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首页> 外文期刊>International immunopharmacology >S-Allyl cysteine reduces eosinophilic airway inflammation and mucus overproduction on ovalbumin-induced allergic asthma model
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S-Allyl cysteine reduces eosinophilic airway inflammation and mucus overproduction on ovalbumin-induced allergic asthma model

机译:S-烯丙基半胱氨酸减少嗜酸性气道炎症和粘液过度生产对卵巢蛋白诱导的过敏性哮喘模型

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摘要

S-Allyl cysteine (SAC) is an active component in garlic and has various pharmacological effects, such as anti-inflammatory, anti-oxidant, and anti-cancer activities. In this study, we explored the suppressive effects of SAC on allergic airway inflammation induced in an ovalbumin (OVA)-induced asthma mouse model. To induce asthma, BALB/c mice were sensitized to OVA on days 0 and 14 by intraperitoneal injection and exposed to OVA from days 21 to 23 using a nebulizer. SAC was administered to mice by oral gavage at a dose of 10 or 20 mg/kg from days 18 to 23. SAC significantly reduced airway hyperresponsiveness, inflammatory cell counts, and Th2 type cytokines in bronchoalveolar lavage fluid induced by OVA exposure, which was accompanied by reduced serum OVA-specific immunoglobulin E. In histological analysis of the lung tissue, administration of SAC reduced inflammatory cell accumulation into lung tissue and mucus production in airway goblet cells induced by OVA exposure. Additionally, SAC significantly decreased MUC5AC expression and nuclear factor-KB phosphorylation induced by OVA exposure. In summary, SAC effectively suppressed allergic airway inflammation and mucus production in OVA-challenged asthmatic mice. Therefore, SAC shows potential for use in treating allergic asthma.
机译:S-烯丙基半胱氨酸(SAC)是大蒜中的活性成分,具有各种药理作用,例如抗炎,抗氧化剂和抗癌活动。在这项研究中,我们探讨了SAC对卵磷酸酯(OVA)诱导的哮喘小鼠模型中诱导的过敏气道炎症的抑制作用。为了诱导哮喘,通过腹膜内注射在第0天和14天和14天中敏感BALB / C小鼠,并使用喷雾器从21至23天暴露于OVA。通过10或20mg / kg的口服饲喂的小鼠从18至23天的剂​​量给予小鼠。囊肿显着降低了通过OVA暴露诱导的支气管肺泡灌洗液中的气道高反应性,炎症细胞计数和Th2型细胞因子。通过减少血清ova特异性免疫球蛋白E.在肺组织的组织学分析中,将SAC降低炎症细胞积累的肺组织和OVA暴露诱导的气道脚轮细胞中的粘液产生。另外,SAC显着降低了OVA暴露诱导的MUC5AC表达和核因子-KB磷酸化。总之,囊有效地抑制了OVA挑战哮喘小鼠的过敏气道炎症和粘液生产。因此,囊显示用于治疗过敏性哮喘的可能性。

著录项

  • 来源
    《International immunopharmacology 》 |2019年第2019期| 共7页
  • 作者单位

    Chonnam Natl Univ Coll Vet Med BK21 Plus Project Team 77 Yongbong Ro Gwangju 61186 South Korea;

    Korea Res Inst Biosci &

    Biotechnol Nat Prod Res Ctr Jeonbuk Branch Ipsingil 181 Jeongeup 56212;

    Chonnam Natl Univ Coll Vet Med BK21 Plus Project Team 77 Yongbong Ro Gwangju 61186 South Korea;

    Korea Inst Oriental Med Herbal Med Resources Res Ctr Geonjae Ro 177 Naju 58245 Jeollanam Do;

    Korea Res Inst Biosci &

    Biotechnol Nat Prod Res Ctr Jeonbuk Branch Ipsingil 181 Jeongeup 56212;

    Chonnam Natl Univ Coll Vet Med BK21 Plus Project Team 77 Yongbong Ro Gwangju 61186 South Korea;

    Korea Inst Toxicol Jeonbuk Dept Inhalat Res 30 Baekhakl Gil Jeongeup 56212 Jeollabuk Do South;

    Chonnam Natl Univ Coll Vet Med BK21 Plus Project Team 77 Yongbong Ro Gwangju 61186 South Korea;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学 ;
  • 关键词

    S-Allyl cysteine; Asthma; Airway inflammation; Mucus production; Mice;

    机译:S-烯丙基半胱氨酸;哮喘;气道炎症;粘液生产;小鼠;

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