Zare Shahneh Fatemeh, Valiyari Samira, Baradaran Behzad, Abdolalizadeh Jalal, Bandehagh Ali, Azadmehr Abass, Hajiaghaee Reza
Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Adv Pharm Bull. 2013;3(1):51-5. doi: 10.5681/apb.2013.009. Epub 2013 Feb 7.
Salvia officinalis L., also known as Maryam Goli, is one of the native plants used to Persian medicinal herbs. Hence, the objective of this study was to examine the in vitro cytotoxic activities of a standardized crude methanol extracts prepared from Salvia officinalis L., on a non-Hodgkin's B-cell lymphoma (Raji) and human leukemic monocyte lymphoma (U937), Human acute myelocytic leukemia (KG-1A) and Human Umbilical Vein Endothelial (HUVEC) cell lines.
The effect of methanolic extract on the inhibition of cell proliferation and cytotoxic activity was evaluated by Dye exclusion and Micro culture tetrazolium test (MTT) cytotoxicity assay. Cell death ELISA was employed to quantify the nucleosome production result from nuclear DNA fragmentation during apoptosis and determined whether the mechanism involves induction of apoptosis or necrosis.
The present results demonstrated that methanolic extract at 50 to 800 μg/ml dose and time-dependently suppressed the proliferation of KG-1A, U937 and Raji cells by more than 80% (p<0.01), with ascending order of IC50 values in 24: KG-1A (214.377 μg/ml), U937 (229.312 μg/ml) and Raji (239.692 μg/ml) when compared with a chemotherapeutic anticancer drug, paclitaxel (Toxol), confirming the tumour-selective cytotoxicity. The crude extract however did not exert any significant cytotoxic effect on normal cell line HUVEC (IC50>800 Ag/ml). Nucleosome productions in KG-1A, Raji and U937 cells were significantly increased respectively upon the treatment of Salvia officinalis L. extract.
The Salvia officinalis L. extract was found dose and time-dependently inhibits the proliferation of lymphoma and leukemic cells possibly via an apoptosis-dependent pathway.
鼠尾草,也被称为玛丽安戈利,是波斯药用草药中使用的本土植物之一。因此,本研究的目的是检测从鼠尾草制备的标准化粗甲醇提取物对非霍奇金B细胞淋巴瘤(Raji)、人白血病单核细胞淋巴瘤(U937)、人急性髓细胞白血病(KG-1A)和人脐静脉内皮细胞(HUVEC)细胞系的体外细胞毒性活性。
通过染料排除法和微量培养四氮唑盐试验(MTT)细胞毒性测定法评估甲醇提取物对细胞增殖抑制和细胞毒性活性的影响。采用细胞死亡ELISA法量化凋亡过程中核DNA片段化产生的核小体,并确定其机制是否涉及凋亡或坏死的诱导。
目前的结果表明,50至800μg/ml剂量的甲醇提取物可剂量和时间依赖性地抑制KG-1A、U937和Raji细胞的增殖超过80%(p<0.01),与化疗抗癌药物紫杉醇(Toxol)相比,24小时时IC50值的升序为:KG-1A(214.377μg/ml)、U937(229.312μg/ml)和Raji(239.692μg/ml),证实了肿瘤选择性细胞毒性。然而,粗提取物对正常细胞系HUVEC没有任何显著的细胞毒性作用(IC50>800μg/ml)。用鼠尾草提取物处理后,KG-1A、Raji和U937细胞中的核小体产量分别显著增加。
发现鼠尾草提取物可剂量和时间依赖性地抑制淋巴瘤和白血病细胞的增殖,并可能通过凋亡依赖性途径发挥作用。