关键词: Cholera toxin KA NMDA excitotoxicity ganglion cells glutamate

Mesh : Amacrine Cells / drug effects pathology physiology Animals Cells, Cultured Excitatory Amino Acid Agonists / toxicity Kainic Acid / toxicity Membrane Potentials Mice Mice, Inbred C57BL N-Methylaspartate / toxicity Photoreceptor Cells / drug effects pathology physiology Retinal Ganglion Cells / drug effects pathology physiology Visual Pathways / drug effects pathology physiology

来  源:   DOI:10.3390/ijms21051570   PDF(Sci-hub)   PDF(Pubmed)

Abstract:
Combined administration of N-Methyl-D-Aspartate (NMDA) and kainic acid (KA) on the inner retina was studied as a model of excitotoxicity. The right eye of C57BL6J mice was injected with 1 µL of PBS containing NMDA 30 mM and KA 10 mM. Only PBS was injected in the left eye. One week after intraocular injection, electroretinogram recordings and immunohistochemistry were performed on both eyes. Retinal ganglion cell (RGC) projections were studied by fluorescent-cholerotoxin anterograde labeling. A clear decrease of the retinal \"b\" wave amplitude, both in scotopic and photopic conditions, was observed in the eyes injected with NMDA/KA. No significant effect on the \"a\" wave amplitude was observed, indicating the preservation of photoreceptors. Immunocytochemical labeling showed no effects on the outer nuclear layer, but a significant thinning on the inner retinal layers, thus indicating that NMDA and KA induce a deleterious effect on bipolar, amacrine and ganglion cells. Anterograde tracing of the visual pathway after NMDA and KA injection showed the absence of RGC projections to the contralateral superior colliculus and lateral geniculate nucleus. We conclude that glutamate receptor agonists, NMDA and KA, induce a deleterious effect of the inner retina when injected together into the vitreous chamber.
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