May 2003
Volume 44, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2003
Effect of Hydrogen Peroxide on Glutamate and Glycine Concentrations in the Bovine Retina and Vitreous Humor
Author Affiliations & Notes
  • K.H. Kulkarni
    College of Pharmacy, University of Houston, Houston, TX, United States
  • A.M. LeDay
    School of Pharmacy & Health Professions, Creighton University, Omaha, NE, United States
  • C.A. Opere
    School of Pharmacy & Health Professions, Creighton University, Omaha, NE, United States
  • A.K. Dash
    School of Pharmacy & Health Professions, Creighton University, Omaha, NE, United States
  • S.E. Ohia
    School of Pharmacy & Health Professions, Creighton University, Omaha, NE, United States
  • Footnotes
    Commercial Relationships  K.H. Kulkarni, None; A.M. LeDay, None; C.A. Opere, None; A.K. Dash, None; S.E. Ohia, None.
  • Footnotes
    Support  NIH Grant EY13266
Investigative Ophthalmology & Visual Science May 2003, Vol.44, 2237. doi:
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      K.H. Kulkarni, A.M. LeDay, C.A. Opere, A.K. Dash, S.E. Ohia; Effect of Hydrogen Peroxide on Glutamate and Glycine Concentrations in the Bovine Retina and Vitreous Humor . Invest. Ophthalmol. Vis. Sci. 2003;44(13):2237.

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

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Abstract

Abstract: : Evidence from our laboratory indicates that hydrogen peroxide (H2O2) can inhibit potassium (K+)-depolarization evoked [3H]D-aspartate release from bovine isolated retinae (Exp. Eye Res. 71: abs. no. 386, 2000). Purpose: In the present study, we investigated the effect of exogenous H2O2 on glutamate and glycine concentrations in the bovine retina and vitreous humor in an ex vivo eye model. It was of interest to determine whether the observed action of H2O2 on K+-evoked [3H]D-aspartate release could be replicated in an ex vivo model. Methods: Whole eye organ cultures were incubated at 37oC for 15 minutes. After incubation, H2O2 (1 – 100 µM) or sterile distilled water (vehicle) was injected intravitreally into each eye. Thirty minutes after injection, the retina and vitreous humor were removed for analysis of glutamate and glycine concentrations by HPLC with fluorescence detection. Results: H2O2 (1-100 µM) caused a concentration-related decrease in glutamate levels reaching a maximum inhibitory response of 63% at 100 µM. Likewise, low concentrations of H2O2 (1-10 µM) caused a decrease in glutamate levels in the vitreous humor. In contrast, a higher concentration of H2O2 (100 µM) caused a significant (p<0.001) increase in glutamate levels in the vitreous humor. H2O2 (1-100 µM) produced a concentration-dependent decrease in glycine levels in the retina reaching a maximum of 35% at 100 µM. H2O2 (1-10 µM) also caused a decrease in glcyine concentrations in the vitreous humor. Conclusion: We conclude that exogenously administered H2O2 can alter the integrity of endogenous pools of both glutamate and glycine in the posterior segment of the eye.

Keywords: pharmacology • retina: neurochemistry • neurotransmitters/neurotransmitter systems 
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