4.7 Article

The protective effect of Sargassum horneri against particulate matter-induced inflammation in lung tissues of an in vivo mouse asthma model

Journal

FOOD & FUNCTION
Volume 10, Issue 12, Pages 7995-8004

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9fo02068c

Keywords

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Funding

  1. Ministry of Oceans and Fisheries, Korea [20172085]
  2. Korea Institute of Marine Science & Technology Promotion (KIMST) [201702852] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Sargassum horneri is an edible brown seaweed with potential anti-inflammatory properties. The present study was designed to evaluate the anti-inflammatory properties of S. horneri using an in vivo mouse asthma model following exposure to particulate matter (PM). 7-8 week old BALB/c mice (20-25 g) were randomly divided into seven groups (n = 4) as follows: 1: no treatment, 2: OVA (ovalbumin) + PM, 3: OVA + PM + SHE (S. horneri ethanol extract) 200 mg kg(-1), 4: OVA + PM + SHE 400 mg kg(-1), 5: OVA + PM + prednisone 5 mg kg(-1), 6: OVA only, and 7: PM only. All mice (except healthy controls) were sensitized on the first day by intraperitoneal injection of 10 mu g OVA and 2 mg Al(OH)(3) in 200 mu L of saline. Starting from day 15, mice (except groups 1 and 6) were exposed to sonicated PM (5 mg m(-3), 30 min day(-1)) through a nebulizer daily for 7 consecutive days. Mice exposed to PM and OVA showed up-regulated expression of MAPKs and pro-inflammatory cytokine production in the lungs. Furthermore, PM-exposed lungs had significantly reduced expression of Nrf2 and HO-1 genes. However, oral administration of the SHE reduced the phosphorylation levels of MAPKs, iNOS and COX2 expression levels, and mRNA expression levels of pro-inflammatory cytokines. In addition, SHE treated group mice had up-regulated anti-oxidant gene expression levels in the lungs compared to group 2. These findings demonstrate that oral administration of the SHE re-establishes PM-induced inflammation and oxidative stress in the lungs. Taken together, the SHE has therapeutic potential in preventing PM-induced inflammation and oxidative stress.

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