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乙醇诱导的大鼠脊髓胶状质抑制性突触传递增强。

Ethanol-induced enhancement of inhibitory synaptic transmission in the rat spinal substantia gelatinosa.

机构信息

1 Department of Neurophysiology, Hyogo College of Medicine, Nishinomiya, Japan.

2 Department of Neuropharmacology, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya, Japan.

出版信息

Mol Pain. 2018 Jan-Dec;14:1744806918817969. doi: 10.1177/1744806918817969. Epub 2018 Nov 19.

Abstract

Recent studies have shown that ethanol produces a widespread modulation of neuronal activity in the central nervous system. It is not fully understood, however, how ethanol changes nociceptive transmission. We investigated acute effects of ethanol on synaptic transmission in the substantia gelatinosa (lamina II of the spinal dorsal horn) and mechanical responses in the spinal dorsal horn. In substantia gelatinosa neurons, bath application of ethanol at low concentration (10 mM) did not change the frequency and amplitude of spontaneous inhibitory postsynaptic currents. At medium to high concentrations (20-100 mM), however, ethanol elicited a barrage of large amplitude spontaneous inhibitory postsynaptic currents. In the presence of tetrodotoxin, such enhancement of spontaneous inhibitory postsynaptic currents was not detected. In addition, ethanol (20-100 mM) increased the frequency of spontaneous discharge of vesicular GABA transporter-Venus-labeled neurons and suppressed the mechanical nociceptive response in wide-dynamic range neurons in the spinal dorsal horn. The present results suggest that ethanol may reduce nociceptive information transfer in the spinal dorsal horn by enhancement of inhibitory GABAergic and glycinergic synaptic transmission.

摘要

最近的研究表明,乙醇会在中枢神经系统中广泛调节神经元的活动。然而,乙醇如何改变伤害性传递还不完全清楚。我们研究了乙醇对脊髓背角胶状质(背角 II 层)中突触传递和机械反应的急性影响。在胶状质神经元中,低浓度(10 mM)的乙醇浴应用并未改变自发性抑制性突触后电流的频率和幅度。然而,在中高浓度(20-100 mM)下,乙醇会引发一连串大振幅的自发性抑制性突触后电流。在加入河豚毒素的情况下,未检测到这种自发性抑制性突触后电流的增强。此外,乙醇(20-100 mM)增加了囊泡 GABA 转运体-Venus 标记神经元的自发性放电频率,并抑制了脊髓背角宽动态范围神经元的机械伤害性反应。本研究结果表明,乙醇可能通过增强抑制性 GABA 能和甘氨酸能突触传递来减少脊髓背角中的伤害性信息传递。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc0f/6293375/65da7caf314e/10.1177_1744806918817969-fig1.jpg

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