Yıldırım Metin, Binzet Gun, Binzet Rıza, Yabalak Erdal
Faculty of Pharmacy, Department of Biochemistry, Harran University, Şanlıurfa, Turkey.
Department of Elementary Science Education, Faculty of Education, Mersin University, Mersin, Turkey.
Int J Environ Health Res. 2024 Nov;34(11):3784-3797. doi: 10.1080/09603123.2024.2326182. Epub 2024 Mar 11.
Hausskn. ex Bornm. () belongs to the Boraginaceae family and it is an endemic species from Irano-turanian phytogeographical region (central and eastern Anatolia) that distributes in steppe areas. This study aimed to investigate the chemical composition, antioxidant, in vitro cytotoxic and apoptosis induction of methanol extract of aerial parts of . As a result of GC/MS analysis, 14 components were identified, and the major compounds of the extracts are retronecine (13.94%), α.-D-Glucopyranosiduronic acid (10.86%), melaniline (7.5%) and 1,2-Butanediol (4.02%), respectively. Antioxidant properties of were determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity, ferric reducing antioxidant power (FRAP) and superoxide radical scavenging activity methods. While the DPPH free radical scavenging activity results of extract varied between 62.49% and 32.27%, reducing power activity and superoxide radical scavenging activity were found to be low. The result of the MTT assay revealed strong anticancer activity of extract. The most significant cytotoxic effect was noted at a concentration of 1000 µg/mL after 48 hours. These findings together with flow cytometry analysis suggest that apoptosis can be the main mechanism underlying cell death after extract treatment.
豪斯肯草(Hausskn. ex Bornm.)属于紫草科,是一种来自伊朗 - 图兰植物地理区域(安纳托利亚中部和东部)的特有物种,分布于草原地区。本研究旨在调查豪斯肯草地上部分甲醇提取物的化学成分、抗氧化活性、体外细胞毒性及凋亡诱导作用。通过气相色谱/质谱联用(GC/MS)分析,鉴定出14种成分,提取物的主要化合物分别为倒千里光裂碱(13.94%)、α - D - 吡喃葡萄糖醛酸(10.86%)、黑素宁(7.5%)和1,2 - 丁二醇(4.02%)。采用2,2 - 二苯基 - 1 - 苦基肼(DPPH)自由基清除活性、铁离子还原抗氧化能力(FRAP)和超氧阴离子自由基清除活性方法测定了豪斯肯草的抗氧化性能。豪斯肯草提取物的DPPH自由基清除活性结果在62.49%至32.27%之间变化,而还原能力活性和超氧阴离子自由基清除活性较低。MTT法检测结果显示豪斯肯草提取物具有较强的抗癌活性。在48小时后,浓度为1000μg/mL时观察到最显著的细胞毒性作用。这些发现与流式细胞术分析表明,凋亡可能是豪斯肯草提取物处理后细胞死亡的主要机制。