Abstract

The aseptic trauma of peripheral surgery activates a systemic inflammatory response that results in neuro-inflammation; the microglia, the resident immunocompetent cells in the brain, are a key element of the neuroinflammatory response. In most settings microglia perform a surveillance role in the brain detecting and responding to “invaders” to maintain homeostasis. However, microglia have also been implicated in producing harm possibly by changing its phenotype from its beneficial, anti-inflammatory state (termed M2) into an injurious pro-inflammatory state (termed M1); it is likely that there are intermediates states between these polar phenotypes and some consider that a gradient exists with a number of intermediates, rather than a strict dichotomy between M1 and M2. In the pro-inflammatory phenotypes, microglia can disrupt synaptic plasticity such as long- term potentiation that can result in disorders of learning and memory of the type observed in Peri-operative Neurocognitive Disorders. Therefore, investigators have sought strategies to prevent microglia from provoking this adverse event in the perioperative period. In preclinical studies microglia can be depleted by removing trophic factors required for its maintenance; subsequent repopulation with a more beneficial microglial phenotype may result in memory enhancement, improved sensory motor function, as well as suppression of neuroinflammatory and oxidative stress pathways. Another approach consists of preventing microglial activation using the non-specific P38 MAP kinase blockers such as minocycline. Perhaps a more physiologic approach is the use of inhibitors of potassium (K+) channels that are required to convert the microglia into an active state. In this context the specific K+ channels that are implicated are termed Kv1.3 and KCa3.1 and high selective inhibitors for each have been developed. Data are accumulating demonstrating the utility of these K+ channel blockers in preventing Perioperative Neurocognitive Disorders.

Highlights

  • The aseptic trauma of surgery initiates an inflammatory cascade leading to neuroinflammation that culminates in microglial activation

  • Microglia are the resident macrophages of the central nervous system (CNS) parenchyma and share the same yolk sac origin as other long-lived tissue macrophages (Ginhoux et al, 2010; Perdiguero et al, 2015)

  • Using a rodent model of aseptic trauma, we have investigated the potential role of microglia for cognitive decline assessed as a decrease in freezing behavior to a previously trained aversive stimulus

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Summary

INTRODUCTION

The aseptic trauma of surgery initiates an inflammatory cascade leading to neuroinflammation that culminates in microglial activation. When an engineered virus that expresses CD55, an inhibitor of complement activation, was injected into the brains of these mice there was an increase in freezing behavior (i.e., improvement in memory) at day 35 after contextual fear conditioning in association with higher levels of activation (using c-fos) of engram cells and decreased levels of synaptic proteins within microglia (Wang C. et al, 2020). Following depletion of microglial by a 21-day course of PLX3397, an ischemic-reperfusion injury from transient middle cerebral artery occlusion (MCAO) resulted in enhancement of the neurological deficit and infarct size; these changes were associated with higher ROS, and pro-inflammatory cytokines (IL1α, IL-1β, IL-6, and TNF-α) and down-regulation of growth factors such as IGF-1 were down-regulated in brain tissues. In both the slice preparation as well as in the mouse AD model, the application of senicapoc, an inhibitor of KCa3.1, prevented proinflammatory and hLTP-impairing activities of AβO and neuroinflammation, amyloid load, and improved synaptic plasticity (Jin et al, 2019)

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