# Effect of inspired oxygen fraction during anesthesia on inflammation and antioxidant enzyme activity in the mouse cortex and hippocampus

## TL;DR

This study investigates how different oxygen levels during anesthesia affect brain inflammation and antioxidant activity in young and aged mice.

## Contribution

The study reveals region-specific effects of high oxygen levels on hippocampal inflammation in mice during anesthesia.

## Key findings

- FiO₂ 80% increased IL-1β levels in the hippocampus compared to controls.
- No significant differences in cytokine levels or SOD activity were observed between FiO₂ 30% and controls.
- The study suggests limited neuroinflammatory impact of 3 h anesthesia with different oxygen fractions.

## Abstract

Although high inspired oxygen fraction (FiO₂) is used during anesthesia to prevent hypoxemia, the effect of different oxygen fraction on the brain remains unclear. This study aims to evaluate whether different inspired oxygen fractions (FiO₂ 30% vs. 80%) during anesthesia affect inflammation and antioxidant enzyme activity in the cortex and hippocampus of young and aged mice.

Young and old mice were anesthetized with sevoflurane at FiO₂ 30% or 80% for 3 h. Mice in the control group were exposed to medical air (FiO₂ 21%) for 3 h. Cytokine and superoxide dismutase (SOD) assays were performed on the cortex and hippocampus samples after anesthesia.

The IL-1β level in the hippocampus was significantly higher in the FiO₂ 80% group compared with controls [5.0 (4.0–6.9) pg. mL−1 vs. 2.3 (1.6–2.7) pg. mL−1; adjusted p = 0.032], whereas no significant differences were observed in IL-1β levels between the control and FiO₂ 30% groups [adjusted p = 0.164] or the FiO₂ 30% and FiO₂ 80% groups [adjusted p = 0.390]. Except for IL-1β in the hippocampus, no significant differences in the cytokine levels and SOD activities were observed among the groups according to the inspired oxygen fraction in either brain region or age group [p > 0.05].

Only 80% oxygen increased hippocampal IL-1β compared with controls, suggesting region-specific vulnerability to oxygen-induced neuroinflammation. However, no significant differences between FiO₂ levels (30% vs. 80%) indicate a limited neuroinflammatory impact under 3 h of anesthesia. Further studies with longer exposure and surgical conditions are needed to clarify the clinical implications.