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大鼠脑膜白血病的实验模型(L5222)。卡莫司汀和环磷酰胺治疗的效果。

An experimental model for meningeal leukemia in rats (L5222). Effect of treatment with BCNU and cyclophosphamide.

作者信息

Fiebig H H, Zeller W H, Schmähl D

出版信息

Int J Cancer. 1976 Nov 15;18(5):710-6. doi: 10.1002/ijc.2910180521.

Abstract

An experimental model of meningeal leukemia in rats is developed by intracerebral (IC) inoculation of leukemic cells from the transplantable acute leukemia L5222. The L5222 proliferates exponentially in the central nervous system (CNS) and the disease becomes systemic 2 days following IC inoculation. Chemotherapeutic studies with BCNU and cyclophosphamide yielded cures in a high percentage of cases when treatment began at an early stage of meningeal leukemia. When treatment was started at the advanced stage, only BCNU showed a large number of cures. However, cyclophosphamide resulted in a marked increase of life-span. The activity of cyclophosphamide against meningeal leukemia, which is in contrast to the results obtained by Skipper et. al. (1961) in the L1210 mouse leukemia, suggests that cyclophosphamide crosses in part the blood--brain barrier in a rat bearing meningeal leukemia. After subcutaneous inoculation, BCNU and cyclophosphamide showed the same rate of cures.

摘要

通过向大鼠脑内(IC)接种可移植性急性白血病L5222的白血病细胞,建立了大鼠脑膜白血病的实验模型。L5222在中枢神经系统(CNS)中呈指数增殖,脑内接种后2天疾病变为全身性。当在脑膜白血病早期开始治疗时,用卡莫司汀(BCNU)和环磷酰胺进行的化疗研究在高比例病例中实现了治愈。当在晚期开始治疗时,只有BCNU显示出大量治愈病例。然而,环磷酰胺使寿命显著延长。环磷酰胺对脑膜白血病的活性与Skipper等人(1961年)在L1210小鼠白血病中获得的结果相反,这表明环磷酰胺在患有脑膜白血病的大鼠中部分穿过血脑屏障。皮下接种后,BCNU和环磷酰胺显示出相同的治愈率。

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