Evaluation of the effects of ozone therapy in the treatment of intra-abdominal infection in rats

BASIC RESEARCH

Evaluation of the effects of ozone therapy in the treatment of intra-abdominal infection in rats

Yglesio Moyses de Souza^I; Belchor Fontes^I; Joilson O Martins^II; Paulina Sannomiya^III; Glacus S. Brito^I; Riad N. Younes^I; Samir Rasslan^I

^IFaculdade de Medicina da Universidade de São Paulo - São Paulo/SP, Brazil

^IIDepartment of Immunology, Institute of Biomedical Sciences, Faculdade de Medicina da Universidade de São Paulo - São Paulo/SP, Brazil

^IIIResearch Division, Heart Institute (INCOR), LIM-11, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo - São Paulo/SP, Brazil. Email: [e-mail]. Tel.: [phone]

ABSTRACT

INTRODUCTION: The antibacterial effect of ozone (O₃) has been described in the extant literature, but the role of O₃ therapy in the treatment of certain types of infection remains controversial.

OBJECTIVES: To evaluate the effect of intraperitoneal (i.p.) O₃ application in a cecal ligation/puncture rat model on interleukins (IL-6, IL-10) and cytokine-induced neutrophil chemoattractant (CINC)-1 serum levels, acute lung injury and survival rates.

METHODS: Four animal groups were used for the study: a) the SHAM group underwent laparotomy; b) the cecal ligation/puncture group underwent cecal ligation/puncture procedures; and c) the CLP+O₂ and CLP+O₃ groups underwent CLP+ corresponding gas mixture infusions (i.p.) throughout the observation period. IL-6, CINC-1 and IL-10 concentrations were determined by enzyme-linked immunosorbent assay (ELISA). Acute lung injury was evaluated with the Evans blue dye lung leakage method and by lung histology. P<0.05 was considered significant.

RESULTS: CINC-1 was at the lowest level in the SHAM group and was lower for the CLP+O₃ group vs. the CLP+O₂ group and the cecal ligation/puncture group. IL-10 was lower for the SHAM group vs. the other three groups, which were similar compared to each other. IL-6 was lower for the SHAM group vs. all other groups, was lower for the CLP+O₃ or CLP+O₂ group vs. the cecal ligation/puncture group, and was similar for the CLP+O₃ group vs. the CLP+O₂ group. The lung histology score was lower for the SHAM group vs. the other groups. The Evans blue dye result was lower for the CLP+O₃ group vs. the CLP+O₂ group and the cecal ligation/puncture group but similar to that of the SHAM group. The survival rate for the CLP+O₃ group was lower than for the SHAM group and similar to that for the other 2 groups (CLP and CLP+O₂).

CONCLUSION: Ozone therapy modulated the inflammatory response and acute lung injury in the cecal ligation/puncture infection model in rats, although there was no improvement on survival rates.

Keywords: IL-6; IL-10; CINC-1; Sepsis; ALI; CLP.

INTRODUCTION

Despite the latest advances in antimicrobial therapy and intensive care, peritonitis and sepsis remain important causes of mortality. Infectious peritonitis can be due to intestinal perforation resulting from various conditions, including trauma, inflammatory diseases, ischemia and perforated neoplasms.¹ Local infection triggers a massive release of interleukin (IL)-1β, tumor necrosis factor (TNF)-α, IL-10, platelet activating factor (PAF), leukotrienes, and thromboxane, all of which participate in the development of sepsis syndrome and septic shock.^2,3

After initiation of the infection process, regardless of the optimal treatment, the inflammatory cascade is sometimes irreversible and results in patient death. Extensive research has focused on elucidating the mechanisms of the inflammatory cascade and modulation of these responses to prevent and treat Systemic Inflammatory Response Syndrome (SIRS) and Multiple Organ Dysfunction Syndrome (MODS)^4,5.

Ozone (O₃) is a potent oxidizing agent and an important disinfectant. The bactericidal effect of O₃ is based on a direct attack on microorganisms by oxidation of biological materials. In fact, O₃ antibacterial activity can be more effective than iodine and chlorine.^6,7 Data reported in the literature have shown that bacteria, spores, and viruses are inactivated by ozone after only few minutes of exposure^8,9. O₃ may act through mechanisms other than oxidation, including the activation of erythrocyte metabolism and immune cells.^10,11

Toxic effects of O₃, caused by excessive doses of inhaled ozone in the airways, as well as toxicity to the endocrine, reproductive, and central nervous systems have been described^7,12. Nevertheless, little is known about the intraperitoneal (i.p.) application of ozone or the repercussions that ozone has on intra-abdominal organs and tissues.

Two studies^13,14 tested a preconditioning O₂ /O₃ pneumoperitoneum in rats submitted to peritonitis. The former study¹³ added an antibiotic regimen to the preconditioning pneumoperitoneum, and both found an increased survival rate in rats after the treatments. However, another study¹⁵ that evaluated preconditioning O₂/O₃ pneumoperitoneum demonstrated a pro-inflammatory effect of O₃, with a tendency to reduce survival rates.

In this context, beyond these controversial results, the real effects of ozone therapy as a single therapeutic agent, not as a preconditioning treatment or as an adjuvant to antibiotics, have not been clearly determined. Thus, the objective of this study was to evaluate the effect of i.p. O₃ application in a cecum ligation/puncture (CLP) rat model on the markers of the inflammatory response, on acute lung injury (ALI) parameters (pulmonary vascular permeability and histology), and on an animal's survival rate.

MATERIALS AND METHODS

This study was performed in the Laboratory of Medical Investigation (LIM)-62 of the third Division of Surgical Clinic of the Hospital das Clinicas and the LIM 11 - University of São Paulo Medical School. Wistar male rats (250-350 g) were utilized throughout the experiments. This study was approved by our Institutional Ethics Committee and performed according to the National Institutes of Health (NIH) guidelines on the experimental use of animals.¹⁶

Four groups of rats were employed in this study:

1) SHAM group animals were submitted only to laparotomy (hereafter this group is referred to as "group SHAM");

2) CLP group animals were submitted to laparotomy + CLP procedures (hereafter this group is referred to as "group CLP");

3) CLP+O₂ group animals were submitted to laparotomy + CLP + O₂ treatment (hereafter this group is referred to as "group CLP+O₂");

4) CLP+O₃ group animals were submitted to laparotomy + CLP + O₃/O₂ treatment (hereafter this group is referred to as "group CLP+O₃").

The lengths of the observation periods varied and are specified in the respective descriptive topics in this Methods section. The study design and distribution of the animals are shown in Figure 1. All of the animals fasted for 8 h before the surgical procedure. Laparotomy and cecal ligation/puncture were performed under general anesthesia with inhalatory halothane, followed by i.p. pentobarbital injection (50 mg/kg).^17-19

During the procedures, the animals were randomized to the 4 groups immediately after cecum exposure was accomplished. The SHAM rats were submitted to a 2-cm laparotomy, followed by exposure of the cecum and closure of the abdominal wall incision with a 4.0 nylon 2-layer running suture.

Cecum ligation and puncture and treatment with O₂ or O₂/O₃

After a 2-cm laparotomy on groups CLP, CLP+O₂, and CLP+O₃, the cecum was exposed, ligated with a 3.0 silk suture just distal to the ileocecal valve to avoid intestinal obstruction, and punctured once with a 22 g needle in its antimesenteric border. The cecum was then squeezed to expel a small amount of fecal material through the puncture site. The bowel was returned to the abdominal cavity, and the abdominal wall incision was closed, as described for group SHAM. The animals were kept warm (37º C) in the postoperative period. Food and water (with dipyrone 0.5%) were offered ad libitum after this procedure.^18,20 For the treatment with O₂ or O₂/O₃, the animals were anesthetized with halothane before the injection procedure. On group CLP+O₂, 100% O₂ (20 ml/kg) was insufflated (i.p.) every 12 h through a puncture in the right lower abdomen with a 22 gauge needle, starting 1 hour after the laparotomy closure. Similarly, group CLP+O₃ received a gas mixture (20 ml/kg, i.p.) containing 5% ozone (102 µg/mL) and 95% oxygen, generated by a MVM™ ozone generator (Multivácuo^®, Campinas, Brazil) , every 12 h, starting 1 hour after laparotomy closure. After recovery from anesthesia recovery, the animals were allowed to have food and water (with dipyrone 0.5%) ad libitum during the observation period.

Enzyme-immuno assays for cytokines and chemokine

Serum levels of the markers of the inflammatory response as well as the pulmonary histology changes were simultaneously evaluated in 44 animals (SHAM=10, CLP=11, CLP+O₂=13, CLP+O₃=10).

The serum concentrations of cytokines and chemokines (IL-6, IL-10 and CINC-1) were determined by enzyme-immuno assay (ELISA) using commercially available kits, according to the manufacturer's instructions (R & D Systems Inc., Minneapolis, MN, USA). The sensitivity of the assay was 15 pg/mL.²¹

Pulmonary Histology

Twenty-four h after the initial procedure (laparotomy for group SHAM or CLP for the other groups), all of the animals were anesthetized with an injection of sodium pentobarbital (50 mg/kg, i.p.). A median sternotomy provided access to the thoracic cavity, and 5 ml of blood was collected from an intracardiac punction (22 gauge needle). This sample was used for cytokines and chemokine analysis. Euthanasia was then performed by cutting the left ventricle with scissors. A piece of the lower lobe of the left lung was fixed in 4% formaldehydum polymerisatum. Paraffin-embedded sections (5 µm) were stained with hematoxylin-eosin and submitted to morphological analysis, including extension (EX) of pulmonary involvement, edema (ED), hemorrhage (H), congestion (C), polymorphonuclear (PO) cell infiltrate and mononuclear (MO) cell infiltrate. A semi-quantitative analysis was performed, due to heterogeneous morphological changes and pulmonary involvement. A score (S) was calculated that combined the extension of pulmonary involvement and intensity of each morphological change, resulting in a final score [S= EX x (ED+H+C+PO+MO)]²². Two different pathologists conducted a blind histological analysis.

Pulmonary vascular permeability evaluation

Acute lung injury was determined in 40 animals (SHAM=10, CLP=10, CLP+O₂=10, CLP+O₃=10) by evaluating the lung vascular permeability with the Evans blue dye (EBD) lung leakage method. Twenty-four h after the initial procedure (laparotomy for group SHAM or CLP in the other groups), the animals were anesthetized with an injection of sodium pentobarbital (50 mg/kg, i.p.), followed by the injection of 20 mg/kg EBD (delivered at a concentration of 25 mg/ml EBD in water,intravenous- (i.v.).

Fifteen minutes after the initial procedure, the laparotomy incision was reopened in all of the animals. Euthanasia was conducted by cutting the inferior vena cava. The thoracic cavity was then opened, and the lungs were perfused for 3 min with 50 ml phosphate-buffered saline (PBS) (pH 7.4) injected through a cannula inserted into the pulmonary artery. After dissection and en block removal of the heart and lungs, the left lung lobe was divided into two samples that were weighed to obtain the wet weight (WW) of each specimen. One sample was held in an oven at 100°C for 24 h and then weighed to determine its dry weight (DW). The dry to wet weight ratio (% DW/WW) of the lung tissue was then calculated. The other sample was submersed in formamide (4 ml formamide/g wet tissue) for 24 h to extract the dye from the tissue. The dye absorbance value in the solution was then detected by a microplate reader (wave length, 620 nm), compared with a series of standard EBD dilutions in formamide, and converted to mg of EBD/mL of the solution. Based on this value, the amount of EBD that had been in the wet lung sample (µg EBD/g wet tissue) was then determined. Finally, the %DW/WW was used to convert the wet tissue value into a µg EBD/g dry lung tissue value, which was recorded as the EBD lung leakage value.^23,24

Survival analysis

For survival rate determination, the animals were observed until the 5^th day post procedure. The survival rates were analyzed in 50 animals (SHAM=10, CLP=12, CLP+O₂=14, CLP+O₃=14), and all of the groups were observed for 5 days. The period of time from the initial procedure until death was annotated in h, and a Log-rank test was performed.

Statistical Methods

The Kolmogorov-Smirnov test was used to determine normality. The data are presented as the mean ± SEM (when a normal distribution was found), or as the median (Md) plus the 25^th and 75^th percentiles [Md (P25;P75)] when the normality test failed. The parametric data were analyzed by ANOVA followed by the Bonferroni multiple comparisons test, when appropriate. The Kruskal-Wallis test was used to analyze the non-parametric data followed by the Student-Newman-Keuls test, when necessary. A Log-rank test was used for survival analysis. A p value < 0.05 was considered to be significant. Statistical analyses were conducted with Sigmastat^® version 3.5 (Systat Software, Inc., Point Richmond, CA, USA).

RESULTS

Cytokines and chemokine analysis

The levels of CINC-1 and IL-10 were expressed as medians (P25; P75), and the level of IL-6 was expressed as the mean ± SEM. CINC-1 levels (pg/mL) were significantly lower for group CLP+O₃ [951.3 (582.6; 1111.5)] than for group CLP+O₂ [1700 (1300; 3928.1)] and group CLP [3555 (3066.8; 4404)]. Group SHAM had the lowest CINC-1 values [47 (43.2; 53.8)] (p<0.01). The Kruskal-Wallis test, followed by the Student-Newman-Keuls test, found no significant difference between groups CLP and CLP+O₂ (Figure 2).

IL-6 levels (pg/mL) were significantly lower for group SHAM (30.8 ± 4.8) than for all the other groups (p<0.001). Groups CLP+O₃ (321.3 ± 35.2) and CLP+O₂ (386.3 ± 40.9) had lower levels than group CLP (695 ± 65.3) (p<0.01). A comparison between groups CLP+O₃ and CLP+O₂ showed no significant difference (p=0.54).

IL-10 levels (pg/mL) for the four groups were 50.1 (38.8; 67) for group SHAM, 98.1 (56.1; 598) for group CLP, 273.6 (152; 314.8) for group CLP+O₂, and 199.5 (107; 289) for group CLP+O₃. The Kruskal-Wallis test showed that IL-10 levels were lower for group SHAM (p=0.02) than for the other groups. There was no difference between the other 3 groups (p=0.85) (Figure 3).

Pulmonary Histology

For lung histology and cytokines analysis, we used 10 rats for group SHAM and, initially, 13 animals in each CLP procedure group. Two animals of group CLP and 3 animals of the group CLP+O₃ had an inadequate blood sample (hemolyzed plasma), so we eliminated these animals. SHAM rats had the lowest histology score [3(2; 4)] of all groups (p=0.002). The pulmonary histology scores were similar in groups CLP+O₂ [6 (3.7; 10.5)], CLP+O₃ [8 (6; 8)], and CLP [10 (5; 12)]. The Kruskal-Wallis test showed no differences between the three groups (p=0.31).

EBD lung leakage method

The EBD lung leakage values were 62.5 (39; 71.3) for group SHAM, 56.1 (52.7; 109.1) for group CLP, 88.2 (53.6; 151.1) for group CLP+O_2, and 28.4 (18.4; 51.3) for group CLP+O₃. There was a significant difference when we compared group CLP+O₃ with groups CLP+O₂ and CLP (p=0.02). A comparison of groups CLP+O₃ and SHAM showed no significant difference.

Survival Analysis

For the survival analysis, we used 10 animals for group SHAM because of the low morbidity of the procedure. The groups with the CLP procedures initially had 14 animals, but 2 animals of group CLP died right after anesthesia and then were eliminated from the analysis.

Only one animal of group SHAM died during the observation period (110 ± 10 h). All of the other groups had a decreased survival time compared to group SHAM (p=0.002). The observed death rates were: 1/10 (10%) for group SHAM, 9/12 (75%) for group CLP, 6/14 (42.8%) for group CLP+ O₂, and 10/14 (71.4%) for group CLP+O₃. Animals of group CLP+O₂ had a survival time that was not significantly different from that of group CLP+O₃ (71 h ± 12.9 vs. 52.1 ± 8 h, p=0.4). Animals of group CLP had a mean survival time of 57.4 ± 10.3 h. The Log-rank test performed between groups CLP, CLP+O₂, and CLP+O₃ showed that there was no statistical difference (p=0.4). These results are illustrated in Figure 4.

DISCUSSION

The utilization of O₃ as a potent antimicrobial agent has been the object of many studies.^25-30 The use of ozone in humans and animals is still considered controversial because of its side effects that are specifically related to free radical formation and irritation of the respiratory system.^{12, 31} For these reasons, ozone therapy has had limited acceptance in clinical practice, and most of the studies on O₃ therapy have been experimental. Despite this fact, ozonized oxygen exhibits various effects on the immune system, such as the modulation of phagocytic activity on the peritoneal³² and alveolar³³ macrophages that generate the first line of defense against bacteria and/or its toxins.

Bette et al. (2006)¹³ tested a preconditioning O₂/O₃ pneumoperitoneum, followed by a tazobactam/piperacilin regimen in Wistar rats submitted to peritonitis, and found an increase in survival rates and a decrease in pro-inflammatory cytokines (TNF-α and IL-1β). Promisingly, Schulz et al. (2003)¹⁴ found that after a repetitive pre-treatment using ozonized oxygen (i.p.), mortality in animals submitted to lethal polymicrobial peritonitis was reduced. Rodriguez et al. (2009)¹ verified that there was an increase of superoxide dismutase (SOD) and glutathione peroxidase (GPx) in rats submitted to ozone oxidative preconditioning (OOP) prior to a fecal peritonitis induction, suggesting that there was a protective effect of OOP. However, in a model of peritoneal sepsis in rats submitted to a 5-day preconditioning period with O₃ (i.p), Torossian et al. (2004)¹⁵ found that survival was reduced from 50% to 35% (p=0.1). In addition, ozone therapy increased TNF-α and macrophageal inflammatory protein (MIP)-2. From this, the authors concluded that O₃ therapy (i.p.) was proinflammatory ¹⁵.

The previous studies with O₃ preconditioning^1,14,15 or preconditioning plus antibiotics¹³ may not have correctly estimated the true impact of ozone therapy in the treatment of septic rats. Therefore, we conducted this study to evaluate the isolated effect of intraperitoneal ozone as a single therapeutic agent in intra-abdominal infections.

In this study, the variables were chosen based on the previous reports in the literature^{1,7, 13,14,15,20} and for their applicability for the evaluation of SIRS.^1,21,24

The CLP procedure groups were substantially affected for CINC-1 elevation compared to group SHAM. Group CLP+O₃ had a significant decrease in CINC-1 levels when compared to all of the CLP-procedure groups. CINC-1 plays an important role in the inflammatory response as an attractant and activator of neutrophils and macrophages.^34,35 However, a previous in vitro study³⁶ demonstrated that adhesion and chemotaxis of neutrophils were independent of exposure to ozone when peripheral blood was used. CINC-1 levels rapidly increase after induction of inflammation in rats, especially 8 hrs after the injury³⁵, and the levels reach concentrations significantly different from those of controls at 4, 8, and 24 hrs after LPS infusion in blood samples.³⁷ The possible mechanism by which CINC-1 expression was modulated in this study remains to be determined. We hypothesize that inactivation of bacteria, as a result of topical (i.p.) application of ozone, could attenuate the migration of macrophages, decreasing CINC-1 expression at 24 h. A histological analysis of the peritoneum after euthanasia by counting the macrophages could provide additional evidence for this hypothesiIL-6 is secreted from T-cells and macrophages and stimulates the immune response to trauma, leading to inflammation. In mice, IL-6 has been shown to be required for resistance against certain species of bacteria, acting as a weak pyrogen.³⁸ The CLP procedures increased IL-6 values compared to group SHAM, but groups CLP+O₃ and CLP+O₂ had lower levels of IL-6 than group CLP, and no difference was observed when group CLP+O₃ was compared to group CLP+O₂. Inactivation of bacteria by ozone could explain this decrease in IL-6 levels for group CLP+O₃, but there is no clear mechanism to explain the similar expression of IL-6 for group CLP+O₂ compared to CLP+O₃ .

Intraperitoneal administration of O₂ and O₃ did not have a significant impact on IL-10 levels after 24 h of observation. An IL-10 peak can be observed as much as 24 h after systemic injury.³⁹ Anti-inflammatory IL-10 production is known to be part of a protective mechanism that suppresses the induction of proinflammatory cytokines such as TNF-α and IL-1 and is itself induced by monocytes and macrophages during sepsis.^{40, 41} Sewnath et al. (2001)⁴² found a role of endogenous IL-10 in local antibacterial host defense and in the development of SIRS during abdominal sepsis, indicating that endogenous IL-10 increases bacterial clearance.

Previously, it has been shown that an increased histology score is associated with the presence of ALI.⁴³ In the CLP groups, the increased histology scores indicate that the CLP procedures provoked pulmonary tissue injury. However, there was no beneficial effect of O₃ therapy on the lung histology score. Hyaline membranes were not found in any of the animals, and this compromised the characterization of ALI by histological methods in this study. This might be attributed to the short time interval (24 h) between the CLP procedures and euthanasia of the animals. Hyaline membranes can be identified by optical microscopy 24 to 48 h after initial injury.⁴³ The presence of edema in the samples that were evaluated 24 h post-injury was uniformly discreet, and thus we decided to eliminate it in calculating the histology score. The ALI analysis might have been more accurate if pulmonary histology had been performed 48 h later.

The EBD lung leakage method was chosen because it is an early marker of lung vascular injury.^23,24 Differences in pulmonary vascular permeability can be observed as soon as 2 h after procedures such as gut ischemia/reperfusion and lipopolysaccharide (LPS) infusion.^23,24 Moreover, accumulation of macrophages at sites of tissue injury can be observed after acute inhalation of ozone.^44,45 These cells, along with resident alveolar epithelial cells, become activated and release cytotoxic and proinflammatory mediators, such as nitric oxide (NO), which increase of pulmonary vascular permeability and to the development of ALI.^44,45 However, in the present study (with i.p. administration of O₃), there was a less pronounced capillary permeability (quantified by means of EBD lung leakage) for group CLP+O_3, and this might suggest that O₃ therapy had an anti-inflammatory effect. The administration route (i.p.) might have better controlled the intraperitoneal infection⁷ without the undesirable side effects of ozone inhalation. The modulation of the inflammatory cascade might explain the lower EBD lung leakage values for group CLP+O₃ vs. groups CLP+O₂ and CLP. There was no difference between groups CLP+O₃ and SHAM. This might be due to the small influence that laparotomy and cecal exposure have on pulmonary vascular permeability for group SHAM.

We evaluated the survival rate 5 days after procedure, quantified the survival time in h for each animal, and performed a Log-rank test. We used a concentration of 102 µg/ml O₃ with a lower volume of the O₂/O₃ gas mixture (20 ml/kg). We used a different concentration from that used by Schulz et al.¹⁴ (80 mL/kg) to avoid any potential side effects of massive pneumoperitoneum, but the final concentration of infused ozone was similar. The CLP groups had increased mortality compared to group SHAM (p=0.002), but no difference was observed when each group was compared to the other (p=0.12). We observed that group CLP had a similar lethality rate (84%) compared to the classic study by Wichterman et al. (1980)²⁰ on survival rates after CLP. Thus, in the present study, ozone treatment did not influence survival rates.

In conclusion, the results of our study suggest that intraperitoneal ozone therapy has a possible benefit in attenuating the inflammatory response and acute lung injury resulting from intra-abdominal infection in rats, although there was no improvement in survival rates.

Received for publication on September 14, 2009

Accepted for publication on November 04, 2009

• 1. Rodríguez ZZ, Guanche A, Álvarez RG, Rosales FH, Alonso Y, Schulz S. Preconditioning with ozone/oxygen mixture induces reversion of some indicators of oxidative stress and prevents organic damage in rats with fecal peritonitis. Inflamm Res. 2009;58:371-5.
• 2. Annane D, Bellisant E, Cavaillon JM. Septic shock. Lancet. 2005;365:63-78.
• 3. Flowers F, Zimmerman J. Reactive oxygen species in the cellular pathophysiology of shock. New Horiz. 1998;6:169-80.
• 4. Freitas FG, Salomão R, Tereran N, Mazza BF, Assunção M, Jackiu M, et al. The impact of duration of organ dysfunction on the outcome of patients with severe sepsis and septic shock. Clinics.2008;63:483-8.
• 5. Rezende E, Silva Junior JM, Isola AM, Campos EV, Amendola CP, Almeida SL. Epidemiology of severe sepsis in the emergency department and difficulties in the initial assistance. Clinics. 2008;63:57-64.
• 6. Mehlman MA, Borek C. Toxicity and biochemical mechanisms of ozone. Environ Res. 1987; 42:36-53.
• 7. Silva RA, Garotti JEG, Silva RS, Navarini A, Pacheco Jr A. Analysis of the bactericidal effect of ozone pneumoperitoneum. Acta Cir Bras. 2009;24:124-7.
• 8. Bocci V, Paulesu L. Studies on the biological effects of ozone: induction of interferon on human leucocytes. Haematologica.1990;75:510-5.
• 9. Bocci V. Ozone as bioregulator: pharmacology and toxicology of ozonetherapy today. J Biol Regul Homeost Agents. 1996;10:31-53.
• 10. Buckley RD, Hackney JD, Clark K, Posin C. Ozone and human blood. Arch Environ Health. 1975;30:40-3.
• 11. Zimran A, Wasser G, Forman L, Gelbart T, Beutler E. Effect of ozone on red blood cell enzymes and intermediates. Acta Haematol. 2000;102:148-51.
• 12. Bhalla DK, Gupta SK, Reinhart PG. Alteration of epithelial integrity, alkaline phosphatase activity, and fibronectin expression in lungs of rats exposed to ozone. J Toxicol Environ Health A. 1999;57:329-43.
• 13. Bette M, Nuesing RM, Mutters R, Menendez S, Schulz S. Efficiency of tazobactam/piperacilin in lethal peritonitis is enhanced after preconditioning of rats with O₃/O₂ pneumoperitoneum. Shock. 2006;1:26-9.
• 14. Schulz S, Rodriguez ZZ, Mutters R, Menendez S, Bette M. Repetitive pneumoperitoneum with ozonized oxygen as a preventive in lethal polymicrobial sepsis in rats. Eur Surg Res. 2003;35:26-34.
• 15. Torossian A, Ruehlmann S, Eberhart L, Middeke M, Wulf H, Bauhofer A. Pre-treatment with ozonized oxygen (O₃) aggravates inflammation in septic rats. Inflamm Res. 2004;53:S122-5.
• 16. Institute of Laboratory Animals Resources. Guide for the Care and Use of Laboratory Animals. Washington, DC, USA: National Academy Press, 1996.
• 17. Arruda MJC de, Poggetti RS, Fontes B, Lima WT de, Trezena AG, Birolini D. Intestinal ischemia/reperfusion induces bronchial hyperreactivity and increases serum TNF-alpha in rats.. Clinics. 2006;61:21-8.
• 18. Nakagawa, NK, Jukemura J, Aikawa P, Nogueira RA, Poli-de-Figueredo IF, Sannomiya P. In vivo observation of mesenteric leukocyte-endothelial interactions after cecal ligation/puncture and surgical sepsis source control. Clinics. 2007;62:321-6.
• 19. Lee DK, Terrazas RG, Votto LG, Arenson-Pandikow H. Techniques of inhalatory induction in rats: a comparative study. Acta Cir Bras.1994;9:34-7
• 20. Wichterman, KA, Baue AE, Chaudry IH. Sepsis and septic shocka review of laboratory models and a proposal. J Surg Res. 1980;29:189-201.
• 21. Martins JO, Zanoni FL, Martins DO, Coimbra R, Krieger JE, Jancar S, et al. Insulin regulates cytokines and intercellular adhesion molecule-1 gene expression through nf-kb activation in lipopolysaccaride-induced acute lung injury in rats. Shock. 2009;31:404-9.
• 22. Capelozzi VL, Saldiva PH, Antonângelo L, de Carvalho TS, Logulo A, de Carvalho CR, et al. Quantitation in inflammatory pleural disease to distinguish tuberculous and paramalignant from chronic non-specific pleuritis. J Clin Pathol.1997;50:935-40.
• 23. Dallal MM, Chang SW. Evans blue dye in the assessment of permeability surface area product in perfused rat lungs. J Appl Physiol. 1994;77:1030-5.
• 24. Moraes LB, Murakami AH, Fontes B, Poggetti RS, Van Roojen N, Younes RN, Heimbecker AM, Birolini D. Gut ischemia/reperfusion induced acute lung injury is an alveolar macrophage dependent event. J Trauma Inj Inf Crit Care. 2008; 64:1196-200.
• 25. Roy D, Wong PK, Engelbrecht RS, Chian ES. Mechanism of enteroviral inactivation by ozone. Appl Environ Microbiol. 1981;41:718-23.
• 26. Dyas A, Boughton BJ, Das BC. Ozone killing action against bacterial and fungal species:microbiological testing of a domestic ozone generator. J Clin Pathol. 1983;36:1102-4.
• 27. Olson WP. Ozone. PDA J Pharm Sci Technol. 1999;53:125-8.
• 28. Steinhart H, Schulz S, Mutters R. Evaluation of ozonated oxygen in an experimental animal model of osteomyelitis as a further treatment option for skull-base osteomyelitis. Eur Arch Otorhinolaryngol.1999;256:153-7.
• 29. Sechi LA, Lezcano I, Nunez N, Espim M, Dupre I, Pinna A, et al. Antibacterial activity of ozonized sunflower oil(oleozon). J Appl Microbiol. 2001;90:279-84.
• 30. Fan L, Song J, McRae KB, Walker BA, Sharpe D. Gaseous ozone treatment inactivates Listeria innocua in vitro. J Appl Microbio.2007;103:2657-63.
• 31. Pryor, WA. Mechanisms of radical formation from reactions of ozone with target molecules in the lung. Free Radic Biol Med. 1994;17:451-65.
• 32. Canning BJ, Hmieleski RR, Spannhake EW, Jakab GJ. Ozone reduces murine alveolar and peritoneal macrophage phagocytosis: the role of prostanoids. Am J Physiol. 1991;261:L277-82.
• 33. Chatterjee D, Mukherjee SK. Destruction of phagocytosis-supressing activity of aflatoxin B1 by ozone. Lett Appl Microbiol. 1993;17:52-4.
• 34. Shibata F, Kato H, Konishi K, Okumura A, Ochiai H, Katsuhisa N, et al. Differential changes in the concentrations of cytokine induced neutrophil chemoattractant (CINC)-1 and CINC-2 in exudate during rat lipolysccharide-induced inflammation. Cytokine. 1996;8:222-6.
• 35. Kunkel SL, Lukacs NW, Strieter RM. The role of interleukin-8 in the infectious process. Ann N Y Acad Sci.1994;730:134-43.
• 36. Margalit M , Attias E , Attias D, Elstein D , Zimran A, Matzner Y. Effect of ozone on neutrophil function in vitro. Clin Lab Haematol.2002; 23:243-7.
• 37. Focà A, Berlinghieri MC, Barreca GS, Placanica PM, Diana R, Liberto MC, et al. Kinetics of IL-8, MIP-1 alpha, TNF alpha, IL-1 beta, IL-1ra and IL-10 in human whole blood samples triggered by smooth and rough LPS. New Microbiol. 1998;21:123-30.
• 38. Nilsberth C, Elander L, Hamzic N, Norell M, Lönn J, Engström L, et al. The role of interleukin-6 in lipopolysaccharide-induced fever by mechanisms independent of prostaglandin E2. Endocrinology.2009;150:1850-60.
• 39. Seghaye MC, Duchateau J, Bruniaux J, Demontoux S, Bosson C, Serraf A, et al. Interleukin-10 release related to cardiopulmonary bypass in infants undergoing cardiac operations. J Thorac Cardiovasc Surg. 1996;111:545-53.
• 40. Kato T, Murata A, Ishida H, Toda H, Tanaka N, Hayashida H, et al. Interleukin 10 reduces mortality from severe peritonitis in mice. Antimicrob Agents Chemother. 1995;39:1336-40.
• 41. van der Poll T, Marchant A, Buurman WA, Berman L, Keogh CV, Lazarus DD, et al. Endogenous IL-10 protects mice from death during septic peritonitis. J Immunol. 1995; 155:5397-401.
• 42. Sewnath ME, Olszyna DP, Birjmohun R, ten Kate FJ, Gouma DJ, van Der Poll T. IL-10-deficient mice demonstrate multiple organ failure and increased mortality during Escherichia coli peritonitis despite an accelerated bacterial clearance. J Immunol. 2001;166:6323-31.
• 43. Menezes SLS, Bozza PT, Faria Neto HCC, Laranjeira AP, Negri EM, Capelozzi VL, et al. Pulmonary and extrapulmonary acute lung injury: inflammatory and ultrastructural analyses J Appl Physiol. 2005;98:1777-83.
• 44. Laskin DL, Sunil V, Guo Y, Heck DE, Laskin JD. Increased Nitric Oxide Synthase in the Lung after Ozone Inhalation Is Associated with Activation of NF-kB. Environ Health Perspect Suppl.1998;106(S5):1175-9.
• 45. Cerqueira NF, Yoshida WB. Óxido nítrico: revisão Cerqueira NF, Yoshida WB. Óxido nítrico: Revisão. 2002. Acta Cir Bras;17:417-23.

Publication Dates

• Publication in this collection
  03 Mar 2010
• Date of issue
  2010

History

• Received
  14 Sept 2009
• Accepted
  04 Nov 2009