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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Quinidine-induced decrease of intracellular esterase activity in a hepatoma cell line.
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Quinidine-induced decrease of intracellular esterase activity in a hepatoma cell line.

机译:奎尼丁诱导的肝癌细胞系细胞内酯酶活性降低。

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Using image-analyzing equipment, we measured the effect of quinidine on the activity of naphthol AS-D chloroacetate esterase, alpha-naphthyl butyrate esterase, alpha-naphthyl acetate esterase, and acid phosphatase in individual cells of a human Hep G2 hepatoma cell line. The impact of the drug on the morphology of the cells was also observed. Depending on the concentration of quinidine applied, various changes occurred, the most extreme being cell death. However, at some drug concentrations that did not appear to affect visible cell structures, the activity of the esterases was decreased. This lessened enzyme activity did not seem to be related to the enzymes leaking from the cells, because the activity of acid phosphatase was unaffected. Inhibition of the esterase activity was related to the interval of exposure to quinidine in the perfusing medium and to the concentration of the drug. We consider the system described here to be a potential replacement for experiments with animals in the study of hepatotoxicity.
机译:使用图像分析设备,我们测量了奎尼丁对人Hep G2肝癌细胞系单个细胞中萘酚AS-D氯乙酸酯酶,α-萘甲酸丁酯酯酶,α-萘乙酸酯酯酶和酸性磷酸酶活性的影响。还观察到药物对细胞形态的影响。根据所施加的奎尼丁浓度,会发生各种变化,最极端的是细胞死亡。但是,在某些似乎不影响可见细胞结构的药物浓度下,酯酶的活性降低了。这种降低的酶活性似乎与从细胞中泄漏的酶无关,因为酸性磷酸酶的活性不受影响。酯酶活性的抑制与在灌注介质中暴露于奎尼丁的间隔以及药物的浓度有关。我们认为,此处描述的系统可以替代肝毒性研究中的动物实验。

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