• 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

成瘾性脊柱

The "addicted" spine.

机构信息

Department of Animal Biology and Ecology, University of Cagliari Cagliari, Italy.

Department of Animal Biology and Ecology, University of Cagliari Cagliari, Italy ; "G.Minardi" Laboratory of Cognitive Neuroscience, Department of Chemistry and Pharmacy, University of Sassari Sassari, Italy.

出版信息

Front Neuroanat. 2014 Oct 2;8:110. doi: 10.3389/fnana.2014.00110. eCollection 2014.

DOI:10.3389/fnana.2014.00110
PMID:25324733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4183114/
Abstract

Units of dendritic branches called dendritic spines represent more than simply decorative appendages of the neuron and actively participate in integrative functions of "spinous" nerve cells thereby contributing to the general phenomenon of synaptic plasticity. In animal models of drug addiction, spines are profoundly affected by treatments with drugs of abuse and represent important sub cellular markers which interfere deeply into the physiology of the neuron thereby providing an example of the burgeoning and rapidly increasing interest in "structural plasticity". Medium Spiny Neurons (MSNs) of the Nucleus Accumbens (Nacc) show a reduced number of dendritic spines and a decrease in TH-positive terminals upon withdrawal from opiates, cannabinoids and alcohol. The reduction is localized "strictly" to second order dendritic branches where dopamine (DA)-containing terminals, impinging upon spines, make synaptic contacts. In addition, long-thin spines seems preferentially affected raising the possibility that cellular learning of these neurons may be selectively hampered. These findings suggest that dendritic spines are affected by drugs widely abused by humans and provide yet another example of drug-induced aberrant neural plasticity with marked reflections on the physiology of synapses, system structural organization, and neuronal circuitry remodeling.

摘要

被称为树突棘的树突分支单位不仅仅代表神经元的简单装饰附属物,它们还积极参与“棘突”神经细胞的整合功能,从而促进突触可塑性的普遍现象。在药物成瘾的动物模型中,刺突受到滥用药物治疗的深刻影响,并且是重要的亚细胞标志物,它们深入干扰神经元的生理学,从而为“结构可塑性”的新兴和快速增长的兴趣提供了一个例子。伏隔核(Nacc)中的中脑导水管周围灰质(MSNs)在戒断阿片类药物、大麻素和酒精后表现出树突棘数量减少和 TH 阳性终末减少。这种减少是“严格”局限于第二级树突分支的,多巴胺(DA)含有终末的地方,影响树突棘,进行突触接触。此外,长而细的棘突似乎更容易受到影响,这增加了这些神经元的细胞学习可能会被选择性阻碍的可能性。这些发现表明,树突棘受到人类广泛滥用的药物的影响,并提供了另一个药物引起的异常神经可塑性的例子,对突触生理学、系统结构组织和神经元电路重塑有明显的反映。

相似文献

1
The "addicted" spine.成瘾性脊柱
Front Neuroanat. 2014 Oct 2;8:110. doi: 10.3389/fnana.2014.00110. eCollection 2014.
2
Differential striatal spine pathology in Parkinson's disease and cocaine addiction: a key role of dopamine?帕金森病和可卡因成瘾中纹状体棘突的差异病理学:多巴胺的关键作用?
Neuroscience. 2013 Oct 22;251:2-20. doi: 10.1016/j.neuroscience.2013.07.011. Epub 2013 Jul 16.
3
Dopamine facilitates dendritic spine formation by cultured striatal medium spiny neurons through both D1 and D2 dopamine receptors.多巴胺通过 D1 和 D2 多巴胺受体促进培养的纹状体中型多棘神经元的树突棘形成。
Neuropharmacology. 2013 Apr;67:432-43. doi: 10.1016/j.neuropharm.2012.11.030. Epub 2012 Dec 8.
4
Hampered long-term depression and thin spine loss in the nucleus accumbens of ethanol-dependent rats.乙醇依赖大鼠伏隔核中长时程抑制受损及棘突丢失
Proc Natl Acad Sci U S A. 2014 Sep 2;111(35):E3745-54. doi: 10.1073/pnas.1406768111. Epub 2014 Aug 13.
5
Stress and Cocaine Trigger Divergent and Cell Type-Specific Regulation of Synaptic Transmission at Single Spines in Nucleus Accumbens.应激和可卡因引发伏隔核单个棘突处突触传递的不同及细胞类型特异性调节。
Biol Psychiatry. 2016 Jun 1;79(11):898-905. doi: 10.1016/j.biopsych.2015.05.022. Epub 2015 Jun 6.
6
An embryonic culture system for the investigation of striatal medium spiny neuron dendritic spine development and plasticity.用于研究纹状体中间神经元树突棘发育和可塑性的胚胎培养系统。
J Neurosci Methods. 2011 Aug 30;200(1):1-13. doi: 10.1016/j.jneumeth.2011.05.029. Epub 2011 Jun 13.
7
Response learning stimulates dendritic spine growth on dorsal striatal medium spiny neurons.反应学习促进背侧纹状体中间神经元树突棘生长。
Neurobiol Learn Mem. 2018 Nov;155:50-59. doi: 10.1016/j.nlm.2018.06.008. Epub 2018 Jun 23.
8
Dendritic and somatic appendages of identified rubrospinal neurons of the cat.猫红核脊髓神经元的树突和胞体附属结构。
Neuroscience. 1987 Jul;22(1):113-30. doi: 10.1016/0306-4522(87)90202-8.
9
Adolescent nicotine-induced dendrite remodeling in the nucleus accumbens is rapid, persistent, and D1-dopamine receptor dependent.青少年尼古丁诱导的伏隔核树突重塑迅速、持久且依赖于D1-多巴胺受体。
Brain Struct Funct. 2016 Jan;221(1):133-45. doi: 10.1007/s00429-014-0897-3. Epub 2014 Sep 26.
10
Effects of ethanol exposure and withdrawal on dendritic morphology and spine density in the nucleus accumbens core and shell.乙醇暴露和戒断对伏隔核核心区和壳区树突形态及棘密度的影响。
Brain Res. 2015 Jan 12;1594:125-35. doi: 10.1016/j.brainres.2014.10.036. Epub 2014 Oct 27.

引用本文的文献

1
Effects of Chronic Social Isolation Stress and Alcohol on the Reinforcing Properties of Ketamine in Male and Female Rats.慢性社会隔离应激和酒精对雄性和雌性大鼠氯胺酮强化特性的影响。
eNeuro. 2025 Mar 3;12(3). doi: 10.1523/ENEURO.0452-24.2025. Print 2025 Mar.
2
Motivational dysregulation with melanocortin 4 receptor haploinsufficiency.伴有黑皮质素4受体单倍剂量不足的动机调节障碍。
NeuroImmune Pharm Ther. 2024 Nov 20;3(3-4):237-250. doi: 10.1515/nipt-2024-0011. eCollection 2024 Sep.
3
The Role of Acid-Sensing Ion Channel 1A (ASIC1A) in the Behavioral and Synaptic Effects of Oxycodone and Other Opioids.

本文引用的文献

1
Hampered long-term depression and thin spine loss in the nucleus accumbens of ethanol-dependent rats.乙醇依赖大鼠伏隔核中长时程抑制受损及棘突丢失
Proc Natl Acad Sci U S A. 2014 Sep 2;111(35):E3745-54. doi: 10.1073/pnas.1406768111. Epub 2014 Aug 13.
2
A new automated 3D detection of synaptic contacts reveals the formation of cortico-striatal synapses upon cocaine treatment in vivo.一种新的突触接触自动三维检测方法揭示了可卡因体内治疗后皮质-纹状体突触的形成。
Brain Struct Funct. 2015 Sep;220(5):2953-66. doi: 10.1007/s00429-014-0837-2. Epub 2014 Jul 8.
3
The neural rejuvenation hypothesis of cocaine addiction.
酸敏离子通道 1A(ASIC1A)在羟考酮和其他阿片类药物的行为和突触效应中的作用。
Int J Mol Sci. 2024 Oct 29;25(21):11584. doi: 10.3390/ijms252111584.
4
Post-transcriptional regulation and subcellular localization of G-protein γ7 subunit: implications for striatal function and behavioral responses to cocaine.G蛋白γ7亚基的转录后调控与亚细胞定位:对纹状体功能及可卡因行为反应的影响
Front Neuroanat. 2024 May 2;18:1394659. doi: 10.3389/fnana.2024.1394659. eCollection 2024.
5
EcoHIV Infection Modulates the Effects of Cocaine Exposure Pattern and Abstinence on Cocaine Seeking and Neuroimmune Protein Expression in Male Mice.EcoHIV感染调节可卡因暴露模式和戒断对雄性小鼠可卡因觅求行为及神经免疫蛋白表达的影响。
bioRxiv. 2024 Apr 19:2024.04.15.589615. doi: 10.1101/2024.04.15.589615.
6
Conditioned morphine tolerance promotes neurogenesis, dendritic remodelling and pro-plasticity molecules in the adult rat hippocampus.条件性吗啡耐受促进成年大鼠海马中的神经发生、树突重塑和促可塑性分子。
Addict Biol. 2024 Mar;29(3):e13377. doi: 10.1111/adb.13377.
7
Commentary: Effects of acid-sensing ion channel-1A (ASIC1A) on cocaine-induced synaptic adaptations.述评:酸敏感离子通道1A(ASIC1A)对可卡因诱导的突触适应性的影响
Front Physiol. 2023 Dec 4;14:1295561. doi: 10.3389/fphys.2023.1295561. eCollection 2023.
8
Learning to become addicted, one synapse at a time.一次一个突触,学着上瘾。
Neural Regen Res. 2024 Feb;19(2):401-402. doi: 10.4103/1673-5374.379046.
9
Effects of acid-sensing ion channel-1A (ASIC1A) on cocaine-induced synaptic adaptations.酸敏感离子通道1A(ASIC1A)对可卡因诱导的突触适应性的影响。
Front Physiol. 2023 Jun 14;14:1191275. doi: 10.3389/fphys.2023.1191275. eCollection 2023.
10
Proteomics and weighted gene correlated network analysis reveal glutamatergic synapse signaling in diazepam treatment of alcohol withdrawal.蛋白质组学和加权基因共表达网络分析揭示地西泮治疗酒精戒断中的谷氨酸能突触信号传导。
Front Pharmacol. 2023 Jan 11;13:1111758. doi: 10.3389/fphar.2022.1111758. eCollection 2022.
可卡因成瘾的神经修复假说。
Trends Pharmacol Sci. 2014 Aug;35(8):374-83. doi: 10.1016/j.tips.2014.05.005. Epub 2014 Jun 20.
4
Negative reinforcement via motivational withdrawal is the driving force behind the transition to addiction.通过动机撤回进行的负强化是成瘾转变背后的驱动力。
Psychopharmacology (Berl). 2014 Oct;231(19):3911-7. doi: 10.1007/s00213-014-3623-1. Epub 2014 Jun 13.
5
Phasic mesolimbic dopamine signaling encodes the facilitation of incentive motivation produced by repeated cocaine exposure.阶段性中脑边缘多巴胺信号编码了重复接触可卡因所产生的动机强化。
Neuropsychopharmacology. 2014 Sep;39(10):2441-9. doi: 10.1038/npp.2014.96. Epub 2014 May 7.
6
Cellular basis of memory for addiction.成瘾记忆的细胞基础。
Dialogues Clin Neurosci. 2013 Dec;15(4):431-43. doi: 10.31887/DCNS.2013.15.4/enestler.
7
The addicted brain.成瘾的大脑。
Front Psychiatry. 2013 Jun 3;4:40. doi: 10.3389/fpsyt.2013.00040. eCollection 2013.
8
The energy cost of action potential propagation in dopamine neurons: clues to susceptibility in Parkinson's disease.动作电位在多巴胺神经元中传播的能量成本:帕金森病易感性的线索。
Front Comput Neurosci. 2013 Mar 18;7:13. doi: 10.3389/fncom.2013.00013. eCollection 2013.
9
Differential modulation of drug-induced structural and functional plasticity of dendritic spines.药物诱导的树突棘结构和功能可塑性的差异调节。
Mol Pharmacol. 2012 Aug;82(2):333-43. doi: 10.1124/mol.112.078162. Epub 2012 May 17.
10
Subregional, dendritic compartment, and spine subtype specificity in cocaine regulation of dendritic spines in the nucleus accumbens.可卡因对伏隔核树突棘的调节中,亚区、树突分支隔室和棘突亚型特异性。
J Neurosci. 2012 May 16;32(20):6957-66. doi: 10.1523/JNEUROSCI.5718-11.2012.