人参
一氧化氮合酶
p38丝裂原活化蛋白激酶
一氧化氮
MAPK/ERK通路
激酶
肿瘤坏死因子α
药理学
化学
脂多糖
NF-κB
信号转导
NFKB1型
生物化学
生物
免疫学
医学
转录因子
有机化学
病理
替代医学
基因
作者
Chan‐Woo Lee,Seul Lee,Young Pyo Jang,Junseong Park
出处
期刊:Journal of Microbiology and Biotechnology
[Journal of Microbiology and Biotechnology]
日期:2024-01-12
卷期号:34 (2): 262-269
被引量:3
标识
DOI:10.4014/jmb.2312.12001
摘要
Panax ginseng has been widely applied as an important herb in traditional medicine to treat numerous human disorders. However, the inflammatory regulation effect of P. ginseng distillate (GSD) has not yet been fully assessed. To determine whether GSD can ameliorate inflammatory processes, a GSD was prepared using the vacuum distillation process for the first time, and the regulation effect on lipopolysaccharide-induced macrophages was assessed. The results showed that GSD effectively inhibited nitric oxide (NO) formation and activation of inducible nitric oxide synthase (iNOS) mRNA in murine macrophage cell, but not cyclooxygenase-2 production. The mRNA expression pattern of tumor necrosis factor alpha and IL-6 were also reduced by GSD. Furthermore, we confirmed that GSD exerted its anti-inflammatory effects by downregulating c-Jun NH2-terminal kinase (JNK) phosphorylation, the extracellular signal-regulated kinase phosphorylation, and signaling pathway of nuclear factor kappa B (NF-κB). Our findings revealed that the inflammatory regulation activity of GSD could be induced by iNOS and NO formation inhibition mediated by regulation of nuclear factor kappa B and p38/JNK MAPK pathways.
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