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Noisy Spiking in Visual Area V2 of Amblyopic Monkeys

机译:弱视猴子的视觉区域V2中的尖峰噪声

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摘要

Interocular decorrelation of input signals in developing visual cortex can cause impaired binocular vision and amblyopia. Although increased intrinsic noise is thought to be responsible for a range of perceptual deficits in amblyopic humans, the neural basis for the elevated perceptual noise in amblyopic primates is not known. Here, we tested the idea that perceptual noise is linked to the neuronal spiking noise (variability) resulting from developmental alterations in cortical circuitry. To assess spiking noise, we analyzed the contrast-dependent dynamics of spike counts and spiking irregularity by calculating the square of the coefficient of variation in interspike intervals (CV2) and the trial-to-trial fluctuations in spiking, or mean matched Fano factor (m-FF) in visual area V2 of monkeys reared with chronic monocular defocus. In amblyopic neurons, the contrast versus response functions and the spike count dynamics exhibited significant deviations from comparable data for normal monkeys. The CV2 was pronounced in amblyopic neurons for high-contrast stimuli and the m-FF was abnormally high in amblyopic neurons for low-contrast gratings. The spike count, CV2, and m-FF of spontaneous activity were also elevated in amblyopic neurons. These contrast-dependent spiking irregularities were correlated with the level of binocular suppression in these V2 neurons and with the severity of perceptual loss for individual monkeys. Our results suggest that the developmental alterations in normalization mechanisms resulting from early binocular suppression can explain much of these contrast-dependent spiking abnormalities in V2 neurons and the perceptual performance of our amblyopic monkeys.>SIGNIFICANCE STATEMENT Amblyopia is a common developmental vision disorder in humans. Despite the extensive animal studies on how amblyopia emerges, we know surprisingly little about the neural basis of amblyopia in humans and nonhuman primates. Although the vision of amblyopic humans is often described as being noisy by perceptual and modeling studies, the exact nature or origin of this elevated perceptual noise is not known. We show that elevated and noisy spontaneous activity and contrast-dependent noisy spiking (spiking irregularity and trial-to-trial fluctuations in spiking) in neurons of visual area V2 could limit the visual performance of amblyopic primates. Moreover, we discovered that the noisy spiking is linked to a high level of binocular suppression in visual cortex during development.
机译:视觉皮层发育过程中输入信号的眼间去相关会导致双眼视力受损和弱视。尽管人们认为固有噪声的增加是弱视人类一系列感知缺陷的原因,但尚不清楚弱视灵长类动物的感知噪声升高的神经基础。在这里,我们测试了感知噪声与皮层电路发育变化导致的神经元尖峰噪声(变异性)有关的想法。为了评估尖峰噪声,我们通过计算尖峰间间隔(CV 2 )的方差变异系数的平方和从尖峰到尖峰的不规则性,分析了尖峰计数和尖峰不规则性的对比相关动力学。在患有慢性单眼散焦的猴子的视觉区域V2中出现峰值或均值匹配的Fano因子(m-FF)。在弱视神经元中,对比函数与响应函数以及峰值计数动力学表现出与正常猴子的可比数据显着不同。对于高对比度刺激,弱视神经元中的CV 2 明显,对于低对比度光栅,弱视神经元中的m-FF异常高。弱视神经元的峰值计数,CV 2 和自发活动的m-FF也升高。这些依赖于对比的尖峰不规则现象与这些V2神经元的双眼抑制水平以及单个猴子的知觉丧失严重程度相关。我们的结果表明,早期双眼抑制导致归一化机制的发展变化可以解释V2神经元中这些依赖于对比的尖峰异常以及弱视猴子的感知能力。>重要意义声明人类的发育性视觉障碍。尽管对弱视如何出现进行了广泛的动物研究,但我们对人类和非人类灵长类动物的弱视的神经基础知之甚少。尽管通过感知和模型研究通常将弱视人类的视觉描述为嘈杂的,但这种未知感知噪声的确切性质或来源尚不清楚。我们显示视觉区域V2的神经元中升高的嘈杂的自发活动和依赖于对比的嘈杂的尖峰(尖峰的不规则性和从试验到试验的波动)可能会限制弱视灵长类动物的视觉表现。此外,我们发现,嘈杂的尖峰与发育过程中视皮层的高双目抑制有关。

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