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神经性疼痛期间脊髓背角浅层突触前电压门控钙通道的功能重塑

Functional remodeling of presynaptic voltage-gated calcium channels in superficial layers of the dorsal horn during neuropathic pain.

作者信息

Ferron Laurent, Harding Erika K, Gandini Maria A, Brideau Craig, Stys Peter K, Zamponi Gerald W

机构信息

Department of Clinical Neurosciences, Hotchkiss Brain Institute, Calgary Cumming School of Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta T2N 4N1, Canada.

出版信息

iScience. 2024 May 14;27(6):109973. doi: 10.1016/j.isci.2024.109973. eCollection 2024 Jun 21.

Abstract

N- and P/Q-type voltage-gated Ca channels are critical for synaptic transmission. While their expression is increased in the dorsal root ganglion (DRG) neuron cell bodies during neuropathic pain conditions, less is known about their synaptic remodeling. Here, we combined genetic tools with 2-photon Ca imaging to explore the functional remodeling that occurs in central presynaptic terminals of DRG neurons during neuropathic pain. We imaged GCaMP6s fluorescence responses in an spinal cord preparation from mice expressing GCaMP6s in Trpv1-Cre lineage nociceptors. We show that Ca transient amplitude is increased in central terminals of these neurons after spared nerve injury, and that this increase is mediated by both N- and P/Q-type channels. We found that GABA-B receptor-dependent inhibition of Ca transients was potentiated in the superficial layer of the dorsal horn. Our results provide direct evidence toward nerve injury-induced functional remodeling of presynaptic Ca channels in Trpv1-lineage nociceptor terminals.

摘要

N型和P/Q型电压门控钙通道对突触传递至关重要。虽然在神经性疼痛状态下它们在背根神经节(DRG)神经元胞体中的表达会增加,但对其突触重塑的了解较少。在这里,我们将基因工具与双光子钙成像相结合,以探索神经性疼痛期间DRG神经元中枢突触前终末发生的功能重塑。我们在表达Trpv1-Cre谱系伤害感受器中表达GCaMP6s的小鼠脊髓标本中对GCaMP6s荧光反应进行成像。我们发现,在 spared nerve injury后,这些神经元的中枢终末中钙瞬变幅度增加,并且这种增加由N型和P/Q型通道介导。我们发现,在背角浅层中,GABA-B受体依赖性对钙瞬变的抑制作用增强。我们的结果为神经损伤诱导Trpv1谱系伤害感受器终末突触前钙通道的功能重塑提供了直接证据。

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