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Carbohydrate research · 2024

Structural characterization of a sulfated polysaccharide from Gracilariadomingensis and potential anti-inflammatory and antinociceptive effects.

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da Silva Prudêncio Rafael, Sousa Antonio Kleiton de, Silva Denise Mayara Melo, Santos Ferreira Jayro Dos, Rocha Danyela Maria Leal, Almeida Viviane Pinheiro Alves de, Silva Sousa João Janilson da, Sousa Stefany Guimarães, da Silva Tino Marcos Lino, Dos Santos Carvalho André, Cruz Júnior José Simião da, Alves Even Herlany Pereira, Vasconcelos Daniel Fernando Pereira, Bezerra Roosevelt D S, França Dourado Flaviane de, Oliveira Aline Lima de, Cabral Wanessa Feliz, Souza de Almeida Leite José Roberto de, da Silva Durcilene Alves, Nascimento Junior Elias Borges do, Brito Tarcísio Vieira de, Aguiar Magalhães Diva de, Barbosa André Luiz Dos Reis

Аннотация

Seaweeds are natural sources of sulfated polysaccharides (SPs), biopolymers with remarkable pharmacological properties, including biological actions capable of attenuating components of the inflammatory process such as edema, cytokines, cell migration and pain. Our results confirm that SPs obtained from Gracilaria domingensis (SP-GD) are agarans, primarily composed of residues of β-d-galactopyranose 6-sulfate and 3,6-anhydro-α-l-galactopyranose. Specifically, SP-GD at a dose of 10 mg/kg was effective in significantly reducing paw edema induced by carrageenan or histamine, serotonin, bradykinin, 48/80 and prostaglandin E2. SP-GD (10 mg/kg) was also able to reduce neutrophil migration and the activity of the myeloperoxidase enzyme in carrageenan-induced peritonitis, as well as conserve glutathione concentration and reduce malondialdehyde levels in the animals' peritoneal fluid. Furthermore, it showed antinociceptive action in the abdominal writhing test induced by acetic acid and in the paw licking test induced by formalin. Thus, the results obtained allow us to infer that SPs extracted from G. domingensis at a dose of 10 mg/kg have anti-inflammatory effects by reducing neutrophil migration and modulating the activity of vasoactive mediators and antinociceptive effects by acting, at least in part, through a peripheral mechanism dependent on the negative modulation of inflammatory mediators.

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