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温度对小鼠听觉和运动皮层中 FAD 和 NADH 衍生信号及神经代谢偶联的影响。

Effect of temperature on FAD and NADH-derived signals and neurometabolic coupling in the mouse auditory and motor cortex.

机构信息

Department of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

The Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, 405 North Mathews Avenue, Urbana, IL, 61801, USA.

出版信息

Pflugers Arch. 2017 Dec;469(12):1631-1649. doi: 10.1007/s00424-017-2037-4. Epub 2017 Aug 7.

Abstract

Tight coupling of neuronal metabolism to synaptic activity is critical to ensure that the supply of metabolic substrates meets the demands of neuronal signaling. Given the impact of temperature on metabolism, and the wide fluctuations of brain temperature observed during clinical hypothermia, we examined the effect of temperature on neurometabolic coupling. Intrinsic fluorescence signals of the oxidized form of flavin adenine dinucleotide (FAD) and the reduced form of nicotinamide adenine dinucleotide (NADH), and their ratios, were measured to assess neural metabolic state and local field potentials were recorded to measure synaptic activity in the mouse brain. Brain slice preparations were used to remove the potential impacts of blood flow. Tight coupling between metabolic signals and local field potential amplitudes was observed at a range of temperatures below 29 °C. However, above 29 °C, the metabolic and synaptic signatures diverged such that FAD signals were diminished, but local field potentials retained their amplitude. It was also observed that the declines in the FAD signals seen at high temperatures (and hence the decoupling between synaptic and metabolic events) are driven by low FAD availability at high temperatures. These data suggest that neurometabolic coupling, thought to be critical for ensuring the metabolic health of the brain, may show temperature dependence, and is related to temperature-dependent changes in FAD supplies.

摘要

神经元代谢与突触活动的紧密偶联对于确保代谢底物的供应能够满足神经元信号传递的需求至关重要。鉴于温度对代谢的影响,以及在临床低温期间观察到的脑温广泛波动,我们研究了温度对神经代谢偶联的影响。通过测量黄素腺嘌呤二核苷酸(FAD)氧化形式和烟酰胺腺嘌呤二核苷酸(NADH)还原形式的固有荧光信号及其比值,评估神经代谢状态,并记录局部场电位以测量小鼠大脑中的突触活动。使用脑切片制备物来消除血流的潜在影响。在低于 29°C 的一系列温度下,观察到代谢信号和局部场电位幅度之间的紧密偶联。然而,在 29°C 以上,代谢和突触特征出现分歧,使得 FAD 信号减弱,但局部场电位保持其幅度。还观察到,在高温下(因此,突触和代谢事件之间的解偶联)观察到的 FAD 信号下降是由高温下 FAD 供应不足驱动的。这些数据表明,神经代谢偶联被认为对于确保大脑的代谢健康至关重要,但可能表现出温度依赖性,并且与 FAD 供应的温度依赖性变化有关。

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本文引用的文献

1
Translational MR Neuroimaging of Stroke and Recovery.
Transl Stroke Res. 2017 Feb;8(1):22-32. doi: 10.1007/s12975-016-0497-z. Epub 2016 Aug 31.
2
Realistic Numerical and Analytical Modeling of Light Scattering in Brain Tissue for Optogenetic Applications(1,2,3).
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3
Neurovascular coupling in humans: Physiology, methodological advances and clinical implications.
J Cereb Blood Flow Metab. 2016 Apr;36(4):647-64. doi: 10.1177/0271678X15617954. Epub 2015 Nov 24.
6
Specific distribution of non-phosphorylated neurofilaments characterizing each subfield in the mouse auditory cortex.
Neurosci Lett. 2015 Oct 8;606:182-7. doi: 10.1016/j.neulet.2015.08.055. Epub 2015 Sep 2.
7
MITOCHONDRIAL REDOX IMAGING FOR CANCER DIAGNOSTIC AND THERAPEUTIC STUDIES.
J Innov Opt Health Sci. 2009 Oct;2(4):325-341. doi: 10.1142/S1793545809000735.
8
A cellular perspective on brain energy metabolism and functional imaging.
Neuron. 2015 May 20;86(4):883-901. doi: 10.1016/j.neuron.2015.03.035.
9
A reliable model for gamma oscillations in hippocampal tissue.
J Neurosci Res. 2015 Jul;93(7):1067-78. doi: 10.1002/jnr.23590. Epub 2015 Mar 24.
10
Temperature controls oxidative phosphorylation and reactive oxygen species production through uncoupling in rat skeletal muscle mitochondria.
Free Radic Biol Med. 2015 Jun;83:12-20. doi: 10.1016/j.freeradbiomed.2015.02.012. Epub 2015 Feb 17.

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