Inflammopharmacology · 2018
Orofacial antinociceptive effect of sulphated polysaccharide from the marine algae Hypnea pseudomusciformis in rodents.
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Souza Caio Átila Prata Bezerra, de Oliveira Breytiner Amaro, Santos Sacha Aubrey Alves Rodrigues, Batista Francisco Lucas Alves, Andrade Francisco Regivânio Nascimento, Neto Eugênio Januário Ramos, de Melo Júnior José de Maria Albuquerque, Silva Mendes Francisco Rogenio da, Barroso Lana Karine Vasconcelos, Canuto Kirley Marques, Magalhães Francisco Ernani Alves, E Silva Angelo Roncalli Alves, Farias Wladimir Ronald Lobo, Campos Adriana Rolim
Аннотация
This study aimed to evaluate the antinociceptive effect of sulphated polysaccharide from the marine algae Hypnea pseudomusciformis (PLS) using rodent models of orofacial pain. Acute pain was induced by formalin, capsaicin, cinnamaldehyde, acidified saline or glutamate (cutaneous modes) and hypertonic saline (corneal model). In one experiment, animals were pretreated with ruthenium red, glibenclamide, naloxone, L-NAME, methylene blue or ketamine to investigate the mechanism of antinociception. In another experiment, animals pretreated with PLS or saline were submitted to the temporomandibular joint formalin test. In yet another, animals were submitted to craniofacial pain induced by mustard oil. Motor activity was evaluated with the open-field test. Cytotoxicity and antioxidant activities were also assessed. Pre-treatment with PLS significantly reduced nociceptive behavior associated with acute pain. Antinociception was effectively reduced, but not inhibited, by ruthenium red and ketamine. L-NAME and glibenclamide enhanced the PLS effect. PLS antinociception was resistant to methylene blue, naloxone and heating. PLS presented no cytotoxicity or antioxidant properties. Our results confirm the potential pharmacological relevance of PLS as an inhibitor of orofacial nociception in acute pain probably mediated by glutamatergic, nitrergic, TRPs and K + ATP pathways.