Open Access

Hyperoxia provokes a time- and dose-dependent inflammatory response in mechanically ventilated mice, irrespective of tidal volumes

  • Hendrik J. F. Helmerhorst1, 2, 3Email author,
  • Laura R. A. Schouten3, 4,
  • Gerry T. M. Wagenaar5,
  • Nicole P. Juffermans3, 4,
  • Joris J. T. H. Roelofs6,
  • Marcus J. Schultz3, 4,
  • Evert de Jonge1 and
  • David J. van Westerloo1
Intensive Care Medicine Experimental20175:27

https://doi.org/10.1186/s40635-017-0142-5

Received: 27 January 2017

Accepted: 18 May 2017

Published: 26 May 2017

Abstract

Background

Mechanical ventilation and hyperoxia have the potential to independently promote lung injury and inflammation. Our purpose was to study both time- and dose-dependent effects of supplemental oxygen in an experimental model of mechanically ventilated mice.

Methods

Healthy male C57Bl/6J mice, aged 9–10 weeks, were intraperitoneally anesthetized and randomly assigned to the mechanically ventilated group or the control group. In total, 100 mice were tracheotomized and mechanically ventilated for either 8 or 12 h after allocation to different settings for the applied fractions of inspired oxygen (FiO2, 30, 50, or 90%) and tidal volumes (7.5 or 15 ml/kg). After euthanisation arterial blood, bronchoalveolar lavage fluid (BALf) and tissues were collected for analyses.

Results

Mechanical ventilation significantly increased the lung injury score (P < 0.05), mean protein content (P < 0.001), and the mean number of cells (P < 0.01), including neutrophils in BALf (P < 0.001). In mice ventilated for 12 h, a significant increase in TNF-α, IFN-γ, IL-1β, IL-10, and MCP-1 (P < 0.01) was observed with 90% FiO2, whereas IL-6 showed a decreasing trend (P for trend = 0.03) across FiO2 groups. KC, MIP-2, and sRAGE were similar between FiO2 groups. HMGB-1 was significantly higher in BALf of mechanically ventilated mice compared to controls and showed a gradual increase in expression with increasing FiO2. Cytokine and chemokine levels in BALf did not markedly differ between FiO2 groups after 8 h of ventilation. Differences between the tidal volume groups were small and did not appear to significantly interact with the oxygen levels.

Conclusions

We demonstrated a severe vascular leakage and a pro-inflammatory pulmonary response in mechanically ventilated mice, which was enhanced by severe hyperoxia and longer duration of mechanical ventilation. Prolonged ventilation with high oxygen concentrations induced a time-dependent immune response characterized by elevated levels of neutrophils, cytokines, and chemokines in the pulmonary compartment.

Keywords

Hyperoxia Mechanical ventilation mice VILI Inflammation Oxygen toxicity

Background

Supplemental oxygen administration is essential to enhance survival in respiratory impaired and mechanically ventilated patients. Inspiratory fractions of oxygen (FiO2) typically exceed concentrations of atmospheric air and are frequently applied for prolonged periods during mechanical ventilation in patients suffering from severe respiratory distress. However, both mechanical ventilation and hyperoxia can promote lung injury and induce adverse effects through diverse mechanisms. Clinical studies have retrospectively shown associations between arterial hyperoxia and poor outcomes during specific cardiovascular, neurological, respiratory, and traumatic events [14]. Accumulating evidence indicates a U-shaped survival curve of critically ill and mechanically ventilated patients in relation to arterial oxygen levels in the first 24 h of admission [58].

Impaired lung function may be caused by the adverse hemodynamic effects that are mainly imputed to direct vasoconstrictive actions of high oxygen concentrations, and atelectasis which may be aggravated by local and systemic inflammatory responses. These responses have repeatedly been documented in rodents following hyperoxic exposure in inhalation chambers [915]. Although hyperoxia has been suggested to induce time-dependent inflammatory responses [10], studies in animals are usually restricted to periods of up to 6 h of mechanical ventilation, limiting its clinical applicability [1619]. Furthermore, the interaction between mechanical ventilation and concurrent hyperoxia may transcend lung injury by alveolar distention alone [9, 17, 2022]. Given that oxygen therapy cannot altogether be avoided, we aimed to increase knowledge on the host response to different levels of oxygen. Hypothesizing that hyperoxia induces a dose-dependent gradual inflammatory response that may be aggravated by prolonged periods of mechanical ventilation, our purpose was to induce hyperoxia in mice and study both time- and dose-dependent inflammation effects of supplemental oxygen during prolonged ventilatory support with protective and injurious tidal volumes.

Methods

The Animal Care and Use Committee of the Academic Medical Center of the University of Amsterdam, The Netherlands, approved the study protocol in accordance with applicable research and ethical protocols. Animal procedures were performed in consistence with Institutional Standards for Care and Use of Laboratory Animals.

Animals

Healthy male C57Bl/6J mice were obtained from Charles River (Maastricht, The Netherlands) and housed in a temperature- and light-controlled room. The animals were acclimatized at the animal facility for at least 7 days and had free access to rodent chow and water. Animal welfare was warranted throughout the experiment [23]. Conscious animals were injected twice for intraperitoneal prehydration and anesthesia induction. Thereafter, mice were regularly checked on pain stimuli and discomfort. The titration scheme for adequate anesthesia was determined in pilot experiments.

Design

At baseline, 109 mice aged 9–10 weeks (20–28 g) were intraperitoneally prehydrated with a bolus of 1 ml normal saline and randomly assigned to the mechanical ventilation (MV) group (n = 100) or the control group (n = 9). All mice in the MV group were randomized to subgroups (n = 8–9 per subgroup) by allocating different settings for the applied fractions of inspired oxygen (FiO2 = 30, 50, or 90%), tidal volume (TV = 7.5 or 15 ml/kg), and MV duration (8 or 12 h). The control group mice were spread over multiple days along with the instrumentation of the MV groups during the whole experimental period.

Experimental procedures have been described in detail previously [24, 25]. One hour after prehydration, mice assigned to the MV groups (n = 8–9 per group) were anesthetized with a 0.15–0.21 ml intraperitoneal bolus of 126 mg/kg ketamine (Eurovet Animal Health BV, Bladel, The Netherlands), 0.1 mg/kg dexmedetomidine 0.5 mg/ml (Elanca Animal Health, Houten, The Netherlands), 0.5 mg/kg atropine sulfate (Centrafarm BV, Etten-Leur, The Netherlands), and 5 ml/kg 0.9% saline. Maintenance anesthesia was injected hourly through an intraperitoneal catheter (PE 10 tubing, BD, Breda, The Netherlands) and consisted of 36 mg/kg ketamine, 0.02 mg/kg dexmedetomidine, 0.075 mg/kg atropine sulfate, and 9.45 ml/kg 0.65% saline. A 1:5 mix of 0.65% saline and 8.4% sodium bicarbonate was intraperitoneally administered through the catheter every 30 min in order to compensate for fluid loss and maintain physiological bicarbonate levels [25]. Body temperature was strictly controlled between 36.5 and 37.5 °C. Systolic blood pressure and heart rate were noninvasively measured using a murine tail pressure cuff with pulse transducer and monitored on a data acquisition system (LabChart, ADInstruments Ltd, Oxford, UK). Tidal volumes were monitored using a calibrated pneumotachometer (tracheal cannula OD = 1.3 mm, PTM type 378/0.9, HSE-Harvard Apparatus GmbH, March-Hugstetten, Germany) and respiration data acquisition software (BDAS, HSE-Harvard Apparatus GmbH).

Anesthetized mice were tracheotomized, and a Y-tube connector (OD 1.0 mm, ID 0.6 mm) was surgically inserted in the trachea and fixed above the carina. Subsequently, animals were placed on a heating plate in supine position and connected to the ventilator (Babylog 8000 plus, Dräger Medical, Lübeck, Germany). Ventilator settings were pre-determined in pilot experiments and targeted at normal acid–base balance [24]. Ventilators were pressure-controlled and set to deliver low tidal volume (LTV, 7.5 ml/kg) or high tidal volume (HTV, 15 ml/kg). In both ventilation strategies, positive end-expiratory pressure (PEEP) levels were set at 3 cmH2O and the inspiration to expiration ratio at 1:2.8. Respiratory rates were controlled at 160 (LTV) or 52 (HTV) breaths per minute. Recruitment maneuvers were performed every 30 (LTV) or 60 (HTV) minutes by means of inspiratory holds with a pressure of 20 mbar during 5 s.

Immediately after randomization, ventilators were adjusted to the assigned settings by an independent biotechnician. Inspiratory pressures were adjusted and regulated to achieve appropriate TV throughout the experiment. At the end of the experiment, ventilated mice were euthanized by withdrawing blood from the carotid artery. Researchers were blinded for administered FiO2 levels during the experimental procedures. The allocation code of randomization was supplied by the time all data and assay results were collected.

Measurements

After euthanization, arterial blood was collected in heparin-coated syringes and used for blood gas analysis (Rapidpoint 405, Siemens Healthcare, Tarrytown, NY, USA). Lungs were resected en bloc, and the right lung was instilled with normal saline (3 × 0.5 ml) to obtain bronchoalveolar lavage fluid (BALf), which was used for automated cell counting (Z2 Beckman Coulter Counter, Brea, USA). Differential counts were performed on Giemsa stained cytospin slides. BALf was centrifuged, and the supernatant was stored at −80 °C for assessment of protein levels and cytokines. The left lung was weighed and thereafter fixed in 4% formalin and embedded in paraffin. Lung sections were stained with hematoxylin eosin (H&E) to analyze lung histopathology. A dedicated pathologist determined the histopathological lung injury score on a nominal scale by the sum of the score for four pathologic parameters: edema, hemorrhage, interstititial cell infiltration, and hyaline membranes as described previously [24]. Relative lung weight, expressed as lung weight corrected for total body weight at baseline, was used as surrogate for lung tissue edema.

Cytokines (IL-1β, IL-6, IL-10, MCP-1, MIP-2, KC, TNF-α, IFN-γ) were measured in BALf by Luminex (Merck Millipore Chemicals BV, Amsterdam, The Netherlands). High-mobility group box-1 (HMGB-1, IBL International BV, Amersfoort, The Netherlands) and the soluble receptor for advanced glycation end products (sRAGE, R&D Systems, Abingdon, UK) were determined by enzyme-linked immunosorbent assays (ELISA) according to the manufacturer’s protocols. Total protein levels were determined in serum and BALf (Oz Biosciences, Marseille, France), using bovine serum albumin as reference.

The right lung was used for total RNA isolation from tissue homogenates (RNA-Bee, Tel-Test Inc, Bio-Connect BV, Huissen, The Netherlands), first-strand cDNA synthesis (SuperScript Choice System, Life Technologies, Breda, The Netherlands), and real-time quantitative PCR (TNF-α, IL-6, MMP-12, MCP-1, TF, PAI-1), using β-actin as a housekeeping gene reference, were performed on a LightCycler 480 (Roche, Almere, The Netherlands) of the Leiden Genome Technology Center (Leiden, The Netherlands) as described previously [26].

Statistical analysis

The partial pressure of arterial oxygen (PaO2) at the end of the experiment was defined as the primary outcome. Inflammatory markers and markers of lung injury were assessed as secondary outcomes. Based on previous pilot results and with a group size of eight animals per group the Wilcoxon rank-sum test ensures 80% power using a two-sided significance level of 0.05 to detect an estimated effect size of 1.85 that the observed parameter differs between groups. With an anticipated dropout rate of one per group, nine animals were initially assigned to each group. Differences between study groups were tested with one-way analysis of variance or Kruskal Wallis as appropriate. Cuzick’s test was used to test for trends across different FiO2 groups. Statistical analyses were performed using R version 3.2.1 (R Foundation for Statistical Computing, Vienna, Austria) and STATA/SE 10.1 (StataCorp LP, College Station, TX, USA).

Results

All mice survived mechanical ventilation with the applied settings in a volume-targeted approach (Table 1). Mean systolic blood pressures decreased gradually during 8 or 12 h of mechanical ventilation (145 to 90 mmHg) and were slightly higher in the 90% FiO2 group (Table 1, Additional file 1 Figure S1). Heart rates and body temperatures remained stable throughout the experiment.
Table 1

Ventilation and hemodynamic parameters

 

8 h

12 h

30%

50%

90%

30%

50%

90%

LTV

 TV (μl)

181 (0)

182 (0)

179 (0)

176 (0)

178 (1)

176 (0)

 Pinsp (mbar)

13 (0)

14 (0)

12 (0)

12 (0)

13 (0)

12 (0)

 SBP (mmHg)

116 (7)

128 (7)

123 (5)

103 (4)

102 (5)

112 (4)

HTV

 TV (μl)

351 (0)

379 (1)

372 (1)

366 (2)

371 (1)

360 (1)

 Pinsp (mbar)

20 (0)

21 (0)

20 (0)

20 (0)

20 (0)

20 (0)

 SBP (mmHg)

114 (6)

136 (8)

124 (7)

104 (4)

110 (6)

113 (5)

Data are means ± SD. TV = tidal volume, Pinsp = inspiratory pressure, SBP = systolic blood pressure. All indicated parameters were measured hourly.

Oxygenation and ventilation

The partial pressure of oxygen in the carotid arterial blood at the end of mechanical ventilation was distinctly higher with increasing fractions of supplied oxygen (P < 0.001, Fig. 1a). Partial pressure of arterial carbon dioxide (PaCO2) was in general lower for the HTV groups but did not show a trend across FiO2 groups (Fig. 1b). The PaO2/FiO2 ratio decreased for mechanically ventilated mice in comparison to controls and was markedly higher for HTV groups after 12 h of mechanical ventilation (Fig. 1c). Dynamic lung compliance decreased gradually over the study interval for all study groups, but the decrease was nearly complete after 3 h of mechanical ventilation and was larger for the HTV groups (Fig. 1d).
Fig. 1

Arterial oxygenation and ventilation parameters. Data are means ± SEM. Arterial oxygenation in carotid blood (a, upper left panel), arterial carbon dioxide in carotid blood (b, upper right panel), PaO2/FiO2 ratio (c, lower left panel), and dynamic compliance (d, lower right panel). Facets within the panels represent mechanical ventilation time. Different colors represent different tidal volume groups, and different transparency levels represent different FiO2 groups. 0h no mechanical ventilation time, control group; 8h 8 h of mechanical ventilation, 12h 12 h of mechanical ventilation, LTV low tidal volumes, HTV high tidal volumes. Dynamic lung compliance (tidal volume size/(peak inspiratory pressure − PEEP) was measured hourly. PaO2 and PaCO2 were measured once in the arterial blood gas sample taken from the carotid artery at the end of the experiment

Markers of lung injury

Mechanical ventilation significantly increased the lung injury score (Fig. 2a, 1.6-fold at 8 h, P < 0.01; and 1.5-fold at 12 h, P < 0.05), mean protein content (Fig. 2b, 2.6-fold at 8 h, P < 0.001; and 2.2-fold at 12 h, P < 0.001), and the mean number of cells (Fig. 2c, 1.7-fold at 8 h, P < 0.01; and 2.0-fold at 12 h, P < 0.001), including neutrophils in BALf (Fig. 2d, 132-fold at 8 h, P < 0.001; and 180-fold at 12 h, P < 0.001), demonstrating vascular leakage and inflammation as a result of mechanical ventilation even at relatively low hyperoxic conditions of 30% FiO2 and low tidal volumes. Increased hyperoxia up to 90% FiO2 did not further increase protein content or the total number of cells in BALf but showed an increased trend in the percentage of neutrophils towards higher FiO2 levels (P for trend = 0.03). Histopathology showed a decrease in air restraint, suggesting progressive alveolar collapse, with higher oxygen levels (Additional file 1 Figure S2), but this was not translated in a significant difference in the lung injury score between the different FiO2 groups (Fig. 2a).
Fig. 2

Markers of lung injury in BALf after indicated study interval. Data are means ± SEM. Lung injury score (a, upper left panel), total protein content (b, upper right panel), total cell counts (c, lower left panel), and proportion of neutrophils (d, lower right panel) in BALf obtained after the study interval. Facets within the panels represent mechanical ventilation time. Different colors represent different tidal volume groups, and different transparency levels represent different FiO2 groups. 0h no mechanical ventilation time, control group; 8h 8 h of mechanical ventilation, 12h 12 h of mechanical ventilation, LTV low tidal volumes, HTV high tidal volumes

Markers of inflammation

Cytokine and chemokine levels in BALf increased at 8 and 12 h after mechanical ventilation but did not markedly differ between FiO2 groups at 8 h of ventilation (P for trend >0.05, Additional file 1 Figure S3). In mice ventilated for 12 h, a significantly increasing trend in TNF-α, IFN-γ, IL-1β, IL-10, and MCP-1 (Fig. 3, P for trend <0.01) was observed with increasing FiO2, whereas IL-6 showed a decreasing trend (P for trend = 0.03). KC, MIP-2, and sRAGE were similar between FiO2 groups. HMGB-1 was significantly higher in BALf of mechanically ventilated mice compared to controls and showed a gradual increase in expression with increasing FiO2. Almost no differences in cytokine and chemokine levels in the BALf were observed between the 30 and 50% oxygen groups.
Fig. 3

Inflammatory mediators in BALf in controls and after 12 h of mechanical ventilation. Cytokine and chemokine levels in BALf obtained after 12 h of mechanical ventilation. Data are means ± SEM. Facets within the panels represent mechanical ventilation time. Different colors represent different tidal volume groups, and different transparency levels represent different FiO2 groups. 0h no mechanical ventilation time, control group; 12h 12 h of mechanical ventilation, LTV low tidal volumes, HTV high tidal volumes. Cuzick’s P for trend in increasing oxygen levels at 12 h of mechanical ventilation: IL-1β, <0.001; MIP-2, 0.27; IL-6, 0.03; KC, 0.22; IL-10, 0.001; MCP-1, <0.001; TNF-α, 0.001; IFN-γ, 0.001; sRAGE, 0.11; HMGB-1, 0.001. *P for trend <0.05; **P for trend <0.01; ***P for trend <0.001

Differences between the tidal volume groups were small (Additional file 1 Figure S4) and did not appear to significantly interact with the oxygen levels (P > 0.50 for the interaction term for each inflammatory mediator, except for IL-6, P = 0.03). Inflammatory markers were also measured at 12 h of mechanical ventilation in the serum and are shown in Additional file 1 Figure S5.

The RNA expression of selected markers showed an increased relative expression of TNF-α, IL-6, and MCP-1 in lung homogenate of mice that were mechanically ventilated with high tidal volumes compared to controls (Additional file 1 Figure 6).

Discussion

In this experimental study, we demonstrated a severe vascular leakage and a pro-inflammatory pulmonary response in mechanically ventilated mice, which was enhanced by severe hyperoxia and longer duration of mechanical ventilation. Prolonged ventilation with high oxygen concentrations induced a time-dependent immune response characterized by elevated levels of neutrophils, cytokines, and chemokines in the pulmonary compartment.

Although most studies in mechanically ventilated animals are restricted to short exposure periods, recent experiments in mechanically ventilated rodents, rabbits, and pigs, mimicking the clinical environment of critically ill patients, showed that hyperoxia serves as an important cofactor in acute lung injury, bacterial dissemination, progression of multiple system organ dysfunction, and lethality [1315] but can also improve organ function and attenuate tissue apoptosis during shock [27]. In our study, divergent effects were observed in the expression of selected inflammatory markers across the experimental groups, which may be explained by the complex kinetics and dynamics of the immune response due to the concurrent exposure to anesthesia, mechanical ventilation, and hyperoxia. Interaction between pro- and anti-inflammatory cytokines may contribute to the differences in cytokine levels in the experimental groups. Rapid upregulation of TNF-α was seen even in the acute phase reaction after induction of anesthesia in control mice. Cytokine concentrations may decrease after long-term hyperoxic exposure, and a fast upregulation of inflammatory action can be followed by a gradual impairment or suppression of the innate immune system [28], which may in turn make the lung more susceptible to injury and infection. Differences in cytokine levels between the FiO2 groups were relatively mild. We observed a strong inflammatory effect at very high oxygen concentrations (FiO2 90%) while the increase from 30 to 50% did not make a large difference. Indeed, 50% of inspired oxygen may not be as detrimental as 90% as evidenced by the clear increase in neutrophils and most cytokines during 90% oxygen administration, which was also described in other studies [2932]. In addition, ventilation with 30% may actually be a model of relative tissue hypoxia in mice following progressive lung injury during the experiment, although this was not reflected by the PaO2 levels. Comparison with control groups suggests that mechanical ventilation itself was very harmful, possibly not allowing additional damage by increasing oxidative stress. Both hypoxia and hyperoxia may induce oxidative stress, and relative changes in hyperoxia may trigger upregulation of the hypoxia inducible factor (HIF) [33].

Furthermore, damage-associated molecular pattern (DAMP) molecules play a key role in the inflammatory response to injury and have been suggested to modulate the effects of hyperoxia and oxidative stress [34, 35]. In this matter, HMGB-1 has been described as the archetypal chemokine that is upregulated by the innate immune system in response to cell stress [36]. We also observed increased levels of this protein in the lungs of mechanically ventilated mice, particularly after concurrent exposure to high FiO2. The overall protein content did not significantly increase with severe hyperoxia, but this interpretation may be limited as we did not correct the protein in BALf for urea (epithelial lining fluid). The expression of most cytokines in BALf was not essentially different than in the serum, which may be a result of extended duration of mechanical ventilation causing systemic inflammation. In line with previous experiments, the presence of cytokines with short term ventilation was definitely more pronounced in the pulmonary compartment compared to circulating blood of rodents [25, 37].

Our study and others generated conflicting data regarding the inflammatory response after hyperoxic ventilation describing both pro- [15, 17, 38, 39] and anti-inflammatory [40, 41] responses. Kiers et al. recently demonstrated that, in the absence of systemic inflammation, short-term hyperoxia without mechanical ventilation does not result in increased levels of inflammatory cytokines, neutrophil phagocytosis, nor ROS generation in both mice and healthy volunteers [42]. In the present study, the expression of inflammatory markers was shown to be divergent after mechanical ventilation and with increasing FiO2, which is consistent with previous research [16]. Bailey et al. concluded that prolonged mechanical ventilation of healthy rat lungs with a physiological strategy can contribute to the inflammatory response and cause alterations to pulmonary surfactant [43]. Lung injury due to continuous hyperoxic exposure has also been shown to be dose-dependent in rats [12, 15].

Some clinical scenarios may dictate non-protective ventilation, both with high pressures and high levels of inspired oxygen in patients with heavily injured lungs. However, it is not exactly known whether this combination works synergistically in causing lung injury. Our data do not imply such an “add-on effect,” but the discrepancy with a previous study [20] may be explained by the use of lower tidal volumes in our study. It is also possible that the extended duration of mechanical ventilation alone was enough to cause ventilator-induced lung injury (VILI) without an additional effect of tidal volume size. An alternative explanation may be that lower respiratory rates compensated for high tidal volumes, while higher respiratory rates increased the risk of lung injury in the lower tidal volume groups. Also, some of the deleterious properties of hyperoxia may be overcome by applying PEEP, as it may counteract alveolar collapse from progressive nitrogen washout and mitigate the effects of atelectrauma [44].

In our study, lung injury scores did not reveal any histopathological difference between study groups. However, in previous work using a high tidal volume strategy with zero PEEP, total histopathology scores were shown to be higher compared to low tidal volumes and 3 cmH2O PEEP with a marginal additive effect of ventilation duration [24]. This was in accordance with a study reporting that pre-exposure to hyperoxia increases the susceptibility to VILI before initiation of mechanical ventilation [22]. Others documented that short-term exposure to levels of oxygen up to 100% does not increase the changes in respiratory system mechanics induced by mechanical ventilation [16]. The progressive airway collapse and inflammation with increasing FiO2 may not have been severe enough to induce histopathological changes and affect lung function in our model. The striking heterogeneity that exists between experimental studies may be explained by differences in subjects (e.g., species, strains, genetical modification, age, sex), and exposure (e.g., pre-exposure, severity, duration, anesthesia, ventilation).

Although the experiments were performed according to the high standards for methodological quality of animal research [45], several limitations may apply to our experimental procedures. The lavage technique of the lungs may induce subtle differences in the dilution of returned fluid, although saline injection volumes were standardized. Storage of biological specimens was secured according to high-quality protocols. Our analyses were restricted to specific features of injurious ventilation and hyperoxia, yet other underlying mechanisms affecting reactive oxygen species and mitochondrial damage have not been considered. Other covariates such as PaCO2 may have influenced the results, even though this cannot be seen separate from ventilation settings and was inherent to adjusting tidal volumes and FiO2. Furthermore, low respiratory rates, especially in the LTV group, are subphysiological for mice and may cause relative hypercapnia.

The experimental setting may hamper translation of study results to the clinical setting. Indeed, smaller species, such as mice have different lung mechanics and immune reactions than humans [46, 47]. Healthy mice may also respond differently than critically ill patients, especially in case of injured lungs prior to the start of mechanical ventilation. Interestingly, moderate hyperoxia in mechanically ventilated patients without severe respiratory failure does not appear to increase systemic or pulmonary inflammation [48].

Further, the C57Bl/6J type mice that we used are the most widely used strain of mice for experimental research but have been shown to carry a spontaneous mutation, which can result in mitochondrial redox abnormalities and may influence the functionality of the hyperoxia defense [49].

Strengths of this study include the prolonged duration of mechanical ventilation which may be representative of the intensive care unit (ICU) setting, where hyperoxia acts as a second hit on top of VILI. Indeed, we showed that the immune response was considerably stronger at 12 h of mechanical ventilation compared to 8 h, which may imply that models applying mechanical ventilation for extended duration more accurately reflect the underlying mechanisms and long-term effects. Demonstrable lung injury may follow the inflammatory response even later than after 12 h of hyperoxic mechanical ventilation. As such, our results further accentuate that we should limit the exposure to supraphysiological oxygen levels from excessive oxygen supply when prolonged periods of mechanical ventilation are anticipated.

Conclusions

Prolonged experimental hyperoxic mechanical ventilation was associated with a significant inflammatory response in the lung as evidenced by an influx of neutrophils in the pulmonary compartment and upregulation of specific inflammatory markers, which was not directly translated into extensive tissue lung injury or a change in lung compliance. The present experimental data may aid to determine optimal ventilator strategies in mechanically ventilated patients, but the dynamics and kinetics of hyperoxic ventilation need further exploration in order to characterize the long-term effects and investigate protective measures.

Abbreviations

BALf: 

Bronchoalveolar lavage fluid

DAMP: 

Damage associated molecular pattern

ELISA: 

Enzyme-linked immunosorbent assays

FiO2

Fraction of inspired oxygen

HIF: 

Hypoxia inducible factor

HMGB-1: 

High-mobility group box-1

HTV: 

High tidal volume

ICU: 

Intensive care unit

IFN-γ: 

Interferon-γ

IL-10: 

Interleukin-10

IL-1β: 

Interleukin-1β

IL-6: 

Interleukin-6

KC: 

Kupffer Cell

LTV: 

Low tidal volume

MCP-1: 

Monocyte Chemoattractant Protein-1

MIP-2: 

Macrophage Inflammatory Protein-2

MV: 

Mechanical ventilation

PaCO2

Partial pressure of arterial carbon dioxide

PaO2

Partial pressure of arterial oxygen

PEEP: 

Positive end-expiratory pressure

sRAGE: 

soluble Receptor for Advanced Glycation End products

TNF-α: 

Tumor necrosis factor-α

TV: 

Tidal volume

VILI: 

Ventilator-induced lung injury

Declarations

Acknowledgements

Biotechnical and bio-analytical assistance by Jacoline Buchner-Doeven and Anita Tuip-de Boer is gratefully acknowledged.

Funding

Hendrik J.F. Helmerhorst is supported by the ESICM Young Investigator Award.

Availability of data and materials

All data are presented within the manuscript or in the additional files.

Authors’ contributions

HH had full access to the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. LS assisted in the execution of the experimental procedures and contributed to the critical revision of the manuscript. GW assisted in analysis and interpretation of the RNA data from tissue homogenate and contributed to the critical revision of the manuscript. JR assisted in the analysis and interpretation of lung histopathology and contributed to the critical revision of the manuscript. HH, NJ, MS, EdJ, and DvW contributed substantially to the study design, interpretation of the data, and writing and critical revision of the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval

The Animal Care and Use Committee of the Academic Medical Center of the University of Amsterdam, The Netherlands, approved the study protocol in accordance with applicable research and ethical protocols. Animal procedures were performed in consistence with Institutional Standards for Care and Use of Laboratory Animals.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors’ Affiliations

(1)
Department of Intensive Care Medicine, Leiden University Medical Center
(2)
Department of Anesthesiology, Leiden University Medical Center
(3)
Laboratory of Experimental Intensive Care and Anesthesiology, Academic Medical Center
(4)
Department of Intensive Care Medicine, Academic Medical Center
(5)
Department of Pediatrics, Laboratory of Neonatology, University Medical Center Leiden
(6)
Department of Pathology, Academic Medical Center

References

  1. Austin MA, Wills KE, Blizzard L, Walters EH, Wood-Baker R (2010) Effect of high flow oxygen on mortality in chronic obstructive pulmonary disease patients in prehospital setting: randomised controlled trial. BMJ 341:c5462View ArticlePubMedPubMed CentralGoogle Scholar
  2. Farquhar H, Weatherall M, Wijesinghe M, Perrin K, Ranchord A, Simmonds M, Beasley R (2009) Systematic review of studies of the effect of hyperoxia on coronary blood flow. Am Heart J 158(3):371–377View ArticlePubMedGoogle Scholar
  3. Kilgannon JH, Jones AE, Shapiro NI, Angelos MG, Milcarek B, Hunter K, Parrillo JE, Trzeciak S, EMSRN E (2010) Association between arterial hyperoxia following resuscitation from cardiac arrest and in-hospital mortality. JAMA 303(21):2165–2171View ArticlePubMedGoogle Scholar
  4. Helmerhorst HJ, Roos-Blom MJ, van Westerloo DJ, de Jonge E (2015) Association between arterial hyperoxia and outcome in subsets of critical illness: a systematic review, meta-analysis, and meta-regression of cohort studies. Crit Care Med 43(7):1508–1519View ArticlePubMedGoogle Scholar
  5. de Jonge E, Peelen L, Keijzers PJ, Joore H, de Lange D, van der Voort PH, Bosman RJ, de Waal RA, Wesselink R, de Keizer NF (2008) Association between administered oxygen, arterial partial oxygen pressure and mortality in mechanically ventilated intensive care unit patients. Crit Care 12(6):R156View ArticlePubMedPubMed CentralGoogle Scholar
  6. Eastwood G, Bellomo R, Bailey M, Taori G, Pilcher D, Young P, Beasley R (2012) Arterial oxygen tension and mortality in mechanically ventilated patients. Intensive Care Med 38(1):91–98View ArticlePubMedGoogle Scholar
  7. Helmerhorst HJ, Roos-Blom MJ, van Westerloo DJ, Abu-Hanna A, de Keizer NF, de Jonge E (2015) Associations of arterial carbon dioxide and arterial oxygen concentrations with hospital mortality after resuscitation from cardiac arrest. Crit Care 19:348View ArticlePubMedPubMed CentralGoogle Scholar
  8. Helmerhorst HJ, Arts DL, Schultz MJ, van der Voort PH, Abu-Hanna A, de Jonge E, van Westerloo DJ (2017) Metrics of arterial hyperoxia and associated outcomes in critical care. Crit Care Med 45(2):187–195View ArticlePubMedGoogle Scholar
  9. Bailey TC, Martin EL, Zhao L, Veldhuizen RA (2003) High oxygen concentrations predispose mouse lungs to the deleterious effects of high stretch ventilation. J Appl Physiol (1985) 94(3):975–982View ArticleGoogle Scholar
  10. Nagato AC, Bezerra FS, Lanzetti M, Lopes AA, Silva MA, Porto LC, Valenca SS (2012) Time course of inflammation, oxidative stress and tissue damage induced by hyperoxia in mouse lungs. Int J Exp Pathol 93(4):269–278View ArticlePubMedPubMed CentralGoogle Scholar
  11. Martin EL, McCaig LA, Moyer BZ, Pape MC, Leco KJ, Lewis JF, Veldhuizen RA (2005) Differential response of TIMP-3 null mice to the lung insults of sepsis, mechanical ventilation, and hyperoxia. Am J Physiol Lung Cell Mol Physiol 289(2):L244–251View ArticlePubMedGoogle Scholar
  12. Nagato A, Silva FL, Silva AR, Bezerra FS, Oliveira ML, Bello-Klein A, Cristovao Porto L, Santos Valenca S (2009) Hyperoxia-induced lung injury is dose dependent in Wistar rats. Exp Lung Res 35(8):713–728View ArticlePubMedGoogle Scholar
  13. Kikuchi Y, Tateda K, Fuse ET, Matsumoto T, Gotoh N, Fukushima J, Takizawa H, Nagase T, Standiford TJ, Yamaguchi K (2009) Hyperoxia exaggerates bacterial dissemination and lethality in Pseudomonas aeruginosa pneumonia. Pulm Pharmacol Ther 22(4):333–339View ArticlePubMedGoogle Scholar
  14. Tateda K, Deng JC, Moore TA, Newstead MW, Paine R 3rd, Kobayashi N, Yamaguchi K, Standiford TJ (2003) Hyperoxia mediates acute lung injury and increased lethality in murine Legionella pneumonia: the role of apoptosis. J Immunol 170(8):4209–4216View ArticlePubMedGoogle Scholar
  15. Rodriguez-Gonzalez R, Martin-Barrasa JL, Ramos-Nuez A, Canas-Pedrosa AM, Martinez-Saavedra MT, Garcia-Bello MA, Lopez-Aguilar J, Baluja A, Alvarez J, Slutsky AS et al (2014) Multiple system organ response induced by hyperoxia in a clinically relevant animal model of sepsis. Shock 42(2):148–153View ArticlePubMedGoogle Scholar
  16. Cannizzaro V, Berry LJ, Zosky GR, Turner DJ, Hantos Z, Sly PD (2009) Impact of supplemental oxygen in mechanically ventilated adult and infant mice. Respir Physiol Neurobiol 165(1):61–66View ArticlePubMedGoogle Scholar
  17. Li LF, Liao SK, Ko YS, Lee CH, Quinn DA (2007) Hyperoxia increases ventilator-induced lung injury via mitogen-activated protein kinases: a prospective, controlled animal experiment. Crit Care 11(1):R25View ArticlePubMedPubMed CentralGoogle Scholar
  18. Andrade PV, Dos Santos JM, Silva HC, Wilbert DD, Cavassani SS, Oliveira-Junior IS (2013) Influence of hyperoxia and mechanical ventilation in lung inflammation and diaphragm function in aged versus adult rats. Inflammation 37(2):486–494View ArticleGoogle Scholar
  19. Cavassani SS, Junqueira VB, Moraes JB, Luzo KK, Silva CM, Barros M, Marinho M, Simoes RS, Oliveira-Junior IS (2011) Short courses of mechanical ventilation with high-O2 levels in elderly rat lungs. Acta Cir Bras 26(2):107–113View ArticlePubMedGoogle Scholar
  20. Sinclair SE, Altemeier WA, Matute-Bello G, Chi E (2004) Augmented lung injury due to interaction between hyperoxia and mechanical ventilation. Crit Care Med 32(12):2496–2501View ArticlePubMedGoogle Scholar
  21. Altemeier WA, Sinclair SE (2007) Hyperoxia in the intensive care unit: why more is not always better. Curr Opin Crit Care 13(1):73–78View ArticlePubMedGoogle Scholar
  22. Makena PS, Luellen CL, Balazs L, Ghosh MC, Parthasarathi K, Waters CM, Sinclair SE (2010) Preexposure to hyperoxia causes increased lung injury and epithelial apoptosis in mice ventilated with high tidal volumes. Am J Physiol Lung Cell Mol Physiol 299(5):L711–719View ArticlePubMedPubMed CentralGoogle Scholar
  23. Huet O, de Haan JB (2014) The ethical dimension in published animal research in critical care: the dark side of our moon. Crit Care 18(1):120View ArticlePubMedPubMed CentralGoogle Scholar
  24. Hegeman MA, Hemmes SN, Kuipers MT, Bos LD, Jongsma G, Roelofs JJ, van der Sluijs KF, Juffermans NP, Vroom MB, Schultz MJ (2013) The extent of ventilator-induced lung injury in mice partly depends on duration of mechanical ventilation. Crit Care Res Pract 2013:435236PubMedPubMed CentralGoogle Scholar
  25. Wolthuis EK, Vlaar AP, Choi G, Roelofs JJ, Juffermans NP, Schultz MJ (2009) Mechanical ventilation using non-injurious ventilation settings causes lung injury in the absence of pre-existing lung injury in healthy mice. Crit Care 13(1):R1View ArticlePubMedPubMed CentralGoogle Scholar
  26. Wagenaar GT, ter Horst SA, van Gastelen MA, Leijser LM, Mauad T, van der Velden PA, de Heer E, Hiemstra PS, Poorthuis BJ, Walther FJ (2004) Gene expression profile and histopathology of experimental bronchopulmonary dysplasia induced by prolonged oxidative stress. Free Radic Biol Med 36(6):782–801View ArticlePubMedGoogle Scholar
  27. Barth E, Bassi G, Maybauer DM, Simon F, Groger M, Oter S, Speit G, Nguyen CD, Hasel C, Moller P et al (2008) Effects of ventilation with 100% oxygen during early hyperdynamic porcine fecal peritonitis. Crit Care Med 36(2):495–503View ArticlePubMedGoogle Scholar
  28. Baleeiro CE, Wilcoxen SE, Morris SB, Standiford TJ, Paine R 3rd (2003) Sublethal hyperoxia impairs pulmonary innate immunity. J Immunol 171(2):955–963View ArticlePubMedGoogle Scholar
  29. Okuma T, Terasaki Y, Sakashita N, Kaikita K, Kobayashi H, Hayasaki T, Kuziel WA, Baba H, Takeya M (2006) MCP-1/CCR2 signalling pathway regulates hyperoxia-induced acute lung injury via nitric oxide production. Int J Exp Pathol 87(6):475–483View ArticlePubMedPubMed CentralGoogle Scholar
  30. Chen CM (2015) Interluekin-10 for hyperoxia-induced acute lung injury: a new direction? Exp Physiol 100(3):229View ArticlePubMedGoogle Scholar
  31. Min JH, Codipilly CN, Nasim S, Miller EJ, Ahmed MN (2012) Synergistic protection against hyperoxia-induced lung injury by neutrophils blockade and EC-SOD overexpression. Respir Res 13:58View ArticlePubMedPubMed CentralGoogle Scholar
  32. Yamada M, Kubo H, Kobayashi S, Ishizawa K, Sasaki H (2004) Interferon-gamma: a key contributor to hyperoxia-induced lung injury in mice. Am J Physiol Lung Cell Mol Physiol 287(5):L1042–1047View ArticlePubMedGoogle Scholar
  33. Asikainen TM, Schneider BK, Waleh NS, Clyman RI, Ho WB, Flippin LA, Gunzler V, White CW (2005) Activation of hypoxia-inducible factors in hyperoxia through prolyl 4-hydroxylase blockade in cells and explants of primate lung. Proc Natl Acad Sci U S A 102(29):10212–10217View ArticlePubMedPubMed CentralGoogle Scholar
  34. Helmerhorst HJ, Schultz MJ, van der Voort PH, de Jonge E, van Westerloo DJ (2015) Bench-to-bedside review: the effects of hyperoxia during critical illness. Crit Care 19(1):284View ArticlePubMedPubMed CentralGoogle Scholar
  35. Krysko DV, Agostinis P, Krysko O, Garg AD, Bachert C, Lambrecht BN, Vandenabeele P (2011) Emerging role of damage-associated molecular patterns derived from mitochondria in inflammation. Trends Immunol 32(4):157–164View ArticlePubMedGoogle Scholar
  36. Kang R, Chen R, Zhang Q, Hou W, Wu S, Cao L, Huang J, Yu Y, Fan XG, Yan Z et al (2014) HMGB1 in health and disease. Mol Aspects Med 40:1–116View ArticlePubMedGoogle Scholar
  37. Beurskens CJ, Aslami H, Kuipers MT, Horn J, Vroom MB, van Kuilenburg AB, Roelofs JJ, Schultz MJ, Juffermans NP (2012) Induced hypothermia is protective in a rat model of pneumococcal pneumonia associated with increased adenosine triphosphate availability and turnover*. Crit Care Med 40(3):919–926View ArticlePubMedGoogle Scholar
  38. Thiel M, Chouker A, Ohta A, Jackson E, Caldwell C, Smith P, Lukashev D, Bittmann I, Sitkovsky MV (2005) Oxygenation inhibits the physiological tissue-protecting mechanism and thereby exacerbates acute inflammatory lung injury. PLoS Biol 3(6):e174View ArticlePubMedPubMed CentralGoogle Scholar
  39. Nagato AC, Bezerra FS, Talvani A, Aarestrup BJ, Aarestrup FM (2015) Hyperoxia promotes polarization of the immune response in ovalbumin-induced airway inflammation, leading to a TH17 cell phenotype. Immun Inflamm Dis 3(3):321–337View ArticlePubMedPubMed CentralGoogle Scholar
  40. Waisman D, Brod V, Rahat MA, Amit-Cohen BC, Lahat N, Rimar D, Menn-Josephy H, David M, Lavon O, Cavari Y et al (2012) Dose-related effects of hyperoxia on the lung inflammatory response in septic rats. Shock 37(1):95–102View ArticlePubMedGoogle Scholar
  41. Waisman D, Brod V, Wolff R, Sabo E, Chernin M, Weintraub Z, Rotschild A, Bitterman H (2003) Effects of hyperoxia on local and remote microcirculatory inflammatory response after splanchnic ischemia and reperfusion. Am J Physiol Heart Circ Physiol 285(2):H643–652View ArticlePubMedGoogle Scholar
  42. Kiers D, Gerretsen J, Janssen E, John A, Groeneveld R, van der Hoeven JG, Scheffer G-J, Pickkers P, Kox M (2015) Short-term hyperoxia does not exert immunologic effects during experimental murine and human endotoxemia. Sci Rep 5:17441View ArticlePubMedPubMed CentralGoogle Scholar
  43. Bailey TC, Maruscak AA, Martin EL, Forbes AR, Petersen A, McCaig LA, Yao LJ, Lewis JF, Veldhuizen RA (2008) The effects of long-term conventional mechanical ventilation on the lungs of adult rats. Crit Care Med 36(8):2381–2387View ArticlePubMedGoogle Scholar
  44. Lutz D, Gazdhar A, Lopez-Rodriguez E, Ruppert C, Mahavadi P, Gunther A, Klepetko W, Bates JH, Smith B, Geiser T et al (2015) Alveolar derecruitment and collapse induration as crucial mechanisms in lung injury and fibrosis. Am J Respir Cell Mol Biol 52(2):232–243View ArticlePubMedGoogle Scholar
  45. Bara M, Joffe AR (2014) The methodological quality of animal research in critical care: the public face of science. Ann Intensive Care 4:26View ArticlePubMedPubMed CentralGoogle Scholar
  46. Zosky GR, Janosi TZ, Adamicza A, Bozanich EM, Cannizzaro V, Larcombe AN, Turner DJ, Sly PD, Hantos Z (2008) The bimodal quasi-static and dynamic elastance of the murine lung. J Appl Physiol (1985) 105(2):685–692View ArticleGoogle Scholar
  47. Seok J, Warren HS, Cuenca AG, Mindrinos MN, Baker HV, Xu W, Richards DR, McDonald-Smith GP, Gao H, Hennessy L et al (2013) Genomic responses in mouse models poorly mimic human inflammatory diseases. Proc Natl Acad Sci U S A 110(9):3507–3512View ArticlePubMedPubMed CentralGoogle Scholar
  48. Fernandez R, Gili G, Villagra A, Lopez-Aguilar J, Artigas A (2013) Assessment of the inflammatory effect of low-dose oxygen in mechanically ventilated patients. Intensive Care Med 39(4):711–716View ArticlePubMedGoogle Scholar
  49. Ronchi JA, Figueira TR, Ravagnani FG, Oliveira HC, Vercesi AE, Castilho RF (2013) A spontaneous mutation in the nicotinamide nucleotide transhydrogenase gene of C57BL/6J mice results in mitochondrial redox abnormalities. Free Radic Biol Med 63:446–456View ArticlePubMedGoogle Scholar

Copyright

© The Author(s). 2017