Volume 70, Issue 6 pp. 986-995
Original Article

Resolving postoperative neuroinflammation and cognitive decline

Niccolò Terrando PhD

Niccolò Terrando PhD

Department of Anesthesia and Perioperative Care, University of California at San Francisco, San Francisco, CA

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Lars I. Eriksson MD, PhD

Lars I. Eriksson MD, PhD

Department of Anesthesia and Perioperative Care, University of California at San Francisco, San Francisco, CA

Department of Physiology and Pharmacology, Section for Anesthesiology and Intensive Care Medicine, Karolinska Institute, Stockholm, Sweden

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Jae Kyu Ryu PhD

Jae Kyu Ryu PhD

Gladstone Institute of Neurological Disease, University of California at San Francisco, San Francisco, CA

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Ting Yang MD, PhD

Ting Yang MD, PhD

Department of Anesthesia and Perioperative Care, University of California at San Francisco, San Francisco, CA

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Claudia Monaco MD, PhD

Claudia Monaco MD, PhD

Kennedy Institute of Rheumatology, Faculty of Medicine, Imperial College London, London, United Kingdom

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Marc Feldmann FMedSci, FAA, FRS

Marc Feldmann FMedSci, FAA, FRS

Kennedy Institute of Rheumatology, Faculty of Medicine, Imperial College London, London, United Kingdom

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Malin Jonsson Fagerlund MD, PhD

Malin Jonsson Fagerlund MD, PhD

Department of Physiology and Pharmacology, Section for Anesthesiology and Intensive Care Medicine, Karolinska Institute, Stockholm, Sweden

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Israel F. Charo MD, PhD

Israel F. Charo MD, PhD

Gladstone Institute of Cardiovascular Disease, University of California at San Francisco, San Francisco, CA

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Katerina Akassoglou PhD

Katerina Akassoglou PhD

Gladstone Institute of Neurological Disease, University of California at San Francisco, San Francisco, CA

Department of Neurology, University of California at San Francisco, San Francisco, CA

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Mervyn Maze MB, ChB

Corresponding Author

Mervyn Maze MB, ChB

Department of Anesthesia and Perioperative Care, University of California at San Francisco, San Francisco, CA

Department of Anesthesia and Perioperative Care, 521 Parnassus Avenue, C455, San Francisco, CA 94143-0648Search for more papers by this author
First published: 31 October 2011
Citations: 460

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, Ccr2RFP/+Cx3cr1GFP/+, IkkF/F mice and LysM-Cre/IkkF/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. ANN NEUROL 2011;70:986–995

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