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The multi-focal electroretinography (mERG)is a new technique to evaluate objectively the visual function and characterized by observing the function change in focal retina quantitatively. The recording condition is very rigorous and the relative position between the eye and stimuli field must be kept to obtain accurate results. In experiments, the albino Sprague-Dawley rats were kept on a special platform, which can be moved in three dimensions, and the distance between the tested eye and CRT were controlled by a self made apparatus. A silver chloride loop electrode was contacted with corneal limbus as recording electrode. The waveforms of dark-adapted mERG in albino rats were stable, clear and repeatable in focal retina. The amplitudes of a and b waves in upper field were greater than those in lower field while the latencies were shorter. There was no large-amplitude area just like the human macular. This procedure paves the way for evaluating objectively functional change in focal retina in laboratory anima

作者:张作明;顾永昊;李莉;龙潭

来源:第四军医大学学报 2002 年 23卷 11期

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作者:
张作明;顾永昊;李莉;龙潭
来源:
第四军医大学学报 2002 年 23卷 11期
标签:
多焦视网膜电图 大鼠 眼电生理
The multi-focal electroretinography (mERG)is a new technique to evaluate objectively the visual function and characterized by observing the function change in focal retina quantitatively. The recording condition is very rigorous and the relative position between the eye and stimuli field must be kept to obtain accurate results. In experiments, the albino Sprague-Dawley rats were kept on a special platform, which can be moved in three dimensions, and the distance between the tested eye and CRT were controlled by a self made apparatus. A silver chloride loop electrode was contacted with corneal limbus as recording electrode. The waveforms of dark-adapted mERG in albino rats were stable, clear and repeatable in focal retina. The amplitudes of a and b waves in upper field were greater than those in lower field while the latencies were shorter. There was no large-amplitude area just like the human macular. This procedure paves the way for evaluating objectively functional change in focal retina in laboratory anima