Evidence map›Paper›PMID 41580860›Full record

ArticleParasites & vectors2026

Evaluation of the potential therapeutic efficacy of Cerastes cerastes venom in acute experimental toxoplasmosis.

Lobna A El-Zawawy, Doaa E Said, Rana Abdelghaffar, Nehal A Khalil, Sara A Abdel Salam

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Article in Parasites & vectors, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lobna A El-ZawawyDepartment of Medical Parasitology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Doaa E SaidDepartment of Medical Parasitology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Rana AbdelghaffarDepartment of Medical Parasitology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Nehal A KhalilDepartment of Medical Biochemistry, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Sara A Abdel SalamDepartment of Medical Parasitology, Faculty of Medicine, Alexandria University, Alexandria, Egypt. sara.abdelsalam@alexmed.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe control of toxoplasmosis relies on conventional chemotherapeutics, which have hitherto unresolved concerns.

methodsSwiss albino mice were intraperitoneally (IP) infected with 5 × 10

resultsCCV induced an insignificant reduction in mortality rate (MR) and a significant increase in survival time of mice. A statistically significant decrease in the mean peritoneal parasite burden with 89.8% and 90.8% reduction (%R) was observed in both IC and IS-treated subgroups compared with their controls, respectively. This reduction was consistent with 88% and 86% decrease in liver parasite load, respectively, and obvious ultrastructural alterations in treated tachyzoites. Concerning the infectivity study, the percent reduction was 78.8% and 85.5% in the peritoneal fluid and 71.1% and 60.4% in the liver tissues of IC and IS subgroups, respectively. The biochemical safety of the used dose and its high antioxidant activity were verified.

conclusionsThus, one-fourth LD50 of CCV can be considered a promising, effective natural alternative to standard chemotherapy for acute toxoplasmosis.

Indexed as

Antiprotozoal AgentsToxoplasmaToxoplasmosis, AnimalViper VenomsAnimalsCerastesDisease Models, AnimalFemaleKidneyLethal Dose 50LiverMiceParasite LoadSurvival AnalysisTreatment OutcomeAntiprotozoal AgentsViper VenomsAntioxidantCerastes cerastes venomInfectivityMolecularToxoplasma gondiiUltrastructural

Identifiers

PMID41580860
PMCPMC12914995

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