Abstract

We have studied the effect of α2-adrenergic receptor stimulation on the total excitotoxically injured chicken retinal ganglion cell population. N-methyl-D-aspartate (NMDA) was intraocularly injected at embryonic day 18 and Brn3a positive retinal ganglion cells (Brn3a+ RGCs) were counted in flat-mounted retinas using automated routines. The number and distribution of the Brn3a+ RGCs were analyzed in series of normal retinas from embryonic day 8 to post-hatch day 11 retinas and in retinas 7 or 14 days post NMDA lesion. The total number of Brn3a+ RGCs in the post-hatch retina was approximately 1.9x106 with a density of approximately 9.2x103 cells/mm2. The isodensity maps of normal retina showed that the density decreased with age as the retinal size increased. In contrast to previous studies, we did not find any specific region with increased RGC density, rather the Brn3a+ RGCs were homogeneously distributed over the central retina with decreasing density in the periphery and in the region of the pecten oculli. Injection of 5–10 μg NMDA caused 30–50% loss of Brn3a+ cells and the loss was more severe in the dorsal than in the ventral retina. Pretreatment with brimonidine reduced the loss of Brn3a+ cells both 7 and 14 days post lesion and the protective effect was higher in the dorsal than in the ventral retina. We conclude that α2-adrenergic receptor stimulation reduced the impact of the excitotoxic injury in chicken similarly to what has been shown in mammals. Furthermore, the data show that the RGCs are evenly distributed over in the retina, which challenges previous results that indicate the presence of specific high RGC-density regions of the chicken retina.

Highlights

  • Excitotoxic injury has been used extensively to study cell death and proliferation in the retina

  • We have recently shown that activation of α2-adrenergic receptor (α2-ADR) on Müller cells modulates the injury-response by attenuating epidermal growth factor receptor- (EGFR) triggered extracellular signal-regulated kinase (ERK) signaling [18]

  • In this work we have studied the retinal ganglion cell (RGC) population in normal and excitotoxically injured chicken retina after pretreatment with the α2-ADR agonist brimonidine

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Summary

Introduction

Excitotoxic injury has been used extensively to study cell death and proliferation in the retina. Activation of α2-adrenergic receptor (α2-ADR) signaling reduces the adverse effects by different types of injury on retinal neurons This has been studied by analyzing rodent retinal ganglion cell (RGC) loss after injury [6,7,8,9,10,11,12]. The underlying mechanisms for the neuroprotection is not fully understood but is suggested to encompass modulation of excitotoxic signaling directly on RGCs, promotion of neurotrophic factor synthesis in the injured retina or attenuation of the gliotic response by the Müller cells and promotion of neuronal survival by maintenance of retinal homeostasis [6, 13,14,15,16,17,18,19,20]. Because α2-ADR agonists have robust effects on Müller cells as studied in the chicken retina [18, 19] and since it was not known if α2-ADR agonists have similar neuroprotective effects in chicken as in mammals, we studied the effect of brimonidine on chicken RGC loss after an excitoxic lesion by NMDA

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