4.2 Article

Abnormal phosphorylation of tau protein and neuroinflammation induced by laparotomy in an animal model of postoperative delirium

Journal

EXPERIMENTAL BRAIN RESEARCH
Volume 239, Issue 3, Pages 867-880

Publisher

SPRINGER
DOI: 10.1007/s00221-020-06007-2

Keywords

Neuroinflammation; Postoperative delirium; Cognitive dysfunction; Tau phosphorylation

Categories

Funding

  1. National Natural Science Foundation of China [NSFC 81801050]
  2. Basic and clinical cooperative research promotion plan of Anhui Medical University [2019xkjT026]

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Postoperative delirium is an acute neuropsychological disturbance that may be influenced by neuroinflammation and abnormal tau phosphorylation. In a study with mice undergoing laparotomy, significant changes in inflammatory responses and tau protein levels were observed at 4 hours and 24 hours postoperatively, indicating a potential link between these factors and cognitive dysfunction.
Postoperative delirium (POD) is an acute neuropsychological disturbance after surgery, whose prevalence is related with advancing age. Neuroinflammation and abnormal tau phosphorylation that commonly presenting in Alzheimer's disease (AD) may contribute to the progression and duration of POD. To study the acute influence of surgery on cognitive function, wild type male C57BL/6 N mice were randomly divided into three groups: Control (CON), Laparotomy at 4 h and 24 h (LAP-4 h, LAP-24 h), then subjected to laparotomy under sevoflurane anaesthesia. The cognitive performance, peripheral and central inflammatory responses and tau phosphorylation levels were evaluated at 4 h and 24 h postoperatively. When LAP4-hrs displayed anxiety behaviors with high mRNA levels of inflammatory cytokines, such as interleukin-1 beta (IL-1 beta), IL-6, IL-8, TNF-alpha and MCP-1 in the liver, and IL-8 in the hippocampus, results at 24 h were different. In the liver, only IL-10 protein was obviously elevated, but in the hippocampus, both pro- and anti-inflammatory cytokines were significantly decreased whilst the elimination of anxiety. The activity of major related kinases and phosphatases was remarkably changed which may contribute to the dephosphorylated tau protein. With tremendous neuropathological changes and significant numbers of activated microglias and astrocytes observed in the sub-regions of hippocampus, the memory impairment existed at both 4 h and 24 h. Since the association of dephosphorylated tau with POD, these findings may supply novel implications for the understanding of tauopathies and as a theoretical basis for preventions from the postoperative cognitive dysfunction (POCD).

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