PMID- 17804193 OWN - NLM STAT- MEDLINE DCOM- 20081030 LR - 20240109 IS - 0753-3322 (Print) IS - 0753-3322 (Linking) VI - 62 IP - 5 DP - 2008 Jun TI - Effects of Ecklonia cava ethanolic extracts on airway hyperresponsiveness and inflammation in a murine asthma model: role of suppressor of cytokine signaling. PG - 289-96 AB - Ecklonia cava (EC) is a brown alga that evidences radical scavenging activity, bactericidal activity, tyrosinase inhibitory activity, and protease inhibitory activity. However, its anti-allergic effects remain poorly understood. In the current study, we attempted to determine whether pretreatment with EC induces a significant inhibition of asthmatic reactions in a mouse asthma model. Mice sensitized and challenged with ovalbumin (OVA) evidenced typical asthmatic reactions, as follows: an increase in the number of eosinophils in bronchoalveolar lavage fluid; a marked influx of inflammatory cells into the lung around blood vessels and airways, and airway luminal narrowing; the development of airway hyperresponsiveness; the detection of tumor necrosis factor-alpha (TNF-alpha) and Th2 cytokines, including IL-4 and IL-5 in the bronchoalveolar lavage (BAL) fluid; and the detection of allergen-specific immunoglobulin E (IgE) in the serum. However, the administration of EC extract prior to the final airway OVA challenge resulted in a significant inhibition of all asthmatic reactions. We also demonstrated that EC extracts treatment resulted in significant reductions on matrix metalloproteinase-9 (MMP-9) and Suppressor of cytokine signaling-3 (SOCS-3) expression and a reduction in the increased eosinophil peroxidase (EPO) activity. The treatment of animals with EC extracts resulted in a significant reduction in the concentrations of the Th2 cytokine (IL-4 and IL-5) in the airways, without any concomitant increase in the concentration of Th1 cytokines. These findings indicate that EC extracts may prove useful as an adjuvant therapy for allergic airway reactions via the inhibition of the Th2 response. Accordingly, this study may provide evidence that EC extract performs a critical function in the amelioration of the pathogenetic process of asthma in mice. FAU - Kim, Se-Kwon AU - Kim SK AD - Marine Bioprocess Research Center, Pukyong National University, Busan 608-737, Republic of Korea. FAU - Lee, Da-Young AU - Lee DY FAU - Jung, Won-Kyo AU - Jung WK FAU - Kim, Ji-Hye AU - Kim JH FAU - Choi, Inhak AU - Choi I FAU - Park, Sae-Gwang AU - Park SG FAU - Seo, Su-Kil AU - Seo SK FAU - Lee, Soo-Woong AU - Lee SW FAU - Lee, Chang Min AU - Lee CM FAU - Yea, Sung Su AU - Yea SS FAU - Choi, Yung Hyun AU - Choi YH FAU - Choi, Il-Whan AU - Choi IW LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070810 PL - France TA - Biomed Pharmacother JT - Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie JID - 8213295 RN - 0 (Anti-Inflammatory Agents) RN - 0 (Bronchoconstrictor Agents) RN - 0 (Cytokines) RN - 0 (Plant Extracts) RN - 0 (Socs3 protein, mouse) RN - 0 (Socs5 protein, mouse) RN - 0 (Solvents) RN - 0 (Suppressor of Cytokine Signaling 3 Protein) RN - 0 (Suppressor of Cytokine Signaling Proteins) RN - 0W5ETF9M2K (Methacholine Chloride) RN - 37341-29-0 (Immunoglobulin E) RN - 3K9958V90M (Ethanol) RN - 9006-59-1 (Ovalbumin) RN - EC 1.11.1.- (Eosinophil Peroxidase) RN - EC 3.4.24.17 (Matrix Metalloproteinase 3) SB - IM MH - Animals MH - Anti-Inflammatory Agents/immunology/*therapeutic use MH - Asthma/*drug therapy/immunology/metabolism MH - Bronchial Hyperreactivity/*drug therapy/immunology/metabolism MH - Bronchoalveolar Lavage Fluid/chemistry/immunology MH - Bronchoconstrictor Agents/pharmacology MH - Cytokines/*metabolism MH - Eosinophil Peroxidase/metabolism MH - Ethanol MH - Female MH - Immunoglobulin E/blood MH - Matrix Metalloproteinase 3/biosynthesis MH - Methacholine Chloride/pharmacology MH - Mice MH - Mice, Inbred BALB C MH - Ovalbumin MH - Phaeophyceae/*chemistry MH - Phytotherapy MH - Plant Extracts/therapeutic use MH - Solvents MH - Suppressor of Cytokine Signaling 3 Protein MH - Suppressor of Cytokine Signaling Proteins/biosynthesis EDAT- 2007/09/07 09:00 MHDA- 2008/10/31 09:00 CRDT- 2007/09/07 09:00 PHST- 2007/07/02 00:00 [received] PHST- 2007/07/18 00:00 [accepted] PHST- 2007/09/07 09:00 [pubmed] PHST- 2008/10/31 09:00 [medline] PHST- 2007/09/07 09:00 [entrez] AID - S0753-3322(07)00139-4 [pii] AID - 10.1016/j.biopha.2007.07.009 [doi] PST - ppublish SO - Biomed Pharmacother. 2008 Jun;62(5):289-96. doi: 10.1016/j.biopha.2007.07.009. Epub 2007 Aug 10.