Abstract

After the unilateral inflammation or nerve lesion of the ocular surface, the ipsilateral corneal sensory nerve activity is activated and sensitized, evoking ocular discomfort, irritation, and pain referred to the affected eye. Nonetheless, some patients with unilateral ocular inflammation, infection, or surgery also reported discomfort and pain in the contralateral eye. We explored the possibility that such altered sensations in the non-affected eye are due to the changes in their corneal sensory nerve activity in the contralateral, not directly affected eye. To test that hypothesis, we recorded the impulse activity of the corneal mechano- and polymodal nociceptor and cold thermoreceptor nerve terminals in both eyes of guinea pigs, subjected unilaterally to three different experimental conditions (UV-induced photokeratitis, microkeratome corneal surgery, and chronic tear deficiency caused by removal of the main lacrimal gland), and in eyes of naïve animals ex vivo. Overall, after unilateral eye damage, the corneal sensory nerve activity appeared to be also altered in the contralateral eye. Compared with the naïve guinea pigs, animals with unilateral UV-induced mild corneal inflammation, showed on both eyes an inhibition of the spontaneous and stimulus-evoked activity of cold thermoreceptors, and increased activity in nociceptors affecting both the ipsilateral and the contralateral eye. Unilateral microkeratome surgery affected the activity of nociceptors mostly, inducing sensitization in both eyes. The removal of the main lacrimal gland reduced tear volume and increased the cold thermoreceptor activity in both eyes. This is the first direct demonstration that unilateral corneal nerve lesion, especially ocular surface inflammation, functionally affects the activity of the different types of corneal sensory nerves in both the ipsilateral and contralateral eyes. The mechanisms underlying the contralateral affectation of sensory nerves remain to be determined, although available data support the involvement of neuroimmune interactions. The parallel alteration of nerve activity in contralateral eyes has two main implications: a) in the experimental design of both preclinical and clinical studies, where the contralateral eyes cannot be considered as a control; and, b) in the clinical practice, where clinicians must consider the convenience of treating both eyes of patients with unilateral ocular conditions to avoid pain and secondary undesirable effects in the fellow eye.

Highlights

  • The ocular surface (OS) is innervated by different functional types of sensory neurons that evoke conscious sensations and contribute to corneal tissue tropism and initiate protective motor and autonomic reflexes such as blinking and tearing [1,2,3,4,5,6,7]

  • The study was performed in accordance with the Association for Research in Vision and Ophthalmology (ARVO) Statement for the Use of Animals in Ophthalmic and Vision Research, the National Institutes of Health (NIH) Guide for the Care and Use of Laboratory Animals, the European Union Directive (2010/63/EU), and the Spanish regulations on the protection of animals used for research, following protocols approved by the Ethics Committee of the Universidad Miguel Hernández de Elche

  • The corneal nociceptors recorded in the ipsilateral eyes were sensitized, as reflected by the development of spontaneous activity and the significant decrease of the mechanical threshold of mechanonociceptors (0.64 ± 0.04 Mechanical threshold (mN) vs. 0.32 ± 0.03 mN, control vs. UV-irradiated eyes; p < 0.01, Mann-Whitney test)

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Summary

Introduction

The ocular surface (OS) is innervated by different functional types of sensory neurons that evoke conscious sensations and contribute to corneal tissue tropism and initiate protective motor and autonomic reflexes such as blinking and tearing [1,2,3,4,5,6,7]. Cold thermoreceptors express TRPM8 transducing channels and typically respond to decreases in temperature with different thresholds: canonical cold thermoreceptors with high background activity at normal corneal temperature and high sensitivity to cooling, and presumed cold nociceptors, that exhibit a low background activity and requires more intense cooling to increase its firing rate. Their selective stimulation in humans evokes sensations described as freshness/cold or dryness/pain, respectively, depending on the amplitude of temperature decrease [6]. To evoke conscious sensations, the activity of cold thermoreceptors expressing TRPM8 channels contribute to the control of basal tearing and spontaneous blinking [3,4,5, 20]

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