# Silibinin enhanced the efficacy of albendazole in treating the muscular phase of experimental trichinellosis

**Authors:** Mennat-Elrahman A. Fahmy, Marwa Esmat, Manal Badawi, Iman R. Abdel Shafi

PMC · DOI: 10.1007/s11250-025-04429-0 · Tropical Animal Health and Production · 2025-05-07

## TL;DR

Silibinin, when combined with albendazole, improves treatment of the muscular phase of trichinellosis in mice by reducing larvae and inflammation.

## Contribution

Silibinin enhances albendazole's efficacy against the muscular phase of trichinellosis by modulating immune pathways.

## Key findings

- Combined treatment reduced larvae by 69.95% in the diaphragm.
- The combination significantly reduced inflammation and modulated PDL1 expression.
- Monotherapy with albendazole or silibinin alone did not reduce inflammation.

## Abstract

Trichinella spiralis is a parasitic nematode with a special life cycle. Both adults and larvae live in two different niches in the same host (intestinal and muscular). The parasite is known to manipulate the immune system of the host to be able to survive. One of the pathways the parasite modulates is the programmed death 1/ programmed death ligand 1 (PD1/PDL1), a pathway important to maintain the immune homeostasis during chronic infections and cancers. Albendazole (ABZ) shows anti-trichinellosis efficacy, especially against the intestinal phase of the infection. In an attempt to discover a drug that would enhance the efficacy of ABZ against the muscular phase, we used 40 CD1 Swiss-Albino male mice divided into 5 groups: normal, infected, infected ABZ-treated, infected Silymarin (SM)-treated, and the infected-treated with a combination group. After euthanasia, the number of diaphragmatic larvae was estimated in the infected and the infected-treated groups. In addition, the tongues and hearts of all mice were subjected to histopathological and immunohistochemical processing and evaluation. Monotherapy groups showed a significant reduction of both larval count and PD1 local expression compared to the infected-only group, however, neither ABZ nor SM alone could reduce the inflammation accompanying infection. The most significant improvements were recorded in the combined treatment group with a reduction rate of 69.95%, a significant reduction of inflammatory infiltrates (p < 0.05), and significant modulation of PDL1 local expression (p < 0.05). So, Silibinin (the major active ingredient of SM) showed anti-trichinellosis activity and enhanced the efficacy of ABZ against the muscular phase of the infection.

## Linked entities

- **Proteins:** PDCD1 (programmed cell death 1), CD274 (CD274 molecule)
- **Chemicals:** albendazole (PubChem CID 2082), Silibinin (PubChem CID 31553), Silymarin (PubChem CID 5213)
- **Diseases:** trichinellosis (MONDO:0019444)
- **Species:** Trichinella spiralis (taxon 6334)

## Full-text entities

- **Genes:** Cd274 (CD274 antigen) [NCBI Gene 60533] {aka A530045L16Rik, B7h1, Pdcd1l1, Pdcd1lg1, Pdl1}, Pdcd1 (programmed cell death 1) [NCBI Gene 18566] {aka Ly101, PD-1, Pdc1}
- **Diseases:** infected (MESH:D007239), inflammation (MESH:D007249), trichinellosis (MESH:D014235), cancers (MESH:D009369)
- **Chemicals:** ABZ (MESH:D015766), Silibinin (MESH:D000077385), SM (MESH:D012838)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Trichinella spiralis (species) [taxon 6334]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12058922/full.md

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Source: https://tomesphere.com/paper/PMC12058922