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首页> 外文期刊>Journal of biochemical and molecular toxicology >Time- and concentration-dependent production of superoxide anion, nitric oxide, DNA damage and cellular death by ricin in the J774A.1 macrophage cells.
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Time- and concentration-dependent production of superoxide anion, nitric oxide, DNA damage and cellular death by ricin in the J774A.1 macrophage cells.

机译:J774A.1巨噬细胞中蓖麻毒素产生的时间和浓度依赖性的超氧阴离子,一氧化氮,DNA损伤和细胞死亡。

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摘要

The time- and concentration-dependent effects of ricin on some biomarkers of cellular toxicity, including production of superoxide anion (O2-), nitric oxide (NO), and DNA single strand breaks (SSB), as well as cellular death, have been examined in the J774A.1 macrophage cell cultures. Various concentrations of ricin have been added to various cell cultures, and the cells were incubated for 12, 24, 36, and 48 hours. Following 12 hour incubation, ricin did not cause significant increases in any of those biomarkers. However, time- and concentration-dependent increases were observed in the induction of all the biomarkers after incubation for 24-48 hours. Approximately twofold increases in the production of O2- were observed after incubation with 1 and 10 ng/mL of ricin for 24 and 36-48 hours, respectively. The concentrations of ricin that caused approximately twofold increases in the rate of DNA-SSB are 10 and 1-10 ng/mL after 24 and 36-48 hours incubation, respectively. Approximately twofold increases in NO production were only observed after incubation of the cultures with 1-10 ng/mL of ricin for 36-48 hours. Fifty percent reductions in cellular viability were also observed with ricin concentrations of 10-100, 10, and 1-10 ng/mL, after incubation for 24, 36, and 48 hours, respectively.
机译:蓖麻毒素对细胞毒性的某些生物标志物具有时间和浓度依赖性,包括超氧阴离子(O2-),一氧化氮(NO)和DNA单链断裂(SSB)的产生以及细胞死亡。在J774A.1巨噬细胞培养物中进行了检测。各种浓度的蓖麻毒素已添加到各种细胞培养物中,并将细胞孵育12、24、36和48小时。孵育12小时后,蓖麻毒素并未引起任何这些生物标记物的显着增加。然而,在孵育24-48小时后,在所有生物标志物的诱导中观察到时间和浓度依赖性的增加。在分别与1和10 ng / mL的蓖麻蛋白温育24和36-48小时后,观察到O2-的产量增加了大约两倍。孵育24和36-48小时后,引起DNA-SSB速率增加约两倍的蓖麻毒蛋白浓度分别为10和1-10 ng / mL。仅在将培养物与1-10 ng / mL蓖麻毒蛋白温育36-48小时后,才能观察到NO产量大约增加两倍。分别孵育24、36和48小时后,蓖麻毒素浓度为10-100、10和1-10 ng / mL时,细胞活力也降低了50%。

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