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培养的皮质神经元在缺氧时突触小泡循环减少。

Reduced Synaptic Vesicle Recycling during Hypoxia in Cultured Cortical Neurons.

作者信息

Fedorovich Sergei, Hofmeijer Jeannette, van Putten Michel J A M, le Feber Joost

机构信息

Laboratory of Biophysics and Cellular Engineering, Institute of Biophysics and Cell Engineering, National Academy of Sciences of Belarus Minsk, Belarus.

Clinical Neurophysiology, University of TwenteEnschede, Netherlands; Department of Neurology, Rijnstate HospitalArnhem, Netherlands.

出版信息

Front Cell Neurosci. 2017 Feb 16;11:32. doi: 10.3389/fncel.2017.00032. eCollection 2017.

Abstract

Improvement of neuronal recovery in the ischemic penumbra, an area around the core of a brain infarct with some remaining perfusion, has a large potential for the development of therapy against acute ischemic stroke. However, mechanisms that lead to either recovery or secondary damage in the penumbra largely remain unclear. Recent studies in cultured networks of cortical neurons showed that failure of synaptic transmission (referred to as synaptic failure) is a critical factor in the penumbral area, but the mechanisms that lead to synaptic failure are still under investigation. Here we used a Styryl dye, FM1-43, to quantify endocytosis and exocytosis in cultures of rat cortical neurons under normoxic and hypoxic conditions. Hypoxia in cultured cortical networks rapidly depressed endocytosis and, to a lesser extent, exocytosis. These findings support electrophysiological findings that synaptic failure occurs quickly after the induction of hypoxia, and confirms that the failing processes are at least in part presynaptic.

摘要

改善缺血半暗带(即脑梗死核心周围仍有一定灌注的区域)的神经元恢复,对于开发急性缺血性中风的治疗方法具有很大潜力。然而,导致半暗带恢复或继发性损伤的机制在很大程度上仍不清楚。最近在皮质神经元培养网络中的研究表明,突触传递失败(称为突触失效)是半暗带区域的一个关键因素,但导致突触失效的机制仍在研究中。在这里,我们使用一种苯乙烯基染料FM1-43来量化常氧和低氧条件下大鼠皮质神经元培养物中的内吞作用和外排作用。培养的皮质网络中的低氧迅速抑制内吞作用,并在较小程度上抑制外排作用。这些发现支持了电生理研究结果,即低氧诱导后突触失效迅速发生,并证实失效过程至少部分是突触前的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f146/5311063/d1bf051b5118/fncel-11-00032-g0001.jpg

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