Geryani Mohamad Ali, Mahdian Davood, Mousavi Seyed Hadi, Hosseini Azar
Department of Pharmacology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Pharmacology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran; Pharmacological Research Center of Medicinal Plants, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran; Medical Toxicology Research Center, Emam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, Iran.
Avicenna J Phytomed. 2016 Jul-Aug;6(4):410-7.
Perovskia abrotanoides Karel, belongs to the family Lamiaceae and grows wild alongside the mountainous roads inarid and cold climate of Northern Iran. The anti-tumor activity of P. abrotanoides root extract has been shown previously. This study was designed to examine in vitro anti-proliferative and pro-apoptotic effects of flower extract of P. abrotanoides on MCF-7 and Hela cell lines.
Cells were cultured in DMEM medium with 10% fetal bovine serum, 100 units/ml penicillin and 100 µg/ml streptomycin and incubated with different concentrations of plant extracts. Cell viability was quantified by MTT assay. Apoptotic cells were determined using propidium iodide (PI) staining of DNA fragmentation by flow cytometry (sub-G1 peak).
P. abrotanoides extract inhibited the growth of malignant cells in a time and dose-dependent manner and 1000 µg/ml of extract following 48h of incubation was the most cytotoxic dose against Hela cell in comparison with other doses; however, in MCF-7 cells,1000 and 500 µg/ml PA induced toxicity at all time points but with different features.. Analysis of flowcytometry histogram of treated cells compared with control cells indicated that the cytotoxic effect is partly due toapoptosis induction.
Hydro-alcoholic extract of P. abrotanoides flowers inhibits the growth of MCF-7 and HeLa cell lines, partly via inducing apoptosis. Their inhibitory effect was increased in a time and dose-dependent manner, especially in MCF7 cells. However, further studies are needed to reveal the mechanisms of P. abrotanoides extract-induced cell death.
灰毛牡荆属于唇形科,生长于伊朗北部干旱寒冷气候地区的山区道路旁。此前已证明灰毛牡荆根提取物具有抗肿瘤活性。本研究旨在检测灰毛牡荆花提取物对MCF-7和Hela细胞系的体外抗增殖和促凋亡作用。
细胞在含有10%胎牛血清、100单位/毫升青霉素和100微克/毫升链霉素的DMEM培养基中培养,并与不同浓度的植物提取物孵育。通过MTT法对细胞活力进行定量。使用碘化丙啶(PI)染色通过流式细胞术(亚G1峰)测定DNA片段化来确定凋亡细胞。
灰毛牡荆提取物以时间和剂量依赖性方式抑制恶性细胞的生长,与其他剂量相比,孵育48小时后1000微克/毫升的提取物对Hela细胞的细胞毒性最大;然而,在MCF-7细胞中,1000和500微克/毫升的灰毛牡荆提取物在所有时间点均诱导毒性,但具有不同特征。与对照细胞相比,对处理后细胞的流式细胞术直方图分析表明,细胞毒性作用部分归因于凋亡诱导。
灰毛牡荆花的水醇提取物抑制MCF-7和HeLa细胞系的生长,部分是通过诱导凋亡。其抑制作用呈时间和剂量依赖性增加,尤其是在MCF-7细胞中。然而,需要进一步研究以揭示灰毛牡荆提取物诱导细胞死亡的机制。