Binding NF-κB essential modulator (NEMO) to Treat Surgical Pain
Project Number1R21AG086147-01
Former Number1R21TR004954-01
Contact PI/Project LeaderGROSS, ERIC RICHARD
Awardee OrganizationSTANFORD UNIVERSITY
Description
Abstract Text
PROJECT SUMMARY:
Surgical pain is caused by tissue injury and inflammation. To treat surgical pain, people are given opioids
which is leading to secondary health problems after surgery including opioid abuse, dependence, and
overdose that is driving the United States opioid epidemic. This is particularly important for older adults as
treating pain with opioids also present challenges with age-related changes in drug metabolism in addition to
drug-drug interactions due to polypharmacy. Therefore, discovering new non-opioid targets and developing
non-opioid treatments that are as effective in the young and elderly populations to alleviate surgical pain are
urgently needed.
For this HEAL proposal, the goal of the research is to develop a peptidomimetic to block the interaction of
NF-κB essential modulator (IKGKB, UniProt #Q9Y6K9) with IKKβ and further determine whether a peptide
targeting NF-κB essential modulator (NEMO) reduces surgical pain in young and old rodents. NEMO is a
promising non-opioid target to develop drugs to treat pain since NEMO is a critical protein regulating the
canonical pathway of NF-κB-mediated inflammation. Here we will leverage new key findings regarding the
NEMO interaction site with IKKβ based upon the crystal structure to develop a peptidomimetic to block the
NEMO interaction with IKKβ. In order to carry out this work, we developed an assay to screen NEMO peptide
modifications by using a mouse skin fibroblast NIH-3T3 cell line that contains a stable NF-κB luciferase
reporter. Further, we will determine whether a NEMO binding peptide will limit pain and inflammation after
injury using a surgical incision model. To carry out these studies, we developed a rodent paw surgical incision
model that increases phosphorylated NF-κB 3-fold in addition to a 10-fold increase in NF-κB-regulated pro-
inflammatory cytokines including IL-6 and IL-1β. Taken together, this proposal can advance the field by
developing a potential non-opioid therapeutic to treat pain and test whether a peptide binding NEMO is
effective in reducing surgical pain in young and old rodents.
Additionally, since the studies performed for this proposal will determine whether binding NEMO limits NF-κB
activation and production of NF-κB-mediated proinflammatory genes, these studies also have a broad
importance to aging. This is because inflammation is a hallmark of aging and the cellular senescence-
associated secretory phenotype described in aging cells is driven by increases in IL-6 and IL-1β; where IL-6 is
the major driver of this phenotype. Therefore, developing a peptidomimetic that binds NEMO may potentially
have broader implications besides treating surgical pain and useful in limiting inflammatory pain for the elderly.
Public Health Relevance Statement
PROJECT NARRATIVE:
Surgical pain is a major clinical problem requiring new non-opioid treatment strategies. Here we will develop a
peptidomimetic targeting NF-κB essential modulator (IKGKB, UniProt #Q9Y6K9) and test whether a peptide
binding NF-κB essential modulator limits surgical pain in young and old rodents. This proposal can provide a
non-opioid drug to treat surgical pain while also more broadly uncovering how NF-κB essential modulator
contributes to inflammatory pain.
National Institute of Neurological Disorders and Stroke
$427,187
Year
Funding IC
FY Total Cost by IC
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