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Characterization of Tumor-Induced Inflammation and the Effect of Some Anti-Inflammatory Drugs on the Increased Vascular Permeability

机译:肿瘤诱发炎症的表征以及某些抗炎药对血管通透性增加的影响

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References(17) Cited-By(3) The vascular bed in a murine dermal tissue responded to inoculated tumor cells by two-phased changes in the vascular permeability. The initial increase in the vascular permeability was seen in an early stage (1 to 3 day post tumor cells inoculation), and the inflammation was sensitive to glutathione (GSH). Glucocorticoids reduced the increased vascular permeability, but neither acetylsalicylic acid nor indomethacin did. The later vascular response was produced by a growing solid tumor in a continuous mode beginning at 5th to 10th day post inoculation. The degree of the increased vascular permeability in this chronic phase was in direct proportion to the wet weight of the solid tumor, and the inflammation was insensitive to glutathione. Glucocorticoids reduced the increased vascular permeability, but neither acetylsalicylic acid nor indomethacin did. The action of glucocorticoids on the tumor-induced vascular hyper-permeability was discussed in connection with a tumor factor possibly responsible for the vasoexudation.
机译:参考文献(17)被引用的(3)小鼠皮肤组织中的血管床通过血管渗透性的两阶段变化对接种的肿瘤细胞作出反应。在早期阶段(接种肿瘤细胞后1至3天)可以看到血管通透性的最初增加,并且炎症对谷胱甘肽(GSH)敏感。糖皮质激素减少了血管通透性的增加,但是乙酰水杨酸和消炎痛都没有。从接种后第5天到第10天以连续模式生长的实体瘤产生了后来的血管反应。在该慢性期中,血管通透性增加的程度与实体瘤的湿重成正比,并且炎症对谷胱甘肽不敏感。糖皮质激素减少了血管通透性的增加,但是乙酰水杨酸和消炎痛都没有。结合可能引起血管渗出的肿瘤因素,讨论了糖皮质激素对肿瘤引起的血管通透性的作用。

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