Anti-inflammatory effect of the monoterpene myrtenol is dependent on the direct modulation of neutrophil migration and oxidative stress

• Autor(a) principal: Gomes, Bruno S.
• Data de Publicação: 2017
• Outros Autores: S. Neto, Benedito P., Lopes, Everton M., Cunha, Francisco V. M., Araújo, Alyne R., Wanderley, Carlos Wagner de Souza, Wong, Deysi Viviana Tenazoa, Lima Júnior, Roberto César Pereira, Ribeiro, Ronaldo A., Sousa, Damião P., Medeiros, Jand Venes R., Oliveira, Rita C.M., Oliveira, Francisco A.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
• Texto Completo: http://www.repositorio.ufc.br/handle/riufc/26600
• topic: Estresse Oxidativo; Neutrófilos; Neutrophils; Oxidative Stress

Myrtenol is a bicyclic monoterpene with anti-in fl ammatory properties. However, the mechanisms involved are partially unknown. Here, we investigated the effect of myrtenol during experimental chronic arthritis and the possible modulating activity of oxidative stress and neutrophil migration. Complete Freund's Adjuvant (CFA)-sensitized rats were treated with vehicle (1 mL/kg, po), myrtenol (12.5, 25 or 50 mg/kg, po), indomethacin (10 mg/kg, po) or dexamethasone (0.4 mg/kg) followed by intra-articular injection of CFA (0.5 mg/mL, 50 m L per joint). Then, paw edema and articular incapaci- tation (paw elevation time) were evaluated for 14 days. On the last day, a blood concentration superoxide dismutase (SOD) and nitrite was determined. In another experimental setting, human neutrophils were incubated with vehicle (sterile saline, 1 mL) or myrtenol (10 e 100 ng/mL) and the in vitro chemotaxis to N-formylmethionine-leucyl-phenylalanine (fMLP) (10 7 M/well) was evaluated. In addition, antiin- fl ammatory effect of myrtenol was investigated in carrageenan-induced peritonitis. We found that CFA induced a prominent paw swelling and incapacitation of the joint, which were signi fi cantly prevented by myrtenol ( P < 0.05). In addition, blood accumulation nitrite was attenuated by myrtenol when compared with vehicle-treated CFA group ( P < 0.05). Furthermore, plasma levels of SOD were signi fi cantly increased by myrtenol versus vehicle-treated CFA group ( P < 0.05). Moreover, fMLP-triggered neutrophil chemotaxis and carrageenan-induced peritonitis were markedly prevented by myrtenol ( P < 0.05). Therefore, myrtenol showed anti-in fl ammatory and antinociceptive effects on experimental chronic arthritis, which seems to be related to the direct modulation of neutrophil migration and antioxidant activity