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首页> 外文期刊>Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism >Optogenetic assessment of VIP, PV, SOM and NOS inhibitory neuron activity and cerebral blood flow regulation in mouse somato-sensory cortex
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Optogenetic assessment of VIP, PV, SOM and NOS inhibitory neuron activity and cerebral blood flow regulation in mouse somato-sensory cortex

机译:VIP,PV,SOM和NOS抑制神经元活性和小鼠躯体索米感觉皮质中的脑血流量调节的致敏评估

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The impact of different neuronal populations on local cerebral blood flow (CBF) regulation is not well known and insight into these relationships could enhance the interpretation of brain function and dysfunction from brain imaging data. We investigated the role of sub-types of inhibitory neuron activity on the regulation of CBF using optogenetics, laser Doppler flowmetry and different transgenic mouse models (parvalbumin (PV), vasoactive intestinal peptide (VIP), somatostatin (SOM) and nitric oxide synthase (NOS)). Whisker stimulation was used to verify that typical CBF responses were obtained in all mice. Photo-stimulation of SOM-cre and NOS-cre mice produced significant increases in CBF that were similar to whisker responses. In NOS-cre mice, CBF responses scaled with the photo-stimulus pulse duration and frequency. In SOM-cre mice, CBF increases were followed by decreases. In VIP-cre mice, photo-stimulation did not consistently produce significant changes in CBF, while slower increases in CBF that peaked 14-18 s after stimulation onset were observed in PV-cre mice. Control experiments performed in non-expressing regions showed no changes in CBF. These findings suggest that dysfunction in NOS or SOM neurons can have a significant impact on vascular responses that are detected by brain imaging methods like functional magnetic resonance imaging (fMRI).
机译:不同神经元群对局部脑血流量(CBF)调节的影响是不公知的,并且洞察这些关系可以增强脑成像数据的脑功能和功能障碍的解释。我们研究了使用光学机构,激光多普勒流动性和不同转基因小鼠模型(Parvalbumin(PV),血管活性肠肽(VIP),生长抑素(SOM)和一氧化氮合酶( nos))。晶须刺激用于验证所有小鼠中获得典型的CBF响应。 SOM-CRE和NOS-CRE小鼠的光刺激在类似于晶须反应的CBF产生显着增加。在NoS-Cre小鼠中,CBF响应缩放了光刺激脉冲持续时间和频率。在Som-Cre小鼠中,随后CBF增加。在VIP-CRE小鼠中,光刺激并未始终产生CBF的显着变化,而在PV-CRE小鼠中观察到在刺激发作后达到14-18秒的CBF的较慢增加。在非表达区域中进行的对照实验表明CBF没有变化。这些发现表明,NOS或SOM神经元中的功能障碍可以对由脑成像方法(如功能磁共振成像(FMRI)等)检测的血管响应产生显着影响。

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