• 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
Post-trauma administration of the pifithrin-α oxygen analog improves histological and functional outcomes after experimental traumatic brain injury.创伤后给予pifithrin-α氧类似物可改善实验性创伤性脑损伤后的组织学和功能结果。
Exp Neurol. 2015 Jul;269:56-66. doi: 10.1016/j.expneurol.2015.03.015. Epub 2015 Mar 24.
2
Post-traumatic administration of the p53 inactivator pifithrin-α oxygen analogue reduces hippocampal neuronal loss and improves cognitive deficits after experimental traumatic brain injury.创伤后给予p53抑制剂pifithrin-α氧类似物可减少实验性创伤性脑损伤后海马神经元丢失并改善认知缺陷。
Neurobiol Dis. 2016 Dec;96:216-226. doi: 10.1016/j.nbd.2016.08.012. Epub 2016 Aug 20.
3
The p53 inactivators pifithrin-μ and pifithrin-α mitigate TBI-induced neuronal damage through regulation of oxidative stress, neuroinflammation, autophagy and mitophagy.p53 失活剂 pifithrin-μ 和 pifithrin-α 通过调节氧化应激、神经炎症、自噬和线粒体自噬减轻 TBI 诱导的神经元损伤。
Exp Neurol. 2020 Feb;324:113135. doi: 10.1016/j.expneurol.2019.113135. Epub 2019 Nov 26.
4
Neuroprotective effects of pifithrin-α against traumatic brain injury in the striatum through suppression of neuroinflammation, oxidative stress, autophagy, and apoptosis.吡非尼酮-α通过抑制神经炎症、氧化应激、自噬和细胞凋亡对纹状体创伤性脑损伤的神经保护作用。
Sci Rep. 2018 Feb 5;8(1):2368. doi: 10.1038/s41598-018-19654-x.
5
Cognitive impairments accompanying rodent mild traumatic brain injury involve p53-dependent neuronal cell death and are ameliorated by the tetrahydrobenzothiazole PFT-α.伴随啮齿类轻度创伤性脑损伤的认知障碍涉及 p53 依赖性神经元细胞死亡,并可被四氢苯并噻唑 PFT-α改善。
PLoS One. 2013 Nov 28;8(11):e79837. doi: 10.1371/journal.pone.0079837. eCollection 2013.
6
Delayed neuronal death after brain trauma involves p53-dependent inhibition of NF-kappaB transcriptional activity.脑外伤后迟发性神经元死亡涉及p53依赖的NF-κB转录活性抑制。
Cell Death Differ. 2007 Aug;14(8):1529-41. doi: 10.1038/sj.cdd.4402159. Epub 2007 Apr 27.
7
Effects of p53 inhibitor on survival and death of cells subjected to oxidative stress.p53抑制剂对遭受氧化应激的细胞存活与死亡的影响。
J Physiol Pharmacol. 2005 Sep;56 Suppl 4:215-21.
8
Targeting the p53 pathway to protect the neonatal ischemic brain.靶向 p53 通路以保护新生儿脑缺血。
Ann Neurol. 2011 Aug;70(2):255-64. doi: 10.1002/ana.22413. Epub 2011 Jun 14.
9
MiR-125b blocks Bax/Cytochrome C/Caspase-3 apoptotic signaling pathway in rat models of cerebral ischemia-reperfusion injury by targeting p53.微小RNA-125b通过靶向p53阻断大鼠脑缺血再灌注损伤模型中的Bax/细胞色素C/半胱天冬酶-3凋亡信号通路。
Neurol Res. 2018 Oct;40(10):828-837. doi: 10.1080/01616412.2018.1488654. Epub 2018 Jun 29.
10
Delayed treatment with a p53 inhibitor enhances recovery in stroke brain.使用p53抑制剂进行延迟治疗可促进中风后脑的恢复。
Ann Neurol. 2009 May;65(5):520-30. doi: 10.1002/ana.21592.

引用本文的文献

1
Fool's gold standard? Immunoperoxidase staining with the mouse monoclonal antibody (Clone 22C11) for detecting axonal pathology after traumatic brain injury.愚人金标准?用小鼠单克隆抗体(克隆号22C11)进行免疫过氧化物酶染色以检测创伤性脑损伤后的轴突病变。
Front Neurosci. 2025 Jun 2;19:1613172. doi: 10.3389/fnins.2025.1613172. eCollection 2025.
2
Pomalidomide Improves Motor Behavioral Deficits and Protects Cerebral Cortex and Striatum Against Neurodegeneration Through a Reduction of Oxidative/Nitrosative Damages and Neuroinflammation After Traumatic Brain Injury.泊马度胺通过降低创伤性脑损伤后的氧化/硝化损伤和神经炎症改善运动行为缺陷并保护大脑皮层和纹状体免受神经退行性变。
Cell Transplant. 2024 Jan-Dec;33:9636897241237049. doi: 10.1177/09636897241237049.
3
Temporal and structural sensitivities of major biomarkers for detecting neuropathology after traumatic brain injury in the mouse.小鼠创伤性脑损伤后检测神经病理学主要生物标志物的时间和结构敏感性
Front Neurosci. 2024 Jan 30;18:1339262. doi: 10.3389/fnins.2024.1339262. eCollection 2024.
4
Detection and verification of neurodegeneration after traumatic brain injury in the mouse: Immunohistochemical staining for amyloid precursor protein.检测和验证创伤性脑损伤后的神经退行性变:淀粉样前体蛋白的免疫组织化学染色。
Brain Pathol. 2023 Nov;33(6):e13163. doi: 10.1111/bpa.13163. Epub 2023 May 8.
5
Ultrasound stimulation improves inflammatory resolution, neuroprotection, and functional recovery after spinal cord injury.超声刺激可改善脊髓损伤后的炎症消退、神经保护和功能恢复。
Sci Rep. 2022 Mar 7;12(1):3636. doi: 10.1038/s41598-022-07114-6.
6
17β-Estradiol Abrogates Oxidative Stress and Neuroinflammation after Cortical Stab Wound Injury.17β-雌二醇可减轻皮质刺伤损伤后的氧化应激和神经炎症。
Antioxidants (Basel). 2021 Oct 25;10(11):1682. doi: 10.3390/antiox10111682.
7
3,6'-Dithiopomalidomide Ameliorates Hippocampal Neurodegeneration, Microgliosis and Astrogliosis and Improves Cognitive Behaviors in Rats with a Moderate Traumatic Brain Injury.3,6'-二硫苯并二氧戊吡咯并苯并二氮杂卓改善中度创伤性脑损伤大鼠海马神经退行性变、小胶质细胞增生和星形胶质细胞增生,并改善认知行为。
Int J Mol Sci. 2021 Jul 31;22(15):8276. doi: 10.3390/ijms22158276.
8
Neuroprotective effect of hydrogen sulfide against glutamate-induced oxidative stress is mediated via the p53/glutaminase 2 pathway after traumatic brain injury.硫化氢通过 p53/谷氨酰胺酶 2 通路对谷氨酸诱导的氧化应激的神经保护作用在创伤性脑损伤后发挥作用。
Aging (Albany NY). 2021 Feb 26;13(5):7180-7189. doi: 10.18632/aging.202575.
9
Histone deacetylase inhibitor MPT0B291 suppresses Glioma Growth and partially through acetylation of p53.组蛋白去乙酰化酶抑制剂 MPT0B291 抑制神经胶质瘤生长,部分通过乙酰化 p53 实现。
Int J Biol Sci. 2020 Oct 19;16(16):3184-3199. doi: 10.7150/ijbs.45505. eCollection 2020.
10
3,6'-dithiopomalidomide reduces neural loss, inflammation, behavioral deficits in brain injury and microglial activation.3,6'-二硫代苯并二茂寡核苷酸可减少脑损伤中的神经丢失、炎症、行为缺陷和小胶质细胞活化。
Elife. 2020 Jun 26;9:e54726. doi: 10.7554/eLife.54726.

本文引用的文献

1
Transiently lowering tumor necrosis factor-α synthesis ameliorates neuronal cell loss and cognitive impairments induced by minimal traumatic brain injury in mice.短暂降低肿瘤坏死因子-α的合成可改善小鼠轻度创伤性脑损伤所致的神经元细胞丢失和认知障碍。
J Neuroinflammation. 2015 Mar 7;12:45. doi: 10.1186/s12974-015-0237-4.
2
Incretin mimetics as pharmacologic tools to elucidate and as a new drug strategy to treat traumatic brain injury.肠促胰岛素类似物作为阐明创伤性脑损伤的药理工具和一种新的药物治疗策略。
Alzheimers Dement. 2014 Feb;10(1 Suppl):S62-75. doi: 10.1016/j.jalz.2013.12.011.
3
Network dysfunction after traumatic brain injury.创伤性脑损伤后的网络功能障碍。
Nat Rev Neurol. 2014 Mar;10(3):156-66. doi: 10.1038/nrneurol.2014.15. Epub 2014 Feb 11.
4
Cognitive impairments accompanying rodent mild traumatic brain injury involve p53-dependent neuronal cell death and are ameliorated by the tetrahydrobenzothiazole PFT-α.伴随啮齿类轻度创伤性脑损伤的认知障碍涉及 p53 依赖性神经元细胞死亡,并可被四氢苯并噻唑 PFT-α改善。
PLoS One. 2013 Nov 28;8(11):e79837. doi: 10.1371/journal.pone.0079837. eCollection 2013.
5
Selective TNF inhibition for chronic stroke and traumatic brain injury: an observational study involving 629 consecutive patients treated with perispinal etanercept.鞘内注射依那西普治疗慢性卒中和创伤性脑损伤:一项纳入 629 例连续患者的观察性研究
CNS Drugs. 2012 Dec;26(12):1051-70. doi: 10.1007/s40263-012-0013-2.
6
In vivo contributions of BH3-only proteins to neuronal death following seizures, ischemia, and traumatic brain injury.在癫痫发作、缺血和创伤性脑损伤后,BH3 仅蛋白对神经元死亡的体内贡献。
J Cereb Blood Flow Metab. 2011 May;31(5):1196-210. doi: 10.1038/jcbfm.2011.26. Epub 2011 Mar 2.
7
Enhanced survival of dopaminergic neuronal transplants in hemiparkinsonian rats by the p53 inactivator PFT-α.p53 抑制剂 PFT-α 增强半帕金森病大鼠多巴胺能神经元移植的存活率。
Cell Transplant. 2011;20(9):1351-9. doi: 10.3727/096368910X557173. Epub 2011 Feb 3.
8
Animal modelling of traumatic brain injury in preclinical drug development: where do we go from here?创伤性脑损伤的动物模型在临床前药物研发中的应用:我们从何处着手?
Br J Pharmacol. 2011 Oct;164(4):1207-29. doi: 10.1111/j.1476-5381.2010.01163.x.
9
Pathologies associated with the p53 response.与 p53 反应相关的病变。
Cold Spring Harb Perspect Biol. 2010 Jul;2(7):a001180. doi: 10.1101/cshperspect.a001180. Epub 2010 Apr 7.
10
Distinct time courses of secondary brain damage in the hippocampus following brain concussion and contusion in rats.大鼠脑震荡和挫伤后海马体继发性脑损伤的时间进程不同。
Tohoku J Exp Med. 2010 Jul;221(3):229-35. doi: 10.1620/tjem.221.229.

创伤后给予pifithrin-α氧类似物可改善实验性创伤性脑损伤后的组织学和功能结果。

Post-trauma administration of the pifithrin-α oxygen analog improves histological and functional outcomes after experimental traumatic brain injury.

作者信息

Yang L-Y, Chu Y-H, Tweedie D, Yu Q-S, Pick C G, Hoffer B J, Greig N H, Wang J-Y

机构信息

Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.

Drug Design & Development Section, Translational Gerontology Branch, Intramural Research Program, National Institute on Aging, National Institutes of Health, Baltimore, USA.

出版信息

Exp Neurol. 2015 Jul;269:56-66. doi: 10.1016/j.expneurol.2015.03.015. Epub 2015 Mar 24.

DOI:10.1016/j.expneurol.2015.03.015
PMID:25819102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5193498/
Abstract

Traumatic brain injury (TBI) is a major cause of death and disability worldwide. Programmed death of neuronal cells plays a crucial role in acute and chronic neurodegeneration following TBI. The tumor suppressor protein p53, a transcription factor, has been recognized as an important regulator of apoptotic neuronal death. The p53 inactivator pifithrin-α (PFT-α) has been shown to be neuroprotective against stroke. A previous cellular study indicated that PFT-α oxygen analog (PFT-α (O)) is more stable and active than PFT-α. We aimed to investigate whether inhibition of p53 using PFT-α or PFT-α (O) would be a potential neuroprotective strategy for TBI. To evaluate whether these drugs protect against excitotoxicity in vitro, primary rat cortical cultures were challenged with glutamate (50mM) in the presence or absence of various concentrations of the p53 inhibitors PFT-α or PFT-α (O). Cell viability was estimated by LDH assay. In vivo, adult Sprague Dawley rats were subjected to controlled cortical impact (CCI, with 4m/s velocity, 2mm deformation). Five hours after injury, PFT-α or PFT-α (O) (2mg/kg, i.v.) was administered to animals. Sensory and motor functions were evaluated by behavioral tests at 24h after TBI. The p53-positive neurons were identified by double staining with cell-specific markers. Levels of mRNA encoding for p53-regulated genes (BAX, PUMA, Bcl-2 and p21) were measured by reverse transcription followed by real time-PCR from TBI animals without or with PFT-α/PFT-α (O) treatment. We found that PFT-α(O) (10 μM) enhanced neuronal survival against glutamate-induced cytotoxicity in vitro more effectively than PFT-α (10 μM). In vivo PFT-α (O) treatment enhanced functional recovery and decreased contusion volume at 24h post-injury. Neuroprotection by PFT-α (O) treatment also reduced p53-positive neurons in the cortical contusion region. In addition, p53-regulated PUMA mRNA levels at 8h were significantly reduced by PFT-α (O) administration after TBI. PFT-α (O) treatment also decreased phospho-p53 positive neurons in the cortical contusion region. Our data suggest that PFT-α (O) provided a significant reduction of cortical cell death and protected neurons from glutamate-induced excitotoxicity in vitro, as well as improved neurological functional outcome and reduced brain injury in vivo via anti-apoptotic mechanisms. The inhibition of p53-induced apoptosis by PFT-α (O) provides a useful tool to evaluate reversible apoptotic mechanisms and may develop into a novel therapeutic strategy for TBI.

摘要

创伤性脑损伤(TBI)是全球范围内死亡和残疾的主要原因。神经元细胞的程序性死亡在TBI后的急性和慢性神经退行性变中起关键作用。肿瘤抑制蛋白p53作为一种转录因子,已被公认为凋亡性神经元死亡的重要调节因子。p53灭活剂pifithrin-α(PFT-α)已被证明对中风具有神经保护作用。先前的细胞研究表明,PFT-α氧类似物(PFT-α(O))比PFT-α更稳定且活性更高。我们旨在研究使用PFT-α或PFT-α(O)抑制p53是否会成为TBI的一种潜在神经保护策略。为了评估这些药物在体外是否能预防兴奋性毒性,在存在或不存在不同浓度的p53抑制剂PFT-α或PFT-α(O)的情况下,用谷氨酸(50mM)刺激原代大鼠皮质培养物。通过乳酸脱氢酶(LDH)测定评估细胞活力。在体内,成年Sprague Dawley大鼠接受控制性皮质撞击(CCI,速度为4m/s,变形2mm)。损伤后5小时,给动物静脉注射PFT-α或PFT-α(O)(2mg/kg)。在TBI后24小时通过行为测试评估感觉和运动功能。通过与细胞特异性标记物双重染色鉴定p53阳性神经元。通过逆转录随后对未接受或接受PFT-α/PFT-α(O)治疗的TBI动物进行实时PCR,测量p53调节基因(BAX、PUMA、Bcl-2和p21)的mRNA水平。我们发现,在体外,PFT-α(O)(10μM)比PFT-α(10μM)更有效地提高神经元对谷氨酸诱导的细胞毒性的存活率。在体内,PFT-α(O)治疗可增强损伤后24小时的功能恢复并减小挫伤体积。PFT-α(O)治疗的神经保护作用还减少了皮质挫伤区域的p53阳性神经元。此外,TBI后给予PFT-α(O)可使8小时时p53调节的PUMA mRNA水平显著降低。PFT-α(O)治疗还减少了皮质挫伤区域磷酸化p53阳性神经元。我们的数据表明,PFT-α(O)可显著减少皮质细胞死亡,并在体外保护神经元免受谷氨酸诱导的兴奋性毒性,以及通过抗凋亡机制在体内改善神经功能结局并减轻脑损伤。PFT-α(O)对p53诱导的凋亡的抑制作用为评估可逆性凋亡机制提供了一种有用的工具,并可能发展成为TBI的一种新型治疗策略。