Topical Cannabinoids and Ocular Pain Relief

There are three essential components of the ocular ECS: receptors, endogenous cannabinoids, and enzymes responsible for synthesis and degradation of receptors and cannabinoids. Acting to regulate pain transmission, cannabinoid 1 receptor (CB1R) has been identified throughout ocular tissues, whereas the cannabinoid 2 receptor (CB2R) is primarily localized to the surface of immune cells (3). Since ocular inflammation can result in both acute and chronic pain, the anti-inflammatory actions of CB2R modulation can have an indirect effect on improving ocular comfort. Reducing the release of noxious inflammatory mediators helps ameliorate acute pain, and prevention of neuronal sensitization by these mediators reduces the possibility of developing chronic neuropathic pain.

Since pain and inflammation often accompany DED, topical cannabinoids could also represent an important therapeutic approach to this condition. Because CB1R is present on the corneal epithelium, topical cannabinoids can easily access a desiccated epithelium – which can be a source of both acute and chronic ocular pain for DED patients – providing significant pain relief.

Interestingly, CB1R is also expressed in neurons innervating the lacrimal gland. Usually the expression is low, but this expression increases during DED-associated inflammation. McDowell et. al highlighted how CB1R activation reduces sensitization of lacrimal gland nerves, potentially reducing chronic neurotrophic pain (4). Tran et. al also demonstrated improvement in corneal fluorescence, and reduction of corneal and conjunctival inflammation after topical application of cannabinoids in experimentally induced dry eye models (5).

Other methods of ECS modulation are currently under investigation. One uses modulators that increase the binding affinity of cannabinoids to the receptors, allowing for a smaller dose of cannabinoid to achieve the desired effect; another method uses enzyme inhibitors that increase levels of endocannabinoids by inhibiting the actions of enzymes that degrade them. Treatment with enzyme inhibitors has been shown to reduce pain and inflammation in several preclinical models, including for chronic neuropathic pain (3).

There are challenges though; ECS modulators are hydrophobic, so the potential bottleneck of ocular penetration and bioavailability needs to be considered; here, nanotechnology-based drug delivery methods may prove useful.

The ubiquitous presence of the endocannabinoid system in ocular tissues, its role in ocular analgesia, and its demonstrated responsiveness to topical modulators represent a unique opportunity to continue developing a novel class of ECS ocular pain relief medications. These medications could either be used alone or in conjunction with other ocular analgesics to optimize ocular comfort, relieving both acute and chronic pain for patients.