Introduction
Peroxisome proliferator-activated receptors (PPARs) are nuclear hormone receptors, i.e. ligand-dependent intracellular proteins that stimulate transcription of specific genes by binding to specific DNA sequences, following activation by an appropriate ligand. When activated, the transcription factors exert several functions in development and metabolism [
2]. There are three PPAR subtypes encoded by separate genes, showing distinct but overlapping tissue distribution, and commonly designated as PPAR-α (NR1C1), PPAR-γ (NR1C3) and PPAR-β/δ (NUC1, NR1C2), or merely -δ [
2,
3]. In particular, PPAR-β/δ is an ubiquitous receptor, especially expressed in white adipose tissue, heart, muscle, intestine, placenta and macrophages [
4]. It is activated by unsaturated or saturated long-chain fatty acids [
5], prostacyclin, retinoic acid, and some eicosanoids [
6]. Several animal studies reveal that PPAR-β/δ plays an important role in the metabolic adaptation of many tissues to environmental changes [
2]. It appears to be implicated in the regulation of fatty acid metabolism of skeletal muscle and adipose tissue by controlling the expression of a gene involved in fatty acid uptake, β-oxidation and energy uncoupling [
7‐
9].
In this study we wished to investigate the potential therapeutic role of PPAR-β/δ activation during an inflammatory process such as, multiple organ dysfunction syndrome (MODS, also known as multiple organ failure (MOF) or multiple organ system failure [
10]) caused by zymosan. Multiple organ dysfunction syndrome is a cumulative sequence of progressive deterioration in function occurring in several organ systems, frequently seen after septic shock, multiple trauma, severe burns, or pancreatitis [
11‐
13]. Zymosan is a non-bacterial, non-endotoxic agent derived from the cell wall of the yeast
Saccharomyces cerevisiae. When injected into animals, it induces inflammation by inducing a wide range of inflammatory mediators [
14‐
20]. It produces acute peritonitis and multiple organ failure characterized by functional and structural changes in liver, intestine, lung, and kidneys [
16,
18,
21,
22].
It is known that zymosan administration, in mice, within 18 h causes both signs of peritonitis and organ injury [
23,
24]. The onset of the inflammatory response caused by zymosan in the peritoneal cavity was associated with systemic hypotension, high peritoneal and plasma levels of NO, maximal cellular infiltration, exudate formation, cyclooxygenase activity and pro-inflammatory cytokines production [
23,
24]. In this model, we have studied the effect of GW0742, a synthetic high affinity ligand for PPAR-β/δ, after zymosan-induced injury.
Materials and methods
Animals
Male CD mice (20-22 g; Charles River; Milan; Italy) were housed in a controlled environment and provided with standard rodent chow and water. The study was approved by the University of Messina Review Board for the care of animals. Animal care was in compliance with Italian regulations on protection of animals used for experimental and other scientific purposes (D.M.116192) as well as with the EEC regulations (O.J. of E.C. L 358/1 12/18/1986)
Zymosan-induced shock
Mice were randomly allocated into the following groups: (1) Zymosan + vehicle group. Mice were treated intraperitoneally (i.p.) with zymosan (500 mg/kg, suspended in saline solution, i.p.) and with the vehicle for GW0742 (10% dimethylsulfoxide (DMSO) (v/v) i.p), 1 and 6 h after zymosan administration, n = 10; (2) Zymosan + GW0742 group. Identical to the Zymosan + vehicle group but were administered GW0742 (0,3 mg/kg 10% DMSO i.p) at 1 and 6 hour after zymosan instead of vehicle, n = 10; (3) Sham + vehicle group. Identical to the Zymosan + vehicle group, except for the administration of saline instead of zymosan, n = 10; (4) Sham + GW0742 group. Identical to Sham + vehicle group, except for the administration of GW0742 (0,3 mg/kg in 10% DMSO i.p) 1 and 6 hour after saline administration, n = 10. Eighteen hours after administration of zymosan, animals were assessed for shock as described below. In another set of experiments, animals (n = 30 for each group) were randomly divided as described above and monitored for loss of body weight and mortality for 7 days after zymosan or saline administration.
Clinical scoring of systemic toxicity
Clinical severity of systemic toxicity in the mice was scored during the experimental period, (7 days) after zymosan or saline injection, on a subjective scale ranging from 0 to 3; 0 = absence, 1 = mild, 2 = moderate, 3 = serious. The scale was used for each of the toxic signs (conjunctivitis, ruffled fur, diarrhea and lethargy) observed in the animals. The final score was produced upon totaling each evaluation (maximum value 12). All clinical score measurements were performed by an independent investigator, who had no knowledge of the treatment received by each respective animal.
Assessment of acute peritonitis
Eighteen hours after zymosan or saline injection, all animals (n = 10 for each group) were killed under ether anesthesia in order to evaluate the development of acute inflammation in the peritoneum. Through an incision in the linea alba, 5 ml of phosphate buffered saline (PBS, composition in mM: NaCl 137, KCl 2.7, NaH2PO4 1.4, Na2HPO4 4.3, pH 7.4) was injected into the abdominal cavity. Washing buffer was removed with a plastic pipette and was transferred into a 10 ml centrifuge tube. The amount of exudate was calculated by subtracting the volume injected (5 ml) from the total volume recovered. Peritoneal exudate was centrifuged at 7000 × g for 10 min at room temperature.
Peritoneal cell exudate collection and differential staining
At 18 h after treatment, the mice were anesthetized with intramuscular injection of ketamine/xylazine. The mice were injected with 5 mL of ice-cold RPMI-1640 medium (Gibco Inc., Grand Island, NY) with 10% heparin (50 U.I./ml), into the abdominal cavity. The peritoneal cavities were massaged for 1 min and the lavage fluid was collected. Peritoneal exudates cell (PEC) counts were carried out in a hemocytometer by mixing 100 μL of peritoneal cell exudate and 100 μL of eosin. The PEC was spin in a cytocentrifuge at 50 × g for 5 min onto a slide for the differential count. The slides were carefully removed and allowed to air dry briefly. PEC cytospins were stained with Wright-Giemsa stain. PEC cytospins were also stained with neutrophil/mast cell-specific chloroacetate esterase staining and macrophage/monocyte-specific alpha naphthyl butyrate esterase stains for the differential count.
Measurement of nitrite/nitrate concentrations
Nitrite/nitrate (NO
2/NO
3) production, an indicator of NO synthesis, was measured in plasma and in the exudate samples collected 18 hours after zymosan or saline administration, as previously described [
23,
25]. Nitrate concentrations were calculated by comparison with OD550 of standard solutions of sodium nitrate prepared in saline solution.
Immunohistochemical localization of nitrotyrosine, PARP, ICAM-1, P-Selectin, Bax, Bcl-2, TNF-α, IL-1β and FasL
Tyrosine nitration and PARP activation were detected, as previously described [
26], in lung, liver and intestine sections using immunohistochemistry. At 18 hours after zymosan or saline injection, tissues were fixed in 10% (w/v) PBS-buffered formalin and 8 μm sections were prepared from paraffin embedded tissues. After deparaffinization, endogenous peroxidase was quenched with 0.3% (v/v) hydrogen peroxide in 60% (v/v) methanol for 30 min. The sections were permeabilized with 0.1% (v/v) Triton X-100 in PBS for 20 min. Non-specific adsorption was minimized by incubating the section in 2% (v/v) normal goat serum in PBS for 20 min. Endogenous biotin or avidin binding sites were blocked by sequential incubation for 15 min with avidin and biotin (Vector Laboratories, Burlingame, CA). The sections were then incubated overnight with 1:1000 dilution of primary anti-nitrotyrosine antibody (Millipore, 1:500 in PBS, v/v), anti-poly(ADP)-ribose (PAR) antibody (Santa Cruz Biotechnology, 1:500 in PBS, v/v), purified hamster anti-mouse ICAM-1 (CD54) (1:500 in PBS, w/v) (DBA, Milan, Italy), purified goat polyclonal antibody directed towards P-selectin which reacts with mice, anti-Bax rabbit polyclonal antibody (1:500 in PBS, v/v), anti-Bcl-2 polyclonal antibody rat (1:500 in PBS, v/v), anti-TNF-α antibody (Santa Cruz Biotechnology, 1:500 in PBS, v/v), anti-IL-1β antibody (Santa Cruz Biotechnology, 1:500 in PBS, v/v), or anti-Fas Ligand antibody (Abcam,1:500 in PBS, v/v). Controls included buffer alone or non-specific purified rabbit IgG. Specific labeling was detected with a biotin-conjugated specific secondary anti-IgG and avidin-biotin peroxidase complex (Vector Laboratories, Burlingame, CA). To verify the binding specificity for nitrotyrosine, PARP, ICAM-1, P-Selectin, Bax, Bcl-2, TNF-α and IL-1β and FasL, some sections were also incubated with primary antibody only (no secondary antibody) or with secondary antibody only (no primary antibody). In these situations, no positive staining was found in the sections indicating that the immunoreactions were positive in all the experiments carried out. In order to confirm that the immunoreactions for the nitrotyrosine were specific some sections were also incubated with the primary antibody (anti-nitrotyrosine) in the presence of excess nitrotyrosine (10 mM) to verify the binding specificity.
Terminal deoxynucleotidyl transferase-mediated dUTP-biotin end labeling assay
Terminal deoxynucleotidyl transferase-mediated dUTP-biotin end labeling assay (TUNEL) was conducted by using a TUNEL detection kit according to the manufacturer's instruction (Apotag horseradish peroxidase kit; DBA, Milan, Italy). Briefly, sections were incubated with 15 2 g/Ml proteinase K for 15 min at room temperature and then washed with PBS. Endogenous peroxidase was inactivated by 3% H2O2 for 5 min at room temperature and then washed with PBS. Sections were immersed in terminal deoxynucleotidyl transferase (TdT) buffer containing deoxynucleotidyl transferase and biotinylated deoxyuridine 5-triphosphate in TdT buffer, incubated in a humid atmosphere at 37-C for 90 min, and then washed with PBS. The sections were incubated at room temperature for 30 min with anti-fluorescein isothiocyanate horseradish peroxidase-conjugated antibody, and the signals were visualized with diaminobenzidine.
Subcellular fractionation, nuclear protein extraction and Western blot analysis for iNOS, IκB-α, NF-κB p65, Bax and Bcl-2
Tissues were homogenized in cold lysis buffer A (HEPES 10 mM pH = 7.9; KCl 10 mM;EDTA 0.1 mM; EGTA 0.1 mM; DTT 1 mM; PMSF 0.5 mM; Trypsin inhibitor 15 μg/ml; PepstatinA 3 μg/ml; Leupeptin 2 μg/ml; Benzamidina 40 μM). Homogenates were centrifuged at 12000 g for 3 min at 4°C, and the supernatant (cytosol + membrane extract) was collected to evaluate contents of iNOS, IkB-α, Bax, Bcl-2 and β-actin. The pellet was resuspended in buffer C (HEPES 20 mM; MgCl2 1.5 mM; NaCl 0.4 mM; EDTA 1 mM; EGTA 1 mM; DTT 1 mM; PMSF 0.5 μg/ml; Leupeptin 2 μg/ml; Benzamidina 40 μM; NONIDET P40 1%; Glicerolo 20%) and centrifuged at 12000 g for 12 min at 4°C, and the supernatant (nuclear extract) was collected to evaluate the content of NF-kB p65 and LaminB1. Protein concentration in the homogenate was determined by Bio-Rad Protein Assay (BioRad, Richmond CA) and 50 μg of cytosol and nuclear extract from each sample was analysed. Proteins were separated by 12% SDS-polyacrylamide gel electrophoresis and transferred on a PVDF membrane (Hybond-P Nitrocellulose, Amsherman Biosciences, UK). The membrane was blocked with 0.1% TBS-Tween containing 5% non fat milk for 1 h at room temperature. After the blocking, the membranes were incubated with the relative primary antibody overnight at 4°C; anti-iNOS TYPE II diluted 1:1000 (Transduction Laboratories), anti-IkB-α diluted 1:1000, anti-Bax diluted 1:500, anti-Bcl2 diluted 1:1000, anti-NFkB p65 diluted 1:250, anti-β-actin 1:5000 (Santa Cruz Biotechnology, CA) and anti-Laminin B1. After the incubation, the membranes were washed three times for ten minutes with 0.1% TBS Tween and were then incubated for one hour with peroxidase-conjugated anti- mouse or anti-rabbit secondary antibodies (Jackson ImmunoResearch Laboratories, USA) diluted 1:2000, the membranes were then washed three times for ten minutes and protein bands were detected with SuperSignal West Pico Chemioluminescent (PIERCE). Densitometric analysis was performed with a quantitative imaging system (ImageJ).
Cytokines Production
The levels of TNF and IL-1β were evaluated in the plasma at 18 hours after zymosan or saline administration. The assay was conducted using a colorimetric commercial kit (Calbiochem-Novabiochem, La Jolla, CA). The ELISA has a lower detection limit of 10 pg/ml.
Measurement of myeloperoxidase activity
Myeloperoxidase (MPO) activity, which was used as an indicator of PMN infiltration into the lung and intestinal tissues, was measured as previously described [
27].
Quantification of organ function and injury
Blood samples were taken at 18 h after zymosan or saline injection and centrifuged (1610 ×
g for 3 min at room temperature) to separate plasma. Levels of amylase, lipase, creatinine, alanine aminotransferase (ALT), aspartate aminotransferase (AST), bilirubine and alkaline phosphatase were measured by a veterinary clinical laboratory using standard laboratory techniques. For the evaluation of acid base balance and blood gas analysis (indicator of lung injury) arterial blood levels of pH, PaO
2 and PaCO
2 and bicarbonate ion (HCO
3-) were determined by pH/Blood gases Analyser as previously described [
28].
Light microscopy
Lung, liver and small intestine samples were taken 18 hours after zymosan or saline injection. The tissue slices were fixed in Dietric solution [14.25% (v/v) ethanol, 1.85% (w/v) formaldehyde, 1% (v/v) acetic acid] for 1 week at room temperature, dehydrated by graded ethanol and embedded in Paraplast (Sherwood Medical, Mahwah, New Jersey, USA). Sections (thickness 7 μm) were deparaffinized with xylene, stained with hematoxylin and eosin and observed in Dialux 22 Leitz microscope.
Materials
Unless stated otherwise, all reagents and compounds were obtained from Sigma Chemical Company (Milan, Italy).
Data analysis
All values in the figures and text are expressed as mean ± standard error of the mean (s.e.m.) of n observations. For the in vivo studies, n represents the number of animals studied. In the experiments involving histology or immunohistochemistry, the figures shown are representative of at least three experiments (histological or immunohistochemistry coloration) performed on different experimental days on the tissue sections collected from all animals in each group. The results were analyzed by one-way ANOVA followed by a Bonferroni's post-hoc test for multiple comparisons. A p-value of less than 0.05 was considered significant. Statistical analysis for survival data was calculated by Kaplan-Meier survival analysis The Mann-Whitney U test (two-tailed, independent) was used to compare medians between the body weight and the clinical score. For such analyses, p < 0.05 was considered significant.
Discussion
Little is known about the peroxisome proliferator-activated receptor (PPAR)-β/δ compared to the other members of the steroid hormone nuclear receptor family, PPAR-α and PPAR-γ [
30]. Recently, preclinical
in vivo studies, using high-affinity PPAR-β/δ agonists, have demonstrated efficacy in models of diabetes as well as obesity β-oxidation, suggesting that modulation of the beta/delta isoform may have a role in treating these diseases as well as the metabolic syndrome [
30]. Though the mechanism by which PPAR-β/δ acts remains largely unknown and not yet fully characterized, we wanted to demonstrate a possible therapeutic involvement of the PPAR-β/δ isoform in an acute inflammatory disease such as zymosan-induced multiple organ failure. We demonstrated a beneficial role of the PPAR-β/δ agonist, GW0742, as its treatment decreased the development of acute peritonitis, organ dysfunction and injury, which was associated with a severe illness, a survival approximately of 60% and characterized by systemic toxicity, and significant loss of body weight.
Our results demonstrate that GW0742, through the activation of its PPAR-β/δ receptor, not only mediates anti-inflammatory effects but also attenuates cell death and apoptosis processes, ameliorating organ dysfunction and/or improving survival. We clearly demonstrate that GW0742 significantly reduced exudate formation and the degree of PEC count. Moreover, during the study of other inflammatory diseases, it been shown that several transcription factors, important to the regulation of acute inflammation, serve as substrates for PPARs [
31,
32]. These include the transcription factor NF-κB (Nuclear Factor Kappa-light-chain-enhancer of activated B cells), a protein complex that is found in almost all animal cell types and is involved in cellular responses to stimuli such as stress, cytokines, free radicals, ultraviolet irradiation, oxidized LDL, and bacterial or viral antigens [
33‐
37]. NF-κB plays a key role in regulating the immune response to infection. Consistent with this role, incorrect regulation of NF-κB has been linked to cancer, inflammatory and autoimmune diseases, septic shock, viral infection, and improper immune development [
38]. In concurrence with this, multiple organ dysfunction syndrome (MODS) causes liberation of NF-κB p65 by its physiological inhibitor, IκBα, and hence nuclear translocation where it activates the inflammatory pathway. NF-κB p65 function is strikingly altered by PPAR activation. By Western Blot analysis, we report here that zymosan-induced non-septic shock was associated with significant IκB-α degradation as well as increased nuclear localization of NF-kB p65 in the lung at 18 h after zymosan administration. GW0742-treatment significantly reduced IκBα degradation as well as nuclear translocation of p65. Thus, in this
in vivo model system, GW0742 appeared to inhibit NF-κB activation, maintaining high cytoplasm levels of IkBα.
PPAR-β/δ activation also attenuates the increase of many cytokines, such as TNF-α and IL-1β, involved in the inflammatory response. There is evidence that the pro-inflammatory cytokines, TNF-α and IL-1β help to propagate the extension of a local or systemic inflammatory process [
39,
40]. In the present study, zymosan-induced shock causes a substantial increase in the levels of both TNF-α and IL-1β in the plasma after 18 h, while it is clear that GW0742 blocks the mechanisms generating an overproduction of TNF-α and IL-1β. These data are confirmed by immunohistochemical localization of these cytokines. Indeed, the assessment of pancreatic, pulmonary and intestinal tissue sections have revealed a higher presence of TNF-α and IL-1β in samples obtained from zymosan-injected mice, while GW0742 treatment exhibited a fall in the immunohistochemical levels. Moreover, the result of high circulating TNF and IL-1β plasma levels is the expression of endothelial adhesion molecules, such as ICAM-1 and P-selectin that play a pivotal role in the rolling and firm attachment of neutrophils to the endothelium [
28], regulating the process of neutrophil chemoattraction, adhesion, and emigration from the vasculature to the tissues [
41,
42]. In this study, we observed that, 18 h after administration, zymosan induced the expression of P-selectin in the endothelium of small vessels and upregulated the surface expression of ICAM-1 and P-Selectin on endothelial cells in the pancreas, lung and gut. In contrast, there was significantly less expression of P-selectin and ICAM-1 in the pancreas, lung and gut obtained from mice treated with GW0742. Accordingly, we found, by assessment of MPO levels, that neutrophil infiltration was significantly reduced upon GW0742 treatment in zymosan-induced injured mice.
Moreover, in zymosan-induced shock and inflammation the role of nitric oxide (NO), a reactive nitrogen species, has been demonstrated [
43] because of the induction of iNOS, which contributes to the inflammatory process [
24]. NO levels assessed in exudates and plasma, were increased at 18 h after zymosan-injection, while GW0742 decreased the levels of NO. By Western Blot analysis, we have detected the anti-inflammatory action of GW0742 on iNOS expression, which was reduced when compared with zymosan-only injected mice.
Nitrotyrosine formation, along with its detection by immunostaining, was initially proposed as a relatively specific marker for the detection of the endogenous formation "footprint" of peroxynitrite [
44] and an increased nitrotyrosine staining is considered as an indication of increased nitrosative stress [
45]. Thus, by immunohistochemical localization, we have seen an increase in nitrotyrosine staining in samples of pancreas, lung and gut obtained from zymosan-induced injured mice, while an improvement was due to GW0742 administration.
Therefore, in this experiment, it is not unexpected that we found that multiple organ failure results also in the formation of peroxynitrite and it is well known that the nuclear enzyme poly (ADP-Ribose) synthetase (PARS) activation can be a consequence of peroxynitrite production [
46,
47]. A novel pathway of inflammation has been proposed in relation to ROS (hydroxyl radical and peroxynitrite) induced strand breaks in DNA, which trigger energy-consuming DNA repair mechanisms and activates PARP, resulting in the depletion of its substrate NAD
+in vitro and a reduction in the rate of glycolysis. As NAD
+ functions as a cofactor in glycolysis and the tricarboxylic acid cycle, NAD
+ depletion leads to a rapid fall in intracellular ATP. This process has been termed '
the PARP Suicide Hypothesis'. Thus, a markedly immunohistochemical staining of PARP was detected in sections of pancreas, lung and gut from zymosan-treated mice, while, here, we have observed a decrease of PARP activity in samples of mice treated with GW0742.
The processes that lead to the activation of inflammatory mediators, such as NF-kB p65 or TNF-α are also crucially involved and closely associated to apoptotic processes, that occur in FasL expression induced by DNA-damaging agents, such as a genotoxic drug and UV radiation [
48]. Fas forms the Death Inducing Signaling Complex (DISC) upon ligand binding, a multi-protein complex formed by members of the
death receptor family of apoptosis-inducing cellular receptors [
49]. In this study, we have clearly shown the degree of cell death, assessed by immunohistochemical localization of FasL and TUNEL staining, which highlights the presence of apoptotic cell bodies. In either case, we found that zymosan-injection causes an increase of FasL expression in tissue sections of pancreas, lung and gut and TUNEL-positive staining with a marked appearance of dark brown apoptotic cells and intercellular apoptotic fragments in pancreas and lung tissues. On the other hand, the GW0742-mediated activation of PPAR-β/δ confirms the beneficial role in multiple organ failure, decreasing the value of previous apoptotic parameters. Apoptosis manifests itself in two major execution programs downstream of the death signal: the caspase pathway and organelle dysfunction, of which mitochondrial dysfunction is the best characterized [
50,
51]. As the Bcl-2 family members reside upstream of irreversible cellular damage and focus' much of their efforts at the level of the mitochondria, it plays a pivotal role in deciding whether a cell will live or die. The Bcl-2 family of proteins has expanded significantly and includes both pro- as well as anti-apoptotic molecules. Indeed, the ratio between these two subsets helps determine, in part, the susceptibility of cells to a death signal [
52].
Thus, the Western Blot analysis on sections of lung tissue to detect Bax and Bcl-2 expression, supported the idea that the zymosan-injection causes an increase of mitochondrial permeability and severe cellular injury, which leads to a higher expression of Bax than Bcl-2 production, whereas GW0742 administration reduced the apoptosis-induced cell death.
Also the immunohistochemical localization of Bax on sections of pancreatic, pulmonary and intestinal tissue has revealed a loss of physiological balance between pro- and anti-apoptotic factors with an increase of Bax and a decrease of Bcl-2 expression in zymosan-administered mice and, in contrast, a reduction of Bax levels in GW0742-treated animals.
To further confirm these data, we found that GW0742 treatment not only prevents lung dysfunction, and reduces zymosan-induced loss of blood PaO2, PCO2, HCO3- and pH levels, but also diminishes other blood parameters, such as the levels of AST, ALT, bilirubin and alkaline phosphatase that are altered after the onset of zymosan-induced MOF. Furthermore, high concentrations of lipase, amylase and creatinine, indicating the degree of MODS, are all reduced by GW0742, as shown here on liver, pancreas, kidney and lung, is significantly attenuated by PPAR-β/δ activation by GW0742, reducing the pathophysiology of MOF. A histological resolution of organ damage to administration of GW0742 was highlighted in pancreas, lung and gut by haematoxylin-eosin staining too. Indeed, the degree of histoarchitectural modifications in these tissues decreased significantly after treatment with GW0742.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
MG, CC have carried out the molecular biology studies; RDP. IP, TG have carried out the animal studies; EM has carried out the histological/immunohistochemical studies; EC, AK have drafted the manuscript and performed the statistical analysis. SC, CT, PB have participated in the design of the study, have coordinated the study and have finalized the manuscript. All authors have read and approved the final manuscript.