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首页> 外文期刊>Nutrition Research >Inhibitory effect of glycoprotein isolated from Ulmus davidiana Nakai on caspase 3 activity in 12-O-tetradecanoylphorbol 13-acetate-treated liver cells through the reduction of intracellular reactive oxygen species
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Inhibitory effect of glycoprotein isolated from Ulmus davidiana Nakai on caspase 3 activity in 12-O-tetradecanoylphorbol 13-acetate-treated liver cells through the reduction of intracellular reactive oxygen species

机译:通过降低细胞内活性氧,分离自中美洲榆树糖蛋白对12-O-十四烷酰佛波醇13-乙酸处理的肝细胞中胱天蛋白酶3活性的抑制作用

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Ulmus davidiana Nakai (UDN) has traditionally been used for healing of inflammation, ulcers, and cancers as a folk medicine. This experiment was carried out to evaluate the hepatoprotective activity of UDN glycoprotein (molecular weight, 116 kd) in 12-O-tetradecanoylphorbol 13-acetate (TPA)-treated BNL CL.2 (murine embryonic liver) cells. We evaluated the changes of activity in apoptosis-related signals (cytochrome c, caspase 9, and caspase 3), cleavage of poly(adenosine diphosphate-ribose) polymerase (PARP), and nuclei staining for apoptosis after cotreatment with UDN glycoprotein in the presence of TPA (200 nmol/L). The results showed that UDN glycoprotein (200 micro g/mL) does not have any cytotoxic effect and decreases intracellular reactive oxygen species (ROS) in a dose-dependent manner. When cells were treated with TPA (200 nmol/L) alone, the activities of the apoptotic-related signals (cytochrome c, caspase 9, and caspase 3) were activated. However, their activities were inhibited through the reduction of intracellular ROS after treatment with UDN glycoprotein (200 micro g/mL) in the presence of TPA (200 nmol/L). Also, the results indicate that UDN glycoprotein prevents PARP cleavage and DNA fragmentation. These findings suggest that UDN glycoprotein protects from TPA-induced apoptosis through modulating intracellular ROS in BNL CL.2 cells, and UDN may be a nutraceutical supplement for liver health..
机译:传统上,榆木中草药(UDN)已被用于治疗炎症,溃疡和癌症。进行该实验以评估在12-O-十四烷酰佛波醇13-乙酸酯(TPA)处理的BNL CL.2(鼠胚胎肝)细胞中UDN糖蛋白(分子量,116 kd)的肝保护活性。我们评估了细胞凋亡相关信号(细胞色素c,胱天蛋白酶9和胱天蛋白酶3),多聚腺苷二磷酸核糖核糖聚合酶(PARP)的裂解以及细胞核染色与UDN糖蛋白共同处理后细胞凋亡的变化。 TPA(200 nmol / L)。结果表明,UDN糖蛋白(200 micro g / mL)没有任何细胞毒性作用,并且以剂量依赖的方式降低了细胞内活性氧(ROS)。当仅用TPA(200 nmol / L)处理细胞时,凋亡相关信号(细胞色素c,胱天蛋白酶9和胱天蛋白酶3)的活性被激活。但是,在TPA(200 nmol / L)存在下,用UDN糖蛋白(200 micro g / mL)处理后,通过减少细胞内ROS抑制了它们的活性。同样,结果表明UDN糖蛋白可防止PARP裂解和DNA片段化。这些发现表明,UDN糖蛋白可通过调节BNL CL.2细胞中的细胞内ROS来防止TPA诱导的细胞凋亡,并且UDN可能是肝脏健康的营养补充品。

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