Du Kun, De Mieri Maria, Saxena Priyanka, Phungula Khanya V, Wilhelm Anke, Hrubaru Madalina Marina, van Rensburg Elmarie, Zietsman Pieter C, Hering Steffen, van der Westhuizen Jan H, Hamburger Matthias
Department of Chemistry, University of the Free State, Bloemfontein, South Africa.
Division of Pharmaceutical Biology, University of Basel, Basel, Switzerland.
Planta Med. 2015 Aug;81(12-13):1154-62. doi: 10.1055/s-0035-1545929. Epub 2015 Apr 29.
The human ether-a-go-go-related gene channel is a voltage-activated K(+) channel involved in cardiac action potential. Its inhibition can lead to QT prolongation, and eventually to potentially fatal arrhythmia. Therefore, it is considered a primary antitarget in safety pharmacology. To assess the risk of human ether-a-go-go-related gene channel inhibition by medicinal plants, 700 extracts from different parts of 142 medicinal plants collected in Southern Africa were screened on Xenopus laevis oocytes. A CH2Cl2 extract from the stems and leaves of Galenia africana (Aizoaceae) reduced the peak tail human ether-a-go-go-related gene current by 50.4 ± 5.5 % (n = 3) at a concentration of 100 µg/mL. By means of high-performance liquid chromatography-based activity profiling, nine flavonoids were identified in the active time windows. However, the human ether-a-go-go-related gene channel inhibition of isolated compounds was less pronounced than that of extract and active microfractions (human ether-a-go-go-related gene inhibition between 10.1 ± 5 and 14.1 ± 1.6 at 100 µM). The two major constituents, 7,8-methylenedioxyflavone (1) and 7,8-dimethoxyflavone (13), were quantified (4.3 % and 9.4 %, respectively, in the extract). Further human ether-a-go-go-related gene inhibition tests for compounds 1 and 13 at 300 µM showed a concentration-dependent inhibitory activity (33.2 ± 12.4 and 30.0 ± 7.4, respectively). In a detailed phytochemical profiling of the active extract, a total of 20 phenolic compounds, including six new natural products, were isolated and identified.
人醚 - 去极化相关基因通道是一种参与心脏动作电位的电压激活钾通道。对其抑制可导致QT间期延长,并最终引发潜在致命性心律失常。因此,它被视为安全药理学中的主要非靶向靶点。为评估药用植物对人醚 - 去极化相关基因通道的抑制风险,对从非洲南部采集的142种药用植物不同部位提取的700种提取物在非洲爪蟾卵母细胞上进行了筛选。来自非洲伽蓝菜(番杏科)茎叶的二氯甲烷提取物在浓度为100μg/mL时,使人类醚 - 去极化相关基因电流峰值尾电流降低了50.4±5.5%(n = 3)。通过基于高效液相色谱的活性图谱分析,在活性时间窗口内鉴定出9种黄酮类化合物。然而,分离化合物对人醚 - 去极化相关基因通道的抑制作用不如提取物和活性微组分明显(在100μM时人醚 - 去极化相关基因抑制率在10.1±5至14.1±1.6之间)。两种主要成分,7,8 - 亚甲二氧基黄酮(1)和7,8 - 二甲氧基黄酮(13),被定量(提取物中分别为4.3%和9.4%)。对化合物1和13在300μM下进一步的人醚 - 去极化相关基因抑制试验显示出浓度依赖性抑制活性(分别为33.2±12.4和30.0±7.4)。在对活性提取物进行详细的植物化学分析时,共分离并鉴定出20种酚类化合物,包括6种新的天然产物。