• 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

MPTP处理的C57BL/6小鼠中黑质纹状体多巴胺能神经元的自发再生

Spontaneous regeneration of nigrostriatal dopaminergic neurons in MPTP-treated C57BL/6 mice.

作者信息

Mitsumoto Y, Watanabe A, Mori A, Koga N

机构信息

Tokushima New Drug Research Institute, Otsuka Pharmaceutical Co., Ltd., Japan.

出版信息

Biochem Biophys Res Commun. 1998 Jul 30;248(3):660-3. doi: 10.1006/bbrc.1998.8986.

DOI:10.1006/bbrc.1998.8986
PMID:9703982
Abstract

The spontaneous recovery of nigrostriatal dopaminergic neurons was quantitatively analyzed with tyrosine hydroxylase (TH)-immunocytochemistry in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated C57BL/6 young mice. A substantial reduction of striatal dopamine (DA) level was observed until 24 days following MPTP treatment. The TH-immunoreactive (IR) fibers and number of TH-positive cell bodies were also markedly reduced at 3 days after the toxin treatment. Thereafter, TH-IR fiber densities showed to progressively recover through the examining period. The number of TH-positive cell bodies in substantia nigra pars compacta were not changed during the recovery period. These results indicate that MPTP-treated mice have a potential for spontaneous regenerative sprouting in nigrostriatal dopaminergic system.

摘要

利用酪氨酸羟化酶(TH)免疫细胞化学方法,对1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)处理的C57BL/6幼鼠黑质纹状体多巴胺能神经元的自发恢复情况进行了定量分析。在MPTP处理后24天内,观察到纹状体多巴胺(DA)水平显著降低。毒素处理3天后,TH免疫反应性(IR)纤维和TH阳性细胞体数量也明显减少。此后,在整个观察期内,TH-IR纤维密度逐渐恢复。黑质致密部TH阳性细胞体数量在恢复期没有变化。这些结果表明,MPTP处理的小鼠黑质纹状体多巴胺能系统具有自发再生芽生的潜力。

相似文献

1
Spontaneous regeneration of nigrostriatal dopaminergic neurons in MPTP-treated C57BL/6 mice.MPTP处理的C57BL/6小鼠中黑质纹状体多巴胺能神经元的自发再生
Biochem Biophys Res Commun. 1998 Jul 30;248(3):660-3. doi: 10.1006/bbrc.1998.8986.
2
Effect of angiotensin-converting enzyme inhibitor perindopril on interneurons in MPTP-treated mice.血管紧张素转换酶抑制剂培哚普利对MPTP处理小鼠中间神经元的影响。
Eur Neuropsychopharmacol. 2005 Jan;15(1):57-67. doi: 10.1016/j.euroneuro.2004.05.007.
3
Differences in nigral neuron number and sensitivity to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in C57/bl and CD-1 mice.C57/bl和CD-1小鼠黑质神经元数量及对1-甲基-4-苯基-1,2,3,6-四氢吡啶敏感性的差异。
Exp Neurol. 1994 Apr;126(2):195-204. doi: 10.1006/exnr.1994.1058.
4
Tyrosine hydroxylase and dopamine transporter expression following 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurodegeneration of the mouse nigrostriatal pathway.1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导小鼠黑质纹状体通路神经变性后酪氨酸羟化酶和多巴胺转运体的表达
J Neurosci Res. 2004 May 15;76(4):539-50. doi: 10.1002/jnr.20114.
5
Neuroprotective effects of genistein on dopaminergic neurons in the mice model of Parkinson's disease.金雀异黄素对帕金森病小鼠模型中多巴胺能神经元的神经保护作用。
Neurosci Res. 2008 Feb;60(2):156-61. doi: 10.1016/j.neures.2007.10.005. Epub 2007 Oct 23.
6
Social enrichment attenuates nigrostriatal lesioning and reverses motor impairment in a progressive 1-methyl-2-phenyl-1,2,3,6-tetrahydropyridine (MPTP) mouse model of Parkinson's disease.社交丰富化可减轻黑质纹状体损伤,并逆转进行性 1-甲基-2-苯基-1,2,3,6-四氢吡啶(MPTP)帕金森病小鼠模型的运动障碍。
Neurobiol Dis. 2012 Mar;45(3):1051-67. doi: 10.1016/j.nbd.2011.12.024. Epub 2011 Dec 14.
7
Stereotaxic injection of GD1a ganglioside induces limited recovery of striatal dopaminergic system in MPTP-treated aging mice.立体定向注射GD1a神经节苷脂可诱导MPTP处理的衰老小鼠纹状体多巴胺能系统有限恢复。
J Neurosci Res. 1991 Apr;28(4):525-30. doi: 10.1002/jnr.490280409.
8
Pharmacokinetic, neurochemical, stereological and neuropathological studies on the potential effects of paraquat in the substantia nigra pars compacta and striatum of male C57BL/6J mice.百草枯对雄性 C57BL/6J 小鼠黑质致密部和纹状体潜在影响的药代动力学、神经化学、立体学和神经病理学研究。
Neurotoxicology. 2013 Jul;37:1-14. doi: 10.1016/j.neuro.2013.03.005. Epub 2013 Mar 21.
9
Spontaneous long-term compensatory dopaminergic sprouting in MPTP-treated mice.MPTP 处理的小鼠中自发的长期多巴胺能代偿性发芽
Synapse. 2000 Dec 1;38(3):363-8. doi: 10.1002/1098-2396(20001201)38:3<363::AID-SYN16>3.0.CO;2-A.
10
Neuroprotection in Parkinson models varies with toxin administration protocol.帕金森病模型中的神经保护作用因毒素给药方案而异。
Eur J Neurosci. 2006 Dec;24(11):3174-82. doi: 10.1111/j.1460-9568.2006.05192.x.

引用本文的文献

1
The therapeutic use of clonal neural stem cells in experimental Parkinson´s disease.克隆神经干细胞在实验性帕金森病中的治疗应用。
Stem Cell Res Ther. 2024 Oct 9;15(1):356. doi: 10.1186/s13287-024-03965-0.
2
Dopaminergic neurons lacking Caspase-3 avoid apoptosis but undergo necrosis after MPTP treatment inducing a Galectin-3-dependent selective microglial phagocytic response.缺乏 Caspase-3 的多巴胺能神经元在 MPTP 处理后避免凋亡,但会发生坏死,从而引发 Galectin-3 依赖性选择性小胶质细胞吞噬反应。
Cell Death Dis. 2024 Aug 27;15(8):625. doi: 10.1038/s41419-024-07014-9.
3
Dose-Ranging Effects of the Intracerebral Administration of Atsttrin in Experimental Model of Parkinson's Disease Induced by 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in Mice.
阿替瑞林在 MPTP 诱导的帕金森病小鼠模型中脑内给药的剂量效应。
Mol Neurobiol. 2024 Nov;61(11):9432-9458. doi: 10.1007/s12035-024-04161-0. Epub 2024 Apr 20.
4
An optimized Nurr1 agonist provides disease-modifying effects in Parkinson's disease models.优化后的 Nurr1 激动剂可在帕金森病模型中产生疾病修饰作用。
Nat Commun. 2023 Jul 18;14(1):4283. doi: 10.1038/s41467-023-39970-9.
5
Antioxidative Activities of Micronized Solid-State Cultivated Rich in Erinacine A against MPTP-Induced Damages.富恩酰胺 A 固态发酵微米化产物对 MPTP 诱导损伤的抗氧化活性。
Molecules. 2023 Apr 12;28(8):3386. doi: 10.3390/molecules28083386.
6
DAT and TH expression marks human Parkinson's disease in peripheral immune cells.多巴胺转运体(DAT)和酪氨酸羟化酶(TH)表达在外周免疫细胞中标记人类帕金森病。
NPJ Parkinsons Dis. 2022 Jun 7;8(1):72. doi: 10.1038/s41531-022-00333-8.
7
Multifactoriality of Parkinson's Disease as Explored Through Human Neural Stem Cells and Their Transplantation in Middle-Aged Parkinsonian Mice.通过人类神经干细胞及其在中年帕金森病小鼠中的移植探索帕金森病的多因素性
Front Pharmacol. 2022 Jan 19;12:773925. doi: 10.3389/fphar.2021.773925. eCollection 2021.
8
Neurorestorative Effects of a Novel Fas-Associated Factor 1 Inhibitor in the MPTP Model: An [F]FE-PE2I Positron Emission Tomography Analysis Study.新型Fas相关因子1抑制剂在MPTP模型中的神经修复作用:一项[F]FE-PE2I正电子发射断层扫描分析研究。
Front Pharmacol. 2020 Jun 25;11:953. doi: 10.3389/fphar.2020.00953. eCollection 2020.
9
mGluR5 Allosteric Modulation Promotes Neurorecovery in a 6-OHDA-Toxicant Model of Parkinson's Disease.代谢型谷氨酸受体 5 的变构调节促进了 6-羟基多巴胺中毒帕金森病模型中的神经恢复。
Mol Neurobiol. 2020 Mar;57(3):1418-1431. doi: 10.1007/s12035-019-01818-z. Epub 2019 Nov 21.
10
The second generation mixed lineage kinase-3 (MLK3) inhibitor CLFB-1134 protects against neurotoxin-induced nigral dopaminergic neuron loss.第二代混合谱系激酶-3(MLK3)抑制剂 CLFB-1134 可防止神经毒素诱导的黑质多巴胺能神经元丢失。
Exp Neurol. 2019 Aug;318:157-164. doi: 10.1016/j.expneurol.2019.05.002. Epub 2019 May 8.