Long-term spontaneous membrane currents in DRG neurons.

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Receptors and Signal Transduction Pub Date : 2025-06-01 Epub Date: 2025-04-05 DOI:10.1080/10799893.2025.2477925
Sodikdjon A Kodirov, Vera B Plakhova, Owen P Hamill, Boris V Krylov
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Abstract

We have experimented with freshly isolated single DRG neurons from neonatal (P0-5) rats to study currents mediated by voltage dependent Na+ (Nav) channels. All experiments were performed using the whole-cell mode of patch-clamp electrophysiology and following the standard steps of this technique. However, in a subgroup of neurons, spontaneous events resembling neurotransmitter release were observed under conditions optimized for whole-cell patch-clamp recordings of INa. All events have a fast rise phase (similar to responses of receptor channels), but decay in a heterogeneous manner. The waveform of the event closely matches that of the response of the purinergic receptor P2X type to ATP. This new activity in neurons was observed at -60 mV and was facilitated during relatively strong hyperpolarization. Although spontaneous fluctuations, termed membrane potential instabilities, are described in DRG neurons, the observed inward currents at more hyperpolarized states are distinct and novel. The spontaneous heterogeneous activities could be relevant to the elucidation of pain mechanisms by distinct pharmacological tools.

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DRG神经元的长期自发膜电流。
我们用新生(P0-5)大鼠新鲜分离的单DRG神经元进行实验,研究电压依赖性Na+ (Nav)通道介导的电流。所有实验均采用膜片钳电生理全细胞模式,并按照该技术的标准步骤进行。然而,在一组神经元中,在优化的全细胞膜片钳记录INa的条件下,观察到类似神经递质释放的自发事件。所有事件都有一个快速上升阶段(类似于受体通道的反应),但以异质方式衰减。该事件的波形与嘌呤能受体P2X型对ATP的响应密切匹配。神经元的这种新活动在-60毫伏时被观察到,并在相对强的超极化时被促进。虽然自发波动,称为膜电位不稳定性,描述了在DRG神经元,观察到的内向电流在更多的超极化状态是独特的和新颖的。自发的异质性活动可能与不同的药理工具阐明疼痛机制有关。
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来源期刊
Journal of Receptors and Signal Transduction
Journal of Receptors and Signal Transduction 生物-生化与分子生物学
CiteScore
6.60
自引率
0.00%
发文量
19
审稿时长
>12 weeks
期刊介绍: Journal of Receptors and Signal Tranduction is included in the following abstracting and indexing services: BIOBASE; Biochemistry and Biophysics Citation Index; Biological Abstracts; BIOSIS Full Coverage Shared; BIOSIS Previews; Biotechnology Abstracts; Current Contents/Life Sciences; Derwent Chimera; Derwent Drug File; EMBASE; EMBIOLOGY; Journal Citation Reports/ Science Edition; PubMed/MedLine; Science Citation Index; SciSearch; SCOPUS; SIIC.
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