Rufino Ana T, Ferreira Isabel, Judas Fernando, Salgueiro Lígia, Lopes M Celeste, Cavaleiro Carlos, Mendes Alexandrina F
Center for Neuroscience and Cell Biology, University of Coimbra , Coimbra , Portugal .
Pharm Biol. 2015 Aug;53(8):1220-30. doi: 10.3109/13880209.2014.970701. Epub 2015 Jan 23.
Effective drugs to treat osteoarthritis (OA) and inflammatory bowel disease (IBD) are needed.
To identify essential oils (EOs) with anti-inflammatory activity in cell models of OA and IBD.
EOs from Eryngium duriaei subsp. juresianum (M. Laínz) M. Laínz (Apiaceae), Laserpitium eliasii subsp. thalictrifolium Sennen & Pau (Apiaceae), Lavandula luisieri (Rozeira) Rivas-Martínez (Lamiaceae), Othantus maritimus (L.) Hoff. & Link (Asteraceae), and Thapsia villosa L. (Apiaceae) were analyzed by GC and GC/MS. The anti-inflammatory activity of EOs (5-200 μg/mL) was evaluated by measuring inducible nitric oxide synthase (iNOS) and nuclear factor-κB (NF-κB) activation (total and phosphorylated IκB-α), in primary human chondrocytes and the intestinal cell line, C2BBe1, stimulated with interleukin-1β (IL-1β) or interferon-γ (IFN-γ), IL-1β and tumor necrosis factor-α (TNF-α), respectively.
The EO of L. luisieri significantly reduced iNOS (by 54.9 and 81.0%, respectively) and phosphorylated IκB-α (by 87.4% and 62.3%, respectively) in both cell models. The EO of E. duriaei subsp. juresianum caused similar effects in human chondrocytes, but was inactive in intestinal cells, even at higher concentrations. The EOs of L. eliasii subsp. thalictrifolium and O. maritimus decreased iNOS expression by 45.2 ± 8.7% and 45.2 ± 6.2%, respectively, in C2BBe1 cells and were inactive in chondrocytes. The EO of T. villosa was inactive in both cell types.
This is the first study showing anti-inflammatory effects of the EOs of L. luisieri and E. duriaei subsp. juresianum. These effects are specific of the cell type and may be valuable to develop new therapies or as sources of active compounds with improved efficacy and selectivity towards OA and IBD.
需要有效的药物来治疗骨关节炎(OA)和炎症性肠病(IBD)。
在骨关节炎和炎症性肠病的细胞模型中鉴定具有抗炎活性的精油(EOs)。
采用气相色谱(GC)和气相色谱-质谱联用(GC/MS)分析法对硬叶刺芹亚种朱雷西亚刺芹(M. Laínz)M. Laínz(伞形科)、埃利亚斯刺芹亚种唐松叶刺芹Sennen & Pau(伞形科)、路易斯薰衣草(Rozeira)Rivas-Martínez(唇形科)、海滨奥特罕草(L.)Hoff. & Link(菊科)和绒毛毒参L.(伞形科)的精油进行分析。通过检测诱导型一氧化氮合酶(iNOS)和核因子-κB(NF-κB)的激活情况(总IκB-α和磷酸化IκB-α),评估精油(5 - 200μg/mL)在分别用白细胞介素-1β(IL-1β)或干扰素-γ(IFN-γ)、IL-1β和肿瘤坏死因子-α(TNF-α)刺激的原代人软骨细胞和肠细胞系C2BBe1中的抗炎活性。
路易斯薰衣草精油在两种细胞模型中均显著降低了iNOS(分别降低54.9%和81.0%)和磷酸化IκB-α(分别降低87.4%和62.3%)。硬叶刺芹亚种朱雷西亚刺芹精油在人软骨细胞中产生了类似的效果,但在肠细胞中即使在较高浓度下也无活性。埃利亚斯刺芹亚种唐松叶刺芹和海滨奥特罕草的精油在C2BBe1细胞中分别使iNOS表达降低了45.2±8.7%和45.2±6.2%,而在软骨细胞中无活性。绒毛毒参精油在两种细胞类型中均无活性。
这是第一项显示路易斯薰衣草和硬叶刺芹亚种朱雷西亚刺芹精油具有抗炎作用的研究。这些作用具有细胞类型特异性,对于开发新疗法或作为对骨关节炎和炎症性肠病具有更高疗效和选择性的活性化合物来源可能具有重要价值。