• 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

甲基强的松龙治疗严重脊髓损伤后持续输注脑源性神经营养因子(BDNF)

Continuous brain-derived neurotrophic factor (BDNF) infusion after methylprednisolone treatment in severe spinal cord injury.

作者信息

Kim Daniel H, Jahng Tae-Ahn

机构信息

Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

J Korean Med Sci. 2004 Feb;19(1):113-22. doi: 10.3346/jkms.2004.19.1.113.

DOI:10.3346/jkms.2004.19.1.113
PMID:14966352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2822246/
Abstract

Although methylprednisolone (MP) is the standard of care in acute spinal cord injury (SCI), its functional outcome varies in clinical situation. Recent report demonstrated that MP depresses the expression of growth-promoting neurotrophic factors after acute SCI. The present study was designed to investigate whether continuous infusion of brain-derived neurotrophic factor (BDNF) after MP treatment promotes functional recovery in severe SCI. Contusion injury was produced at the T10 vertebral level of the spinal cord in adult rats. The rats received MP intravenously immediately after the injury and BDNF was infused intrathecally using an osmotic mini-pump for six weeks. Immunohistochemical methods were used to detect ED-1, Growth associated protein-43 (GAP-43), neurofilament (NF), and choline acethyl transferase (ChAT) levels. BDNF did not alter the effect of MP on hematogenous inflammatory cellular infiltration. MP treatment with BDNF infusion resulted in greater axonal survival and regeneration compared to MP treatment alone, as indicated by increases in NF and GAP-43 gene expression. Adjunctive BDNF infusion resulted in better locomotor test scores using the Basso-Beattie-Bresnahan (BBB) test. This study demonstrated that continuous infusion of BDNF after initial MP treatment improved functional recovery after severe spinal cord injury without dampening the acute effect of MP.

摘要

尽管甲基强的松龙(MP)是急性脊髓损伤(SCI)的标准治疗药物,但其功能结果在临床情况下存在差异。最近的报告表明,MP会抑制急性脊髓损伤后促进生长的神经营养因子的表达。本研究旨在探讨MP治疗后持续输注脑源性神经营养因子(BDNF)是否能促进严重脊髓损伤后的功能恢复。在成年大鼠脊髓的T10椎体水平制造挫伤损伤。大鼠在受伤后立即静脉注射MP,并使用渗透微型泵鞘内输注BDNF六周。采用免疫组织化学方法检测ED-1、生长相关蛋白-43(GAP-43)、神经丝(NF)和胆碱乙酰转移酶(ChAT)水平。BDNF并未改变MP对血源性炎性细胞浸润的影响。与单独使用MP治疗相比,MP治疗联合BDNF输注导致轴突存活和再生增加,这通过NF和GAP-43基因表达的增加得以体现。使用Basso-Beattie-Bresnahan(BBB)试验,辅助输注BDNF导致更好的运动测试评分。本研究表明,在初始MP治疗后持续输注BDNF可改善严重脊髓损伤后的功能恢复,而不会减弱MP的急性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/fce78eb6b969/jkms-19-113-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/fb403f923514/jkms-19-113-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/d6407bea6eb8/jkms-19-113-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/4e3001f4b97d/jkms-19-113-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/379f13e9bd56/jkms-19-113-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/fce78eb6b969/jkms-19-113-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/fb403f923514/jkms-19-113-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/d6407bea6eb8/jkms-19-113-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/4e3001f4b97d/jkms-19-113-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/379f13e9bd56/jkms-19-113-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2be5/2822246/fce78eb6b969/jkms-19-113-g005.jpg

相似文献

1
Continuous brain-derived neurotrophic factor (BDNF) infusion after methylprednisolone treatment in severe spinal cord injury.甲基强的松龙治疗严重脊髓损伤后持续输注脑源性神经营养因子(BDNF)
J Korean Med Sci. 2004 Feb;19(1):113-22. doi: 10.3346/jkms.2004.19.1.113.
2
Combined therapy of methylprednisolone and brain-derived neurotrophic factor promotes axonal regeneration and functional recovery after spinal cord injury in rats.甲基强的松龙与脑源性神经营养因子联合治疗促进大鼠脊髓损伤后轴突再生和功能恢复。
Chin Med J (Engl). 2003 Mar;116(3):414-8.
3
Brain-derived neurotrophic factor stimulates hindlimb stepping and sprouting of cholinergic fibers after spinal cord injury.脑源性神经营养因子可刺激脊髓损伤后后肢迈步及胆碱能纤维的发芽。
Exp Neurol. 1998 Nov;154(1):170-84. doi: 10.1006/exnr.1998.6924.
4
Pegylated brain-derived neurotrophic factor shows improved distribution into the spinal cord and stimulates locomotor activity and morphological changes after injury.聚乙二醇化脑源性神经营养因子在损伤后显示出更好地分布到脊髓中,并刺激运动活性和形态学变化。
Exp Neurol. 2001 Jul;170(1):85-100. doi: 10.1006/exnr.2001.7699.
5
[Effect of Gold Belt combined with methylprednisolone on motor function and brain-derived neurotrophic factor expression in rats following traumatic spinal cord injury].金腰带联合甲泼尼龙对创伤性脊髓损伤大鼠运动功能及脑源性神经营养因子表达的影响
Nan Fang Yi Ke Da Xue Xue Bao. 2015 Feb;35(2):276-80.
6
Effect of infliximab combined with methylprednisolone on expressions of NF-κB, TRADD, and FADD in rat acute spinal cord injury.英夫利昔单抗联合甲泼尼龙对大鼠急性脊髓损伤中 NF-κB、TRADD 和 FADD 表达的影响。
Spine (Phila Pa 1976). 2013 Jun 15;38(14):E861-9. doi: 10.1097/BRS.0b013e318294892c.
7
Effect of brain-derived neurotrophic factor, nerve growth factor, and neurotrophin-3 on functional recovery and regeneration after spinal cord injury in adult rats.脑源性神经营养因子、神经生长因子和神经营养素-3对成年大鼠脊髓损伤后功能恢复和再生的影响。
J Neurotrauma. 2000 Dec;17(12):1219-31. doi: 10.1089/neu.2000.17.1219.
8
[Effect of Herba Lycopodii Alcohol Extracted Granule Combined Methylprednisolone on Expression Levels of BDNF and NMDA and Behavior of Traumatic Spinal Cord Injury Rats].[伸筋草醇提颗粒联合甲泼尼龙对创伤性脊髓损伤大鼠脑源性神经营养因子和N-甲基-D-天冬氨酸表达水平及行为的影响]
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2015 Aug;35(8):1004-10.
9
Brain-derived neurotrophic factor gene transfer with adeno-associated viral and lentiviral vectors prevents rubrospinal neuronal atrophy and stimulates regeneration-associated gene expression after acute cervical spinal cord injury.腺相关病毒和慢病毒载体介导的脑源性神经营养因子基因转移可预防急性颈脊髓损伤后红核脊髓束神经元萎缩并刺激再生相关基因表达。
Spine (Phila Pa 1976). 2007 May 15;32(11):1164-73. doi: 10.1097/BRS.0b013e318053ec35.
10
[Expression of neurotrophin and IL-1 beta mRNAs following spinal cord injury and the effects of methylprednisolone treatment].[脊髓损伤后神经营养因子和白细胞介素-1β mRNA 的表达及甲基强的松龙治疗的影响]
Kaibogaku Zasshi. 1997 Jun;72(3):209-13.

引用本文的文献

1
Different macaque brain network remodeling after spinal cord injury and NT3 treatment.脊髓损伤和NT3治疗后不同猕猴脑网络重塑
iScience. 2023 Apr 29;26(6):106784. doi: 10.1016/j.isci.2023.106784. eCollection 2023 Jun 16.
2
GSK-3 Inhibitor Promotes Neuronal Cell Regeneration and Functional Recovery in a Rat Model of Spinal Cord Injury.GSK-3 抑制剂促进脊髓损伤大鼠模型中的神经元细胞再生和功能恢复。
Biomed Res Int. 2019 Aug 4;2019:9628065. doi: 10.1155/2019/9628065. eCollection 2019.
3
Combined application of Rho-ROCKII and GSK-3β inhibitors exerts an improved protective effect on axonal regeneration in rats with spinal cord injury.

本文引用的文献

1
Guidelines for the management of acute cervical spine and spinal cord injuries.急性颈椎和脊髓损伤管理指南
Clin Neurosurg. 2002;49:407-98.
2
Brain-derived neurotrophic factor in astrocytes, oligodendrocytes, and microglia/macrophages after spinal cord injury.脊髓损伤后星形胶质细胞、少突胶质细胞和小胶质细胞/巨噬细胞中的脑源性神经营养因子
Neurobiol Dis. 2000 Dec;7(6 Pt B):574-85. doi: 10.1006/nbdi.2000.0318.
3
A critical appraisal of the reporting of the National Acute Spinal Cord Injury Studies (II and III) of methylprednisolone in acute spinal cord injury.
Rho-ROCKII与GSK-3β抑制剂联合应用对脊髓损伤大鼠的轴突再生具有更好的保护作用。
Mol Med Rep. 2016 Dec;14(6):5180-5188. doi: 10.3892/mmr.2016.5918. Epub 2016 Nov 1.
4
An update on spinal cord injury research.脊髓损伤研究的最新进展。
Neurosci Bull. 2013 Feb;29(1):94-102. doi: 10.1007/s12264-012-1277-8. Epub 2012 Nov 3.
5
Correlation between cortical plasticity, motor learning and BDNF genotype in healthy subjects.健康受试者皮质可塑性、运动学习与 BDNF 基因型的相关性。
Exp Brain Res. 2011 Jul;212(1):91-9. doi: 10.1007/s00221-011-2700-5. Epub 2011 May 3.
6
BDNF-hypersecreting human mesenchymal stem cells promote functional recovery, axonal sprouting, and protection of corticospinal neurons after spinal cord injury.BDNF 分泌亢进型人骨髓间充质干细胞促进脊髓损伤后功能恢复、轴突再生和皮质脊髓神经元的保护。
J Neurosci. 2009 Nov 25;29(47):14932-41. doi: 10.1523/JNEUROSCI.2769-09.2009.
7
Increased susceptibility of annexin-A1 null mice to nociceptive pain is indicative of a spinal antinociceptive action of annexin-A1.膜联蛋白A1基因敲除小鼠对伤害性疼痛的易感性增加,表明膜联蛋白A1具有脊髓抗伤害感受作用。
Br J Pharmacol. 2008 Jul;154(5):1135-42. doi: 10.1038/bjp.2008.166. Epub 2008 May 12.
8
Effects of methylprednisolone on the neural conduction of the motor evoked potentials in spinal cord injured rats.甲基强的松龙对脊髓损伤大鼠运动诱发电位神经传导的影响。
J Korean Med Sci. 2005 Feb;20(1):132-8. doi: 10.3346/jkms.2005.20.1.132.
对国家急性脊髓损伤研究(II和III)中甲基强的松龙治疗急性脊髓损伤报告的批判性评价。
J Spinal Disord. 2000 Jun;13(3):185-99. doi: 10.1097/00002517-200006000-00001.
4
Sequential mRNA expression for immediate early genes, cytokines, and neurotrophins in spinal cord injury.脊髓损伤中即刻早期基因、细胞因子和神经营养因子的序列性mRNA表达。
J Neurotrauma. 2000 Mar;17(3):203-18. doi: 10.1089/neu.2000.17.203.
5
Pathogenesis and pharmacological strategies for mitigating secondary damage in acute spinal cord injury.急性脊髓损伤中减轻继发性损伤的发病机制及药理学策略
Neurosurgery. 1999 May;44(5):1027-39; discussion 1039-40. doi: 10.1097/00006123-199905000-00052.
6
Brain-derived neurotrophic factor stimulates hindlimb stepping and sprouting of cholinergic fibers after spinal cord injury.脑源性神经营养因子可刺激脊髓损伤后后肢迈步及胆碱能纤维的发芽。
Exp Neurol. 1998 Nov;154(1):170-84. doi: 10.1006/exnr.1998.6924.
7
Spontaneous longitudinally orientated axonal regeneration is associated with the Schwann cell framework within the lesion site following spinal cord compression injury of the rat.大鼠脊髓压迫性损伤后,自发的纵向轴突再生与损伤部位的雪旺细胞框架有关。
J Neurosci Res. 1998 Jul 1;53(1):51-65. doi: 10.1002/(SICI)1097-4547(19980701)53:1<51::AID-JNR6>3.0.CO;2-I.
8
Long-distance axonal regeneration in the transected adult rat spinal cord is promoted by olfactory ensheathing glia transplants.嗅鞘胶质细胞移植可促进成年大鼠横断脊髓的长距离轴突再生。
J Neurosci. 1998 May 15;18(10):3803-15. doi: 10.1523/JNEUROSCI.18-10-03803.1998.
9
Functional evidence that BDNF is an anterograde neuronal trophic factor in the CNS.脑源性神经营养因子(BDNF)是中枢神经系统(CNS)中一种顺行性神经营养因子的功能证据。
J Neurosci. 1998 Apr 15;18(8):2808-21. doi: 10.1523/JNEUROSCI.18-08-02808.1998.
10
BDNF and NT-4/5 prevent atrophy of rat rubrospinal neurons after cervical axotomy, stimulate GAP-43 and Talpha1-tubulin mRNA expression, and promote axonal regeneration.脑源性神经营养因子(BDNF)和神经营养素-4/5(NT-4/5)可预防大鼠颈髓离断后红核脊髓神经元萎缩,刺激生长相关蛋白43(GAP-43)和α1微管蛋白(Tα1-tubulin)mRNA表达,并促进轴突再生。
J Neurosci. 1997 Dec 15;17(24):9583-95. doi: 10.1523/JNEUROSCI.17-24-09583.1997.