紫杉醇化疗破坏雌性小鼠视交叉上核的昼夜节律基因转录和功能。

IF 2.7 3区 医学 Q3 NEUROSCIENCES
eNeuro Pub Date : 2025-09-22 Print Date: 2025-09-01 DOI:10.1523/ENEURO.0061-25.2025
Zoe M Tapp, Melina M Seng, Amiya K Ghosh, Karl H Obrietan, Leah M Pyter
{"title":"紫杉醇化疗破坏雌性小鼠视交叉上核的昼夜节律基因转录和功能。","authors":"Zoe M Tapp, Melina M Seng, Amiya K Ghosh, Karl H Obrietan, Leah M Pyter","doi":"10.1523/ENEURO.0061-25.2025","DOIUrl":null,"url":null,"abstract":"<p><p>Cancer patients experience circadian rhythm disruptions during and after chemotherapy that can contribute to debilitating side effects. It is unknown how chemotherapy mediates circadian disruptions and specifically the extent to which these disruptions occur at the level of the principal clock, the suprachiasmatic nuclei (SCN) of the hypothalamus. In the present study, we assessed how the commonly used chemotherapeutic, paclitaxel, impacts the SCN molecular clock and SCN-dependent behavioral adaptations to circadian challenges in female mice. Following a repeated chemotherapy regimen, we measured rhythmic SCN expression of molecular clock and circadian-associated transcripts. Paclitaxel chemotherapy disrupted the SCN molecular clock through abolished rhythmicity (<i>Bmal1</i>, <i>Nr1d2</i>) and damped rhythmic transcription (<i>Ciart</i>, <i>Dbp</i>, <i>Nr1d1</i>, <i>Per2</i>) of key molecular clock genes. We further determined chemotherapy-induced changes to SCN function by measuring circadian wheel running adaptations to a jet lag phase-delay or phase-advance paradigm and by generating a phase response curve (PRC). Chemotherapy did not alter re-entrainment to a 6 h phase-advance, but after a 6 h phase-delay, chemotherapy-treated mice had a more stable and robust circadian rhythm than vehicle-treated mice, possibly indicative of a weakened or decoupled SCN. In the PRC, chemotherapy blunted light-induced phase-shift delays during subjective night compared with vehicle controls, also indicative of disrupted SCN-dependent entrainment. Together, this work demonstrates that paclitaxel chemotherapy disrupts both the molecular clock and functional re-entrainment of the SCN that could cause or contribute to observed circadian rhythm disruptions after treatment. This research could help guide application of circadian-mediated therapies to mitigate side effects of chemotherapy.</p>","PeriodicalId":11617,"journal":{"name":"eNeuro","volume":" ","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12453581/pdf/","citationCount":"0","resultStr":"{\"title\":\"Paclitaxel Chemotherapy Disrupts Circadian Gene Transcription and Function of the Suprachiasmatic Nuclei in Female Mice.\",\"authors\":\"Zoe M Tapp, Melina M Seng, Amiya K Ghosh, Karl H Obrietan, Leah M Pyter\",\"doi\":\"10.1523/ENEURO.0061-25.2025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cancer patients experience circadian rhythm disruptions during and after chemotherapy that can contribute to debilitating side effects. It is unknown how chemotherapy mediates circadian disruptions and specifically the extent to which these disruptions occur at the level of the principal clock, the suprachiasmatic nuclei (SCN) of the hypothalamus. In the present study, we assessed how the commonly used chemotherapeutic, paclitaxel, impacts the SCN molecular clock and SCN-dependent behavioral adaptations to circadian challenges in female mice. Following a repeated chemotherapy regimen, we measured rhythmic SCN expression of molecular clock and circadian-associated transcripts. Paclitaxel chemotherapy disrupted the SCN molecular clock through abolished rhythmicity (<i>Bmal1</i>, <i>Nr1d2</i>) and damped rhythmic transcription (<i>Ciart</i>, <i>Dbp</i>, <i>Nr1d1</i>, <i>Per2</i>) of key molecular clock genes. We further determined chemotherapy-induced changes to SCN function by measuring circadian wheel running adaptations to a jet lag phase-delay or phase-advance paradigm and by generating a phase response curve (PRC). Chemotherapy did not alter re-entrainment to a 6 h phase-advance, but after a 6 h phase-delay, chemotherapy-treated mice had a more stable and robust circadian rhythm than vehicle-treated mice, possibly indicative of a weakened or decoupled SCN. In the PRC, chemotherapy blunted light-induced phase-shift delays during subjective night compared with vehicle controls, also indicative of disrupted SCN-dependent entrainment. Together, this work demonstrates that paclitaxel chemotherapy disrupts both the molecular clock and functional re-entrainment of the SCN that could cause or contribute to observed circadian rhythm disruptions after treatment. This research could help guide application of circadian-mediated therapies to mitigate side effects of chemotherapy.</p>\",\"PeriodicalId\":11617,\"journal\":{\"name\":\"eNeuro\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12453581/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"eNeuro\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1523/ENEURO.0061-25.2025\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/9/1 0:00:00\",\"PubModel\":\"Print\",\"JCR\":\"Q3\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"eNeuro","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1523/ENEURO.0061-25.2025","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/1 0:00:00","PubModel":"Print","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

癌症患者在化疗期间和之后会经历昼夜节律紊乱,这可能会导致衰弱的副作用。目前尚不清楚化疗如何介导昼夜节律中断,特别是这些中断在主要时钟水平上发生的程度,即下丘脑的视交叉上核(SCN)。在本研究中,我们评估了常用的化疗药物紫杉醇如何影响雌性小鼠的SCN分子钟和SCN依赖的行为适应昼夜节律挑战。在重复化疗方案后,我们测量了分子钟和昼夜节律相关转录物的SCN节律性表达。紫杉醇化疗通过破坏关键分子钟基因的节律性(Bmal1, Nr1d2)和抑制节律性转录(Ciart, Dbp, Nr1d1, Per2)来破坏SCN分子钟。我们通过测量昼夜节律轮对时差相延迟或提前范式的适应,并通过生成相响应曲线(PRC),进一步确定了化疗诱导的SCN功能变化。化疗并没有改变6小时阶段提前的再携带,但在6小时阶段延迟后,化疗小鼠的昼夜节律比药物治疗小鼠更稳定和强健,这可能表明SCN减弱或去偶联。在PRC中,与车辆对照相比,化疗在主观夜间减弱了光诱导的相移延迟,这也表明scn依赖性夹带被破坏。总之,这项工作表明紫杉醇化疗破坏了分子钟和SCN的功能性再夹带,这可能导致或促成治疗后观察到的昼夜节律中断。这项研究可以帮助指导昼夜节律疗法的应用,以减轻化疗的副作用。昼夜节律紊乱是化疗的普遍副作用,多达一半的癌症患者表现出与治疗引起的副作用和生活质量下降相关的昼夜节律紊乱。导致化疗诱导的昼夜节律中断的机制仍然难以捉摸,例如下丘脑的视交叉上核(SCN)的中央时钟在多大程度上参与其中。在这里,我们评估了常用的紫杉醇化疗对SCN分子钟和SCN功能的影响。我们发现紫杉醇化疗强有力地破坏了与SCN依赖性行为适应改变相关的SCN分子钟。了解化疗改变SCN功能的程度将为潜在靶点提供信息,以减少化疗的衰弱性副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paclitaxel Chemotherapy Disrupts Circadian Gene Transcription and Function of the Suprachiasmatic Nuclei in Female Mice.

Cancer patients experience circadian rhythm disruptions during and after chemotherapy that can contribute to debilitating side effects. It is unknown how chemotherapy mediates circadian disruptions and specifically the extent to which these disruptions occur at the level of the principal clock, the suprachiasmatic nuclei (SCN) of the hypothalamus. In the present study, we assessed how the commonly used chemotherapeutic, paclitaxel, impacts the SCN molecular clock and SCN-dependent behavioral adaptations to circadian challenges in female mice. Following a repeated chemotherapy regimen, we measured rhythmic SCN expression of molecular clock and circadian-associated transcripts. Paclitaxel chemotherapy disrupted the SCN molecular clock through abolished rhythmicity (Bmal1, Nr1d2) and damped rhythmic transcription (Ciart, Dbp, Nr1d1, Per2) of key molecular clock genes. We further determined chemotherapy-induced changes to SCN function by measuring circadian wheel running adaptations to a jet lag phase-delay or phase-advance paradigm and by generating a phase response curve (PRC). Chemotherapy did not alter re-entrainment to a 6 h phase-advance, but after a 6 h phase-delay, chemotherapy-treated mice had a more stable and robust circadian rhythm than vehicle-treated mice, possibly indicative of a weakened or decoupled SCN. In the PRC, chemotherapy blunted light-induced phase-shift delays during subjective night compared with vehicle controls, also indicative of disrupted SCN-dependent entrainment. Together, this work demonstrates that paclitaxel chemotherapy disrupts both the molecular clock and functional re-entrainment of the SCN that could cause or contribute to observed circadian rhythm disruptions after treatment. This research could help guide application of circadian-mediated therapies to mitigate side effects of chemotherapy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
eNeuro
eNeuro Neuroscience-General Neuroscience
CiteScore
5.00
自引率
2.90%
发文量
486
审稿时长
16 weeks
期刊介绍: An open-access journal from the Society for Neuroscience, eNeuro publishes high-quality, broad-based, peer-reviewed research focused solely on the field of neuroscience. eNeuro embodies an emerging scientific vision that offers a new experience for authors and readers, all in support of the Society’s mission to advance understanding of the brain and nervous system.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信