June 2023
Volume 64, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2023
Gap junctions as the explanation for a novel retinal response component in the spectral ERG
Author Affiliations & Notes
  • Christopher W. Tyler
    Smith-Kettlewell Eye Research Institute, San Francisco, California, United States
    City University of London, London, London, United Kingdom
  • Russell D Hamer
    Florida Atlantic University, Boca Raton, Florida, United States
  • Michael Liang
    Smith-Kettlewell Eye Research Institute, San Francisco, California, United States
  • Zhangziyi Zhou
    Smith-Kettlewell Eye Research Institute, San Francisco, California, United States
  • Lora Likova
    Smith-Kettlewell Eye Research Institute, San Francisco, California, United States
  • Footnotes
    Commercial Relationships   Christopher Tyler None; Russell Hamer None; Michael Liang None; Zhangziyi Zhou None; Lora Likova None
  • Footnotes
    Support  NH Grant EY13055
Investigative Ophthalmology & Visual Science June 2023, Vol.64, 1639. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Christopher W. Tyler, Russell D Hamer, Michael Liang, Zhangziyi Zhou, Lora Likova; Gap junctions as the explanation for a novel retinal response component in the spectral ERG. Invest. Ophthalmol. Vis. Sci. 2023;64(8):1639.

      Download citation file:


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

      ×
  • Supplements
Abstract

Purpose : Electrical gap junctions are a ubiquitous form of bidirectional synaptic connectivity whose role in visual processing remains underappreciated. Their typical configuration is lateral connectivity between cells in the same neural layer (including the photoreceptor layer of the retina), as opposed to the unidirectional feedforward and feedback connectivity of neurotransmitter-mediated chemical synapses. Although electrical gap junctions are expected to have a rapid response, evidence from studies with gap junction blockers show that their response speed can in fact be slower than for chemical synapses (Cadetti et al., 2005).

Methods : Methods. Full-field spectral ERGs were recorded with a RETeval device for 6 narrowband chromatic stimuli (magenta, red, yellow, green, cyan, blue) plus white, using 250 ms light pulses at 2 Hz for 30 sec (60 full cycles) at 5 intensities from 3 to 300 cd/m2.

Results : The spectral ERGs exhibit three components: 1) Rod-pathway responses (up to ~10 cd/m2) whose a/b-wave complex has a scotopic spectral sensitivity with a b-wave peak time of ~60 ms and typical rod-like saturation attributable to transmitter depletion at the rod/bipolar chemical synapse. 2) Cone pathway responses with a photopic spectral sensitivity and a b-wave peak time of ~40 ms. 3) An unexpected additional response component consisting of a slow scotopic/mesopic response with a b-wave peak time of ~90 ms. Its spectral sensitivity peaks in the yellow-green range, and is measurable up to about 50 cd/m2, well beyond the level of the classic rod response.

Conclusions : The slow component revealed in our spectral ERG protocol appears to reflect activity in a distinct signal processing pathway. It has several paradoxical features: a b-wave even slower than the rod-mediated b-waves, but with a spectral tuning peaking in the yellow-green; light sensitivity comparable to rod-pathway responses but lacking rod-like saturation at high intensities. A hypothetical mechanism for this component could be gap junctions from the M-cones to the rod pathway to account for the yellow-green tuning, with the slower response of the gap junctions accounting for the slower time courses. The lack of saturation could reflect a wide dynamic range of gap junction electrical conductivity.

This abstract was presented at the 2023 ARVO Annual Meeting, held in New Orleans, LA, April 23-27, 2023.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×