Liu Changda, Dunkin David, Lai Joanne, Song Ying, Ceballos Clare, Benkov Keith, Li Xiu-Min
*Department of Pediatrics, Jaffe Food Allergy Institute, Icahn School of Medicine at Mount Sinai, New York, New York; †Division of Gastroenterology, Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, New York; and ‡The Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Inflamm Bowel Dis. 2015 Aug;21(8):1918-25. doi: 10.1097/MIB.0000000000000439.
Crohn's disease (CD) is a chronic inflammatory disease of the gastrointestinal tract. Current medications have potentially serious side effects. Hence, there is increasing interest in alternative therapies. We previously demonstrated the anti-inflammatory effects of Food Allergy Herbal Formula-2 in vitro on peripheral blood mononuclear cells (PBMCs) and mucosa from CD subjects. Here, we investigated the anti-inflammatory effects of a bioactive compound isolated from Ganoderma lucidum (G. lucidum), a key herbal constituent of Food Allergy Herbal Formula-2, in CD in vitro.
Triterpene ganoderic acid C1 (GAC1) was isolated from G. lucidum. Stimulated RAW 264.7 macrophages were treated with GAC1. Human PBMCs and colonic biopsies were obtained from children with CD and cultured with or without GAC1. TNF-α and other proinflammatory cytokine levels were measured in the culture supernatant. NF-κB signaling was investigated in PBMCs and colonic mucosa treated with GAC1 by In-Cell Western and Western blot analysis.
GAC1 decreased TNF-α production by macrophages and PBMCs from CD subjects. GAC1 significantly decreased TNF-α, IFN-γ, and IL-17A production by inflamed colonic biopsies from CD subjects. These effects were due to downregulation of the NF-κB signaling pathway.
GAC1 inhibited production of TNF-α and other proinflammatory cytokines by PBMCs and inflamed CD colonic mucosa due to blockage of NF-κB activation. GAC1 is a key beneficial constituent in G. lucidum and the Food Allergy Herbal Formula-2 in suppressing the inflammatory cytokines found in CD and warrants clinical investigation for the treatment of CD.
克罗恩病(CD)是一种胃肠道慢性炎症性疾病。目前的药物有潜在的严重副作用。因此,人们对替代疗法的兴趣与日俱增。我们之前在体外证明了食物过敏中药配方2对CD患者外周血单个核细胞(PBMC)和黏膜具有抗炎作用。在此,我们研究了从食物过敏中药配方2的关键草药成分灵芝中分离出的一种生物活性化合物在体外对CD的抗炎作用。
从灵芝中分离出三萜类化合物灵芝酸C1(GAC1)。用GAC1处理经刺激的RAW 264.7巨噬细胞。从CD患儿获取人PBMC和结肠活检组织,在有或无GAC1的情况下进行培养。检测培养上清液中肿瘤坏死因子-α(TNF-α)和其他促炎细胞因子水平。通过细胞内western印迹法和western印迹分析研究GAC1处理的PBMC和结肠黏膜中的核因子-κB(NF-κB)信号传导。
GAC1可降低CD患者巨噬细胞和PBMC产生的TNF-α。GAC1显著降低CD患者炎症结肠活检组织产生的TNF-α、干扰素-γ(IFN-γ)和白细胞介素-17A(IL-17A)。这些作用是由于NF-κB信号通路的下调。
GAC1通过阻断NF-κB激活,抑制PBMC和炎症性CD结肠黏膜产生TNF-α和其他促炎细胞因子。GAC1是灵芝和食物过敏中药配方2中抑制CD中发现的炎性细胞因子的关键有益成分,值得进行治疗CD的临床研究。