4.7 Article

Resolution of inflammation is altered in Alzheimer's disease

Journal

Alzheimers & Dementia
Volume 11, Issue 1, Pages 40-50

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jalz.2013.12.024

Keywords

ChemR23; ELISA; FPRL1; Human; Immunohistochemistry; Lipoxin A(4); ALX/FPR2; 15-Lipoxygenase-2; Mild cognitive impairment; Resolvin D1; Specialized pro-resolving mediators; Tau

Funding

  1. Swedish Research Council [072194]
  2. Swedish Brain Power
  3. Chinese Scholarship Council, P.R. China
  4. Knut and Alice Wallenberg foundation
  5. Karolinska Institutet research funds
  6. Stiftelsen for Gamla Tjanarinnor
  7. Swedish Alzheimer Foundation
  8. Gun och Bertil Stohnes Stiftelse
  9. Petrus och Augusta Hedlunds Stiftelse
  10. Gustav V and Queen Victoria's Freemason Foundation
  11. Barmore Foundation (MUSC)
  12. National Institutes of Health [P01GM095467, GM038765]
  13. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R29GM038765, R01GM038765, P01GM095467, R37GM038765] Funding Source: NIH RePORTER
  14. NATIONAL INSTITUTE ON AGING [R21AG046200, R21AG048631] Funding Source: NIH RePORTER

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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 A(4) (LXA(4)) were reduced in AD, both in the CSF and hippocampus. An enzyme involved in LXA(4) synthesis and two SPM receptors were elevated in AD brains. LXA(4) 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. (C) 2015 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.

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