NLRP3 inhib 
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  • ||||||||||  Journal:  Novel Compounds as NLRP3 Inhibitors for Treating Cardiovascular Diseases. (Pubmed Central) -  Aug 14, 2024   
    cells in T2DM by inhibiting NLRP3 signaling through miR-19b-3p/SOCS3/STAT3 axis mediated autophagy. Provided herein are novel compounds as NLRP3 inhibitors, pharmaceutical compositions, use of such compounds in treating cardiovascular diseases, and processes for preparing such compounds.
  • ||||||||||  Journal:  Novel Compounds as NLRP3 Inhibitors for Treating Alzheimer's Disease and Parkinson's Disease. (Pubmed Central) -  Aug 14, 2024   
    Provided herein are novel compounds as NLRP3 inhibitors, pharmaceutical compositions, use of such compounds in treating cardiovascular diseases, and processes for preparing such compounds. Provided herein are novel compounds as NLRP3 inhibitors, pharmaceutical compositions, use of such compounds in treating Alzheimer's disease and Parkinson's disease, and processes for preparing such compounds.
  • ||||||||||  BMS-986299 / BMS, Visudyne (verteporfin) / Novartis
    Journal:  TAOK1-mediated regulation of the YAP/TEAD pathway as a potential therapeutic target in heart failure. (Pubmed Central) -  Aug 9, 2024   
    Furthermore, in the mouse model of adenomyosis, MCC950 exhibited a therapeutic effect by alleviating the severity of adenomyosis. TAOK1 played a crucial role in regulating IL-17-mediated increase in the pyroptosis and decrease in the proliferation of cardiomyocytes by regulating the activities of the NLRP3 inflammasomes and the YAP/TEAD pathway.
  • ||||||||||  The Inhibition of Mitochondrial NLRP3 Inflammasome Decreases Dopaminergic Cell Death in a 6-OHDA Mouse Model of Parkinson's Disease. (Poster Hall (Exhibit Hall A)) -  Aug 9, 2024 - Abstract #MDSCongress2024MDS_Congress_1924;    
    TAOK1 played a crucial role in regulating IL-17-mediated increase in the pyroptosis and decrease in the proliferation of cardiomyocytes by regulating the activities of the NLRP3 inflammasomes and the YAP/TEAD pathway. Inhibition of mitochondrial NLRP3 inflammasome may be neuroprotective to dopaminergic neurons that degenerate during PD, hence, may be used as a novel treatment therapy for patients with early- and/or late-onset PD.
  • ||||||||||  Melatonin Modulates NLRP3 Inflammasome Activation through TLR2 to Protect Against Parkinson's Disease (Poster Hall (Exhibit Hall A)) -  Aug 9, 2024 - Abstract #MDSCongress2024MDS_Congress_1098;    
    In BV2 cells and PFF-induced mouse models, MLT attenuates the activation of the NLRP3 inflammasome in microglia by modulating TLR2 expression, thereby mitigating neuroinflammation and protecting dopaminergic neurons. These findings contribute novel insights into the anti-inflammatory therapeutic mechanism of MLT in PD.(Submitted to IAPRD meeting on January 28th) ?-syn modulates NLRP3 Activation via TLR2 MLT inhibits NLRP3 Inflammasome Activation MLT protects against DA neurons degeneration in PD
  • ||||||||||  nibrozetone (RRx-001) / EpicentRx
    Validating the clinical stage NLRP3 inflammasome inhibitor nibrozetone as a disease-modifying therapeutic for Parkinson's disease (Poster Hall (Exhibit Hall A)) -  Aug 9, 2024 - Abstract #MDSCongress2024MDS_Congress_991;    
    These findings contribute novel insights into the anti-inflammatory therapeutic mechanism of MLT in PD.(Submitted to IAPRD meeting on January 28th) ?-syn modulates NLRP3 Activation via TLR2 MLT inhibits NLRP3 Inflammasome Activation MLT protects against DA neurons degeneration in PD Given the excellent clinical safety record of RRx-001 in human studies to date, our results suggest that RRx-001 could be an attractive neuroprotective strategy for disease modification of PD, with the potential for rapid clinical translation.
  • ||||||||||  Loganic Acid Alleviates the Bidirectional Olfactory-Brain NLRP3 Inflammasome Activation and Rescues Dopaminergic Neurons in Experimental Models of Parkinson's Disease (Poster Hall (Exhibit Hall A)) -  Aug 9, 2024 - Abstract #MDSCongress2024MDS_Congress_968;    
    Given the excellent clinical safety record of RRx-001 in human studies to date, our results suggest that RRx-001 could be an attractive neuroprotective strategy for disease modification of PD, with the potential for rapid clinical translation. Loganic acid treatment showed a prominent neuroprotective effect via regulating cellular redox homeostasis, restricting microglial activation, and supporting neuronal survival by targeting the NLRP3 inflammasome pathway in both cellular and animal model and further reducing neuroinflammation and neuronal damage associated with PD.
  • ||||||||||  Journal:  Eclipta prostrata improves alveolar development of bronchopulmonary dysplasia via suppressing the NLRP3 inflammasome in a DLD-dependent manner. (Pubmed Central) -  Aug 8, 2024   
    Loganic acid treatment showed a prominent neuroprotective effect via regulating cellular redox homeostasis, restricting microglial activation, and supporting neuronal survival by targeting the NLRP3 inflammasome pathway in both cellular and animal model and further reducing neuroinflammation and neuronal damage associated with PD. Our study suggested that EAP could attenuate arrest of alveolar development via inhibiting NLRP3 inflammasome in a DLD-dependent way, and could be a potential therapeutic method for BPD.
  • ||||||||||  Journal:  Angiogenin-mediated tsRNAs control inflammation and metabolic disorder by regulating NLRP3 inflammasome. (Pubmed Central) -  Aug 6, 2024   
    Furthermore, in vivo results showed that Ang deficiency led to the downregulation of tsRNAs, ultimately leading to an exacerbation of NLRP3 inflammasome-dependent inflammation, including lipopolysaccharide-induced systemic inflammation and type-2 diabetes-related inflammation. Altogether, our study sheds a new light on the role of Ang-induced 5'-tsRNAs in regulating NLRP3 inflammasome activation via SGs, and highlights tsRNAs as a promising target for the treatment of NLRP3 inflammasome-related diseases.
  • ||||||||||  NLRP3 inhibition reduces pathogenic IL1-family signalling in Hidradenitis Suppurativa skin (Poster Area) -  Aug 5, 2024 - Abstract #EADV2024EADV_1784;    
    Our findings underscore the significant therapeutic promise of targeting the NLRP3 inflammasome in HS with novel potent small molecule inhibitors and support that IL-1 family cytokines are important disease mediators. Beyond HS, these NLRP3 inhibitors may be efficacious for other skin inflammatory diseases where IL-1 family cytokines and continuous neutrophil infiltration play a key pathogenic role.
  • ||||||||||  Journal:  Gentiopicroside improves NASH and liver fibrosis by suppressing TLR4 and NLRP3 signaling pathways. (Pubmed Central) -  Jul 28, 2024   
    In vitro, GPS attenuated inflammation induced by BMDMs by inhibiting TLR4 and NLRP3 signaling pathways, and Co-culture studies suggested that GPS reduced hepatocyte pyroptosis and HSC activation, which was also confirmed in liver tissues GPS improves NASH and liver fibrosis by inhibiting the TLR4 and NLRP3 signaling pathways. The specific mechanism may be related to the suppression of macrophage-mediated inflammatory responses, thereby reducing hepatocyte pyroptosis and HSC activation.
  • ||||||||||  colchicine / Generic mfg.
    Clinical, Review, Journal:  Colchicine-The Divine Medicine against COVID-19. (Pubmed Central) -  Jul 27, 2024   
    In addition, post-COVID-19 symptoms in those treated with colchicine were significantly rarer. As a large number of viruses can overactivate the NLRP3 inflammasome (like seasonal influenza), we are convinced that higher colchicine doses would be useful in these cases as well.
  • ||||||||||  benfotiamine / Generic mfg.
    Preclinical, Journal:  Benfotiamine protects MPTP-induced Parkinson's disease mouse model via activating Nrf2 signaling pathway. (Pubmed Central) -  Jul 23, 2024   
    Control of Nrf2 proved crucial for BFT, as it facilitated Nrf2 movement to the nucleus, upregulating antioxidant genes and enzymes while mitigating oxidative damage. This study elucidates BFT's neuroprotective effects in a PD mouse model via Nrf2-mediated antioxidant mechanisms and gene expression modulation, underscoring its potential as a therapeutic agent for PD.