October 1993
Volume 34, Issue 11
Free
Articles  |   October 1993
Effects of experimentally induced ischemia on dopamine metabolism in rabbit retina.
Author Affiliations
  • W Cao
    Department of Ophthalmology, Faculty of Medicine, Sherbrooke University, Quebec, Canada.
  • A Drumheller
    Department of Ophthalmology, Faculty of Medicine, Sherbrooke University, Quebec, Canada.
  • M Zaharia
    Department of Ophthalmology, Faculty of Medicine, Sherbrooke University, Quebec, Canada.
  • G Lafond
    Department of Ophthalmology, Faculty of Medicine, Sherbrooke University, Quebec, Canada.
  • J R Brunette
    Department of Ophthalmology, Faculty of Medicine, Sherbrooke University, Quebec, Canada.
  • F B Jolicoeur
    Department of Ophthalmology, Faculty of Medicine, Sherbrooke University, Quebec, Canada.
Investigative Ophthalmology & Visual Science October 1993, Vol.34, 3140-3146. doi:
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      W Cao, A Drumheller, M Zaharia, G Lafond, J R Brunette, F B Jolicoeur; Effects of experimentally induced ischemia on dopamine metabolism in rabbit retina.. Invest. Ophthalmol. Vis. Sci. 1993;34(11):3140-3146.

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

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Abstract

PURPOSE: To determine the role of dopamine in experimentally induced retinal ischemia. Experiment 1 was designed to study the effects of ischemic levels on dopamine (DA) metabolism. Experiment 2 evaluated the effects of ischemic duration on DA metabolism. The effects of recirculation time after ischemia on DA metabolism were investigated in experiment 3. METHODS: Ischemia was produced by raising intraocular pressure (IOP) in rabbits. Three levels of ischemia were used--level A, level B, and level C--representing 50%, 75%, and 100%, respectively, of the IOP necessary to produce total ischemia. Retinal levels of DA and its main metabolites, homovanillic acid (HVA) and 3,4-dihydroxyphenylacetic acid (DOPAC), were measured by high-performance liquid chromatography with electrochemical detection. RESULTS: Experiment 1 showed that at ischemic level B, DA contents were significantly reduced, but neither DOPAC nor HVA concentrations were altered. The reductions of retinal DA, DOPAC, and HVA concentrations were seen at level C without altering the ratio index. Level A ischemia did not alter DA metabolism. In experiment 2, significant reductions in DA, DOPAC, and HVA concentrations were found at both 30 and 60 minutes in the ischemic group, whereas the ratio DOPAC/DA and (HVA + DOPAC)/DA were significantly decreased only in the 60-minute ischemic group. Five-minute total ischemia did not alter DA metabolism. In experiment 3, concentrations of DA were still significantly decreased at 30 minutes of recirculation after ischemia, but DOPAC and HVA levels were back to normal. However, the ratios of DOPAC/DA, HVA/DA, and (HVA + DOPAC)/DA were significantly elevated. After 90 and 240 minutes of recirculation, retinal DA contents had returned to normal values, but DOPAC and HVA concentrations as well as all ratio indices of DA metabolism were still enhanced. CONCLUSION: Dopamine metabolism is altered during and after retinal ischemia. Dopamine may play a contributing role in ischemia.

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