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Phlorofucofuroeckol A inhibits the LPS-stimulated iNOS and COX-2 expressions in macrophages via inhibition of NF-κB, Akt, and p38 MAPK.
Kim, A-Reum; Lee, Min-Sup; Shin, Tai-Sun; Hua, Hong; Jang, Byeong-Churl; Choi, Jae-Sue; Byun, Dae-Seok; Utsuki, Tadanobu; Ingram, Donald; Kim, Hyeung-Rak.
Afiliação
  • Kim AR; Department of Food Science and Nutrition, Pukyong National University, Busan 608-737, South Korea.
Toxicol In Vitro ; 25(8): 1789-95, 2011 Dec.
Article em En | MEDLINE | ID: mdl-21963823
ABSTRACT
We have recently reported that phlorofucofuroeckol A isolated from the edible brown algae Ecklonia stolonifera showed potential antioxidative and anti-inflammatory properties in macrophage stimulated by LPS treatments. In this study, we further investigated the pharmacological characteristic of phlorofucofuroeckol A in regulations of inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2 through regulatory and signaling pathways using LPS-treated RAW 264.7 cells. Treatment with 20 µM of phlorofucofuroeckol A significantly decreased levels of iNOS and COX-2 mRNA induced by LPS stimulation. As results, levels of pro-inflammatory cytokines such as interleukin (IL)-1ß, IL-6 and tumor necrosis factor (TNF)-α were significantly reduced by treatments of phlorofucofuroeckol A in LPS-stimulated RAW 264.7 cells. Phlorofucofuroeckol A inhibited promoter activities of inflammatory-mediators (iNOS and COX-2) and transcriptional factors (nuclear factor-κB, NF-κB, and AP-1) in LPS-treated RAW 264.7 cells. Moreover, phlorofucofuroeckol A inhibited activation of Akt and p38 MAPK in LPS-treated RAW 264.7 cells. These results indicate that the phlorofucofuroeckol A regulates iNOS and COX-2 expressions through the NF-κB-dependent transcriptional control associated with inhibition of multiple signaling proteins, suggesting potential candidates of phloroglucinol derivatives for treatments of inflammatory diseases.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzofuranos / Dioxinas / Óxido Nítrico Sintase Tipo II / Inibidores de Ciclo-Oxigenase 2 / Anti-Inflamatórios Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzofuranos / Dioxinas / Óxido Nítrico Sintase Tipo II / Inibidores de Ciclo-Oxigenase 2 / Anti-Inflamatórios Idioma: En Ano de publicação: 2011 Tipo de documento: Article