首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Neurobiological Mechanisms of Chemotherapy-induced Cognitive Impairment in a Transgenic Model of Breast Cancer
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Neurobiological Mechanisms of Chemotherapy-induced Cognitive Impairment in a Transgenic Model of Breast Cancer

机译:化疗诱导的乳腺癌转基因模型中化疗诱导的认知障碍的神经生物学机制

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Animal studies have reinforced clinical reports of cognitive impairment in cancer survivors following chemotherapy but, until now, all pre-clinical research in this area has been conducted on normal rodents. The present study investigated the effects of chemotherapy on cognition and underlying biological mechanisms in the FVB/N-Tg (MMTV-neu) 202 Mul/J mouse, a well-characterized transgenic model of breast cancer that has similarities to the tumorigenesis which occurs in humans. Tumor-bearing and control mice received three weekly injections of a combination of methotrexate + 5-fluorouracil, or an equal volume of saline. Different aspects of learning and memory were measured before and after treatment. The effects of tumor and chemotherapy on neurogenesis, neuro-inflammatory cytokine activity, and brain volume, as they relate to corresponding cognitive changes, were also measured. The toxic effects of chemotherapy extended to the cancerous model in which substantial cognitive impairment was also associated with the disease. Cognitive deficits were greatest in tumorigenic mice that received the anti-cancer drugs. Both tumor growth and chemotherapy caused significant changes in brain volume, including the hippocampus and frontal lobes, two structures that are directly implicated in cognitive tasks that were shown to be vulnerable. The level of hippocampal neurogenesis in adulthood was suppressed in chemotherapy-treated mice and associated with loss of hippocampus-controlled cognitive function. Dysregulation of cytokine activity was found in tumorigenic mice and associated with impaired cognitive performance. The results show that chemotherapy and tumor development independently contribute to cognitive deficits through different biological mechanisms. (C) 2017 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:动物研究在化疗后,增强了癌症幸存者中的认知障碍的临床报告,但到目前为止,该地区的所有临床研究都在普通啮齿动物上进行。本研究研究了化疗对FVB / N-TG(MMTV-NEU)202 MUL / J小鼠的认知和潜在的生物机制的影响,其具有与发生的肿瘤发生的相似性的良好表征的乳腺癌转基因模型。人类。肿瘤轴承和对照小鼠接受了甲氨蝶呤+ 5-氟尿嘧啶或等体积的盐水组合的三次每周注射。在治疗之前和之后测量学习和记忆的不同方面。还测量了肿瘤和化疗对神经发生,神经炎症细胞因子活性和脑体积的影响,因为它们与相应的认知变化有关。化疗的毒性效应扩展到癌症模型,其中具有重要认知障碍也与疾病有关。在接受抗癌药物的致癌症小鼠中,认知缺陷是最大的。肿瘤生长和化疗均导致脑体积的显着变化,包括海马和额叶,两种结构直接涉及所示易受伤害的认知任务。在化疗处理的小鼠中抑制了成年的海马神经发生水平,并与海马控制的认知功能丧失相关。在致瘤小鼠中发现了细胞因子活性的失调,并且与认知性能受损相关。结果表明,通过不同的生物机制,化疗和肿瘤发展独立地促进了认知缺陷。 (c)2017年IBRO。 elsevier有限公司出版。保留所有权利。

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