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J Neurotrauma. 2020 Aug 1;37(15):1729-1739. doi: 10.1089/neu.2019.6973.
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Learning to promote recovery after spinal cord injury.学习促进脊髓损伤后的恢复。
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Glutamate at the Vertebrate Neuromuscular Junction: From Modulation to Neurotransmission.脊椎动物神经肌肉接点处的谷氨酸:从调制到神经传递。
Cells. 2019 Aug 28;8(9):996. doi: 10.3390/cells8090996.
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Adult spinal motoneurons change their neurotransmitter phenotype to control locomotion.成年脊髓运动神经元改变其神经递质表型以控制运动。
Proc Natl Acad Sci U S A. 2018 Oct 16;115(42):E9926-E9933. doi: 10.1073/pnas.1809050115. Epub 2018 Oct 1.
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Metaplasticity within the spinal cord: Evidence brain-derived neurotrophic factor (BDNF), tumor necrosis factor (TNF), and alterations in GABA function (ionic plasticity) modulate pain and the capacity to learn.脊髓内的形质变化:证据表明脑源性神经营养因子(BDNF)、肿瘤坏死因子(TNF)以及 GABA 功能改变(离子型可塑性)调节疼痛和学习能力。
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Neuromuscular NMDA Receptors Modulate Developmental Synapse Elimination.神经肌肉N-甲基-D-天冬氨酸受体调节发育过程中的突触消除。
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证据表明,中枢神经系统可以在神经肌肉接点诱导一种修饰,有助于维持行为反应。

Evidence That the Central Nervous System Can Induce a Modification at the Neuromuscular Junction That Contributes to the Maintenance of a Behavioral Response.

机构信息

Case Comprehensive Cancer Center/Case Western Reserve School of Medicine, Cleveland, Ohio 44106.

U.S. Army Institute of Surgical Research, JBSA Fort Sam Houston, Houston, Texas 78234.

出版信息

J Neurosci. 2020 Nov 25;40(48):9186-9209. doi: 10.1523/JNEUROSCI.2683-19.2020. Epub 2020 Oct 23.

DOI:10.1523/JNEUROSCI.2683-19.2020
PMID:33097637
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7687054/
Abstract

Neurons within the spinal cord are sensitive to environmental relations and can bring about a behavioral modification without input from the brain. For example, rats that have undergone a thoracic (T2) transection can learn to maintain a hind leg in a flexed position to minimize exposure to a noxious electrical stimulation (shock). Inactivating neurons within the spinal cord with lidocaine, or cutting communication between the spinal cord and the periphery (sciatic transection), eliminates the capacity to learn, which implies that it depends on spinal neurons. Here we show that these manipulations have no effect on the maintenance of the learned response, which implicates a peripheral process. EMG showed that learning augments the muscular response evoked by motoneuron output and that this effect survives a sciatic transection. Quantitative fluorescent imaging revealed that training brings about an increase in the area and intensity of ACh receptor labeling at the neuromuscular junction (NMJ). It is hypothesized that efferent motoneuron output, in conjunction with electrical stimulation of the tibialis anterior muscle, strengthens the connection at the NMJ in a Hebbian manner. Supporting this, paired stimulation of the efferent nerve and tibialis anterior generated an increase in flexion duration and augmented the evoked electrical response without input from the spinal cord. Evidence is presented that glutamatergic signaling contributes to plasticity at the NMJ. Labeling for vesicular glutamate transporter is evident at the motor endplate. Intramuscular application of an NMDAR antagonist blocked the acquisition/maintenance of the learned response and the strengthening of the evoked electrical response. The neuromuscular junction (NMJ) is designed to faithfully elicit a muscular contraction in response to neural input. From this perspective, encoding environmental relations (learning) and the maintenance of a behavioral modification over time (memory) are assumed to reflect only modifications upstream from the NMJ, within the CNS. The current results challenge this view. Rats were trained to maintain a hind leg in a flexed position to avoid noxious stimulation. As expected, treatments that inhibit activity within the CNS, or disrupt peripheral communication, prevented learning. These manipulations did not affect the maintenance of the acquired response. The results imply that a peripheral modification at the NMJ contributes to the maintenance of the learned response.

摘要

脊髓内的神经元对环境关系敏感,可以在没有大脑输入的情况下引起行为改变。例如,接受过胸(T2)横断的大鼠可以学会保持后腿弯曲的姿势,以最大程度地减少对有害电刺激(电击)的暴露。用利多卡因使脊髓内的神经元失活,或切断脊髓与周围神经(坐骨神经横断)的通讯,会消除学习能力,这意味着它依赖于脊髓神经元。在这里,我们表明这些操作对所学反应的维持没有影响,这暗示了一个外周过程。肌电图显示,学习增强了运动神经元输出引起的肌肉反应,并且这种效应在坐骨神经横断后仍然存在。定量荧光成像显示,训练会增加运动终板处乙酰胆碱受体标记的面积和强度。有人假设,传出运动神经元的输出,结合对胫骨前肌的电刺激,以赫布式的方式增强 NMJ 上的连接。支持这一点,传出神经和胫骨前肌的成对刺激产生了弯曲持续时间的增加,并增强了没有脊髓输入的诱发电反应。有证据表明,谷氨酸能信号在 NMJ 处发挥作用。囊泡谷氨酸转运体的标记在运动终板处可见。肌内应用 NMDA 受体拮抗剂阻断了学习反应的获得/维持以及诱发电反应的增强。神经肌肉接头(NMJ)旨在忠实地响应神经输入引起肌肉收缩。从这个角度来看,编码环境关系(学习)和随时间维持行为改变(记忆)被认为仅反映 NMJ 上游、中枢神经系统内的改变。当前的结果挑战了这一观点。大鼠被训练保持后腿弯曲的姿势以避免有害刺激。正如预期的那样,抑制中枢神经系统内活动或破坏周围神经通讯的治疗方法阻止了学习。这些操作不会影响已获得反应的维持。结果表明,NMJ 上的外周改变有助于维持学习反应。