Evidence map›Paper›PMID 40951511›Full record

ArticleThe journal of venomous animals and toxins including tropical diseases2025

Proteasome-driven modulation of immune and oxidative pathways during scorpion envenomation pathogenesis.

Amal Megdad-Lamraoui, Sonia Adi-Bessalem, Fares Daachi, Fatima Laraba-Djebari

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Article in The journal of venomous animals and toxins including tropical diseases, 2025. 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

4 authors.

Amal Megdad-LamraouiLaboratory of Cellular and Molecular Biology-Tamayouz, Department of Cellular and Molecular Biology, Faculty of Biological Sciences, University of Science and Technology Houari Boumediene (USTHB), Algiers, Algeria.ORCID https://orcid.org/0000-0002-8156-4013
Sonia Adi-BessalemLaboratory of Cellular and Molecular Biology-Tamayouz, Department of Cellular and Molecular Biology, Faculty of Biological Sciences, University of Science and Technology Houari Boumediene (USTHB), Algiers, Algeria.ORCID https://orcid.org/0000-0001-8238-2062
Fares DaachiLaboratory of Cellular and Molecular Biology-Tamayouz, Department of Cellular and Molecular Biology, Faculty of Biological Sciences, University of Science and Technology Houari Boumediene (USTHB), Algiers, Algeria.ORCID https://orcid.org/0000-0001-7748-9412
Fatima Laraba-DjebariLaboratory of Cellular and Molecular Biology-Tamayouz, Department of Cellular and Molecular Biology, Faculty of Biological Sciences, University of Science and Technology Houari Boumediene (USTHB), Algiers, Algeria.ORCID https://orcid.org/0000-0003-4641-261X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Scorpion venom contains a variety of toxin molecules that are the drivers of inflammation and oxidative stress, leading to significant tissue damage. While several mechanisms underlying these responses have been studied, the involvement of the proteasome complex - a key regulator of inflammation - remains poorly understood. This study explored the role of the proteasome in modulating inflammatory and oxidative responses to envenomation by Methods: Mice were pretreated intraperitoneally with bortezomib, a proteasome inhibitor, at low (0.05 mg/kg), medium (0.25 mg/kg), or high (0.5 mg/kg) doses, 30 minutes prior to sublethal venom administration (0.5 mg/kg, subcutaneous). Twenty-four hours after venom administration, animals were euthanized, blood and organs were collected to evaluate vascular permeability (via Evans blue dye extravasation), the extent of inflammatory cell infiltration (myeloperoxidase and eosinophil peroxidase enzymatic activities), and oxidative/nitrosative stress markers (nitric oxide, hydrogen peroxide Results: Our findings revealed a dose-dependent immune-modulatory role of the proteasome system. A medium dose of bortezomib reduced inflammatory and oxidative stress markers, such as vascular permeability, eosinophil peroxidase, neutrophil peroxidase, nitric oxide, and malondialdehyde in renal tissue, suggesting a reduction in local inflammation and oxidative damage. In contrast, a higher dose showed pronounced preventive effects in cardiopulmonary and hepatic tissues, significantly reducing inflammatory mediators and oxidative markers, restoring antioxidant enzyme activity (catalase) and glutathione, as well as, improving tissue structure and organ function. Conclusion: These findings underscore the proteasome involvement in inflammatory regulation, likely through modulation of vascular permeability, immune cell activation, and oxidative stress, making it a key target in scorpion envenomation.

Indexed as

Cardiopulmonary tissueHepatorenal tissueImmune-inflammatory responseOxidative stressProteasomeScorpion venom

Identifiers

PMID40951511
PMCPMC12431687

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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 OpenQuestion graph.