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Abstract

Background: The search for effective natural alternatives to synthetic non-steroidal antiinflammatory drugs (NSAIDs), which are often associated with undesirable side effects, is an important axis of current research. The slime of the snail Helix aspersa Müller, is a traditional remedy that deserves scientific investigation for its potential therapeutic properties.

Purpose: This study aimed to comprehensively evaluate the anti-inflammatory effects of Helix aspersa Müller slime using a combination of in vitro, in vivo, and in silico methodologies.

Methods: In vitro analyses included assays for inhibition of protein denaturation, antiprotease and antilipoxygenase activities, and membrane stabilization, with diclofenac and indomethacin as reference standards. The in vivo component involved a rat model of auricular edema to measure the reduction of swelling and attenuation of oxidative stress. Molecular docking simulations were conducted to analyze the binding affinity of slime constituents for key inflammatory targets.

Results: The slime exhibited potent, dose-dependent anti-inflammatory activity. In vitro, it inhibited protein denaturation by up to 90.41% at 500 µg/mL, with antiprotease, antilipoxygenase, and membrane-stabilizing effects comparable to standard drugs. In vivo, it reduced auricular edema in rats by 76.68% at a dose of 500 µg/mL, exceeding the efficacy of diclofenac and reducing oxidative stress. Molecular docking confirmed strong binding affinities with key inflammatory receptors, delineating a multimodal mechanism of action.

Conclusion: The secretion of H. aspersa Müller demonstrates exceptional anti-inflammatory and antioxidant properties, validating its potential as a viable natural alternative to conventional NSAIDs for the management of inflammatory conditions and oxidative stress-related disorders.

Creative Commons License

Creative Commons Attribution 4.0 License
This work is licensed under a Creative Commons Attribution 4.0 License.

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