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dc.contributor.authorRajpoot, Sajjanen_US
dc.contributor.authorJha, Hem Chandraen_US
dc.contributor.authorBaig, Mirza Saqiben_US
dc.date.accessioned2023-06-24T13:06:36Z-
dc.date.available2023-06-24T13:06:36Z-
dc.date.issued2023-
dc.identifier.citationRajpoot, S., Kumar, A., Gaponenko, V., Thurston, T. L. M., Mehta, D., Faisal, S. M., . . . Baig, M. S. (2023). Dorzolamide suppresses PKCδ-TIRAP-p38 MAPK signaling axis to dampen the inflammatory response. Future Medicinal Chemistry, 15(6), 533-554. doi:10.4155/fmc-2022-0260en_US
dc.identifier.issn1756-8919-
dc.identifier.otherEID(2-s2.0-85159204224)-
dc.identifier.urihttps://doi.org/10.4155/fmc-2022-0260-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/12011-
dc.description.abstractBackground: Sepsis is a syndrome due to microbial infection causing impaired multiorgan function. Its underlying cause is immune dysfunction and macrophages play an essential role. Methods: TIRAP interaction with PKCδin macrophage was studied, revealing downstream signaling by Western blot and quantitative reverse transcriptase PCR. Dorzolamide (DZD) disrupting TIRAP-PKCδinteraction was identified by virtual screening and validated in vitro and in septic mice. Results: The study highlights the indispensable role of TIRAP-PKCδin p38 MAPK-activation, NF-κB- and AP-1-mediated proinflammatory cytokines expression, whereas DZD significantly attenuated the signaling. Conclusion: Targeting TIRAP-PKCδinteraction by DZD is a novel therapeutic approach for treating sepsis. © 2023 MS Baig.en_US
dc.language.isoenen_US
dc.publisherNewlands Press Ltden_US
dc.sourceFuture Medicinal Chemistryen_US
dc.subjectAP1en_US
dc.subjectdorzolamide (DZD)en_US
dc.subjectmacrophagesen_US
dc.subjectNF-κBen_US
dc.subjectp38 MAPKen_US
dc.subjectPKCδen_US
dc.subjectpro-inflammatory cytokinesen_US
dc.subjectsepsisen_US
dc.subjectTIRAPen_US
dc.titleDorzolamide suppresses PKCδ-TIRAP-p38 MAPK signaling axis to dampen the inflammatory responseen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Biosciences and Biomedical Engineering

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