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缺氧增强白三烯、氢过氧化二十碳四烯酸或钙离子载体A23187对单层肝细胞的杀伤作用。

Hypoxia potentiates killing of hepatocyte monolayers by leukotrienes, hydroperoxyeicosatetraenoic acids, or calcium ionophore A23187.

作者信息

Trudell J R, Bendix M, Bosterling B

出版信息

Biochim Biophys Acta. 1984 Apr 16;803(4):338-41. doi: 10.1016/0167-4889(84)90126-5.

Abstract

Potentiation of chemical toxicity by hypoxia was studied in confluent hepatocyte monolayers. Addition of either hydroperoxyarachidonic acid (50 micrograms), leukotriene C4 (10 micrograms), or calcium ionophore A23187 (1.8 micrograms) to hepatocyte monolayers followed by incubation in 2% oxygen for 24 h killed 95% of the hypoxic cells, but was without effect on the normoxic cells. The greater than 10-fold increase in toxicity of A23187 suggests that hypoxic cells are less able to regulate intracellular calcium. The increased toxicity of hydroperoxyarachidonic acid and leukotriene C4 may be due to a related reduction in activity of protective enzymes.

摘要

在汇合的肝细胞单层中研究了缺氧对化学毒性的增强作用。向肝细胞单层中添加氢过氧化花生四烯酸(50微克)、白三烯C4(10微克)或钙离子载体A23187(1.8微克),然后在2%氧气中孵育24小时,可杀死95%的缺氧细胞,但对常氧细胞没有影响。A23187毒性增加超过10倍,表明缺氧细胞调节细胞内钙的能力较弱。氢过氧化花生四烯酸和白三烯C4毒性增加可能是由于保护酶活性相关降低所致。

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