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用于实验性神经肿瘤学的可移植犬胶质瘤模型

Transplantable canine glioma model for use in experimental neuro-oncology.

作者信息

Salcman M, Scott E W, Schepp R S, Knipp H C, Broadwell R D

出版信息

Neurosurgery. 1982 Sep;11(3):372-81. doi: 10.1227/00006123-198209000-00007.

Abstract

The need for a large animal tumor model in experimental neuro-oncology led us to re-evaluate and to modify the transplantable canine glioma of Wodinsky and Walker. Successive passages of the original tumor brei were made in purebred beagles, from beagle to mongrel, and between various mongrel strains until an intracerebral injection of 0.1 cc on Days 1 to 3 of life produced a 93% incidence of tumor take in all breeds. The mean survival was 13.5 +/- 1.9 days after injection (range, 10 to 19 days) in 10 litters. The tumor was invariably fatal and possessed many of the histological characteristics of human glioblastoma (i.e., capillary proliferation, pseudopallisading, frequent mitotic figures, and multinucleated giant cells). The animals were large enough to be scanned on the Pfizer 450 scanner, and the tumors were visualized in vivo as typical "ring" lesions after the injection of contrast agent. Intravital staining with Evans blue outlined the areas of contrast enhancement observed in the same tumors by computed tomography. The apparent defect in the blood-brain barrier could be explained in part by the absence of endothelial tight junctions on electron microscopy. Stability in the histology and activity of the tumor could be demonstrated after more than 14 months of storage at -70 degrees C. The transplantable canine glioma model has many advantages including low cost, reproducible morphology, a short survival time, and relative safety for the investigator. The large size of the animal preparation allows the use of complex surgical instrumentation and radiographic study, as well as repeated sampling of cerebrospinal and other fluids.

摘要

实验神经肿瘤学对大型动物肿瘤模型的需求促使我们重新评估并改进了沃丁斯基和沃克的可移植犬胶质瘤模型。将原始肿瘤匀浆在纯种比格犬、从比格犬到杂种犬以及不同杂种犬品系之间连续传代,直至在出生后第1至3天脑内注射0.1 cc,所有品种的肿瘤接种成功率均达到93%。在10窝动物中,注射后平均存活时间为13.5±1.9天(范围为10至19天)。该肿瘤无一例外都是致命的,具有人类胶质母细胞瘤的许多组织学特征(即毛细血管增生、假栅栏状、频繁的有丝分裂象和多核巨细胞)。这些动物体型足够大,可以在辉瑞450扫描仪上进行扫描,注射造影剂后,肿瘤在体内呈现为典型的“环形”病变。用伊文思蓝进行活体染色勾勒出了计算机断层扫描在同一肿瘤中观察到的造影剂增强区域。血脑屏障的明显缺陷部分可以通过电子显微镜下内皮紧密连接的缺失来解释。在-70℃储存超过14个月后,肿瘤的组织学和活性仍能保持稳定。可移植犬胶质瘤模型具有许多优点,包括成本低、形态可重复、存活时间短以及对研究者相对安全。动物标本的大尺寸使得可以使用复杂的手术器械和进行放射学研究,以及对脑脊液和其他液体进行反复采样。

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