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Anti-inflammatory Effects of (Z)-Ligustilide through Suppression of Mitogen-activated Protein Kinases and Nuclear Factor-${kappa}B$ Activation Pathways
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  • Anti-inflammatory Effects of (Z)-Ligustilide through Suppression of Mitogen-activated Protein Kinases and Nuclear Factor-${kappa}B$ Activation Pathways
  • Anti-inflammatory Effects of (Z)-Ligustilide through Suppression of Mitogen-activated Protein Kinases and Nuclear Factor-${kappa}B$ Activation Pathways
저자명
Chung. Ji Won,Choi. Ran Joo,Seo. Eun-Kyoung,Nam. Joo-Won,Dong. Mi-Sook,Shin. Eun Myoung,Guo. Lian Yu,Kim. Yeong Shik
간행물명
Archives of pharmacal research : a publication of the Pharmaceutical Society of Korea
권/호정보
2012년|35권 4호|pp.723-732 (10 pages)
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대한약학회
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정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The roots of Angelica tenuissima have been commonly used for the treatment of cardiovascular diseases and menstrual discomfort in Asian countries, such as China and Korea. The primary volatile flavor components are essential oil ingredients, phthalide lactones. In this study, (Z)-ligustilide was tested for its anti-inflammatory activities in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages. We found that (Z)-ligustilide strongly inhibitis the induction of LPS-induced inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) at both the mRNA and protein levels in a dose-dependent manner. The transcriptional activity of nuclear factor kappa B (NF-${kappa}B$) was also down-regulated in a concentration-dependent manner. Further study revealed that (Z)-ligustilide inhibited the phosphorylation and subsequent degradation of $I{kappa}B{alpha}$, an inhibitor protein of NF-${kappa}B$. In addition, (Z)-ligustilide inhibited the phosphorylation of p38 mitogen-activated protein kinase (p38 MAPK), extracellular signal-regulated kinase (ERK) and c-Jun $NH_2$-terminal kinase (JNK) in a dose-dependent manner. Taken together, these data suggest that (Z)-ligustilide can exert its anti-inflammatory effects by regulating the NF-${kappa}B$ and MAPK signal pathways.