Effects of Mydriatics on Rod/Cone- and Melanopsin-driven Pupil Responses

Optom Vis Sci. 2020 Mar;97(3):198-206. doi: 10.1097/OPX.0000000000001486.

Abstract

Significance: Pupillometry protocols evaluating rod/cone- and melanopsin-driven responses often use mydriatics to ensure maximal stimulus exposure; however, retinal effects of mydriatics are not fully understood. We demonstrate that dilation with either atropine or phenylephrine results in similar enhancements of rod/cone- and melanopsin-driven pupil responses.

Purpose: The purposes of this study were to compare the effects of atropine, a muscarinic antagonist, and phenylephrine, an adrenergic agonist, on consensual pupil responses and to assess the repeatability of pupil metrics without mydriasis.

Methods: Right eye pupil responses of 20 adults aged 21 to 42 years were recorded before and 45 minutes after instillation of 0.5% atropine or 2.5% phenylephrine in the left eye. Stimuli were presented to the left eye and included six alternating 1-second 651-nm "red" and 456-nm "blue" flashes. Metrics included baseline pupil diameter, maximal constriction, 6- and 30-second post-illumination pupil responses, and early (0 to 10 seconds) and late (10 to 30 seconds) areas under the curve.

Results: Dilation of the stimulated eye with either mydriatic significantly increased the 6-second post-illumination pupil response and early and late areas under the curve for blue stimuli, and early area under the curve for red stimuli (P < .05 for all). Melanopsin-driven post-illumination pupil responses, achieved with either phenylephrine or atropine, did not significantly differ from each other (P > .05 for all). Without mydriasis, intersession intraclass correlation coefficients for pupil metrics were 0.63 and 0.50 (6- and 30-second post-illumination pupil responses, respectively) and 0.78 and 0.44 (early and late areas under the curve, respectively) for blue stimuli, with no significant difference between sessions (P > .05 for all).

Conclusions: Dilation with phenylephrine or atropine resulted in similar enhancements of the rod/cone- and melanopsin-driven pupil responses, despite differing mechanisms. Early pupil metrics without mydriasis demonstrated moderate to good intersession repeatability.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Administration, Ophthalmic
  • Adrenergic alpha-1 Receptor Agonists / pharmacology
  • Adult
  • Atropine / pharmacology*
  • Female
  • Humans
  • Male
  • Muscarinic Antagonists / pharmacology
  • Mydriatics / pharmacology*
  • Ophthalmic Solutions
  • Phenylephrine / pharmacology*
  • Photic Stimulation
  • Photoreceptor Cells, Vertebrate / drug effects
  • Photoreceptor Cells, Vertebrate / metabolism
  • Pupil / drug effects*
  • Reflex, Pupillary / physiology
  • Rod Opsins / metabolism*
  • Young Adult

Substances

  • Adrenergic alpha-1 Receptor Agonists
  • Muscarinic Antagonists
  • Mydriatics
  • Ophthalmic Solutions
  • Rod Opsins
  • melanopsin
  • Phenylephrine
  • Atropine