Cyclooxygenase-1-dependent prostaglandins mediate susceptibility to systemic inflammation-induced acute cognitive dysfunction.
about
Non-Neuronal Acetylcholine: The Missing Link Between Sepsis, Cancer, and Delirium?PKR deficiency alters E. coli-induced sickness behaviors but does not exacerbate neuroimmune responses or bacterial loadThe American Geriatrics Society/National Institute on Aging Bedside-to-Bench Conference: Research Agenda on Delirium in Older Adults.Missing link or not, mobilise against delirium.Inflammation biomarkers and delirium in critically ill patients.Acute neuroinflammation impairs context discrimination memory and disrupts pattern separation processes in hippocampus.Possible roles of COX-1 in learning and memory impairment induced by traumatic brain injury in mice.Cerebrospinal fluid markers of neuroinflammation in delirium: a role for interleukin-1β in delirium after hip fractureWorsening cognitive impairment and neurodegenerative pathology progressively increase risk for deliriumPeripherally triggered and GSK-3β-driven brain inflammation differentially skew adult hippocampal neurogenesis, behavioral pattern separation and microglial activation in response to ibuprofen.Systemic lipopolysaccharide administration impairs retrieval of context-object discrimination, but not spatial, memory: Evidence for selective disruption of specific hippocampus-dependent memory functions during acute neuroinflammation.Systemic inflammation and microglial activation: systematic review of animal experimentsThe interface between delirium and dementia in elderly adultsSurgery plus anesthesia induces loss of attention in mice.Growth and adherence of Staphylococcus aureus were enhanced through the PGE2 produced by the activated COX-2/PGE2 pathway of infected oral epithelial cells.Eicosanoids Derived From Arachidonic Acid and Their Family Prostaglandins and Cyclooxygenase in Psychiatric DisordersNew horizons in the pathogenesis, assessment and management of delirium.Systemic TNF-α produces acute cognitive dysfunction and exaggerated sickness behavior when superimposed upon progressive neurodegeneration.The role of neuroinflammation in dementias.Co-morbidity and systemic inflammation as drivers of cognitive decline: new experimental models adopting a broader paradigm in dementia research.The Role of Microglia in Prion Diseases: A Paradigm of Functional Diversity.Serotonin as a putative scavenger of hypohalous acid in the brain.The Severity of Cecal Ligature and Puncture-Induced Sepsis Correlates with the Degree of Encephalopathy, but the Sepsis Does Not Lead to Acute Activation of Spleen Lymphocytes in Mice.Statins for delirium in ICU patients: a negative trial but a positive step.Characterization of Brain-Heart Interactions in a Rodent Model of Sepsis.The contribution of the acute phase response to the pathogenesis of relapse in chronic-relapsing experimental autoimmune encephalitis models of multiple sclerosisDoes prior sepsis alter subsequent circadian and sickness behaviour response to lipopolysaccharide treatment in mice?Obstructive sleep apnoea and the need for its introduction into dental curricula.Factors associated with physical and cognitive fatigue in patients with Crohn's disease: a cross-sectional and longitudinal study.The Period 2 Enhancer Nobiletin as Novel Therapy in Murine Models of Circadian Disruption Resembling Delirium.
P2860
Q26782713-1FEC8589-A7B5-49C5-BAAA-6D529BFF49EFQ30398450-CEC56245-5CAF-43A8-A54F-A79AA80592A8Q33610107-15A593E6-CE92-4BA8-AFAF-CB2D50E4945BQ33754739-1EEA04CF-49AC-4CED-84AD-F580D75015C1Q33821403-4B6E980D-DA2F-4F59-AE63-ADF7AE7EECF1Q34162775-3D9738E7-E159-4316-8367-2C2C4994F565Q34574272-AD94E8D7-D66E-4DCB-B9F2-BF725A52BD03Q34760173-AB169321-FD73-4F5A-A338-6FF7D6E9A8B8Q34784435-F96DBFF5-6AF1-4803-8A24-FB1BE43DA491Q35150206-DB942239-82AC-42D7-A162-1A1C3041B0D9Q35174989-461B0E98-D7FD-4FC8-9E46-6DC465CEEA78Q35750202-E6A2C0CF-6438-48D9-B380-DE6B4067E999Q35949863-8246ECCC-88EB-42F4-B78B-42C0600EA8BFQ36033097-008145CC-6214-48C1-A41F-F2A9570589E3Q36363166-016B9D45-79C9-4AEB-B282-0F19B872DBEEQ36594940-D6FCDB06-4FDD-4366-A92B-E7D23B9356DCQ37259016-01B40AAF-CD54-4753-A580-8A523A20D652Q37524082-6B78046A-155C-4D2A-9BEA-65636340CE20Q38365247-AB6225BE-B34E-4415-B531-7A816C35E7B2Q38388693-B83A8B9D-8139-4AE7-8F50-C28211F2A7D8Q39424451-1996D402-1691-4247-BCAA-2A9073E8A432Q39854722-D3755486-88BE-417F-88F1-67265E164BADQ40829801-7BBD0437-AA6A-489B-B0F0-9EBAF95E8739Q41428461-0A8A15DF-59CB-4558-B8A1-BFD22351565AQ41817617-21A59258-67B0-41B1-A2E4-42618757DA13Q42368148-A93287E0-D8F0-40BC-B88E-394A2572C80CQ42633196-2D9D7A2A-2C78-4BD7-B3AA-E2B2BECB4650Q47631346-64B3D51D-58CC-4774-A64A-5D01D1D0979FQ48124857-09593151-407B-4C10-9D44-B82875FF4306Q50533803-BE72934A-0423-447F-9BE4-B3AB9E1002AE
P2860
Cyclooxygenase-1-dependent prostaglandins mediate susceptibility to systemic inflammation-induced acute cognitive dysfunction.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on September 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Cyclooxygenase-1-dependent pro ...... d acute cognitive dysfunction.
@en
Cyclooxygenase-1-dependent pro ...... d acute cognitive dysfunction.
@nl
type
label
Cyclooxygenase-1-dependent pro ...... d acute cognitive dysfunction.
@en
Cyclooxygenase-1-dependent pro ...... d acute cognitive dysfunction.
@nl
prefLabel
Cyclooxygenase-1-dependent pro ...... d acute cognitive dysfunction.
@en
Cyclooxygenase-1-dependent pro ...... d acute cognitive dysfunction.
@nl
P2860
P50
P1476
Cyclooxygenase-1-dependent pro ...... d acute cognitive dysfunction.
@en
P2093
Carol L Murray
P2860
P304
15248-15258
P356
10.1523/JNEUROSCI.6361-11.2013
P407
P577
2013-09-01T00:00:00Z