Anti-Inflammatory and Immunomodulatory Properties of a Crude Polysaccharide Derived from Green Seaweed Halimeda tuna: Computational and Experimental Evidences

Author:

Kraiem Marwa1,Ben Hamouda Sonia2,Eleroui Malek1,Ajala Marwa1ORCID,Feki Amal1ORCID,Dghim Amel1,Boujhoud Zakaria3ORCID,Bouhamed Marwa4,Badraoui Riadh56,Pujo Jean Marc7,Essafi-Benkhadir Khadija2ORCID,Kallel Hatem89ORCID,Ben Amara Ibtissem1ORCID

Affiliation:

1. Laboratory of Medicinal and Environment Chemistry, Higher Institute of Biotechnology, University of Sfax, PB 261, Sfax 3000, Tunisia

2. Laboratory of Molecular Epidemiology and Experimental Pathology–LR16IPT04, Pasteur Institute of Tunis, University of Tunis El Manar, Tunis 1002, Tunisia

3. Laboratory of Health Sciences and Technologies, Higher Institute of Health Sciences of Settat, Hassan First University of Settat, Settat 26000, Morocco

4. Laboratory of Anatomopathology, CHU Habib Bourguiba, University of Sfax, Sfax 3029, Tunisia

5. Department of General Biology, University of Ha’il, Ha’il 81451, Saudi Arabia

6. Section of Histology–Cytology, Medicine Faculty of Tunis, University of Tunis El Manar, La Rabta 1007, Tunisia

7. Emergency Department, Cayenne General Hospital, Cayenne 97300, French Guiana

8. Intensive Care Unit, Cayenne General Hospital, Cayenne 97300, French Guiana

9. Tropical Biome and Immunopathology CNRS UMR-9017, Inserm U 1019, University of Guiana, Cayenne 97300, French Guiana

Abstract

In this study, we investigated for the first time the anti-inflammatory and immunomodulatory properties of crude polysaccharide (PSHT) extracted from green marine algae Halimeda tuna. PSHT exhibited anti-oxidant activity in vitro through scavenging 1, 1-diphenyl-2-picryl hydroxyl free radical, reducing Fe3+/ferricyanide complex, and inhibiting nitric oxide. PSHT maintained the erythrocyte membrane integrity and prevented hemolysis. Our results also showed that PSHT exerted a significant anti-edematic effect in vivo by decreasing advanced oxidation protein products and malondialdehyde levels and increasing the superoxide dismutase and glutathione peroxidase activities in rat’s paw model and erythrocytes. Interestingly, PSHT increased the viability of murine RAW264.7 macrophages and exerted an anti-inflammatory effect on lipopolysaccharide-stimulated cells by decreasing pro-inflammatory molecule levels, including nitric oxide, granulocyte-macrophage colony-stimulating factor (GM-CSF) and tumor necrosis factor-alpha (TNF-α). Our findings indicate that PSHT could be used as a potential immunomodulatory, anti-inflammatory, anti-hemolytic, and anti-oxidant agent. These results could be explained by the computational findings showing that polysaccharide building blocks bound both cyclooxygenase-2 (COX-2) and TNF-α with acceptable affinities.

Funder

Tuniso-Moroccan project

Publisher

MDPI AG

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