June 2022
Volume 63, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2022
MIF inhibition improves retinal function in NMDA mediated excitotoxic damage
Author Affiliations & Notes
  • Tyler Heisler-Taylor
    Ophthalmology and Visual Sciences, The Ohio State University, Columbus, Ohio, United States
    Biomedical Engineering, The Ohio State University, Columbus, Ohio, United States
  • Elizabeth G Urbanski
    Ophthalmology and Visual Sciences, The Ohio State University, Columbus, Ohio, United States
  • Sumaya Hamadmad
    Ophthalmology and Visual Sciences, The Ohio State University, Columbus, Ohio, United States
  • Claire Landreth
    Ophthalmology and Visual Sciences, The Ohio State University, Columbus, Ohio, United States
  • Hailey Wilson
    Ophthalmology and Visual Sciences, The Ohio State University, Columbus, Ohio, United States
  • Julie Racine
    Nationwide Children's Hospital, Columbus, Ohio, United States
  • Colleen M Cebulla
    Ophthalmology and Visual Sciences, The Ohio State University, Columbus, Ohio, United States
  • Footnotes
    Commercial Relationships   Tyler Heisler-Taylor None; Elizabeth Urbanski None; Sumaya Hamadmad None; Claire Landreth None; Hailey Wilson None; Julie Racine None; Colleen Cebulla None
  • Footnotes
    Support  USAMRAA (DOD) W81XWH1810805
Investigative Ophthalmology & Visual Science June 2022, Vol.63, 3181 – F0455. doi:
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    • Get Citation

      Tyler Heisler-Taylor, Elizabeth G Urbanski, Sumaya Hamadmad, Claire Landreth, Hailey Wilson, Julie Racine, Colleen M Cebulla; MIF inhibition improves retinal function in NMDA mediated excitotoxic damage. Invest. Ophthalmol. Vis. Sci. 2022;63(7):3181 – F0455.

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

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Abstract

Purpose : Inhibition of macrophage migration inhibitory factor (MIF) has shown promise protecting retinal neurons in excitotoxic retinal damage models. We evaluated the ability of three MIF inhibitors (MIFi) to improve electroretinography (ERG) function in the chick excitotoxic retinal damage model.

Methods : Experiments were performed under an IACUC approved protocol. White leghorn chicks (n=3/group) were given intravitreal injections with NMDA (500nmol) at day 0 (D0) plus one of three different MIFi: ibudilast, AV1013, or CPSI-1306 at 1.0 mg/ml or vehicle (sterile water). Injections of MIFi and vehicle was performed on D-1, and D0. ERG waveforms were captured between D10-D14 with the Celeris ERG system. Light adapted ERGs and oscillatory potentials were captured with flash intensities between 0.05 and 25 cd*s/m2. Additionally, 20Hz flicker and long flash ERGs were recorded. Statistics were calculated in Graphpad PRISM using ANOVA with Tukey and Dunnett multiple comparison testing. A p-value ≤ 0.05 was considered statistically significant.

Results : ERG measurements resulted in no significant differences between MIFi-treated and vehicle-treated NMDA-damaged eyes in the CPSI-1306 and AV1013 groups. Ibudilast treatment resulted in significant improvement in two groups: the ERG b-wave and the long flash ERG bipolar-ON wave. NMDA-damaged eyes treated with ibudilast were found to have significantly higher b-wave amplitudes at 3, 8, and 13 cd*s/m2 (177.24±47.04 µV vs 278.60±61.78 µV, p=0.0049; 192.08±64.39 µV vs 279.90±40.62 µV, p=0.0173; 183.16±66.67 µV vs 265.00±27.23 µV, p=0.0288; NMDA+vehicle vs NMDA+ibudilast, respectively). The ON waves were also improved due to statistically higher amplitudes (11.09±5.26 µV vs 35.54±22.68 µV, p=0.0170; NMDA+vehicle vs NMDA+ibudlast). Both of these waveform groups correspond to inner retinal neurons, which are most susceptible to excitotoxic damage caused by NMDA.

Conclusions : Ibudilast is approved in Japan for neurologic and inflammatory indications and is in clinical trials for multiple sclerosis in the US. Preliminary results show ibudilast is promising for excitotoxic retinal damage prevalent in many retinal disorders like blast injury, diabetic retinopathy, vein occlusion and retinal ischemia.

This abstract was presented at the 2022 ARVO Annual Meeting, held in Denver, CO, May 1-4, 2022, and virtually.

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