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1 Department of Ophthalmology, The Jikei University, Tokyo, Nishi-shimbashi, Japan
2 Optometry and Vision Sciences, The University of Melbourne, Melbourne, Victoria, Australia
3 Optometry and Vision Sciences, The University of Melbourne, Corner, Cardigan & Kepple Streets, Melbourne, Victoria, 3010, Australia
* To whom correspondence should be addressed. E-mail: bvb{at}unimelb.edu.au.
| Abstract |
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PURPOSE. Diabetes is known to alter retinal function as measured with the electroretinogram (ERG) where a propensity is found for inner-retinal, oscillatory potential (OPs) abnormalities. However the effect that diabetes has on other ganglion cell-related responses is not known. This study reports a systematic evaluation of streptozotocin (STZ) diabetes related ERG changes in rats for the first 11 weeks post-diabetogenesis.
METHODS. Thirty, Sprague-Dawley rats were randomly assigned to treated (50 mg/kg STZ (n = 16) and control groups (1 mL/kg citrate buffer, n = 14) at 6 weeks of age. Two controls and 4 STZ animals were excluded due to blood glucose criteria or systemic complications. Diabetic animals were given daily subcutaneous injections of 1-2 units of long-acting insulin. ERGs were measured at 4, 8 and 11 weeks after treatment. The a-wave was used as an index of outer-retinal function whereas b-wave, OPs and the scotopic threshold response (STR) were used as indices of inner retinal function.
RESULTS. Photoreceptoral (a-wave) and bipolar cell (b-wave) responses were not significantly reduced by STZ treatment. OPs were significantly reduced by 8 weeks (-25 ± 7%, P
0.05). The most severely affected component was the ganglion cell dominated positive STR, which was significantly decreased from the first time-point (-51 ± 11% at 4 weeks, P
0.05), but the negative component was unaffected over the 11 week period.
CONCLUSIONS. The ganglion cell dominated pSTR showed large losses in STZ treated rats.
Key Words: diabetic retinopathy, electroretinography, ganglion cell
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