认知和星形细胞反应性的变化在雌性啮齿动物模型化疗诱导的认知障碍是可变的急性和慢性。

IF 2.6 3区 心理学 Q2 BEHAVIORAL SCIENCES
Behavioural Brain Research Pub Date : 2025-03-05 Epub Date: 2024-12-10 DOI:10.1016/j.bbr.2024.115391
Olivia J Haller, Ines Semendric, Lyndsey E Collins-Praino, Alexandra L Whittaker, Rebecca P George
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引用次数: 0

摘要

化疗引起的认知障碍(CICI)影响女性癌症幸存者,在乳腺癌幸存者等人群中发现了这种损害,其中三分之一受到影响。障碍包括记忆、学习、注意力和处理速度方面的问题,对生活质量产生负面影响。提出了几种驱动这些的机制,有证据表明神经炎症是一个关键因素。然而,损伤发生的时间过程不太确定,更长期的时间点研究较少。本研究旨在了解甲氨蝶呤(MTX)或5-氟尿嘧啶(5- fu)化疗后认知变化的演变,评估三个时间点:急性(96小时)、亚急性(31天)和慢性(93天)。此外,我们研究了认知的改变是否与星形细胞反应性的伴随变化有关。雌性Sprague Dawley大鼠分别腹腔注射MTX、5-FU或生理盐水,进行新物体识别、5选择序列反应时间任务和巴恩斯迷宫的评估。检测海马和前额皮质组织GFAP表达。在第31天,MTX和5-FU暴露均与空间记忆、任务获取和处理速度损伤相关,第93天损伤有所改善。虽然MTX和5-FU在不同时间点和区域诱导GFAP表达的变化,在96小时的变化最为显著,但5-FU在海马中的表达变化在所有时间点都是一致的。这些结果为了解CICI中神经炎症介质的复杂性提供了有价值的见解。虽然神经炎症可能是一个很有希望的治疗靶点,但应该进一步评估标志物,以阐明完整的神经免疫反应,从而确定哪些方面需要靶向,何时靶向,以确保接受化疗的癌症患者的最佳结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in cognition and astrocytic reactivity in a female rodent model of chemotherapy-induced cognitive impairment are variable both acutely and chronically.

Chemotherapy-induced cognitive impairment (CICI) affects female cancer survivors, with impairment recognised in populations such as breast cancer survivors, where 1 in 3 are affected. Impairments include issues with memory, learning, concentration, and processing speed, negatively impacting quality of life. Several mechanisms are proposed to drive these, with evidence implicating neuroinflammation as a key contributor. However, the time course over which impairments occur is less well-established, with fewer longer-term time-points investigated. This study aimed to understand the evolution of cognitive changes following methotrexate (MTX) or 5- fluorouracil (5-FU) chemotherapy, assessing three time-points: acute (96-hour), sub-acute (31-days) and chronic (93-days). Further, we investigated whether alterations in cognition were associated with concomitant changes in astrocytic reactivity. Female Sprague Dawley rats received two intraperitoneal injections of MTX, 5-FU or saline and were assessed on the novel object recognition, 5-choice serial reaction time task and Barnes maze. Hippocampal and prefrontal cortex tissue was examined for GFAP expression. Both MTX and 5-FU exposure were associated with spatial memory, task acquisition, and processing speed impairments at 31-days, with impairment ameliorated by 93-days. While both MTX and 5-FU induced changes in GFAP expression across various time-points and regions, with most notable changes at 96-hours, 5-FU exhibited expression changes in the hippocampus consistently across all time-points. These results provide valuable insight into the complexity of a mediator of neuroinflammation in CICI. While neuroinflammation may be a promising therapeutic target, further markers should be assessed to elucidate the full neuroimmune response, and thus which aspects to target and when, to ensure optimal outcomes for cancer patients treated with chemotherapy.

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来源期刊
Behavioural Brain Research
Behavioural Brain Research 医学-行为科学
CiteScore
5.60
自引率
0.00%
发文量
383
审稿时长
61 days
期刊介绍: Behavioural Brain Research is an international, interdisciplinary journal dedicated to the publication of articles in the field of behavioural neuroscience, broadly defined. Contributions from the entire range of disciplines that comprise the neurosciences, behavioural sciences or cognitive sciences are appropriate, as long as the goal is to delineate the neural mechanisms underlying behaviour. Thus, studies may range from neurophysiological, neuroanatomical, neurochemical or neuropharmacological analysis of brain-behaviour relations, including the use of molecular genetic or behavioural genetic approaches, to studies that involve the use of brain imaging techniques, to neuroethological studies. Reports of original research, of major methodological advances, or of novel conceptual approaches are all encouraged. The journal will also consider critical reviews on selected topics.
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