대한본초학회지 (The Korea Journal of Herbology)

  • 제28권5호
  • /
  • Pages.45-52
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  • 2013
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  • 1229-1765(pISSN)
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  • 2288-7199(eISSN)
대한본초학회 (The Korea Association of Herbology)
권호 표지
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황금(黃芩) 발효 추출물이 LPS로 유발된 마우스대식세포에서 염증인자증가에 미치는 영향

Effect of Fermented Scutellariae Radix Extract on Production of Inflammatory Mediator in LPS-stimulated Mouse Macrophages

  • 양회정 (가천대학교 한의과대학 본초학교실) ;
  • 한효상 (중부대학교 보건행정학과) ;
  • 이영종 (가천대학교 한의과대학 본초학교실)
  • Yang, Hoi-Jeong (Department of Herbology, College of Oriental Medicine, Gachon University) ;
  • Han, Hyo-Sang (Department of Health Administration, College of Social Sciences, Joongbu University) ;
  • Lee, Young-Jong (Department of Herbology, College of Oriental Medicine, Gachon University)
  • 투고 : 2013.08.15
  • 심사 : 2013.09.17
  • 발행 : 2013.09.30
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초록

Objectives : This study aims at examining the immuno-modulating activity in the fermentative extract of the root of Scutellaria baicalensis Georgi (Scutellariae Radix) on the production of inflammatory mediator in LPS-stimulated RAW264.7 mouse macrophages. Method : Measurements were done for the influences on the cell viability, generation of hydrogen peroxide in cells and nitric oxide (NO) generation using the macrophage of mouse with the specimen SBS as the fermentative extract of Scutellariae Radix (SBS) with Saccharomyces cerevisiae STV89. Result : As a result of carrying out MTT assay to check the cellular toxicity of the fermentative extract of Scutellariae Radix, any excessive toxicity to the macrophage did not occur from treatments by concentration for SBS. SBS increased the generation of hydrogen peroxide in the macrophage. SBS suppressed the NO generated in macrophages and SBS concentration higher than $25{\mu}g/mL$ significantly suppressed the increased NO generated in LPS-stimulated macrophages. SBS concentration higher than $25{\mu}g/mL$ significantly suppressed the generation of IL-6, IL-10, IL-12p40 and MCP-1 in LPS-stimulated macrophages. Conclusion : Our findings indicate that SBS has an immuno-modulating activity in macrophage activation through suppressing the generation of inflammatory substances, NO, IL-6, IL-10, IL-12p40 and MCP-1.

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