Haller Olivia J, Semendric Ines, Collins-Praino Lyndsey E, Whittaker Alexandra L, George Rebecca P
School of Biomedicine, The University of Adelaide, South Australia, Australia.
School of Biomedicine, The University of Adelaide, South Australia, Australia.
Behav Brain Res. 2025 Mar 5;480:115391. doi: 10.1016/j.bbr.2024.115391. Epub 2024 Dec 10.
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.
化疗引起的认知障碍(CICI)会影响女性癌症幸存者,在乳腺癌幸存者等人群中已认识到存在这种障碍,其中三分之一的人会受到影响。认知障碍包括记忆、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。人们提出了几种机制来解释这些问题,有证据表明神经炎症是一个关键因素。然而,认知障碍出现的时间进程尚不太明确,对长期时间点的研究较少。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情况,评估三个时间点:急性(96小时)、亚急性(31天)和慢性(93天)。此外,我们研究了认知改变是否与星形胶质细胞反应性的伴随变化有关。雌性Sprague Dawley大鼠接受两次腹腔注射MTX、5-FU或生理盐水,并在新物体识别、5选串行反应时间任务和巴恩斯迷宫测试中接受评估。检查海马体和前额叶皮质组织中胶质纤维酸性蛋白(GFAP)的表达。MTX和5-FU暴露在31天时均与空间记忆、任务获取和处理速度受损有关,到93天时受损情况有所改善。虽然MTX和5-FU在各个时间点和区域均诱导了GFAP表达的变化,在96小时时变化最为明显,但5-FU在所有时间点海马体中的表达变化都很一致。这些结果为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有前景的治疗靶点,但应评估更多标志物以阐明完整的神经免疫反应,从而确定靶向哪些方面以及何时靶向,以确保接受化疗的癌症患者获得最佳疗效。