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Enhanced Antitumor Effect of Ultrasound in the Presence of Piroxicam in a Mouse Air Pouch Model

机译:在小鼠气袋模型中存在吡罗昔康的超声增强的抗肿瘤作用。

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摘要

The antitumor effects of piroxicam, a non‐steroidal anti‐inflammatory drug, on sarcoma 180 cells under ultrasonic irradiation were examined in a mouse air pouch model. When piroxicam was added to sarcoma 180 suspension under ultrasound irradiation (2 MHz, 10 W, 120 s), the mortality rate of tumor cells immediately after the irradiation and the survival rate of mice were significantly higher than those when ultrasound alone was applied, and these effects of piroxicam were dose‐dependent. When D‐mannitol was used with piroxicam, the mortality rate of the tumors cells after the irradiation was comparable with that when piroxicam alone was applied, but when L‐ histidine was used concurrently, the antitumor effect was significantly lower than that when piroxicam alone was applied. Histological examinations one week after the ultrasound irradiation in the presence of piroxicam showed sparse tumor tissue in the air pouch and normal appearance of the air pouch and surrounding tissue. The findings suggest that piroxicam enhances the anti‐ tumor effects of ultrasound in vivo by increasing the production of singlet oxygen without damage to tissue surrounding the tumor.
机译:在小鼠气囊模型中检查了非甾体类抗炎药吡罗昔康对超声照射下肉瘤180细胞的抗肿瘤作用。在超声照射(2 MHz,10 W,120 s)下向肉瘤180悬浮液中添加吡罗昔康时,照射后立即产生的肿瘤细胞死亡率和小鼠的存活率明显高于单独使用超声时的肿瘤细胞死亡率和存活率。吡罗昔康的这些作用是剂量依赖性的。当D-甘露醇与吡罗昔康一起使用时,放疗后的肿瘤细胞死亡率与单独使用吡罗昔康时相当,但是当同时使用L-组氨酸时,其抗肿瘤作用明显低于单独使用吡罗昔康时。应用。吡罗昔康存在下超声照射一周后的组织学检查显示气囊中的肿瘤组织稀疏,气囊及其周围组织的外观正常。研究结果表明吡罗昔康可通过增加单线态氧的产生而增强对体内超声的抗肿瘤作用,而不会破坏肿瘤周围的组织。

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