# Resource Core > **NIH NIH U19** · MARINE BIOLOGICAL LABORATORY · 2021 · $737,335 ## Abstract Chronic pain is a leading cause of disability, affecting about one-third of adults worldwide, with a prevalence greater than heart disease, cancer, and diabetes combined. Misuse and abuse of opiates have led to a nationwide addiction and overdose crisis. Thus, there is an urgent need for alternative, non-addictive analgesics. Non-selective voltage-gated sodium channel (Nav) blockers are among existing non-addictive FDA-approved drugs which can sometimes provide symptomatic relief for patients. However, their utility is limited by CNS and cardiac side effects. Genetic and functional studies of human pain disorders and animal models of pain have validated NaV1.7, a voltage-gated Na Channel that is preferentially expressed in peripheral neurons, as an attractive target for therapy. Isoform-selective Nav blockers, however, are difficult to generate and those that have been generated are rapidly cleared from the body, limiting their effectiveness. Alternative approaches are needed. We propose a novel, non-addictive approach to treat chronic pain by editing the messages that encode NaV1.7 in order to alter its electrophysiological properties. By changing a single lysine codon to arginine in the ion selectivity filter, the channel will go from being Na+ selective to both Na+ and K+ selective, effectively creating a counter-current shunt that will dampen excitability. Site-Directed RNA Editing (SDRE) refers to novel mechanisms to generate programmed edits within RNAs. It relies on the ADAR (Adenosine Deaminase that Acts on RNA) enzymes, which are endogenously expressed in human cells, including sensory neurons. Directed by a guide RNA (gRNA), SDRE systems convert precisely selected adenosines to inosine, a translational mimic for guanosine, which can recode specific amino acids. Off- target RNA editing is a significant consideration for SDRE that must be taken into account as part of reagent design. For use as an analgesic, editing mRNA is preferable to DNA because it is transient, thus limiting potential off-target effects, including malignant transformations and ADARs are endogenous while enzymes for DNA manipulation (e.g. Cas proteins) are not, thus SDRE will not be as immunogenic. Compared to small molecule channel blockers, SDRE can be more specific, because it relies on Watson-Crick base-pairing of gRNAs for targeting, and its effects are likely longer lasting because they will remain as long as the edited channels are expressed. We propose to use SDRE to edit NaV1.7 K1395R to render the channel permeable to both Na+ and K+. The purpose of the Resource Core is to supply all investigators involved in this project with the required RNA editing quantification and statistical analyses. Primarily, the Resource Core will quantify on-target and off-target RNA editing activity for the various experimental systems to be used by the different research components, from cells to mice. We will introduce off-target analysis as an integral part of the reagent opt... ## Key facts - **NIH application ID:** 10398389 - **Project number:** 1U19NS126038-01 - **Recipient organization:** MARINE BIOLOGICAL LABORATORY - **Principal Investigator:** Eli Eisenberg - **Activity code:** U19 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2021 - **Award amount:** $737,335 - **Award type:** 1 - **Project period:** 2021-09-23 → 2025-08-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10398389 ## Citation > US National Institutes of Health, RePORTER application 10398389, Resource Core (1U19NS126038-01). Retrieved via AI Analytics 2026-05-29 from https://api.ai-analytics.org/grant/nih/10398389. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*