• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Acute Neural and Proteostasis Messenger Ribonucleic Acid Levels Predict Chronic Locomotor Recovery after Contusive Spinal Cord Injury.急性神经和蛋白稳态信使 RNA 水平预测创伤性脊髓损伤后的慢性运动功能恢复。
J Neurotrauma. 2021 Feb;38(3):365-372. doi: 10.1089/neu.2020.7258. Epub 2020 Nov 10.
2
Activating Transcription Factor-6α Deletion Modulates the Endoplasmic Reticulum Stress Response after Spinal Cord Injury but Does Not Affect Locomotor Recovery.激活转录因子 6α 缺失可调节脊髓损伤后的内质网应激反应,但不影响运动功能恢复。
J Neurotrauma. 2018 Feb 1;35(3):486-491. doi: 10.1089/neu.2015.3993. Epub 2017 Nov 1.
3
Attenuating the endoplasmic reticulum stress response improves functional recovery after spinal cord injury.减轻内质网应激反应可改善脊髓损伤后的功能恢复。
Glia. 2011 Oct;59(10):1489-502. doi: 10.1002/glia.21191. Epub 2011 Jun 2.
4
Deletion of the pro-apoptotic endoplasmic reticulum stress response effector CHOP does not result in improved locomotor function after severe contusive spinal cord injury.CHOP(内质网应激反应促凋亡效应因子)缺失并不改善严重创伤性脊髓损伤后的运动功能。
J Neurotrauma. 2012 Feb 10;29(3):579-88. doi: 10.1089/neu.2011.1940. Epub 2011 Nov 21.
5
Restoring endoplasmic reticulum homeostasis improves functional recovery after spinal cord injury.恢复内质网稳态可改善脊髓损伤后的功能恢复。
Neurobiol Dis. 2013 Oct;58:29-37. doi: 10.1016/j.nbd.2013.04.021. Epub 2013 May 6.
6
Inhibition of GADD34, the stress-inducible regulatory subunit of the endoplasmic reticulum stress response, does not enhance functional recovery after spinal cord injury.抑制GADD34(内质网应激反应中应激诱导的调节亚基)并不能增强脊髓损伤后的功能恢复。
PLoS One. 2014 Nov 11;9(11):e109703. doi: 10.1371/journal.pone.0109703. eCollection 2014.
7
Oligodendrocyte-specific deletion of Xbp1 exacerbates the endoplasmic reticulum stress response and restricts locomotor recovery after thoracic spinal cord injury.少突胶质细胞特异性敲除 Xbp1 加剧内质网应激反应,并限制胸段脊髓损伤后的运动功能恢复。
Glia. 2021 Feb;69(2):424-435. doi: 10.1002/glia.23907. Epub 2020 Sep 14.
8
Hypoxia-inducible factor prolyl hydroxylase domain (PHD) inhibition after contusive spinal cord injury does not improve locomotor recovery.创伤性脊髓损伤后缺氧诱导因子脯氨酰羟化酶结构域(PHD)抑制不能改善运动功能恢复。
PLoS One. 2021 Apr 5;16(4):e0249591. doi: 10.1371/journal.pone.0249591. eCollection 2021.
9
Post-spinal cord injury astrocyte-mediated functional recovery in rats after intraspinal injection of the recombinant adenoviral vectors Ad5-VEGF and Ad5-ANG.脊髓内注射重组腺病毒载体Ad5-VEGF和Ad5-ANG后大鼠脊髓损伤后星形胶质细胞介导的功能恢复
J Neurosurg Spine. 2017 Jul;27(1):105-115. doi: 10.3171/2016.9.SPINE15959. Epub 2017 Apr 28.
10
Diffusion tensor imaging at 3 hours after traumatic spinal cord injury predicts long-term locomotor recovery.创伤性脊髓损伤后 3 小时的弥散张量成像预测长期运动功能恢复。
J Neurotrauma. 2010 Mar;27(3):587-98. doi: 10.1089/neu.2009.1063.

引用本文的文献

1
Opposite modulation of functional recovery following contusive spinal cord injury in mice with oligodendrocyte-selective deletions of Atf4 and Chop/Ddit3.在 Atf4 和 Chop/Ddit3 敲除的少突胶质细胞选择性小鼠中,对挫伤性脊髓损伤后的功能恢复进行相反的调节。
Sci Rep. 2023 Jun 6;13(1):9193. doi: 10.1038/s41598-023-36258-2.
2
Acute Pharmacological Inhibition of Protein Kinase R-Like Endoplasmic Reticulum Kinase Signaling After Spinal Cord Injury Spares Oligodendrocytes and Improves Locomotor Recovery.脊髓损伤后蛋白激酶 R 样内质网激酶信号的急性药理学抑制可保护少突胶质细胞并改善运动功能恢复。
J Neurotrauma. 2023 May;40(9-10):1007-1019. doi: 10.1089/neu.2022.0177. Epub 2023 Jan 25.
3
The Proteostasis Network: A Global Therapeutic Target for Neuroprotection after Spinal Cord Injury.蛋白质稳态网络:脊髓损伤后神经保护的全球治疗靶点。
Cells. 2022 Oct 22;11(21):3339. doi: 10.3390/cells11213339.
4
Limited changes in locomotor recovery and unaffected white matter sparing after spinal cord contusion at different times of day.一天中不同时间脊髓挫伤后运动功能恢复变化有限,且白质不受影响。
PLoS One. 2021 Nov 23;16(11):e0249981. doi: 10.1371/journal.pone.0249981. eCollection 2021.
5
Hypoxia-inducible factor prolyl hydroxylase domain (PHD) inhibition after contusive spinal cord injury does not improve locomotor recovery.创伤性脊髓损伤后缺氧诱导因子脯氨酰羟化酶结构域(PHD)抑制不能改善运动功能恢复。
PLoS One. 2021 Apr 5;16(4):e0249591. doi: 10.1371/journal.pone.0249591. eCollection 2021.

急性神经和蛋白稳态信使 RNA 水平预测创伤性脊髓损伤后的慢性运动功能恢复。

Acute Neural and Proteostasis Messenger Ribonucleic Acid Levels Predict Chronic Locomotor Recovery after Contusive Spinal Cord Injury.

机构信息

Kentucky Spinal Cord Injury Research Center and Departments of University of Louisville School of Medicine, Louisville, Kentucky, USA.

Neurological Surgery, University of Louisville School of Medicine, Louisville, Kentucky, USA.

出版信息

J Neurotrauma. 2021 Feb;38(3):365-372. doi: 10.1089/neu.2020.7258. Epub 2020 Nov 10.

DOI:10.1089/neu.2020.7258
PMID:33076743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7826426/
Abstract

One of the difficulties in identifying novel therapeutic strategies to manage central nervous system (CNS) trauma is the need for behavioral assays to assess chronic functional recovery. assays and/or acute behavioral assessments cannot accurately predict long-term functional outcome. Using data from 13 independent T9 moderate contusive spinal cord injury (SCI) studies, we asked whether the ratio of acute (24-72 h post-injury) changes in the levels of neuron-, oligodendrocyte-, astrocyte-specific and/or endoplasmic reticulum stress response (ERSR) messenger ribonucleic acids (mRNAs) could predict the extent of chronic functional recovery. Increased levels of neuron, oligodendrocyte, and astrocyte mRNAs all correlated with enhanced Basso Mouse Scale (BMS) scores. Reduced levels of the ERSR mRNAs and correlate with improved chronic locomotor function. Neither neural or ERSR mRNAs were predictive for chronic recovery across all behavioral changes. The ratio of oligodendrocyte/ERSR mRNAs, however, did predict "improved," "no change," or "worse" functional recovery. Neuronal/ERSR mRNA ratios predicted functional improvement, but could not distinguish between worse or no change outcomes. Astrocyte/ERSR mRNA ratios were not predictive. This approach can be used to confirm biological action of injected drugs and to optimize dose and therapeutic window. It may prove useful in cervical and lumbar SCI and in other traumatic CNS injuries such as traumatic brain injury and stroke, where prevention of neuronal loss is paramount to functional recovery. Although the current analysis was directed toward ERSR whose activity was targeted in all but one study, acute mRNA markers for other pathophysiological cascades may be as predictive of chronic recovery when those cascades are targeted for neuroprotection.

摘要

确定治疗中枢神经系统 (CNS) 创伤的新策略的困难之一是需要行为测定来评估慢性功能恢复。测定和/或急性行为评估不能准确预测长期功能结果。我们利用来自 13 项独立的 T9 中度挫伤性脊髓损伤 (SCI) 研究的数据,询问急性 (损伤后 24-72 小时) 神经元、少突胶质细胞、星形胶质细胞特异性和/或内质网应激反应 (ERSR) 信使核糖核酸 (mRNA) 水平变化的比值是否可以预测慢性功能恢复的程度。神经元、少突胶质细胞和星形胶质细胞 mRNA 水平的升高均与 Basso Mouse Scale (BMS) 评分的提高相关。ERSR mRNA 水平的降低与慢性运动功能的改善相关。无论是神经还是 ERSR mRNA 均不能预测所有行为变化的慢性恢复。然而,少突胶质细胞/ERSR mRNA 的比值可预测“改善”、“无变化”或“恶化”的功能恢复。神经元/ERSR mRNA 比值可预测功能改善,但不能区分恶化或无变化的结果。星形胶质细胞/ERSR mRNA 比值无预测作用。这种方法可用于确认注射药物的生物学作用,并优化剂量和治疗窗口。它可能对颈段和胸段 SCI 以及其他创伤性 CNS 损伤(如创伤性脑损伤和中风)有用,在这些损伤中,预防神经元丢失对于功能恢复至关重要。尽管目前的分析针对的是除一项研究之外的所有研究均靶向的 ERSR,但当针对神经保护靶向其他病理生理级联反应时,急性 mRNA 标志物可能与慢性恢复一样具有预测作用。