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April 6, 2026Journal of Biochemical and Molecular Toxicology3 citations

A Narrative Review of the Pharmacological Potential of Dapansutrile, a Selective NLRP3 Inflammasome Inhibitor

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RARehab S. AbdelrahmanSMSamar F. MiskiTSTahani Saeedi

Key Points

  • This review aims to explore the pharmacological potential of dapansutrile as a selective NLRP3 inflammasome inhibitor.
  • Conducted a narrative review of existing literature on dapansutrile and the NLRP3 inflammasome.
  • Examined both topical and oral formulations of dapansutrile.
  • Summarized evidence on safety, efficacy, and mechanism of action.
  • Dapansutrile demonstrated a satisfactory safety profile and good tolerability in humans.
  • Both formulations reduced target joint pain effectively.
  • NLRP3 inflammasome activation mechanisms highlighted provide insights for treatment strategies.

Abstract

OLT1177™ (Dapansutrile) is a newly developed drug that specifically inhibits the NLRP3 inflammasome and is safe in humans. Initially formulated as a topical treatment for degenerative arthritis, it has since been developed into an oral form. Both topical gel and oral capsules have demonstrated that OLT1177 is safe and well-tolerated in humans, with a satisfactory safety profile and efficacy in reducing target joint pain. Inflammasomes are cytoplasmic proteins that activate caspase-1 in response to microbial invasion and damage signals. The NLRP3 inflammasome is one of the NOD-like receptor family members and is widely studied and activated by various stimuli. NLRP3 inflammasome activation is regulated through a two-step process, with priming at transcriptional and posttranslational levels and assembly by multiple pathways. The NLRP3 inflammasome, which activates inflammation-related diseases, is primarily activated through K+ efflux, mitochondrial dysfunction, and lysosomal rupture. However, its regulation in humans remains unclear. NLRP3 inflammasome composition, downstream pathways, and inhibitor development offer the potential for treating inflammation-related diseases. Several inhibitors have emerged and are currently in clinical trials, with over 10 having completed trials and recruiting participants.

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Cite This Study

Abdelrahman et al. (2026) studied this question.

synapsesocial.com/papers/69d34e1e9c07852e0af97a4fhttps://doi.org/10.1002/jbt.70790
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