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土耳其鸦葱属植物提取物通过抑制核因子κB激活减弱细胞因子分泌,在体外显示出抗炎作用。

Turkish Scorzonera Species Extracts Attenuate Cytokine Secretion via Inhibition of NF-κB Activation, Showing Anti-Inflammatory Effect in Vitro.

作者信息

Bahadır Acikara Özlem, Hošek Jan, Babula Petr, Cvačka Josef, Budešínský Miloš, Dračinský Martin, Saltan İşcan Gülçin, Kadlecová Daniela, Ballová Ludmila, Šmejkal Karel

机构信息

Department of Pharmacognosy, Faculty of Pharmacy, Ankara University, 06100 Ankara, Turkey.

Department of Molecular Biology and Pharmaceutical Biotechnology, Faculty of Pharmacy, University of Veterinary and Pharmaceutical Sciences Brno, Palackého tř. 1946/1, 61242 Brno, Czech Republic.

出版信息

Molecules. 2015 Dec 30;21(1):E43. doi: 10.3390/molecules21010043.

Abstract

Scorzonera species are used in different folk medicines to combat many diseases, including the illnesses connected with inflammation. Previous experiments showed anti-inflammatory activity of Scorzonera extracts in vivo. S. latifolia, S. cana var. jacquiniana, S. tomentosa, S. mollis ssp. szowitsii, S. eriophora, S. incisa, S. cinerea, and S. parviflora extracts were, therefore, evaluated for their inhibitory activities of TNF-α and IL-1β production, and NF-κB nuclear translocation in THP-1 macrophages. The HPLC analysis was carried out to elucidate and to compare the composition of these extracts. Major compounds of the tested extracts have been isolated using different chromatographic techniques and further tested for their inhibitory activities on TNF-α and IL-1β production. Several extracts showed promising anti-inflammatory activity in these in vitro tests. Results of HPLC analysis revealed chlorogenic acid as a compound present in all tested extracts. Hyperoside, quercetin-3-O-β-d-glucoside and rutin were also present in varying amount in some Scorzonera species analyzed. Furthermore, eight phenolics which were identified as quercetin-3-O-β-d-glucoside (1), hyperoside (2), hydrangenol-8-O-glucoside (3), swertisin (4), 7-methylisoorientin (5), 4,5-O-dicaffeoyl-quinic acid (6), 3,5-di-O-caffeoyl-quinic acid (7), and chlorogenic acid (8) have been isolated as major phenolic compounds of the tested extracts and, together with eight terpenoids (9-16) previously obtained from different Scorzonera species, have been tested for the inhibition of TNF-α production, unfortunately with no activity comparable with standard.

摘要

鸦葱属植物被用于不同的民间药物中,以对抗多种疾病,包括与炎症相关的疾病。先前的实验表明鸦葱属植物提取物在体内具有抗炎活性。因此,对宽叶鸦葱、毛果鸦葱变种、绒毛鸦葱、软叶鸦葱亚种、绵毛鸦葱、裂叶鸦葱、灰叶鸦葱和小花鸦葱提取物的肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)产生抑制活性以及在THP-1巨噬细胞中核因子-κB(NF-κB)核转位进行了评估。进行高效液相色谱(HPLC)分析以阐明和比较这些提取物的成分。使用不同的色谱技术分离了受试提取物的主要化合物,并进一步测试了它们对TNF-α和IL-1β产生的抑制活性。在这些体外试验中,几种提取物显示出有前景的抗炎活性。HPLC分析结果显示绿原酸是所有受试提取物中都存在的一种化合物。在一些分析的鸦葱属植物中还不同程度地存在金丝桃苷、槲皮素-3-O-β-D-葡萄糖苷和芦丁。此外,已分离出8种酚类化合物,分别为槲皮素-3-O-β-D-葡萄糖苷(1)、金丝桃苷(2)、水甘草醇-8-O-葡萄糖苷(3)、獐牙菜苷(4)、7-甲基异荭草素(5)、4,5-O-二咖啡酰奎宁酸(6)、3,5-二-O-咖啡酰奎宁酸(7)和绿原酸(8),作为受试提取物的主要酚类化合物,并且与先前从不同鸦葱属植物中获得的8种萜类化合物(9 - 16)一起测试了对TNF-α产生的抑制作用,遗憾的是没有与标准品相当的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/6274538/9ed105c92ef3/molecules-21-00043-g001.jpg

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