Resolving postoperative neuroinflammation and cognitive decline

Ann Neurol. 2011 Dec;70(6):986-995. doi: 10.1002/ana.22664.

Abstract

Objective: Cognitive decline accompanies acute illness and surgery, especially in the elderly. Surgery engages the innate immune system that launches a systemic inflammatory response that, if unchecked, can cause multiple organ dysfunction. We sought to understand the mechanisms whereby the brain is targeted by the inflammatory response and how this can be resolved.

Methods: C57BL/6J, Ccr2(RFP/+)Cx3cr1(GFP/+), Ikk(F/F) mice and LysM-Cre/Ikk(F/F) mice underwent stabilized tibial fracture operation under analgesia and general anesthesia. Separate cohorts of mice were tested for systemic and hippocampal inflammation, integrity of the blood-brain barrier (BBB), and cognition. The putative resolving effects of the cholinergic pathway on these postoperative responses were also studied.

Results: Peripheral surgery disrupts the BBB via release of tumor necrosis factor-alpha (TNFα), which facilitates the migration of macrophages into the hippocampus. Macrophage-specific deletion of Ikappa B kinase (IKK)β, a central coordinator of TNFα signaling through activation of nuclear factor (NF) κB, prevents BBB disruption and macrophage infiltration in the hippocampus following surgery. Activation of the α7 subtype of nicotinic acetylcholine receptors, an endogenous inflammation-resolving pathway, prevents TNFα-induced NF-κB activation, macrophage migration into the hippocampus, and cognitive decline following surgery.

Interpretation: These data reveal the mechanisms for bidirectional communication between the brain and immune system following aseptic trauma. Pivotal molecular mechanisms can be targeted to prevent and/or resolve postoperative neuroinflammation and cognitive decline.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aza Compounds / administration & dosage
  • Behavior, Animal
  • CD11b Antigen / metabolism
  • CX3C Chemokine Receptor 1
  • Cell Movement
  • Cells, Cultured
  • Cognition Disorders / etiology*
  • Cognition Disorders / prevention & control
  • Conditioning, Psychological / physiology
  • Cytokines / metabolism
  • Dioxins / administration & dosage
  • Disease Models, Animal
  • Drug Administration Schedule
  • Encephalitis / etiology*
  • Encephalitis / metabolism*
  • Encephalitis / pathology
  • Encephalitis / prevention & control
  • Fear / physiology
  • HMGB1 Protein / metabolism
  • Hippocampus / pathology
  • I-kappa B Kinase / genetics
  • Luminescent Proteins / genetics
  • Macrophages / metabolism
  • Macrophages / pathology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Motor Activity
  • NF-kappa B / metabolism
  • Nicotinic Agonists / administration & dosage
  • Postoperative Complications / physiopathology*
  • Receptors, CCR2 / genetics
  • Receptors, Chemokine / genetics
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Aza Compounds
  • CD11b Antigen
  • CX3C Chemokine Receptor 1
  • Ccr2 protein, mouse
  • Cx3cr1 protein, mouse
  • Cytokines
  • Dioxins
  • HMGB1 Protein
  • Luminescent Proteins
  • NF-kappa B
  • Nicotinic Agonists
  • PHA-568487E
  • Receptors, CCR2
  • Receptors, Chemokine
  • Tumor Necrosis Factor-alpha
  • I-kappa B Kinase