Matches in SemOpenAlex for { <https://semopenalex.org/work/W2772218995> ?p ?o ?g. }
- W2772218995 endingPage "931" @default.
- W2772218995 startingPage "921" @default.
- W2772218995 abstract "Inflammation initiated by damage-associated molecular patterns has been implicated for the cognitive decline associated with surgical trauma and serious illness. We determined whether resolution of inflammation mediates dexmedetomidine-induced reduction of damage-associated molecular pattern-induced cognitive decline.Cognitive decline (assessed by trace fear conditioning) was induced with high molecular group box 1 protein, a damage-associated molecular pattern, in mice that also received blockers of neural (vagal) and humoral inflammation-resolving pathways. Systemic and neuroinflammation was assessed by proinflammatory cytokines.Damage-associated molecular pattern-induced cognitive decline and inflammation (mean ± SD) was reversed by dexmedetomidine (trace fear conditioning: 58.77 ± 8.69% vs. 41.45 ± 7.64%, P < 0.0001; plasma interleukin [IL]-1β: 7.0 ± 2.2 pg/ml vs. 49.8 ± 6.0 pg/ml, P < 0.0001; plasma IL-6: 3.2 ± 1.6 pg/ml vs. 19.5 ± 1.7 pg/ml, P < 0.0001; hippocampal IL-1β: 4.1 ± 3.0 pg/mg vs. 41.6 ± 8.0 pg/mg, P < 0.0001; hippocampal IL-6: 3.4 ± 1.3 pg/mg vs. 16.2 ± 2.7 pg/mg, P < 0.0001). Reversal by dexmedetomidine was prevented by blockade of vagomimetic imidazoline and α7 nicotinic acetylcholine receptors but not by α2 adrenoceptor blockade. Netrin-1, the orchestrator of inflammation-resolution, was upregulated (fold-change) by dexmedetomidine (lung: 1.5 ± 0.1 vs. 0.7 ± 0.1, P < 0.0001; spleen: 1.5 ± 0.2 vs. 0.6 ± 0.2, P < 0.0001), resulting in upregulation of proresolving (lipoxin-A4: 1.7 ± 0.2 vs. 0.9 ± 0.2, P < 0.0001) and downregulation of proinflammatory (leukotriene-B4: 1.0 ± 0.2 vs. 3.0 ± 0.3, P < 0.0001) humoral mediators that was prevented by α7 nicotinic acetylcholine receptor blockade.Dexmedetomidine resolves inflammation through vagomimetic (neural) and humoral pathways, thereby preventing damage-associated molecular pattern-mediated cognitive decline." @default.
- W2772218995 created "2017-12-22" @default.
- W2772218995 creator A5001585701 @default.
- W2772218995 creator A5004214697 @default.
- W2772218995 creator A5022038749 @default.
- W2772218995 creator A5034128142 @default.
- W2772218995 creator A5041289533 @default.
- W2772218995 creator A5056288565 @default.
- W2772218995 creator A5065301160 @default.
- W2772218995 date "2018-05-01" @default.
- W2772218995 modified "2023-09-27" @default.
- W2772218995 title "Dexmedetomidine Prevents Cognitive Decline by Enhancing Resolution of High Mobility Group Box 1 Protein–induced Inflammation through a Vagomimetic Action in Mice" @default.
- W2772218995 cites W1497700962 @default.
- W2772218995 cites W1539818664 @default.
- W2772218995 cites W1851466778 @default.
- W2772218995 cites W1954619989 @default.
- W2772218995 cites W1973553804 @default.
- W2772218995 cites W1984552110 @default.
- W2772218995 cites W1988468898 @default.
- W2772218995 cites W1997283844 @default.
- W2772218995 cites W2007143131 @default.
- W2772218995 cites W2008778172 @default.
- W2772218995 cites W2017573472 @default.
- W2772218995 cites W2021604439 @default.
- W2772218995 cites W2027848881 @default.
- W2772218995 cites W2028906750 @default.
- W2772218995 cites W2038460368 @default.
- W2772218995 cites W2042821764 @default.
- W2772218995 cites W2043873159 @default.
- W2772218995 cites W2055155423 @default.
- W2772218995 cites W2059718338 @default.
- W2772218995 cites W2070818523 @default.
- W2772218995 cites W2075700581 @default.
- W2772218995 cites W2076263589 @default.
- W2772218995 cites W2082311304 @default.
- W2772218995 cites W2088750369 @default.
- W2772218995 cites W2131024082 @default.
- W2772218995 cites W2135672238 @default.
- W2772218995 cites W2135735522 @default.
- W2772218995 cites W2135781589 @default.
- W2772218995 cites W2139090780 @default.
- W2772218995 cites W2146246868 @default.
- W2772218995 cites W2156100110 @default.
- W2772218995 cites W2162294258 @default.
- W2772218995 cites W2164014399 @default.
- W2772218995 cites W2169358800 @default.
- W2772218995 cites W2293827238 @default.
- W2772218995 cites W2515708122 @default.
- W2772218995 cites W2528679837 @default.
- W2772218995 cites W2531057230 @default.
- W2772218995 cites W2532576306 @default.
- W2772218995 cites W2536199828 @default.
- W2772218995 cites W2549749029 @default.
- W2772218995 cites W2576421220 @default.
- W2772218995 cites W2579756956 @default.
- W2772218995 cites W2592804026 @default.
- W2772218995 cites W2596424855 @default.
- W2772218995 cites W2604235446 @default.
- W2772218995 cites W2623870930 @default.
- W2772218995 cites W2740995713 @default.
- W2772218995 doi "https://doi.org/10.1097/aln.0000000000002038" @default.
- W2772218995 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6445386" @default.
- W2772218995 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29252509" @default.
- W2772218995 hasPublicationYear "2018" @default.
- W2772218995 type Work @default.
- W2772218995 sameAs 2772218995 @default.
- W2772218995 citedByCount "56" @default.
- W2772218995 countsByYear W27722189952018 @default.
- W2772218995 countsByYear W27722189952019 @default.
- W2772218995 countsByYear W27722189952020 @default.
- W2772218995 countsByYear W27722189952021 @default.
- W2772218995 countsByYear W27722189952022 @default.
- W2772218995 countsByYear W27722189952023 @default.
- W2772218995 crossrefType "journal-article" @default.
- W2772218995 hasAuthorship W2772218995A5001585701 @default.
- W2772218995 hasAuthorship W2772218995A5004214697 @default.
- W2772218995 hasAuthorship W2772218995A5022038749 @default.
- W2772218995 hasAuthorship W2772218995A5034128142 @default.
- W2772218995 hasAuthorship W2772218995A5041289533 @default.
- W2772218995 hasAuthorship W2772218995A5056288565 @default.
- W2772218995 hasAuthorship W2772218995A5065301160 @default.
- W2772218995 hasBestOaLocation W27722189952 @default.
- W2772218995 hasConcept C104317684 @default.
- W2772218995 hasConcept C118552586 @default.
- W2772218995 hasConcept C126322002 @default.
- W2772218995 hasConcept C127561419 @default.
- W2772218995 hasConcept C134018914 @default.
- W2772218995 hasConcept C164027704 @default.
- W2772218995 hasConcept C16837860 @default.
- W2772218995 hasConcept C169900460 @default.
- W2772218995 hasConcept C2776814716 @default.
- W2772218995 hasConcept C2776914184 @default.
- W2772218995 hasConcept C2779134260 @default.
- W2772218995 hasConcept C2779144063 @default.
- W2772218995 hasConcept C2779483572 @default.
- W2772218995 hasConcept C2780043718 @default.
- W2772218995 hasConcept C2781302539 @default.
- W2772218995 hasConcept C2984863031 @default.