alexa Spontaneous One-Lung Ventilation Increases the Lung Inflammatory Response: An Experimental Pilot Study | OMICS International
ISSN: 2155-6148
Journal of Anesthesia & Clinical Research
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Spontaneous One-Lung Ventilation Increases the Lung Inflammatory Response: An Experimental Pilot Study

Humberto S Machado1*, Paula Sá1, Catarina S Nunes2, António Couceiro3, Álvaro Moreira da Silva4 and Artur Águas5

1Anesthesiology Department, Centro Hospitalar do Porto, Largo Abel Salazar, 4099-001 Porto, Portugal

2Open University, Department of Science and Technology and Anesthesiology Department, Centro Hospitalar do Porto, Largo Abel Salazar, 4099-001 Porto, Portugal

3Pathological Anatomy service, Gaia/Espinho Hospital Centre, Rua Conceição Fernandes, 4430 Vila Nova de Gaia, Portugal

4Intensive care Service, Port Hospital Center, Largo Abel Salazar, 4099-001 Porto, Portugal

5Department of Normal Anatomy, Abel Salazar Biomedical Sciences Institute-University of Porto and Multidisciplinary Biomedical Research Unit, St. Jorge Viterbo Ferreira, 228, 4050-313 Porto, Portugal

*Corresponding Author:
Humberto S Machado
Department, Centro Hospitalar do Porto
Largo Abel Salazar, 4099-001 Porto, Portugal
Tel: 351 935848475
Fax: 351 220900644
E-mail: [email protected]

Received date: May 28, 2014; Accepted date: August 01, 2014; Published date: August 11, 2014

Citation: Machado HS, Sá P, Nunes CS, Couceiro A, da Silva ÁM, et al. (2014) Spontaneous One-Lung Ventilation Increases the Lung Inflammatory Response: An Experimental Pilot Study. J Anesth Clin Res 5:428. doi: 10.4172/2155-6148.1000428

Copyright: © 2014 Machado HS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

Study objective: The purpose of this study was to investigate if spontaneous one-lung ventilation would induce any type of inflammatory lung response when compared to spontaneous two-lung ventilation and its intensity, by quantification of inflammatory cells in lung histology at the end of the procedure.

Design: In vivo prospective randomised animal study

Setting: University research laboratory

Subjects: New Zealand rabbits Interventions: Rabbits (n=20) were randomly assigned to 4 groups (n=5 each group). Groups 1 and 2 were submitted to one-lung ventilation, during 20 and 75 minutes respectively; groups 3 and 4 were submitted to two-lung ventilation during 20 and 75 minutes and considered controls. Ketamine/xylazine was administered for induction and maintenance of anesthesia. One-lung ventilation was achieved by administration of air into the interpleural space, and left lung collapse was visually confirmed through the centre of the diaphragm.

Measurements: Lung histology preparations were observed under light microscopy for quantification of the inflammatory response (light, moderate and severe).

Main results: All subjects had at least light inflammatory response. However, rabbits submitted to one-lung ventilation had a statistically significant value for the occurrence of moderate inflammation (p<0.05). The inflammatory response found included mainly eosinophils, with an average proportion of 75/25 to other polymorphonuclear cells. No differences between groups were found regarding gas exchange, heart rate and respiratory rate.

Conclusions: In this spontaneous one-lung ventilation model, lung collapse was positively associated with a greater inflammatory response when compared to normal two-lung ventilation.

Keywords

Inflammatory response; One-lung ventilation; Atelectasis

Introduction

Pulmonary complications such as infection and acute lung injury (ALI) may lead to high morbidity rates after thoracic surgery and/or one-lung ventilation (OLV) [1,2]. Inflammation after lung surgery is pointed out as an important cause for the development of ALI [3,4]. The incidence of ALI varies from 2, 5% in patients submitted to thoracic surgery in general to 7, 9% of patients submitted to pneumonectomy [5]. During thoracic surgery several factors can lead to the release of pro-inflammatory mediators (with the subsequent activation of neutrophils that alter endovascular permeability), namely overdistension, hypoxia, hyperoxia and possibly isquemia-reperfusion injury [6]. Also, mechanical ventilation by itself may induce several alveolar changes which are not seen during spontaneous ventilation [6]. In addition, surgical manipulation of the lung may aggravate the alveolar injury with leukocyte recruitment in both lungs during OLV [6]. These findings support the multiple hit hypotheses, in which lung damage during thoracic surgery may be due to: mechanical ventilation, OLV, surgical manipulation, lung overdistension, atelectrauma and reexpansion/ reperfusion injury [7]. However, as far as we know, there are no reported studies that show an independent effect of OLV on lung inflammatory response. Thus, in an experimental controlled animal model with spontaneous ventilation, we hypothesized that lung inflammatory response is not increased by one-lung ventilation itself.

Materials and Methods

Animals

The experimental protocol used in this study was approved by the ethics committee, and carried out according to the European Union Directive nº 63/2010/EU. Twenty adult New Zealand rabbits were purchased from a Portuguese breeder (NORLAP-Rui M.S. Gonçalo, 4825-466 Água-Longa, Portugal) and kept under standard housing conditions with unrestricted access to food and water, with attendance by veterinary doctors and daily inspection. Study inclusion criteria for rabbits were based on general well being status, namely normal food and water ingestion, with absence of self-mutilation and weigh loss.

Study groups

This study was conducted as a prospective randomized animal experiment; with four groups with five rabbits each being studied. Group 1 and 2 had spontaneous OLV during 20 and 75 minutes, respectively; Group 3 and 4 had spontaneous two-lung ventilation (TLV) during 20 and 75 minutes, respectively. All rabbits received 2 litter/minute fresh gas mixture of oxygen and air. Since the TLV group was not submitted to any thoracic instrumentation, just receiving anesthesia as the OLV group, this was assumed to represent the control group.

Instrumentation

The rabbits were anesthetized with intramuscular ketamine 50 mg/kg (Imalgene®, Merial Laboratorios, S.A., and Spain) and xylazine 4 mg/kg (Rompum®, Bayer, Leverkusen, Germany). Anaesthesia maintenance was attained with half the initial dose of ketamine and xylazine every 20 minutes. The anterior region of the neck and the abdomen were shaved, with a 2 cm vertical midline incision being made through the anterior cervical region; after exposing the trachea, an incision was made to allow the introduction of a 2.5 tracheal tube to be connected to a spontaneous breathing system (Jackson-Rees type) with 2 litters per minute flow of a fresh oxygen/air mixture

Monitoring

During the procedure non-invasive monitoring was used to monitor heart rate (HR) and peripheral arterial saturation (SpO2) (Nellcor Oximax N600X®,Tyco Healthcare group LP, Nellcor Puritan Bennett Division, Pleasanton, CA 94588, USA); respiratory rate (RR) was monitored by direct observation. First and last measurements were obtained at five minutes after setup and five minutes before the end of the procedure. We developed an OLV model using spontaneous ventilation in order to avoid pro-inflammatory situations previously described as the multiple hit hypotheses (such as mechanical ventilation, surgical manipulations and re-expansion/reperfusion). In all rabbits, a left subcostal incision was performed; In Groups 1 and 2 air injection (10 ml/kg) was administered through the left costal-diaphragmatic recess into the intra-pleural cavity. Left lung collapse was confirmed by visual observation through the centre of diaphragm (by way of its transparency), as was right lung spontaneous ventilation (Figure 1). Groups 3 and 4 were maintained on spontaneous bilateral ventilation (control groups). The rabbit was identified as a suitable model for the study since its anatomy allows OLV due to the anatomic-physiological pleural separation of both sides of the thorax. At the end of procedure all rabbits were euthanized with ketamine (100 mg/kg) and xylazine (8 mg/kg), followed by section of abdominal aorta for exsanguination.

anesthesia-clinical-research-Rabbit-Lung

A–Basal view of right hemithorax, B–Basal view of left hemithorax, C– Inflatted right lung, D– Collapsed left lung, E–left pneumotorax

Figure 1: Rabbit Lung (diaphragmatic ventral aspect).

Tissue samples

The rabbits’ lungs were harvested and fixed in 10% formaldehyde and embedded in paraffin for a light microscopy (LM) study. Three micra sections from the left and right lungs (superior, middle and lower lobe) were obtained from all rabbits. Lung sections were stained in haematoxylin and eosin.

Histopathology

An arbitrarily defined four level inflammatory score was assigned to the lungs depending on the intensity of inflammatory infiltrates in each lung plate: no inflammation, light, moderate and severe inflammation.

Infrequent inflammatory cells and/or inflammation confined to a few areas (corresponding to less than 15 cells per high magnification field of 40x) [8] were defined as a light inflammatory response. Multiple areas in the tissue or a large area of inflammatory cells (corresponding to an average of 16 to 25 cells per high magnification field 40x) [8] were defined as a moderate inflammatory response. Large multifocal areas of tissue with inflammatory cells or almost all areas of tissue affected (corresponding to more than 25 cells per high magnification field 40x) [8] were defined as severe inflammation. Thus, rabbits were classified as light, moderate or severe inflammatory responders according to the intensity of inflammation assessed by total plate visualization. Staff investigators who collected data during the procedure were aware of the group assignments. An independent and experienced pathologist (unaware of which subject was being evaluated) classified all plates accordingly to the criteria set.

Statistical analysis

The Resource Equation method [9] was used to determine if the sample size was appropriate for the experiment, considering a laboratory animal study with a controlled set-up. A sample size of 5 rabbits per group with a total of 4 groups (n=20) were considered adequate for the questions being asked, resulting in an adequate error component (df) between 10 and 20. Odds ratio (OR) was used as a measure of association. Kruskal-Wallis non-parametric test was used to compare variables between groups. Friedman test (Nonparametric two-way ANOVA) was used to compare variations within groups. Spearman’s rho was used as a measure of correlation between the different variables and the level of inflammation. Pearson’s chisquared test was used to test for independence in inflammation. The statistical hypothesis is that the occurrence of moderate inflammation is independent of the technique (OLV or TLV). A p-value<0.05 was considered statically significant. The Statistics Matlab® Toolbox from Mathworks, and Microsoft Excel 2013 were used for all calculations. Data is presented with median and range variables.

Results

All rabbits fulfilled the inclusion criteria for the study; daily visits to vivarium demonstrated animal wellbeing, with normal feeding, absence of self-mutilation, or weight loss.

Weight, heart rate (HR), respiratory rate (RR), oxygenation (SpO2)

The median weight was 1975 g (min 1378; max 3790) in the OLV Group and 1912.5 g (min 1400; max 2433) in the TLV Group, with no statistical difference between the two.

Table 1 summarizes values for all the parameters. During the procedure SpO2 significantly increased in both groups (p<0.05). In the OLV Group, SpO2 had a median increase of 4.5% and in the TLV Group SpO2 increased by 5.2%, with no differences between the groups. Initial SpO2, HR and RR values are not correlated with the level of inflammation. When considering all rabbits, only the percentage change in RR had a negative correlation with the level of inflammation (R=-0.512, p<0.05).

  OLV (One-lung ventilation) TLV (Two-lung ventilation)
1st recording Last recording 1st recording Last recording
HR, bpm 190 (120-235) 197.5 (125-235) 152.5 (125-205) 163.5 (130-225)
RR, b/m 85 (56-95) 92.5 (50-100) 82 (61-88) 90 (60-95)
SpO2, % 91 (79-100) 96 (91-100) 89 (68-95) 94.5 (80-99)

Table 1: Physical parameters.

Lung inflammation

Rabbits in Group 1 and 2 were found to be equally likely to have moderate inflammation (OR=1, Chi-square p=0.53). The same was also found in rabbits from Group 3 and 4 (OR=1, Chi-square p=0.53). Since the degree of inflammatory response was not influenced by the length of the procedure, we aggregated the rabbits in only two groups: those submitted to OLV (group 1 and 2-OLV Group, n=10) and those submitted to TLV (group 3 and 4–TLV Group, n=10), so as to analyse the influence of OLV versus TLV, independently of procedure duration. As expected, all rabbits had some degree of inflammation. The OLV Group showed moderate inflammation in 4 subjects, whereas the TLV Group only did so in 2 rabbits. Our hypothesis was that the occurrence of moderate inflammation was independent of the technique used (OLV or TLV), but this was rejected (Chi-square p<0.05). In the OLV Group, inflammation results were compared between left (collapsed) and right lungs; there was moderate inflammation in 4 of the left lungs, whereas only 2 right lungs presented moderate inflammation. This contradicts the hypotheses that the occurrence of moderate inflammation is independent of the lung being collapsed or being ventilated (Chi-square p<0.05). The inflammatory cells found in these plates were neutrophils and eosinophils; the proportion found showed approximately 75% eosinophils and 25% neutrophils (Figure 2).

anesthesia-clinical-research-Light-inflammation

Legend: arrow-eosinophil

Figure 2: A-Light inflammation (12 eosinophils), B-moderate inflammation (23 eosinophils).

Discussion

In our study, rabbits submitted to one-lung ventilation (OLV) had greater degree of inflammatory response than did animals submitted to two-lung ventilation (TLV); this fact was shown in more rabbits having moderate inflammation response in the OLV group. In OLV animals, the inflammatory response was more intense in the left lung (collapsed) than in the ventilated lung, suggesting that OLV is not an indifferent factor to the occurrence of more intense inflammation. However, moderate inflammation also appeared in TLV group, which may raise the possibility of a cause also present in the TLV rabbits, but to a lesser extent than in OLV, possibly implicating a systemic effect in these findings. These facts draw our attention to a physiological situation that is present in the collapsed lung without any doubt, and might be present in the ventilated lung with lower intensity, namely areas of atelectasis. Based on this assumption, we may explain why even in a non-surgical spontaneous ventilation model (without interference of mechanical ventilation and surgical manipulation) the local acidic environment induced by atelectasis might induce inflammation, this finding being more pronounced when these areas are more extensive as is the case with whole lung collapse (such as in OLV). In this regard, one might assume that a major local event, such as a collapsed lung, might have the ability to induce a systemic effect affecting both lungs.

No high plateau pressures (barotrauma), no overdistension (volutrauma), nor the shear stress of repetitive opening (atelectotrauma) were present, since the model only included spontaneous ventilation with oxygen/air supplementation of 2 litters/minute. However, as demonstrated in some literature, when these factors were present the length of the procedure may be associated with a greater inflammatory response [10-12]. In all rabbits, spontaneous ventilation set up included a fixed volume of fresh gas flow of 2 litters per minute; this volume allowed visual control of spontaneous ventilation by means of Jackson- Rees balloon self-inflation and deflation observation. It was assumed that this fact implied that a certain degree of continuous positive airway pressure (CPAP) was applied to all animals, which could hypothetically prevent local atelectasis formation. Lung surgery has a 2-6% mortality rate, according to the complexity of the surgical procedures [13]. At the present time, mortality rates have shifted away from the cardiac and surgical causes and are more related to pulmonary problems, such as infection and ALI in its most severe form, the acute respiratory distress syndrome (ARDS) [10,14]. The strongest predictors of ALI are related to the pre-operative condition of the patient, extent of lung resection, “injurious” mechanical ventilation and fluid therapy during the surgical procedure [13]. It is known that controlled OLV with higher tidal volumes (10 ml/kg) may produce a significant rise of inflammatory markers, including increased cellular infiltration [15]. Other causes of release of inflammatory mediators are hyperoxia and high levels of positive pressure at the end of inspiration [16,17]. In addition, studies showed that biochemical and histological lesions occur both in the collapsed and in the ventilated lung during OLV [18,19]. The ventilated lung may be subjected to a combination of volutrauma, hyperinflation, and hyperoxia that represents a potential source of oxidative stress and inflammatory response [20]. However, none of the situations previously described have been applied in this study. This draws attention to the possibility that the occurrence of moderate inflammatory response might be linked to the OLV status itself. Inflammation is characterized by profound changes in metabolic activity, tissue hypoxia and metabolic acidosis. These shifts in tissue metabolism are frequently associated with vasculitis and intense recruitment of various inflammatory cell types [21]. Furthermore, it is clear that oxygen supplementation in all subjects may increase the possibility of inflammation, since oxygen itself may induce the occurrence of atelectatic areas [22,23]. These areas are poorly ventilated and induce local hypoxia, with the consequent signalling of inflammatory mediators. However, both groups had oxygen supplementation, but the OLV group had higher moderate inflammation scores, implying that OLV clearly augments inflammatory response. The overall inflammatory response cell population found was composed of neutrophil and eosinophil leukocytes. However, in all plates the percentage of eosinophil leukocytes reached 75%, which was an unexpected inflammation pattern. Eosinophils are involved in several inflammatory processes that imply a certain degree of pro-fibrogenic and pro-angiogenic activity, namely in some chronic allergic conditions such as asthma. This angiogenesis is often linked to hypoxic conditions present in inflamed tissues. Since eosinophils respond to hypoxia by up-regulation and other pro-angiogenic functions, this indicates that there may be a correlation between eosinophilic inflammation and hypoxia [23,24]. In our study, we did not suspect allergic conditions since all rabbits were considered healthy by the overall clinical analysis made at arrival and during quarantine time; with no abnormal clinical signs or symptoms being detected during the whole housing period. In addition, all rabbits had an official health certificate from the producer certifying the animals’ wellbeing. Thus, eosinophilic predominance may be related to local hypoxic conditions. The results of this study show that some factors linked to the oxygen supply during OLV (and subsequent set up of oxygenation variability) may play a role not only in the occurrence of inflammatory response, but also on the type of cells encountered. Local hypoxia may have prompted inflammatory signalling, which might have been responsible for the appearance of either neutrophils and/or eosinophils. Considering all rabbits, the percentage of change in RR had a negative correlation with the level of inflammation (p<0.05); thus, it may be assumed that this increase in RR may lower systemic carbon dioxide levels and its correspondent contribution to acidity during inflammation.

The main findings in this study include:

• Spontaneous one-lung ventilation in a non-surgical, nonmanipulated lung, induces inflammatory changes in both lungs, with predominance in the collapsed lung.

• Atelectasis is present not only in the collapsed one-lung ventilated lung, but may also be present in two-lung ventilated subjects, however, with a more pronounced inflammatory response in the first.

• Inflammatory cellular infiltrates that result from a certain degree of lung atelectasis and local hipoxia, were predominantly eosinophilic in nature.

The conclusion of this study is that OLV (assumed as a major factor of atelectasis) is a relevant trigger for lung inflammation and, since no controlled ventilation was used, nor surgical manipulation of the lung was performed, this inflammatory response can be a direct physiological consequence. Study limitations were identified during our work and may contribute to plan further investigation. This spontaneous ventilation animal model was created to study the histological consequences of OLV. However, no previous studies were done that established a time limit for an experiment like the one carried out. In this regard, it was assumed that a seventy-five minute limit on the length of procedure was acceptable, as it might represent some similarity to the majority of thoracic procedures; however, further studies might contribute data regarding what is the ideal procedure duration in the study of the effects of OLV. Likewise, this study setup is not comparable to clinical OLV; in which positive pressure ventilation and lung exclusion using double-lumen tracheal tubes or bronchial blockers are used. Thus, further studies should be designed to allow the extrapolation to human clinical practice in order to know how to avoid consequences of atelectasis during and after anesthesia.

Acknowledgements

The authors would like to thank Mr. Costa e Silva for coordinating the housing and husbandry of animals, Mrs. Manuela Silva for help in laboratory tasks, and Dr. Ana Pinto and Dr. Madalena Costa for histological assembling and preparation.

The authors would like to thank Centro Hospitalar do Porto for the funding granted for the purchase of animals, animal food, and other husbandry expenses, as also the Anesthesia Department at Centro Hospitalar do Porto for funding the edition and publication of this study.

Disclosures

This study received funding from Centro Hospitalar do Porto (Largo Abel Salazar, 4099-001 Porto, Portugal) for logistic purposes, animal purchase, housing and husbandry. The Anesthesia Department at Centro Hospitalar do Porto (Largo Abel Salazar, 4099-001 Porto, Portugal) funded expenses regarding edition and publication. No funding was granted to any author.

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