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通过脑内注射肿瘤性神经胶质细胞在大鼠体内产生脑肿瘤的研究:超微结构研究

The development of brain tumours produced in rats by the intracerebral injection of neoplastic glial cells: a fine structural study.

作者信息

Davaki P, Lantos P L

出版信息

Neuropathol Appl Neurobiol. 1981 Jan-Feb;7(1):49-61. doi: 10.1111/j.1365-2990.1981.tb00231.x.

Abstract

Tumours were produced by the intracerebral injection of a clone of glial cells derived from a glioma induced transplacentally by N-ethyl-N-nitrosourea in a BD-IX rat. The injection of 5 X 10(5) cells into the left frontal lobe resulted in a 100% incidence of tumours. To follow the development of the neoplasms, the brains were studied from 1 day to 4 weeks after injection. The tumours maintained their glial characters throughout, but their features changed with time. Ultrastructurally, they were pleomorphic: the proportion of fibrillary astrocytes, undifferentiated and intermediate cell types varied according to tumour size. When smaller (1 and 2 weeks), fibrillary astrocytes predominated, but when larger (3 and 4 weeks), the number of undifferentiated astrocytes considerably increased. A reproducible brain tumour model with a short latency has thus been established and characterized, which may be of use for chemo- and radiotherapeutic studies and for examining the mechanisms of cerebral oedema.

摘要

通过向BD-IX大鼠脑内注射由N-乙基-N-亚硝基脲经胎盘诱导的胶质瘤衍生的神经胶质细胞克隆来产生肿瘤。向左侧额叶注射5×10⁵个细胞导致肿瘤发生率为100%。为了跟踪肿瘤的发展,在注射后1天至4周对大脑进行研究。肿瘤始终保持其神经胶质细胞特征,但其特征随时间变化。在超微结构上,它们是多形性的:纤维性星形胶质细胞、未分化细胞和中间细胞类型的比例根据肿瘤大小而变化。当肿瘤较小时(1周和2周),纤维性星形胶质细胞占主导,但当肿瘤较大时(3周和4周),未分化星形胶质细胞的数量显著增加。因此,已经建立并表征了一种潜伏期短且可重复的脑肿瘤模型,这可能有助于化学治疗和放射治疗研究以及检查脑水肿的机制。

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