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通过向大鼠鞘内注射9L胶质肉瘤和Walker 256癌肉瘤建立脑膜瘤形成的实验模型。

Development of experimental models for meningeal neoplasia using intrathecal injection of 9L gliosarcoma and Walker 256 carcinosarcoma in the rat.

作者信息

Kooistra K L, Rodriguez M, Powis G, Yaksh T L, Harty G J, Hilton J F, Laws E R

出版信息

Cancer Res. 1986 Jan;46(1):317-23.

PMID:3753551
Abstract

Two models for meningeal neoplasia have been developed in rats using intrathecal injection of 9L gliosarcoma and Walker 256 carcinosarcoma cells. Tumor cells were injected in unanesthetized animals through an indwelling catheter inserted at the cisterna magna to the level of the lumbar enlargement of the spinal cord. Survival of rats was dependent on the number of tumor cells injected. Spread of tumor was quantified by histology using a grading scale, and functional and behavioral changes were measured. Rats injected with 10(6) 9L gliosarcoma cells showed progressive weight loss, flaccid paralysis, and neurogenic bladder dysfunction and had a median survival of 11 days. The tumor frequently grew as a mass compressing the spinal cord. The 9L gliosarcoma tumor cells markedly invaded the Virchow-Robin spaces but exhibited only minimal invasion of the central nervous system parenchyma. The tumor reached the brain by day 10. Rats injected with 2 X 10(5) Walker 256 carcinosarcoma cells showed progressive weight loss and weakness and had a median survival of 6 days. The tumor grew within the leptomeninges in a discontinuous multifocal fashion and reached the brain by day 4. There was extensive invasion of the central nervous system parenchyma by Walker 256 tumor cells along the Virchow-Robin spaces resulting in hemorrhage and necrosis of grey and white matter. Hot plate and tail flick response times were significantly delayed only in the days immediately preceding death of animals with either 9L or Walker 256 tumor and were not good indicators of tumor progression. Loss of motor coordination and failure of the stepping and placing reflex on the other hand showed good correlation with spread of tumor measured histologically. Control animals injected with 0.9% NaCl or with lethally irradiated tumor cells showed no significant weight loss or functional or behavioral changes. The intrathecal 9L gliosarcoma and Walker 256 carcinosarcoma models show different characteristics of human meningeal carcinomatosis and will be used for studies of experimental chemotherapy with intrathecally administered antitumor drugs.

摘要

通过向大鼠鞘内注射9L胶质肉瘤细胞和Walker 256癌肉瘤细胞,已建立了两种脑膜瘤形成模型。在未麻醉的动物中,通过插入大池至脊髓腰膨大水平的留置导管注射肿瘤细胞。大鼠的存活取决于注射的肿瘤细胞数量。通过组织学使用分级量表对肿瘤扩散进行量化,并测量功能和行为变化。注射10(6)个9L胶质肉瘤细胞的大鼠出现体重逐渐减轻、弛缓性麻痹和神经源性膀胱功能障碍,中位生存期为11天。肿瘤常呈肿块生长,压迫脊髓。9L胶质肉瘤肿瘤细胞明显侵入血管周围间隙,但对中枢神经系统实质的侵袭仅为轻微。肿瘤在第10天到达脑部。注射2×10(5)个Walker 256癌肉瘤细胞的大鼠出现体重逐渐减轻和虚弱,中位生存期为6天。肿瘤在软脑膜内以不连续的多灶性方式生长,在第4天到达脑部。Walker 256肿瘤细胞沿血管周围间隙广泛侵袭中枢神经系统实质,导致灰质和白质出血和坏死。仅在患有9L或Walker 256肿瘤的动物死亡前几天,热板和甩尾反应时间才显著延迟,且不是肿瘤进展的良好指标。另一方面,运动协调性丧失以及踏步和放置反射消失与组织学测量的肿瘤扩散具有良好的相关性。注射0.9%氯化钠或经致死剂量照射的肿瘤细胞的对照动物未出现明显的体重减轻或功能及行为变化。鞘内9L胶质肉瘤和Walker 256癌肉瘤模型显示了人类脑膜癌病的不同特征,将用于鞘内给药抗肿瘤药物的实验化疗研究。

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