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Mechanisms underlying orientation selectivity of neurons in the primary visual cortex of the macaque.

机译:猕猴初级视觉皮层中神经元定向选择性的潜在机制。

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摘要

1. Effects of blocking intracortical inhibition by microiontophoretic administration of bicuculline methiodide (BMI), a selective antagonist for GABAA receptors, on orientation selectivity of 109 neurones were studied in the primary visual cortex (V1) of anaesthetized and paralysed monkeys. 2. The averaged orientation tuning of visual responses of cells was poor in cytochrome oxidaserich blobs of layer II/III and in layer IVc beta, moderate in layers IVb, IVc alpha and V, and sharp in the interblob region of layer II/III and in layers IVa and VI. 3. Iontophoretic administration of BMI reduced the sharpness of orientation tuning of cells to a varying extent in each layer. In most cells, furthermore, the originally ineffective stimuli induced visual responses during the BMI administration, suggesting that excitatory inputs evoked by the non-optimally oriented stimuli were masked by GABAergic inhibition. Nevertheless, the maximal facilitation was observed in the response to the optimally or near-optimally oriented stimuli. 4. There was a difference in such an effect of BMI among layers. Orientation selectivity of cells in interblobs in layer II/III and in layer IVb was sensitive to BMI whereas that of cells in layer VI was relatively insensitive to BMI, suggesting a larger contribution of excitatory mechanisms to the orientation selectivity in this layer. 5. In the orientation-selective cells, an analysis of the magnitude of excitation and inhibition evoked by stimuli at various orientations suggests that both inputs tune around the optimal orientation and their magnitudes are almost proportional to each other except at the optimal orientation. This analysis also indicates that the orientation tuning of inhibition had a less prominent peak around the optimal orientation than that of excitation. This dominance of excitation over inhibition around the optimal orientation may function to accentuate the response to the optimally oriented stimulus. 6. These results suggest that, in the monkey V1, the orientation selectivity of cells is largely dependent on the orientation-biased excitatory and inhibitory inputs which have a broader tuning profile, covering from the optimal to null-orientation, than that observed in extracellularly recorded responses at the control level.
机译:1.在麻醉和麻痹的猴子的初级视皮层(V1)中,研究了微离子电泳法对GABAA受体的选择性拮抗物双小分子甲硫氨酸(BMI)对109个神经元的定向选择性的抑制作用。 2.在II / III层和IVc beta层的细胞色素氧化酶丰富的斑点中,细胞视觉反应的平均方向调整很差,在IVb,IVc alpha和V层中等,而在II / III和在第IVa和VI层中。 3. BMI的离子电渗疗法在每层中都不同程度地降低了细胞方向调整的清晰度。此外,在大多数细胞中,最初无效的刺激会在BMI给药期间引起视觉反应,这表明由非最佳定向刺激引起的兴奋性输入被GABA能抑制所掩盖。然而,在对最佳或接近最佳定向的刺激的反应中观察到最大的促进作用。 4.各层之间的BMI效果有所不同。 II / III层和IVb层中的blob中的细胞的定向选择性对BMI敏感,而VI层中的细胞对BMI相对不敏感,表明兴奋机制对这一层的定向选择性有较大贡献。 5.在方向选择单元中,对各种方向上的刺激引起的激发和抑制的幅度的分析表明,两个输入都围绕最佳方向进行调整,除了在最佳方向上,它们的大小几乎彼此成比例。该分析还表明,抑制的定向调谐在最佳定向周围的峰不如激发的峰突出。围绕最优定向的抑制上的激发主导作用可以用来增强对最优定向刺激的响应。 6.这些结果表明,在猴子V1中,细胞的方向选择性在很大程度上取决于方向偏向的兴奋性和抑制性输入,这些输入具有比在细胞外观察到的更宽的调节范围,从最佳方向到无效方向。在控制级别记录响应。

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