Evidence map›Paper›PMID 41941084›Full record

ArticleActa parasitologica2026

Marine Biotoxins as Potential Nematocide: Impact of Cassiopea andromeda Venom Against Acute and Chronic Trichinellosis in Murine model.

Rasha A Elmahy, Amina M Salama, Nahla A Radwan, Alaa Y Moustafa, Samar F Harras, Mona M Elwan

Abstract read
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Article in Acta parasitologica, 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

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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

6 authors.

Rasha A ElmahyZoology Department, Faculty of Science, Tanta University, Tanta, Egypt.
Amina M SalamaMedical Parasitology Department, Faculty of Medicine, Tanta University, Tanta, Egypt.
Nahla A RadwanZoology Department, Faculty of Science, Tanta University, Tanta, Egypt. nahla.radwan@science.tanta.edu.eg.
Alaa Y MoustafaZoology Department, Faculty of Science, Sohag University, Sohag, Egypt.
Samar F HarrasZoology Department, Faculty of Science, Tanta University, Tanta, Egypt.
Mona M ElwanZoology Department, Faculty of Science, Tanta University, Tanta, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA significant challenge in the treatment of trichinellosis is addressing theencysted larvae. The efficacy of albendazole on larvae appears to be limited, underscoring theurgent necessity for developing effective alternatives. Recently, marine biotoxins have beeninvestigated as possible substitutes for traditional medications. In the present work, we assessedthe nematocidal potential of the jellyfish Cassiopea andromeda’s venom against the enteral andparenteral phases of Trichinella spiralis in mice.

methodsA total of 115 BALB/c mice werecategorized into two phases: acute and chronic. Each was divided into five groups: uninfecteduntreated group, untreated group infected with T. spiralis , uninfected group and treated withjellyfish venom, infected group and administered albendazole, and infected group and treatedwith jellyfish venom. In vitro study exposed adults and larvae of T. spiralis to the Lethalconcentration (LC90) of C. andromeda venom, and ultrastructural changes were observed. Invivo assay included haematological and biochemical analyses. Histopathological andimmunohistochemical assessments evaluated the host tissue’s alterations. ANOVA and post hoctests were used in the statistical analysis.

resultsThe present results showed that the LC90 ofthe venom caused complete mortality of adults. The infected and venom-treated group of micegained weight, achieved a 85.23% reduction in adult worms, and showed verified structural improvement, diminished degenerative changes, and decreased P53 expression. High levels of oxidative stress indicators and liver enzymes were observed.

conclusionsVenom treatmentdecreased inflammation and restored antioxidant levels. C. andromeda venom may be aninteresting alternative for treating T. spiralis' intestinal and muscle phases; however, furtherresearch is needed to clarify its structure, production, molecular targets, and methods ofadministration.

Indexed as

Antinematodal AgentsCnidarian VenomsScyphozoaTrichinella spiralisTrichinellosisAlbendazoleAnimalsDisease Models, AnimalFemaleLarvaMaleMiceMice, Inbred BALB CAlbendazoleAntinematodal AgentsCnidarian VenomsAlbendazoleCassiopea andromedaHistopathological alterationsImmunohistochemical analysisOxidative stressSEMTrichinella spiralisVenom

Identifiers

PMID41941084
PMCPMC13053410

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.