February 1994
Volume 35, Issue 2
Free
Articles  |   February 1994
Electroretinogram recovery in the rabbit after repetitive short-term ischemia in light and dark.
Author Affiliations
  • S Y Kim
    Department of Ophthalmology, Stanford University School of Medicine, CA 94305-5308.
  • M S Nayak
    Department of Ophthalmology, Stanford University School of Medicine, CA 94305-5308.
  • M Kita
    Department of Ophthalmology, Stanford University School of Medicine, CA 94305-5308.
  • M F Marmor
    Department of Ophthalmology, Stanford University School of Medicine, CA 94305-5308.
Investigative Ophthalmology & Visual Science February 1994, Vol.35, 664-668. doi:
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    • Get Citation

      S Y Kim, M S Nayak, M Kita, M F Marmor; Electroretinogram recovery in the rabbit after repetitive short-term ischemia in light and dark.. Invest. Ophthalmol. Vis. Sci. 1994;35(2):664-668.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: To determine the time course and reproducibility of electroretinogram recovery after short-term (5- to 20-minute) retinal ischemia in the light and in the dark. METHODS: Electroretinogram recovery was measured in Dutch rabbits after 5-, 10-, or 20-minute episodes of ocular ischemia, repeated three times at 1-hour intervals. Results were compared under light- and dark-adapted conditions. RESULTS: The rate of b-wave recovery was highly reproducible after repetitive ischemic insults in the same eye. The rate of b-wave recovery varied in proportion to the duration of ischemia but generally reached 100% of preischemic levels within 45 to 60 minutes. Recovery was slower under dark-adapted conditions than under light-adapted conditions, and 10 minutes of ischemia appeared to be a critical duration to maximize light- and dark-adapted metabolic differences. CONCLUSIONS: Because of the speed and reproducibility of electroretinogram recovery, the use of short-term ischemic episodes may facilitate studies on the pharmacologic therapy of retinal ischemia. It remains to be determined, however, whether the retinal effects of short-term ischemia are mediated by the same mechanisms as the effects of longer-term ischemia.

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