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去甲肾上腺素转运体的膜片钳和安培测量记录:通道活性与电压依赖性摄取

Patch-clamp and amperometric recordings from norepinephrine transporters: channel activity and voltage-dependent uptake.

作者信息

Galli A, Blakely R D, DeFelice L J

机构信息

Department of Pharmacology and Center for Molecular Neuroscience, Vanderbilt University Medical Center, Nashville TN 37232-6600, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13260-5. doi: 10.1073/pnas.95.22.13260.

Abstract

Transporters for the biogenic amines dopamine, norepinephrine, epinephrine and serotonin are largely responsible for transmitter inactivation after release. They also serve as high-affinity targets for a number of clinically relevant psychoactive agents, including antidepressants, cocaine, and amphetamines. Despite their prominent role in neurotransmitter inactivation and drug responses, we lack a clear understanding of the permeation pathway or regulation mechanisms at the single transporter level. The resolution of radiotracer-based flux techniques limits the opportunities to dissect these problems. Here we combine patch-clamp recording techniques with microamperometry to record the transporter-mediated flux of norepinephrine across isolated membrane patches. These data reveal voltage-dependent norepinephrine flux that correlates temporally with antidepressant-sensitive transporter currents in the same patch. Furthermore, we resolve unitary flux events linked with bursts of transporter channel openings. These findings indicate that norepinephrine transporters are capable of transporting neurotransmitter across the membrane in discrete shots containing hundreds of molecules. Amperometry is used widely to study neurotransmitter distribution and kinetics in the nervous system and to detect transmitter release during vesicular exocytosis. Of interest regarding the present application is the use of amperometry on inside-out patches with synchronous recording of flux and current. Thus, our results further demonstrate a powerful method to assess transporter function and regulation.

摘要

生物胺多巴胺、去甲肾上腺素、肾上腺素和5-羟色胺的转运体在递质释放后对递质失活起主要作用。它们也是许多临床相关精神活性药物的高亲和力靶点,包括抗抑郁药、可卡因和安非他明。尽管它们在神经递质失活和药物反应中起着重要作用,但我们对单个转运体水平的渗透途径或调节机制仍缺乏清晰的认识。基于放射性示踪剂的通量技术的分辨率限制了剖析这些问题的机会。在这里,我们将膜片钳记录技术与微电流测定法相结合,以记录去甲肾上腺素通过分离的膜片的转运体介导的通量。这些数据揭示了电压依赖性去甲肾上腺素通量,其在时间上与同一膜片中对抗抑郁药敏感的转运体电流相关。此外,我们解析了与转运体通道开放爆发相关的单位通量事件。这些发现表明,去甲肾上腺素转运体能够以包含数百个分子的离散脉冲形式将神经递质转运过膜。微电流测定法被广泛用于研究神经系统中神经递质的分布和动力学,以及检测囊泡胞吐过程中的递质释放。关于本应用,有趣的是在内外翻转膜片上使用微电流测定法同时记录通量和电流。因此,我们的结果进一步证明了一种评估转运体功能和调节的强大方法。

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