Endogenous carbon monoxide (CO) has been shown to modulate inflammation and inhibit cytokine production both in vivo and in vitro. The aim of this study was to examine whether exogenous carbon monoxide could suppress the vitality of Escherichia coli (E coli) and improve the survival rate in an E coli-induced murine sepsis model.
ICR mice were infected with E coli, and immediately injected intravenously with carbon monoxide releasing molecule-2 (CORM-2, 8 mg/kg) or inactive CORM-2 (8 mg/kg). The survival rate was monitored 6 times daily for up to 36 h. The blood samples, liver and lung tissues were collected at 6 h after the infection. Bacteria in peritoneal lavage fluid, blood and tissues were enumerated following culture. Tissue iNOS mRNA expression was detected using RT-PCR. NF-κB expression was detected with Western blotting.
Addition of CORM-2 (200 and 400 μmol/L) into culture medium concentration-dependently suppressed the growth of E coli and decreased the colony numbers, but inactive CORM-2 had no effect. Treatment of the infected mice with CORM-2 significantly increased the survival rate to 55%, while all the infected mice treated with inactive CORM-2 died within 36 h. E coli infection caused severe pathological changes in liver and lungs, and significantly increased serum transaminases, lipopolysaccharide, TNF-α and IL-1β levels, as well as myeloperoxidase activity, TNF-α and IL-1β levels in the major organs. Meanwhile, E coli infection significantly increased the number of colonies and the expression of iNOS mRNA and NF-κB in the major organs. All these abnormalities were significantly attenuated by CORM-2 treatment, while inactive CORM-2 was ineffective.
In addition directly suppressing E coli, CORM-2 protects the liver and lungs against E coli-induced sepsis in mice, thus improving their survival.
Sepsis is a clinical syndrome that complicates severe infection1. A subset of patients develops multiple organ dysfunction syndrome (MODS) rapidly leading to death, while another subset goes into remission but is more prone to develop secondary life-threatening microbial infections2,3. Sepsis and severe sepsis are leading causes of death in many intensive care units (ICU) all around the world4. Recently in the United States, the incidence of severe sepsis has been estimated to be 3% of the population, with a death rate of 25% among these cases during hospitalization5. Clinically, nearly 95% of sepsis cases are caused by bacterial infection, and 62.2% of these can be attributed to Gram-negative bacteria, with Escherichia coli (E coli) responsible for nearly 16% of these infections6. E coli is an opportunistic pathogen, which migrates by bacterial translocation from the gastrointestinal tract to extra-intestinal sites, where virulence factors are important in establishing infections. In recent years, more frequent use of broad-spectrum antibiotics has increased bacterial resistance7,8; therefore, novel and effective antibacterial agents for use in the clinical are urgently required.
Carbon monoxide (CO) is a stable gas that has long been known as a toxic compound because of its ability to bind hemoglobin. Endogenous carbon monoxide, which is a by-product of inducible heme oxygenase-1 (HO-1), can modulate inflammation and inhibit lipopolysaccharide (LPS)-induced production of cytokines both in vivo and in vitro9,10,11. Recently, transitional metal carbonyls have been identified as potential CO-releasing molecules (CORMs) with the potential to deliver CO to tissues and organs as a therapeutic agent12,13. We have reported that CORM-2 attenuated leukocyte sequestration in some vital organs and the small intestine in burned and cecal ligation and puncture (CLP)-challenged mouse models of sepsis through interfering with nuclear factor-κB (NF-κB) activation and intercellular adhesion molecule-1 (ICAM-1) protein expression and suppressing the endothelial cell pro-adhesive phenotype14,15,16,17. In addition, our earlier studies also showed that CORM-2 inhibits the activity and virulence of E coli in vitro. On the basis of these observations, the aim of the present study was to determine the capacity of exogenous CO, carbon monoxide-releasing molecule II (CORM-2), to suppress E coli ATCC25922 vitality, and to decrease the inflammatory responses in the liver and lung, increase the survival rate in an E coli ATCC25922-induced murine model of sepsis.
Materials and methods
The experimental protocol was approved by the Council on Animal Care at Jiangsu University on the Protection and Welfare of Animals and was conducted according to the National Institutes of Health guidelines for the care and use of experimental animals. Anesthesia consisting of spontaneous inhalation of isoflurane-N2O (Abbott Laboratories, Missisauga, Ontario, Canada) in a 60% oxygen/40% nitrogen mixture was administered when necessary. Mice were euthanized by excessive anesthesia administration for each experiment.
Tricarbonyldichlororuthenium (II) dimer (carbon monoxide releasing molecule-2, CORM-2) was purchased from Sigma (St Louis, Mo, USA) and solubilized in dimethyl sulfoxide (DMSO) to obtain a 40 mmol/L stock solution. Chemical structure of CORM-2 was shown in our published report18. Inactive form of CORM-2 (iCORM-2, negative controls) was prepared as described previously18. E coli ATCC25922 was kindly offered by Department of Microbiological Testing of the Affiliated Hospital of Jiangsu University. Other reagents and instruments included tumor necrosis factor-alpha (TNF-α) and interleukin-1 beta (IL-1β) ELISA kits (Qiaoyi, Shanghai, China), LAL reagents (Houshiji, Fujian, China), a high-speed and low-temperature desktop centrifuge (Beckman, Inc, USA), and a VMR-type small animal anesthesia machine (Matrx, Inc, USA), a CFX96TM Real-Time System (Bio-Rad, Inc, USA). All the other chemicals were of reagent grade and obtained from Sigma unless otherwise stated.
Growth curve measuring and colony counting
Measurement of growth curve was used to dynamically study the growth of bacteria. The bacterial growth data in our preliminary experiments indicated that the consistent major effect of CORM-2 on growth dynamics was an extended lag phase in which entry into exponential growth was delayed that increased with increasing CORM-2 concentrations. Thus, we focused on how CORM-2 altered the duration of the lag phase.
The bacteria were divided into five groups (n=6), including E coli, E coli+200 μmol/L CORM-2, E coli+400 μmol/L CORM-2, E coli+200 μmol/L iCORM-2, and E coli+400 μmol/L iCORM-2. E coli were inoculated and cultured on the Luria-Bertani (LB) medium until they reached peak viability and activity. Single colonies were then inoculated into 2 mL of LB medium, cultured overnight (37 °C at 250 r/min), diluted at the rate of 1:100, and inoculated in 20 mL of LB medium in the following morning. Corresponding concentrations of CORM-2 or iCORM-2 (200 or 400 μmol/L) were added to each group (except E coli group) to intervene, and the values at OD600 were measured at specific time points. In addition, 100 μL of the bacterial culture was appropriately diluted and evenly spread on Mueller-Hinton agar plates. The bacteria were cultured in a CO2 incubator at 37 °C for 48 h and the resulting colonies were then counted.
Infection model and survival rate
Pathogen-free male ICR mice (kindly offered by Laboratory Animal Center, Yangzhou University) aged 6–8 weeks and weighing 20±2 g were fed in laboratory for one week. Mice were housed in standard wire-topped cages and in temperature-controlled units. Food and water were supplied ad libitum. A total of 80 ICR mice were divided into four groups (n=20) as follows: control, E coli, E coli+CORM-2, E coli+iCORM-2. The control group received 0.5 mL saline by intraperitoneal injection, while the other groups received intraperitoneal injections of 0.5 mL E coli (3×108 cfu/mL). Immediately afterwards, the E coli+CORM-2 and E coli+iCORM-2 groups received CORM-2 (8 mg/kg, iv) or iCORM-2 (8 mg/kg, iv), respectively. The concentration of CORM-2 used in the present study was based on a previous report of the use of this compound in mice and our own preliminary experiments that measured the dynamic and peak carboxyhemoglobin (COHb) levels19. Mouse survival was monitored six times daily for up to 36 h.
A total of 32 ICR mice were divided into four groups (n=8) and were infected with E coli with CORM-2 or iCORM-2 intervention as described above. Six hours after the injection, the mice were euthanized by excessive anesthesia administration. The liver and lung specimens harvested from different groups of mice were fixed by immersion in 4% formaldehyde solution. The tissues were embedded in paraffin wax, serially sectioned, and stained with hematoxylin-eosin. Liver and lung morphologic characteristics were evaluated by light microscopy.
LPS concentration assessment
The concentration of LPS in the serum of mice was determined using the Limulus amebocyte lysate (LAL) test (Houshiji, Fujian, China). In accordance with the protocol provided by the manufacturer, 100 μL of each sample was added into 100 μL of the quantitative LAL reagents dissolved in LPS-free water and then incubated in a motionless water bath at 37 °C for 2 h. The formation of gel from the LAL products induced by the existence of non-neutralized LPS was measured utilizing the kinetic turbidimetric assay. The results were analyzed using GEN5 data analysis software.
Serum transaminase levels
Blood samples were obtained by cardiac puncture of the left ventricle. The samples were stored in serum tubes and immediately centrifuged at 3000 g/min for 5 min. Evaluation of hepatocellular injury was performed by determining the enzymatic activity of ALT and AST in serum samples using a commercially available kit (Boehringer Manheim, Munich, Germany) according to the manufacturer's instructions.
TNF-α and IL-1β levels in serum and tissue homogenates
TNF-α and IL-1β levels in serum, and tissue homogenates (liver and lung) were measured by enzyme-linked immunosorbent assay (ELISA) kits following the manufacturer's instructions.
Myeloperoxidase (MPO) activity
MPO activity was measured in liver and lung tissues using a procedure similar to that documented by Hillegas et al20. Tissue samples were homogenized in 50 mmol/L potassium phosphate buffer (PB) (pH 6.0), and centrifuged at 10 000×g (10 min); pellets were suspended in 50 mmol/L PB containing 0.5% hexadecyltrimethylammonium bromide. After sonication, the samples were centrifuged at 10 000×g (10 min). Aliquots (0.3 mL) were added to 2.3 mL of reaction mixture containing 50 mmol/L PB, o-dianisidine, and 20 mmol/L H2O2 solution. One unit of enzyme activity was defined as the amount of MPO present that caused a change in absorbance measured at 460 nm for 3 min. MPO activity was expressed as unit/g tissue.
Mice were infected by E coli followed by immediate intravenous administration of CORM-2 or iCORM-2 as described above. Six hours after the infection, the mice were euthanized by excessive anesthesia administration. Samples (100 μL) of the blood, peritoneal lavage fluid, liver and lung homogenates of the mice were appropriately diluted and evenly spread on Mueller-Hinton agar plates, cultured in a CO2 incubator at 37 °C for 24 h. Finally the resulting colonies were counted.
Semiquantitation of iNOS mRNA by reverse transcription-polymerase chain reaction (RT-PCR)
The liver and lung tissue samples were sheared and treated with Trizol, chloroform, isopropanol, ethanol, and RNase free water in order to extract total RNA. Reversed transcription of RNA to yield cDNA was carried out using Revert Aid First Strand cDNA Synthesis Kit (Thermo, Boston, USA). Quantitative real-time PCR (Maxima SYBR Green/ROX qPCR Kit, Thermo) amplification was performed under the conditions of 95 °C for 10 min and 95 °C for 10 s, followed by 1 min at 60 °C, with data collection during the last 30 s. Primer sequences for the genes of interest and the reference gene (GAPDH) were as follows: for iNOS, forward primer 5′-CTT-CCG-AAG-TTT-CTG-GCA-GCA-GCG-3′ and reverse primer 5′-GAG-CCT-CGT-GGC-TTT-GGG-CTC-CTC-3′; for GAPDH, forward primer 5′-CAC-CCC-ATT-TGA-TGT-TAG-TGC-3′ and reverse primer 5′-CCA-TTT-GCA-GTG-GCA-AAG-3′. The values were standardized by comparing with values from relative expression of GAPDH.
Nucleic proteins were extracted with the nuclear protein extraction buffer kit (Vazyme Biotech, Jiangsu, China). Protein concentration was assayed using the bicinchoninic acid (BCA) protein assay kit (Beyotime, Jiangsu, China) and equal amounts of protein were loaded per well on 7.5%–15% polyacrylamide gels. An anti-mouse NF-κB-specific polyclonal antibody (1:200, Santa Cruz Biotechnology, Santa Cruz, CA, USA) was used as the primary antibody and an HRP-conjugated goat anti-rabbit IgG antibody (Santa Cruz Biotechnology, Santa Cruz, CA, USA) was used as secondary antibody at the appropriate concentration (1:2500). Immunoreactive bands were visualized using an ECL detection system and band intensity was determined using Fluorchem FC3 software.
Statistical analyses were performed by using SPSS 17 software (SPSS, Chicago, IL, USA). Data were expressed as mean±SD. One-way analysis of variance (ANOVA) and the independent-samples t-test was used for the comparisons. A value of P<0.05 was considered to be statistically significant.
Effects of CORM-2 on E coli growth curve and colony counting
E coli were divided into five groups (n=6). Each group (except E coli group) was added with CORM-2 or iCORM-2 to coculture at corresponding concentrations (200 or 400 μmol/L), and strain growth was monitored at hourly intervals until stationary phase was reached. Growth was monitored by both determining the optical density at 600 nm (OD600) and counting the clonal formation unit (CFU). Bacterial growth was markedly suppressed in the presence of CORM-2. This was confirmed by observing growth curve of E coli under intervention of CORM-2 or iCORM-2. When compared with E coli and E coli+iCORM-2 group, the growth of E coli in E coli+200 μmol/L CORM-2 group was suppressed, and the platform phase entering time was significantly delayed, with a decrease in colony numbers (F value in Figure 1A and 1B were 1034.33 and 248.32 respectively, P<0.01). Group E coli+400 μmol/L CORM-2 showed an even more obvious suppression of bacterial growth and decrease in colony numbers (F value in Figure 1C and D were 7087.46 and 11342.67 respectively, P<0.01).
Effect on CORM-2 on survival
All mice that received intraperitoneal injections of E coli alone died within 36 h, while CORM-2 administration significantly increased the survival rate which reached 55% (P<0.05). All mice that received iCORM-2 immediately after intraperitoneal injections of E coli also died within 36 h (Figure 2).
The organ sections of the animals in each group were evaluated microscopically using H+E staining. Histological analysis revealed normal structure in the liver and lung sections from the control group (Figure 3A, 3E). In the E coli infected mice, marked vacuolization and infiltration of the liver by inflammatory cells was observed (Figure 3B). Increased numbers of red blood cells and inflammatory cells were also observed in the lung alveolae (Figure 3F). These morphological changes in both lung and liver suggested the presence of systemic inflammation and multiple organ damage after E coli challenge, and these pathological changes also existed in tissues of E coli+iCORM-2 group (Figure 3D, 3H). After in vivo administration of CORM-2, granulocyte infiltrations were significantly decreased in both liver and lung tissue (Figure 3C, 3G), providing evidence that CORM-2 may be involved in the suppressive effects against E coli vitality and toxicity. The figure is representative of at least three experiments performed on different days.
Effect on CORM-2 on organ function and MPO activity in liver and lung tissues
Hepatocyte injury was evaluated by determining the serum concentrations of ALT and AST. At 6 h after receiving intraperitoneal injections of E coli, serum ALT and AST were found to be significantly elevated in E coli and E coli+iCORM-2 infected mice as compared to the mice of control group (ALT, 131.50±12.93 and 125.00±11.33 vs 44.18±2.76; AST, 244.63±22.61 and 237.75±21.78 vs 55.25±5.01 U/L, P<0.05). In contrast, the corresponding values in the E coli+CORM-2 group were significantly lower than those in the E coli and E coli+iCORM-2 groups (ALT, 87.13±6.42 vs 131.50±12.93 and 125.00±11.33 U/L; AST, 172.68±13.40 vs 244.63±22.61 and 237.75±21.78 U/L, P<0.05, Figure 4A).
The activity of MPO, which is an enzyme in the azurophilic granules of neutrophils, was assessed to determine whether the E coli-induced polymorphonuclear leukocyte (PMN) accumulation in the liver and lung was effectively prevented by treatment with CORM-2. Homogenates of the organ samples were examined for MPO activity at 6 h after bacterial infection. MPO activity in liver and lung homogenates obtained from E coli and E coli+iCORM-2 infected mice was markedly increased compared with control mice (liver, 0.56±0.05 and 0.59±0.04 vs 0.28±0.02 unit/g; lung, 0.99±0.08 and 1.01±0.09 vs 0.39±0.03 unit/g, P<0.05), while this increase was significantly reduced by CORM-2 treatment (liver, 0.34±0.02 vs 0.56±0.05 and 0.59±0.04 unit/g; lung, 0.66±0.06 vs 0.99±0.08 and 1.01±0.09 unit/g, P<0.05, Figure 4B).
Effect of CORM-2 on LPS concentration and cytokines levels in serum, liver and lung
Mice were infected by E coli followed by immediate intravenous administration of CORM-2 or iCORM-2. At 6 h after receiving intraperitoneal injection of E coli, serum concentrations of LPS increased significantly after bacterial infection compared with control group (826.51±71.98 vs 36.35±8.42 eU/mL, P<0.05), while the concentration of LPS in the E coli+CORM-2 group was significantly lower than that detected in the E coli and E coli+iCORM-2 groups (468.97±43.29 vs 826.51±71.98 and 805.39±81.22 eU/mL, P<0.05, Figure 5A). In parallel, the TNF-α and IL-1β levels in the serum as well as in the liver and lung homogenates of E coli and E coli+iCORM-2 mice were significantly increased compared to the levels detected in the control group. In the E coli+CORM-2 group, the elevation in serum and tissue homogenate levels of TNF-α and IL-1β was significantly reduced compared with E coli and E coli+iCORM-2 group mice (P<0.05, Figure 5B–5D).
Detection of colony distribution in major mouse organs after E coli infection
Mice were infected by E coli followed by immediate intravenous administration of CORM-2 or iCORM-2. Six hours after the injection, the mice were killed by excessive anesthesia. The number of colonies in blood, peritoneal lavage fluid (PLF), liver and lung homogenates of E coli infected mice were significantly increased compared with that in the control group (P<0.001), while the number of colonies in the major organs of E coli+CORM-2 group were significantly decreased compared with that in the E coli group [blood, (1.21±0.50)×106 vs (5.25±4.90)×107 and (4.10±3.30)×107 cfu/mL; PLF, (2.16±1.38)×107 vs (2.71±2.00)×1010 and (2.68±2.10)×1010 cfu/mL; liver, (1.47±1.11)×106 vs (4.92±3.20)×107 and (5.40±4.70)×107 cfu/mL; lung, (3.90±3.30)×106 vs (6.94±3.92)×107 and (6.23±4.34) ×107 cfu/mL, P<0.01. Figure 6].
Effect of CORM-2 on iNOS mRNA expression in the liver and lung of E coli infected mice
Mice were infected by E coli followed by immediate intravenous administration of CORM-2 or iCORM-2. Six hours after the injection, the expressions of iNOS mRNA in liver and lung of E coli and E coli+iCORM-2 group mice significantly increased compared to that of the control group (liver, 32.99±2.96 and 33.65±3.29 vs 1±0; lung, 19.01±2.71 and 18.15±2.60 vs 1±0, P<0.05). This increase was significantly reduced in the E coli+CORM-2 group (liver, 13.54±3.17 vs 32.99±2.96; lung, 6.74±0.79 vs 19.01±2.71, P<0.05, Figure 7).
Effect of CORM-2 on NF-κB activation in the liver and lung of E coli infected mice
Mice were infected by E coli followed by immediate intravenous administration of CORM-2 or iCORM-2. Six hours after the injection, NF-κB activation in the liver and lung of E coli and E coli+iCORM-2 group mice were significantly increased compared to those of the control group (liver, 0.98±0.01 and 0.98±0.01 vs 0.53±0.01; lung, 1.10±0.06 and 1.11±0.03 vs 0.54±0.01, P<0.05), while this elevation was significantly inhibited in the E coli+CORM-2 group (liver, 0.77±0.01 vs 0.98±0.01; lung, 0.87±0.01 vs 1.10±0.06, P<0.05, Figure 8).
In the United States, the incidence of severe sepsis is estimated to 3% of the population; septic shock is associated with the highest mortality (approaching 50%)21. Sepsis arises from the complex interactions between the infecting microorganism and the host immune, inflammatory and coagulation responses22. The fundamental pathogenesis of sepsis has not yet been fully elucidated23,24. Sepsis often progresses in cases where the host cannot contain the primary infection, which is commonly related to the characteristics of the microorganism25.
Escherichia coli (E coli), which is an important member of the normal intestinal microflora of humans, typically colonizes the mammalian gut within few hours after birth. E coli and its human host coexist in good health and with mutual benefit for decades26,27. However, during severe sepsis and sepsis shock, human immunity is compromised and the permeability of the intestinal mucosa changes. E coli, as an opportunistic pathogen, can migrate from the gastrointestinal tract to the extra-intestinal sites by bacterial translocation28,29, causing local or disseminated infection and even life-threatening secondary infections.
Many experimental studies have highlighted the specific and independent role of exogenous CO in modulating inflammation30,31. As new metal carbonyl-based compounds, CORMs release CO in biological systems32. CORM-2, a DMSO-soluble CORM, has been shown to exhibit anti-inflammatory actions and to improve the function of many important organs in CLP and thermal injury models of sepsis in our previous studies33,34,35. Therefore, we extended these investigations of the anti-inflammatory effects of exogenous CO in an E coli (ATCC25922)-induced murine sepsis model.
Previously, we confirmed that intravenous administration of CORM-2 effectively inhibited pulmonary and hepatic pathological injury, MPO activity, expression of TNF-α and IL-1β, transcription of iNOS and NF-κB activity in CLP mice. However, whether CORM-2 exerted its effects on directly suppressing the vitality of bacteria remained unknown. To further explore the potential mechanisms, the in vitro growth curve and colony counting of bacteria were investigated. Growth curve and colony counting were typically used to observe the vitality of bacteria, by which we could monitor the real-time growth of bacteria36. Results of growth curve and colony counting showed that bacterial growth was significantly suppressed after CORM-2 intervention when compared with the E coli and E coli+iCORM-2 groups, which implied that CORM-2 directly inhibited the bacterial vitality.
Myeloperoxidase (MPO) is an enzyme that is found predominantly in the azurophilic granules of PMNs. The interaction between leukocytes and endothelial cells plays an important role in inflammation and tissue damage37. Furthermore, the quantitation of tissue MPO activity is a useful biomarker for assessing the influx of PMNs38. In the present study, we found that MPO activity in liver and lung tissues was significantly elevated after bacterial infection and this effect was significantly attenuated after in vivo administration of CORM-2 but not iCORM-2. In accordance with previously reports15,17, this finding indicated that treatment with CORM-2 effectively prevented PMN chemotaxis and infiltration of liver and lung tissues after bacterial infection, consequently decreasing the production of oxidants, and reducing oxidant-mediated injury and inflammatory response in these tissues.
The data from this study showed that infection with a large number of bacteria induced hepatocellular injury as evidenced by increased plasma ALT and AST levels. Serum ALT and AST levels markedly increased in sepsis mice. However, this effect was not observed in sepsis mice treated with CORM-2, indicating CORM-2 attenuates the hepatocellular injury associated with sepsis in this model. Similarly, CORM-2 treatment abolished the elevation in TNF-α and IL-1β levels in the serum and liver and lung tissue homogenates of sepsis mice. TNF-α and IL-1β play a critical roles in the pathogenesis of sepsis and related syndromes. Moreover, infectious diseases can induce exaggerated production of inflammatory cytokines such as TNF-α and IL-1β in the early stages39. Similar protective effects of CORM-2 on inhibiting TNF-α and IL-1β were discovered in CLP-induced peritonitis sepsis and LPS-induced sterile sepsis40. Our results suggested that CORM-2 prevents liver damage, and decreases the production of TNF-α and IL-1β in liver and lung following bacterial infection. These data indicate that the cytoprotective effects of CORM-2 are, at least partly, due to inhibition of the production and secretion of TNF-α and IL-1β during the early period of bacterial infection.
The inducible iNOS, which is expressed in macrophages and neutrophils, is a calcium-independent enzyme that is upregulated in response to inflammation41. Compared with the other isoforms, iNOS activity is more sustained resulting in a concomitant increase in nitric oxide (NO)42. NO plays a major role in cellular injury resulting in the production of reactive oxygen and oxidative stress43. In this study, we found that bacterial infection produced a significant upregulation in iNOS mRNA expression. After administration of CORM-2, the iNOS mRNA expression was significantly decreased. It can be speculated that this effect leads to inhibition of NO production and amelioration of cellular injury in this model.
The NF-κB family members are ubiquitous, rapidly acting transcription factors that modify immune and inflammatory reactions by regulating the expression of some chemokines and cytokines44,45. Previously, we showed that CORM-2 plays a pivotal role in the inhibition of NF-κB activity in the liver in thermal injury model in mice, by decreasing the hepatocellular secretion of inflammatory cytokines and hepatic dysfunction15. Published reports also confirmed that NF-κB activity was significantly down-regulated in LPS-stimulated endothelial cells and macrophages interfered by CORM-246,47. In the present study, NF-κB activity in liver and lung tissues were elevated by bacterial infection, while it was markedly inhibited by administration of CORM-2. All these data showed that CORM-2 plays an even greater role in the inhibition of NF-κB activity, resulting in decreased expression of inflammatory factors such as TNF-α, IL-1β, NO, and improved organ function after bacterial infection.
Interestingly, our results of in vivo experiments showed that there were large numbers of E coli in the blood, peritoneal lavage fluid, liver and lung homogenates of mice following bacterial infection. This was accompanied by markedly increased serum LPS concentrations. After administration of CORM-2, both the number of E coli and the concentration of LPS were significantly decreased. The endotoxin LPS, which is a constituent of the cell wall of Gram-negative bacteria, is released on bacterial death. The presence of endotoxins in the blood, known as endotoxemia, can lead to septic shock48. On the basis of our data, it can be speculated that, rather than causing cell death, CORM-2 inhibits the proliferation of E coli in vivo; however, this remains to be confirmed in future studies.
Here, we observed 100% mortality in mice within 36 h of intraperitoneal injection of E coli. CORM-2 administration immediately after bacterial infection significantly increased the survival rate, which reached 55%. This phenomenon was not observed following administration of iCORM-2 in this model and all mice died within 36 h of bacterial infection. Previously studies and the present data indicated that CORMs might exert a critical therapeutic potential in increasing survival in both sepsis and other severe medical condition such as cardiovascular disease49,50, and organ transplantation and preservation51,52.
Taken together these findings indicate that CORM-released CO suppresses Escherichia coli vitality, protects the liver and lungs against E coli-mediated sepsis, resulting in improved survival. However, there is still a great gap in the respect to applying CORM-2 to treatment in clinical sepsis. E coil-challenged murine sepsis model can't fully mimic the pathophysiology in humans. Besides, although CO gas has already passed safety evaluation in Phase I testing in healthy human beings53, CORM-2 as a kind of transitional metal carbonyls, metabolical and toxicological effects need to be further characterized.
This study was supported by the National Natural Science Foundation of China, No 81071546, No 81272148 and No 81471903; by the Jiangsu Natural Science Foundation, No BK2012703.
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Microbiology and Immunology (2015)