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一种印度药用植物玫瑰铅丹对实验小鼠肿瘤的体内肿瘤抑制和放射增敏作用。

In vivo tumor inhibitory and radiosensitizing effects of an Indian medicinal plant, Plumbago rosea on experimental mouse tumors.

作者信息

Devi P U, Solomon F E, Sharada A C

机构信息

Department of Radiobiology, Kasturba Medical College, Manipal, India.

出版信息

Indian J Exp Biol. 1994 Aug;32(8):523-8.

PMID:7959931
Abstract

Tumor growth inhibitory and radiosensitizing effects of the alcoholic root extract of P. rosea was studied on experimental mouse tumors, S-180 solid tumor and Ehrlich ascites carcinoma in vivo. Intraperitoneal injection of 50 mg/kg of Plumbago extract (PE) for 10 days starting from 24 hr after intradermal inoculation of S-180 cells in BALB/c mice produced about 16% complete response (CR). The CR% increased with increase in drug dose, to 50% at 100 mg/kg for 10 days. As 100 mg/kg produced toxic side effects, lower doses were used with other treatment modalities, radiation (RT) and hyperthermia (HT). Treatment of 50 mm3 tumor with PE (75 mg/kg) for 10 days with local RT (10 Gy) and/or HT (43 degrees C, 30 min) subadditively increased the CR% and tumor free survival. The combination also significantly reduced the growth rates of uncured tumors. The PE significantly reduced the tumor glutathione content and this effect was markedly enhanced by the combination of the three modalities. PE alone was not very effective in preventing the growth of Ehrlich ascites carcinoma in Swiss mice, though it increased mean survival time and ILS% of the mice. But with radiation it produced a synergistic effect in increasing the tumor inhibition and 120 day animal survival from 10% to 50%. The results demonstrate that though PE may have only a weak antitumor effect, it may be a good candidate for use with radiation to enhance the tumor killing effect.

摘要

研究了玫瑰紫茉莉酒精根提取物对实验小鼠肿瘤、S-180实体瘤和艾氏腹水癌的体内肿瘤生长抑制和放射增敏作用。在BALB/c小鼠皮内接种S-180细胞24小时后开始,腹腔注射50mg/kg的紫茉莉提取物(PE),持续10天,产生了约16%的完全缓解(CR)。CR%随着药物剂量的增加而增加,在100mg/kg持续10天时达到50%。由于100mg/kg产生毒性副作用,因此较低剂量与其他治疗方式,如放疗(RT)和热疗(HT)联合使用。用PE(75mg/kg)处理50mm³肿瘤10天,并联合局部放疗(10Gy)和/或热疗(43℃,30分钟),亚相加地增加了CR%和无瘤生存期。该联合治疗还显著降低了未治愈肿瘤的生长速率。PE显著降低了肿瘤谷胱甘肽含量,并且三种治疗方式联合使用时该作用明显增强。单独使用PE对预防瑞士小鼠艾氏腹水癌的生长效果不佳,尽管它增加了小鼠的平均生存时间和ILS%。但与放疗联合使用时,它在增强肿瘤抑制作用方面产生协同效应,使120天动物生存率从10%提高到50%。结果表明,尽管PE可能只有较弱的抗肿瘤作用,但它可能是与放疗联合使用以增强肿瘤杀伤效果的良好候选药物。

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