treatment for T. gondii and several promising drug candidates characterized by a high selectivity, the low IC50 (the half maximal inhibitory concentration) and low cytotoxicity towards host cells are revealed.
Journal ArticleDOI

The pharmacological activities and mechanisms of artemisinin and its derivatives: a systematic review

TL;DR: The proposed mechanisms of action of artemisinins are reviewed with the hope of gaining more insight into the multiple actions of these potent drugs and how they work.
References
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Journal ArticleDOI

Toxoplasma gondii and Other Risk Factors for Schizophrenia: An Update

TL;DR: The failure to find genes of major effect in schizophrenia has refocused attention on nongenetic, including infectious factors, and antibodies to Toxoplasma gondii were found to be elevated in 23 studies of schizophrenia.
Journal ArticleDOI

Results of 20-year follow-up of congenital toxoplasmosis.

TL;DR: Screening of women for toxoplasmosis before pregnancy seems advisable, as new lesions continue to appear well after the age of 5 years, and the impairments can be severe.
Journal ArticleDOI

Induction of dendritic cell migration upon Toxoplasma gondii infection potentiates parasite dissemination

TL;DR: Findings show that Toxoplasma is able to subvert the regulation of host cell motility and likely exploits the host’s natural pathways of cellular migration for parasite dissemination.
Journal ArticleDOI

Recent investigations of artemether, a novel agent for the prevention of schistosomiasis japonica, mansoni and haematobia.

TL;DR: Clinical trials confirmed that artemether, orally administered at a dose of 6 mg/kg once every 2-3 weeks, results in no drug-related adverse effects, and significantly reduces the incidence and intensity of schistosome infections.
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