Resolution of inflammation is altered in Alzheimer's disease. Issue 1 (14th February 2014)

• Record Type: Journal Article
• Authors: Wang, Xiuzhe; Zhu, Mingqin; Hjorth, Erik; Cortés‐Toro, Veronica; Eyjolfsdottir, Helga; Graff, Caroline; Nennesmo, Inger; Palmblad, Jan; Eriksdotter, Maria; Sambamurti, Kumar; Fitzgerald, Jonathan M.; Serhan, Charles N.; Granholm, Ann‐Charlotte; Schultzberg, Marianne
• Is Part Of: Alzheimer's & dementia. Volume 11:Issue 1(2015)
• Page Start: 40
• Page End: 50.e2
• Publication Date: 2014-02-14
• Subjects: ChemR23 -- ELISA -- FPRL1 -- Human -- Immunohistochemistry -- Lipoxin A4 -- ALX/FPR2 -- 15‐Lipoxygenase‐2 -- Mild cognitive impairment -- Resolvin D1 -- Specialized pro‐resolving mediators -- Tau; Alzheimer's disease -- Periodicals; Alzheimer Disease -- Periodicals; Dementia -- Periodicals; Démence; Maladie d'Alzheimer; Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 616.83
• DOI: 10.1016/j.jalz.2013.12.024
• Languages: English
• ISSNs: 1552-5260

Abstract

Abstract: Background: Resolution is the final stage of the inflammatory response, when restoration of tissue occurs. Failure may lead to chronic inflammation, which is known as part of the pathology in the brain of individuals with Alzheimer's disease (AD). Methods: Specialized pro‐resolving mediators (SPMs), receptors, biosynthetic enzyme, and downstream effectors involved in resolution were analyzed in postmortem hippocampal tissue from AD patients and non‐AD subjects. SPMs were analyzed in cerebrospinal fluid (CSF). Results: SPMs and SPM receptors were detected in the human brain. Levels of the SPM lipoxin A4 (LXA4 ) were reduced in AD, both in the CSF and hippocampus. An enzyme involved in LXA4 synthesis and two SPM receptors were elevated in AD brains. LXA4 and RvD1 levels in CSF correlated with Mini‐Mental State Examination (MMSE) scores. Conclusions: A resolution pathway exists in the brain and the alterations described herein strongly suggest a dysfunction of this pathway in AD. MMSE correlations suggest a connection with cognitive function in AD.