April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Retinal Ganglion Cell and Optic Nerve Functional and Structural loss in a Rodent Model of Blast-Induced Traumatic Brain Injury
Author Affiliations & Notes
  • Matthew M. Harper
    Veterans Administration, Ames, Iowa
  • Kabhilan Mohan
    Veterinary Clinical Sciences, Iowa State University, Ames, Iowa
  • Tatjana Lazic
    Veterinary Clinical Sciences, Iowa State University, Ames, Iowa
  • Sinisa D. Grozdanic
    Veterinary Clinical Sciences, Iowa State University, Ames, Iowa
  • Randy H. Kardon
    Ophthalmology and Visual Sciences, University of Iowa, Iowa City, Iowa
  • Footnotes
    Commercial Relationships  Matthew M. Harper, None; Kabhilan Mohan, None; Tatjana Lazic, None; Sinisa D. Grozdanic, Biomed-Vision (C); Randy H. Kardon, None
  • Footnotes
    Support  Department of Veterans Affairs – Center for Prevention and Treatment of Vision Loss Iowa City
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 5906. doi:
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      Matthew M. Harper, Kabhilan Mohan, Tatjana Lazic, Sinisa D. Grozdanic, Randy H. Kardon; Retinal Ganglion Cell and Optic Nerve Functional and Structural loss in a Rodent Model of Blast-Induced Traumatic Brain Injury. Invest. Ophthalmol. Vis. Sci. 2011;52(14):5906.

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

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Abstract

Purpose: : To characterize effects of blast-mediated injury on the structure and function of retinal ganglion cells (RGC) and the optic nerve (ON) in order to improve diagnostic and treatment modalities for soldiers exposed to blast-mediated traumatic brain injury (TBI).

Methods: : Healthy adult C57/Bl6 mice were exposed to a blast wave (137 kPa) using a custom built blast chamber. RGC/ON function and structure were evaluated using the chromatic pupil light reflex (cPLR), pattern electroretinography (pERG) and spectral-domain optical coherence tomography (SD-OCT).

Results: : Assessment of the cPLR demonstrated a decreased maximum pupil constriction diameter in blast-injured mice (n=20) when using red light stimuli of 630 nm wavelength (Ctrl=1.12 ± 0.05 mm; TBI = 1.38 ± mm; p = 0.0063, Student’s t-test) or blue light stimuli of 480 nm wavelength (Ctrl = 0.56 ± 0.02 mm; TBI = 0.71 ± 0.02 mm; p = 0.0008) 24h after injury. Baseline pupil diameters before illumination were not significantly different between control and blast injured animals (Ctrl = 2.11 ± 0.05 mm; TBI = 2.11 ± 0.04 mm; p = 0.9914). Pattern ERG responses 24h after injury were also significantly decreased compared to pre-recorded values (Pre-rec = 7.17 ± 0.34 µV; Post-TBI = 5.34± 0.64 µV; p < 0.05). Three months following injury a significant thinning of the superior retinal nerve fiber layer was observed in animals with blast-injury compared to controls using SD-OCT (Ctrl = 45+4µm, TBI = 32+1µm; p = 0.009). Histological analysis showed loss of retinal ganglion cells and recipient thalamic neurons.

Conclusions: : Blast-induced traumatic brain injury is associated with severe functional and structural retina and optic nerve deficits in this experimental mouse model. Utilization of non-invasive functional (cPLR, pERG) and structural (SD-OCT) diagnostic tests may be useful approach for early detection of visual system abnormalities in blast-injured subjects.

Keywords: optic nerve • electroretinography: non-clinical • ganglion cells 
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