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通过直接、聚焦地沉默神经元活动来进行行为控制。

Behavioral control through the direct, focal silencing of neuronal activity.

机构信息

Department of Chemistry, Stanford University, 333 Campus Drive, Stanford, CA 94305, USA.

Department of Integrative Biology, University of Wisconsin-Madison, 121 Integrative Biology Research Building, 1117 W Johnson St, Madison, WI 53706, USA.

出版信息

Cell Chem Biol. 2024 Jul 18;31(7):1324-1335.e20. doi: 10.1016/j.chembiol.2024.04.003. Epub 2024 May 9.

Abstract

The ability to optically stimulate and inhibit neurons has revolutionized neuroscience research. Here, we present a direct, potent, user-friendly chemical approach for optically silencing neurons. We have rendered saxitoxin (STX), a naturally occurring paralytic agent, transiently inert through chemical protection with a previously undisclosed nitrobenzyl-derived photocleavable group. Exposing the caged toxin, STX-bpc, to a brief (5 ms) pulse of light effects rapid release of a potent STX derivative and transient, spatially precise blockade of voltage-gated sodium channels (Nas). We demonstrate the efficacy of STX-bpc for parametrically manipulating action potentials in mammalian neurons and brain slice. Additionally, we show the effectiveness of this reagent for silencing neural activity by dissecting sensory-evoked swimming in larval zebrafish. Photo-uncaging of STX-bpc is a straightforward method for non-invasive, reversible, spatiotemporally precise neural silencing without the need for genetic access, thus removing barriers for comparative research.

摘要

光学刺激和抑制神经元的能力彻底改变了神经科学研究。在这里,我们提出了一种直接、有效、用户友好的化学方法,用于光沉默神经元。我们通过用以前未公开的硝基苄基衍生的光可裂解基团进行化学保护,使天然存在的麻痹剂石房蛤毒素 (STX) 暂时失活。将笼状毒素 STX-bpc 暴露于短暂(5 毫秒)的光脉冲下,会导致强效 STX 衍生物的快速释放,并瞬时、精确地阻断电压门控钠离子通道 (Nas)。我们证明了 STX-bpc 在哺乳动物神经元和脑片中对动作电位进行参数化操作的有效性。此外,我们还通过剖析幼虫斑马鱼的感觉诱发游泳来展示该试剂用于沉默神经活动的有效性。STX-bpc 的光解笼是一种简单的非侵入性、可逆、时空精确的神经沉默方法,无需遗传操作,从而消除了比较研究的障碍。

相似文献

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Behavioral control through the direct, focal silencing of neuronal activity.通过直接、聚焦地沉默神经元活动来进行行为控制。
Cell Chem Biol. 2024 Jul 18;31(7):1324-1335.e20. doi: 10.1016/j.chembiol.2024.04.003. Epub 2024 May 9.

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