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Updated: Feb 28, 2026

Transretinal ERG Recordings from Mouse Retina: Rod and Cone Photoresponses
Published on: March 14, 2012
A novel intrinsic electroretinogram response in isolated mouse retina
Motoharu Takao1, Yumi Fukuda2, Takeshi Morita2
1Department of Human and Information Science, Tokai University, Hiratsuka, Kanagawa 259-1292, Japan.
Abstract:
Since the discovery of intrinsic photosensitive retinal ganglion cell (ipRGC) was reported in 2002, many features specific to this cell type have been described. However, scare information is available on the retinographic components directly reflecting ipRGC activity. In this study, we identified the electroretinogram (microERG) that reflects the photoresponses by ipRGCs in ex vivo preparations of the mouse retina, in which classical photoreceptors (cones and rods) were ablated mechanically and photochemically. MicroERG consisted of three components: a large transient ON response, a small and lazy hump 19s after the onset of the light, and a large transient OFF response. A complete microERG recording required at least 30s of light exposure. MicroERG showed the highest spectral photosensitivity at 478nm. This wavelength corresponds to the peak wavelength in the ipRGCs' photosensitive curve. The psychophysical test using a blue light-emitting diode (LED) light (470nm) revealed that the absolute threshold illuminance for microERG was greater than 12.26 log photons/s/cm2 in both ON and OFF responses, whereas microERG was not adapted for dark. The amplitude of microERG increased linearly with irradiance. The sensitivity of temporal frequency was high in microERG (at least 100Hz), as suggested by the study on melatonin suppression by flickering light in human subjects (Zelter et al., 2014). Melatonin secretion was suppressed by light via ipRGCs and the suprachiasmatic nucleus. These properties of the photoresponse indicate that microERG may reflect the functions of ipRGC as a luminance detector in the mouse retina.

