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本文引用的文献

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Effects of insertion conditions on tissue strain and vascular damage during neuroprosthetic device insertion.神经假体装置植入过程中植入条件对组织应变和血管损伤的影响。
J Neural Eng. 2006 Sep;3(3):196-207. doi: 10.1088/1741-2560/3/3/002. Epub 2006 Jun 21.
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Brain micromotion around implants in the rodent somatosensory cortex.啮齿动物体感皮层中植入物周围的脑微运动。
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Minocycline treatment prevents cavitation in rats after a cortical devascularizing lesion.米诺环素治疗可预防大鼠皮质去血管化损伤后的空洞形成。
Brain Res. 2006 May 23;1090(1):172-81. doi: 10.1016/j.brainres.2006.03.072. Epub 2006 May 2.
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Response of brain tissue to chronically implanted neural electrodes.脑组织对长期植入神经电极的反应。
J Neurosci Methods. 2005 Oct 15;148(1):1-18. doi: 10.1016/j.jneumeth.2005.08.015. Epub 2005 Sep 27.
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Dexamethasone treatment reduces astroglia responses to inserted neuroprosthetic devices in rat neocortex.地塞米松治疗可降低大鼠新皮质中星形胶质细胞对植入神经假体装置的反应。
Exp Neurol. 2005 Aug;194(2):289-300. doi: 10.1016/j.expneurol.2004.08.037.
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A comparison of chronic multi-channel cortical implantation techniques: manual versus mechanical insertion.慢性多通道皮层植入技术的比较:手动插入与机械插入
J Neurosci Methods. 2005 Mar 30;142(2):169-76. doi: 10.1016/j.jneumeth.2004.08.009.
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An economical multi-channel cortical electrode array for extended periods of recording during behavior.一种经济的多通道皮质电极阵列,用于行为期间的长时间记录。
J Neurosci Methods. 2005 Mar 15;142(1):97-105. doi: 10.1016/j.jneumeth.2004.07.018.
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Neuroprotection in Huntington's disease: a 2-year study on minocycline.亨廷顿舞蹈病中的神经保护作用:米诺环素的两年研究
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Minocycline inhibits apoptotic cell death via attenuation of TNF-alpha expression following iNOS/NO induction by lipopolysaccharide in neuron/glia co-cultures.在神经元/神经胶质细胞共培养物中,脂多糖诱导诱导型一氧化氮合酶/一氧化氮(iNOS/NO)后,米诺环素通过减弱肿瘤坏死因子-α(TNF-α)的表达来抑制凋亡性细胞死亡。
J Neurochem. 2004 Nov;91(3):568-78. doi: 10.1111/j.1471-4159.2004.02780.x.
10
Minocycline inhibits neuronal death and glial activation induced by beta-amyloid peptide in rat hippocampus.米诺环素可抑制大鼠海马中由β-淀粉样肽诱导的神经元死亡和胶质细胞激活。
Glia. 2004 Oct;48(1):85-90. doi: 10.1002/glia.20051.

米诺环素可提高慢性神经记录的质量和时长。

Minocycline increases quality and longevity of chronic neural recordings.

作者信息

Rennaker R L, Miller J, Tang H, Wilson D A

机构信息

School of Aerospace and Mechanical Engineering, The University of Oklahoma, 865 Asp Ave Felgar Hall 210, Norman, OK 73019, USA.

出版信息

J Neural Eng. 2007 Jun;4(2):L1-5. doi: 10.1088/1741-2560/4/2/L01. Epub 2007 Jan 24.

DOI:10.1088/1741-2560/4/2/L01
PMID:17409469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2291199/
Abstract

Brain/machine interfaces could potentially be used in the treatment of a host of neurological disorders ranging from paralysis to sensory deficits. Insertion of chronic micro-electrode arrays into neural tissue initiates a host of immunological responses, which typically leads to the formation of a cellular sheath around the implant, resulting in the loss of useful signals. Minocycline has been shown to have neuroprotective and neurorestorative effects in certain neural injury and neurodegenerative disease models. This study examined the effects of minocycline administration on the quality and longevity of chronic multi-channel microwire neural implants 1 week and 1 month post-implantation in auditory cortex. The mean signal-to-noise ratio for the minocycline group stabilized at the end of week 1 and remained above 4.6 throughout the following 3 weeks. The control group signal-to-noise ratio dropped throughout the duration of the study and at the end of 4 weeks was 2.6. Furthermore, 68% of electrodes from the minocycline group showed significant stimulus-driven activity at week 4 compared to 12.5% of electrodes in the control group. There was a significant reduction in the number of activated astrocytes around the implant in minocycline subjects, as well as a reduction in total area occupied by activated astrocytes at 1 and 4 weeks.

摘要

脑机接口有可能用于治疗从瘫痪到感觉缺陷等一系列神经系统疾病。将慢性微电极阵列插入神经组织会引发一系列免疫反应,这通常会导致在植入物周围形成细胞鞘,从而导致有用信号的丧失。在某些神经损伤和神经退行性疾病模型中,米诺环素已被证明具有神经保护和神经恢复作用。本研究考察了在听觉皮层植入慢性多通道微丝神经植入物后1周和1个月给予米诺环素对植入物质量和寿命的影响。米诺环素组的平均信噪比在第1周结束时稳定下来,并在接下来的3周内保持在4.6以上。对照组的信噪比在整个研究期间下降,在4周结束时为2.6。此外,与对照组12.5%的电极相比,米诺环素组68%的电极在第4周显示出显著的刺激驱动活动。米诺环素治疗的受试者植入物周围活化星形胶质细胞的数量显著减少,在1周和4周时活化星形胶质细胞占据的总面积也减少。