Abstract

Recent studies using full-field electroretinography (ffERG) that triggers a non-specific mass response generated by several retinal sources have attributed an important role for cannabinoid receptors in mediating vision in primates. Specific cone-mediated responses evoked through the photopic flicker ERG appear to be a better way to validate the assumption that endogenous cannabinoids modulate the cone pathway, since FAAH is mainly expressed in the vervet monkey cone photoreceptors. The aim of this study is two-fold: (1) to use the photopic flicker ERG to target the cone pathway specifically, and (2) use URB597 as a selective inhibitor of the endocannabinoid degrading enzyme Fatty Acid Amide Hydrolase (FAAH) to enhance the levels of fatty acid amides, particularly anandamide. We recorded ERGs under four different flicker frequencies (15, 20, 25, and 30 Hz) in light-adapted conditions after intravitreal injections of URB597. Our results show that intravitreal injections of URB597, compared to the vehicle DMSO, increased significantly ffERG amplitudes at 30 Hz, a frequency that solely recruits cone activity. However, at 15 Hz, a frequency that activates both rods and cones, no significant difference was found in the ERG response amplitude. Additionally, we found no differences in implicit times after URB597 injections compared to DMSO vehicle. These results support the role of molecules degraded by FAAH in cone-mediated vision in non-human primates.

Highlights

  • Cannabinoid receptors are localized throughout the retina of several animal species [1,2], including primates [3,4,5,6,7]

  • The degrading fatty acid amide hydrolase (FAAH) and synthesizing (NAPE-PLD) enzymes related to CB1R are expressed in the cone system of several animal species [8,11,12]

  • The Full-field electroretinogram (ffERG) is a nonspecific mass response made out of several retinal sources that are summed throughout the retina, and this method has been used for studying the eCB system in several animal species including mice and primates [1,3,4,14,15,16,17]

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Summary

Introduction

Cannabinoid receptors are localized throughout the retina of several animal species [1,2], including primates [3,4,5,6,7]. The cannabinoid receptor type 1 (CB1R) is mainly expressed in the cones of the central retina [8], whereas the cannabinoid receptor type 2 (CB2R) is localized in the retinal glia (Müller cells) [9]. Manipulating the eCB system by blocking the activity of CB1R using intravitreal injections of the specific antagonist AM251 alters the global ffERG in the vervet monkey [14]. These results led to the suggestion that, in the primate model, CB1R acts as a mediator of central retinal function [4]

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