首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Low-threshold primary afferent drive onto GABAergic interneurons in the superficial dorsal horn of the mouse.
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Low-threshold primary afferent drive onto GABAergic interneurons in the superficial dorsal horn of the mouse.

机译:低阈值初级传入驱动到小鼠浅表背角的GABA能中间神经元。

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摘要

Inhibition in the spinal cord dorsal horn is crucial for maintaining separation of touch and pain modalities. Disruption of this inhibition results in allodynia, allowing low-threshold drive onto pain and temperature-sensitive projection neurons. This low-threshold (LT) excitatory pathway is normally under strong inhibition. We hypothesized that superficial dorsal horn inhibitory neurons, which would be ideally located to suppress LT drive onto projection neurons in a feedforward manner, are driven by LT input. In addition, because disinhibition-induced allodynia shares some features with the immature dorsal horn such as elevated sensitivity to LT input, we also questioned whether LT drive onto inhibitory neurons changes during postnatal maturation. To investigate these questions, slices were made at different ages from transgenic mice with enhanced green fluorescent protein expression in GABAergic neurons and whole-cell recordings were made from these fluorescent neurons. Evoked synaptic activity was measured in response to electrical stimulation of the dorsal root. We demonstrate that Abeta fibers activate a significant proportion of superficial dorsal horn GABAergic neurons. This occurs with similar excitatory synaptic drive throughout postnatal maturation, but with a greater prevalence at younger ages. These GABAergic neurons are well situated to contribute to suppressing LT activation of output projection neurons. In addition, the majority of these GABAergic neurons also had convergent input from high-threshold fibers, suggesting that this novel subclass of GABAergic neurons is important for gating innocuous as well as noxious information.
机译:脊髓背角的抑制对于维持触觉和疼痛模式的分离至关重要。这种抑制的破坏导致异常性疼痛,允许低阈值驱动疼痛和温度敏感的投射神经元。这种低阈值 (LT) 兴奋性通路通常受到强烈抑制。我们假设浅表背角抑制神经元是由 LT 输入驱动的,其理想位置是以前馈方式抑制 LT 驱动到投射神经元上的理想位置。此外,由于去抑制诱导的异常性疼痛与未成熟的背角有一些共同的特征,例如对 LT 输入的敏感性升高,我们还质疑 LT 驱动抑制性神经元在出生后成熟过程中是否发生变化。为了研究这些问题,从GABA能神经元中绿色荧光蛋白表达增强的转基因小鼠中制作了不同年龄的切片,并从这些荧光神经元中进行了全细胞记录。在对背根的电刺激的响应下测量诱发的突触活动。我们证明 Abeta 纤维激活了很大一部分浅表背角 GABA 能神经元。在整个出生后成熟过程中,这发生在类似的兴奋性突触驱动中,但在年轻时患病率更高。这些GABA能神经元处于有利位置,有助于抑制输出投射神经元的LT激活。此外,这些GABA能神经元中的大多数也具有来自高阈值纤维的收敛输入,这表明GABA能神经元的这一新亚类对于门控无害和有害信息很重要。

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