- Open Access
Ethyl pyruvate reduces mortality in an endotoxin-induced severe acute lung injury mouse model
Respiratory Research volume 10, Article number: 91 (2009)
Ethyl pyruvate (EP) was recently identified as an experimental therapeutic agent in a wide variety of model systems for inflammation-mediated tissue and cellular injury.
To evaluate the effect of ethyl EP on improving the survival in mice with LPS-induced acute lung injury (ALI).
ALI was induced by administering lipopolysaccharide (LPS) intratracheally. The mice were treated intraperitoneally (i.p.) with 100, 50 and 10 mg/kg EP immediately before intratracheal instillation of LPS, and 100 mg/kg EP was administered 0, 12, 24 and 48 hours after induction of ALI. The mortality rate was recorded and analyzed by the Kaplan-Meier method. Serum tumor necrosis factor (TNF)-α, interleukin (IL) -6 and IL-1 β were measured in bronchial alveolar lavage fluid using an enzyme-linked immunosorbent assay. High-mobility group box 1 levels were measured by Western immunoblotting.
Treatment with EP significantly inhibited the release of HMGB1, TNF-α, IL-6 and IL-1β into bronchoalveolar lavage (BAL) fluids of ALI mice, and reduced the permeability index of the injured lung. High EP doses reduced the mortality from ALI and the permeability index (100 mg/kg and 50 mg/kg EP versus control; P < 0.0001). Early administration of high-dose EP significantly increased survival rate (0, 12 and 24 h versus control; P < 0.0001, P < 0.0001 and P = 0.01 respectively by log-rank test). There was no survival advantage when EP was initiated at 48 h.
Ethyl pyruvate improves survival and reduces the lung permeability index in mice with LPS-induced ALI.
Despite significant advances in understanding the pathogenesis of acute lung injury (ALI) and its management, the mortality rate from ALI remains unacceptably high [1, 2]. It is well known that the pathogenesis of ALI is mediated by pro-inflammatory cytokines, including tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6 and high-mobility group box (HMGB) 1, which are released from macrophages, neutrophils and other cells of the innate immune system [3, 4]. However, in two large clinical trails, administration of a monoclonal antibody against human TNF-α (TNF-α MAb) and a recombinant human IL-1 (rhIL-1ra) receptor antagonist failed to prolong survival in patients with sepsis syndrome [5, 6].
HMGB1 is a late mediator of lethal systemic inflammation in animal models of cytokine-mediated disease. It is released by macrophages only after a delay of 12-18 h during endotoxemia . Anti-HMGB1 antibodies protect against the lethal effects of LPS-induced endotoxemia in mice when administered 2 h after the onset of endotoxemia . HMGB1 stimulates the release of TNF-α, IL-1β and other inflammatory cytokines from macrophages and pituicytes, and mediates ALI and lethality [8, 9]. Moreover, in patients with severe infection, increased serum HMGB-1 levels correlated with non-survival . These results suggest that HMGB1 is an important mediator in ALI and that its inhibition may be a key to improving clinical outcomes.
Ethyl pyruvate (EP) is a simple derivative of the endogenous metabolite pyruvic acid. Pyruvic acid is an end product of glycolysis, but it is also a potent antioxidant and free-radical scavenger. EP has been shown to improve survival and ameliorate organ dysfunction in a wide variety of animal models of severe sepsis , hemorrhagic shock , ischemia/reperfusion-induced intestinal mucosal injury , and ileus induced by bowel manipulation in mice . EP inhibits lipopolysaccharide (LPS)-induced NF-κB activation in cultured RAW264.7 murine macrophage-like cells, and reduces HMGB1 release and TNF-α gene expression both in vitro and in vivo [10–13]. Therefore, we reasoned that EP might also be protective in established ALI, depending on inhibition of early and late inflammatory cytokines. The present study was designed to evaluate whether EP could be beneficial in a mouse model of LPS-induced ALI.
Materials and methods
Animals and Materials
Adult male BALB/c mice (22-25 g) were allowed to acclimatize for one week housed at 25°C on a 12-h light/12-h dark cycle; all animals were allowed free access to water and standard laboratory chow. All studies were conducted in accordance with the committee of Shandong University School of Medicine on the use and care of animals. The protocols were also approved by the Institutional Animal Care and Use Committee of Shandong University Qilu Hospital. All chemicals were purchased from Sigma-Aldrich (St. Louis, MO). Ethyl pyruvate solution was prepared as 28 mM EP, 130 mM NaCl, 4 mM KCl, 2.7 mM CaCl2 (pH 7.0).
Animal Model of Lung injury
Before the induction of ALI, the mice were fasted overnight but allowed free access to water, then anesthetized with ketamine (100 mg/kg, i.m.) and xylazine (10 mg/kg, i.m.). To create the lung injury, 50 μg LPS from Escherichia coli (serotype O111:B4; Sigma-Aldrich) in 50 μl PBS was given intratracheally. Sham-operated mice underwent the same procedure with intratracheal injection of 50 μl PBS without LPS. To retrieve bronchoalveolar lavage (BAL) fluids, the airways were flushed with 1.0 ml PBS, BAL fluids were collected, and the permeability index as a quantitative marker of vascular leakage was determined as previously described . In brief, bovine serum albumin (BSA) was labeled with 125I by the chloramine T method. A trace amount of 125I-BSA was added to unlabeled BSA (5 mg/ml in PBS), and 200 μl of this solution was injected intravenously. Four hours later, the mice were euthanized with ketamine and blood was collected from the inferior vena cava. The thorax was opened, the left atrium was incised, and the lung was perfused in situ with PBS via the pulmonary artery. The flushed lungs were removed and the permeability index (indicating the extent of pulmonary leakage) was determined using a gamma counter and expressed as the ratio of counts per min (cpm) in the whole lung to radioactivity in 100 μl of blood. BAL fluids were collected and the permeability index was calculated 12 h after ALI induction unless otherwise noted.
In the first experiment, 50 LPS-induced ALI mice were divided randomly into two groups (n = 25, each group). EP was administered intraperitoneally (i.p.) at 100 mg/kg immediately before intratracheal instillation of LPS, and control mice received the same dose of vehicle. HMGB1, TNF-α, IL-1β and IL-6 were measured in BAL fluids and the permeability indices were calculated.
The second experiment was designed to determine the effect on mouse survival of treatment with different doses of EP (100, 50 and 10 mg/kg) starting immediately before intratracheal LPS instillation. Four separate groups of mice (n = 30, each group) were used for this study. Among the 30 mice in each group, 20 were used to record mortality up to a week after the procedure and 10 were killed at 12 h to calculate the permeability index. The mice in these groups were treated with EP at 100, 50 and 10 mg/kg/d (i.p.), and the control mice received the same dose of vehicle until the end of the study. Mortality was recorded up to a week after the procedure (n = 20). Mice (n = 10) were killed and the permeability indices were calculated.
In the third experiment, the experimental and control mice were divided randomly into four treatment groups (n = 20, each group). EP was administered at the same dose (100 mg/kg/d, i.p.), and control mice received the same volume of vehicle beginning at four different time points (0, 12, 24 and 48 h after LPS instillation) until the end of study. Mortality was recorded up to a week after the injection.
The concentrations of TNF-α, IL-6 and IL-1β were measured using commercially available enzyme-linked immunosorbent assay kits (R&D Systems, Minneapolis, MN) according to the manufacturer's instructions. The sensitivities for TNF-α, IL-6 and IL-1β were 15 pg/ml, 5 pg/ml and 5 pg/ml, respectively. Levels of HMGB1 were measured by Western immunoblotting as described by Wang et al. . In brief, serum samples were ultrafiltered with Centricon 100 (Amicon, Millipore, Bedford, MA) to clear them of cell debris and macromolecular complexes, then concentrated 15-fold with Centricon YM-30 and separated on 12% sodium dodecyl sulfate-polyacrylamide gels. The separated proteins were transferred to an immunoblot polymembrane (Bio-Rad, Hercules, Calif), and HMGB1 was measured using polyclonal anti-HMGB1 antibodies (Santa Cruz, America, 1:500 dilution) and secondary anti-rabbit antibodies linked to horseradish peroxidase (Amersham Pharmacia, Buckinghamshire, UK). Standard curves were constructed using r-HMGB1 (Sigma-Aldrich Chemical), and the intensity of the 30-kd band was measured by densitometry.
Data are presented as mean ± SEM unless otherwise indicated. Differences between treatment groups were determined by Student's t test or 1-way analysis of variance (ANOVA) followed by the least-significant difference test, or Fisher's exact test. In the mortality study, time-to-survival data were analyzed by the Kaplan-Meier method and compared with the log-rank test; P < 0.05 was considered statistically significant.
The effect of ethyl pyruvate on pro-inflammatory cytokines in BAL fluids and permeability index of experimental ALI mice
To determine the levels of pro-inflammatory cytokines in BAL fluids, we flushed the airways with 1.0 ml PBS and collected the BAL fluids 12 h after ALI induction. As shown in Table 1, levels of the cytokines HMGB1, TNF-α, IL-6 and IL-1β were substantially elevated in BAL fluids from LPS-induced ALI mice (versus controls; P < 0.001).
Treatment with EP (100 mg/kg, i.p., immediately before intratracheal LPS instillation) significantly inhibited the release of HMGB1, TNF-α, IL-6 and IL-1β into the BAL fluids of ALI mice (Table 1), indicating that EP prevented LPS-induced ALI by attenuating the release of early (TNF-α, IL-6, and IL-1β) and late (HMGB1) systemic pro-inflammatory cytokines associated with lethality. As shown in Fig. 1, EP reduced the permeability indices of the injured lungs (Fig. 1).
Administration of high dose EP prevents the lethality of ALI and reduces the permeability index
To evaluate the protective effect of EP against lethality in LPS-induced ALI mice, the mice received three different doses of EP (100, 50 and 10 mg/kg/d. i.p.) starting immediately before intratracheal LPS instillation. The results showed that the high EP dose (100 mg/kg/d) protected against ALI lethality (survival in 100 mg/kg/d and 50 mg/kg/d of EP versus survival in vehicle-treated controls; P < 0.0001 and P = 0.02 respectively), but the effect was dose dependent; the low dose failed to protect significantly against death (survival in 10 mg/kg/d of EP versus survival in vehicle-treated controls; P = 0.81) (Fig. 2). Also, there was a dose-dependent reduction in the permeability index (100 mg/kg/d and 50 mg/kg/d EP versus vehicle-treated control, P < 0.0001; 10 mg/kg/d versus vehicle-treated control, P = 1.00; Fig. 3).
Early administration of high dose EP prevents ALI lethality
To assess the therapeutic efficacy of early EP treatment against ALI, EP was administered at different time points (0, 12, 24 and 48 h after induction of ALI) at the same single dose of 100 mg/kg/d, i.p. The results showed that early administration of high dose EP (0, 12 or 24 h) significantly increased survival rate in the mice (survival after administration EP at 0, 12 and 24 h versus survival in vehicle-treated controls; P < 0.0001, P < 0.0001 and P = 0.01, respectively) (Fig. 4). However, no survival advantage occurred when EP was initiated at 48 h (survival after EP administration at 48 h versus survival in vehicle-treated controls; P = 0.75) (Fig. 4). Moreover, the animals treated with EP beginning at 0, 12, and 24 h were significantly more active and alert and fed more rapidly than either the animals with treatment beginning at 48 h or controls treated with vehicle.
Acute lung injury (ALI) is an important problem in humans and its pathogenesis is poorly understood. To investigate the molecular mechanisms of ALI, various experimental models have been used; intratracheal administration of LPS induces an ideal model because it results in lung injury without causing systemic inflammation and multi-organ failure. Moreover, the LPS-induced ALI model results in microvascular injury and diffuse alveolar damage with intrapulmonary hemorrhage, edema and fibrin deposition, which are also features of patients with ALI and acute respiratory distress syndrome (ARDS) [15, 16].
In this present study, the levels of both early (TNF-α, IL-1β and IL-6) and late (HMGB1) cytokines in BAL fluids increased in mice with ALI 12 h after induction. Ethyl pyruvate (EP), an experimental pharmacological agent, significantly inhibited the systemic release of these cytokines, which mediate the lethality of ALI and systemic inflammation. Early administration of high-dose EP (0, 12, 24 h) significantly protected against ALI lethality. However, low dose EP or delayed administration gave no advantage in terms of survival. It is likely that pro-inflammatory cytokines, notably TNF-α, IL-1β and IL-6, participate in the early development of inflammation; they have been shown to play a crucial role in ALI and ARDS . Persistent elevation of pro-inflammatory cytokines in serum and BAL fluid in ALI or sepsis patients is associated with a worse outcome . Furthermore, instillation of IL-1β and TNF-α into the lungs leads to neutrophil accumulation, interstitial edema and histological changes consistent with inflammatory lung injury [17–19]. High concentrations of TNF-α are found in BAL fluids from patients with sustained ALI and ARDS, and high levels of IL-6 have been described in a number of acute conditions such as burns, major surgery and sepsis . In patients with ALI and ARDS, non-survivors have significantly higher BAL-fluid-to-plasma cytokine concentration ratios than survivors , indicating the critical role of these cytokines in mortality.
These results suggest that the levels of HMGB1 in BAL fluids were greater in LPS-induced ALI mice than control mice. Moreover, administration of EP reduced the late mediator HMGB1. Unlike other pro-inflammatory cytokines, HMGB1 is a "late-appearing" inflammatory mediator, because its release during endotoxemia is delayed in comparison with the rapid increase of early pro-inflammatory cytokines such as IL-1β, IL-6 and TNF-α [7, 10, 22, 23]. HMGB1 rose in the circulation starting at 8 h, increased until 16 h, and thereafter remained at a high level until 36 h during endotoxemia . Further study showed that administration of anti-HMGB1 antibodies reduced lethality from 100% to 30% . Intratracheal administration of HMGB1 produced acute inflammatory lung injury, and anti-HMGB1 Abs decreased the migration of neutrophils to the lungs as well as lung edema in endotoxin-induced acute lung inflammation . Thus, delayed release of HMGB1 can participate in the downstream development of lung injury, and HMGB1 may be a distal mediator of acute inflammatory lung injury.
Ethyl pyruvate (EP), a very simple aliphatic ester derived from pyruvic acid, has been shown to be an effective anti-inflammatory agent in a wide variety of in vivo and in vitro model systems of inflammation-mediated cellular or tissue injury, including severe sepsis, hemorrhagic shock, ischemia/reperfusion-induced intestinal mucosal injury, and ileus induced by bowel manipulation in mice [10–13, 24, 25]. EP increases survival and reduces circulating levels of IL-6 ., and inhibits activation of NF-κB in Caco-2 human enterocyte-like cells stimulated with a mixture of TNF-α and IL-1β . It blocks the secretion of HMGB1 by LPS-stimulated RAW 264.7 cells and the release of HMGB1 into the circulation in mice . The survival advantage was apparent even when EP was administered 30 min before endotoxin infusion, and the treatment began 24 h after the onset of disease . The molecular mechanism of EP action is to interfere with signal transduction through the p38 MAPK and NF-κB pathways, and to target directly the p65 subunit of the transcription factor [10, 28]. EP inhibition of the p38 MAPK and NF-κB signal transduction pathways effectively induced the release of early (TNF-α, IL-1β and IL-6) and late (HMGB1) inflammatory mediators. Our data showed that administration of EP even when initiated 24 h after induction of ALI significantly increased survival, though no survival advantage occurred when administration was initiated at 48 h, when the levels of these cytokines had decreased significantly; indicating that EP modulation of HMGB1 and other inflammatory cytokines contributes to the beneficial effects on survival.
In conclusion, EP decreased the release of pro-inflammatory cytokines and improved survival in mice with LPS-induced ALI. Thus, EP may be developed as a novel therapeutic adjunct in the treatment of ALI.
acute lung injury
high-mobility group box 1
tumor necrosis factor
Ware LB, Mattay MA: The acute respiratory distress syndrome. N Engl J Med 2000, 342:1334–1349.
Repine JE: Scientific perspective on the adult respiratory distress syndrome. Lancet 1992, 339:466–9.
Gong Q, Yin H, Fang M, Xiang Y, Yuan CL, Zheng GY, Yang H, Xiong P, Chen G, Gong FL, Zheng F: Heme oxygenase-1 upregulation significantly inhibits TNF-alpha and HMGB1 releasing and attenuates lipopolysaccharide-induced acute lung injury in mice. Int Immunopharmacol 2008, 8:792–8.
Kim JY, Park JS, Strassheim D, Douglas I, Diaz del Valle F, Asehnoune K, Mitra S, Kwak SH, Yamada S, Maruyama I, Ishizaka A, Abraham E: HMGB1 contributes to the development of acute lung injury after hemorrhage. Am J Physiol Lung Cell Mol Physiol 2005, 288:L958–65.
Abraham E, Anzueto A, Gutierrez G, Tessler S, San Pedro G, Wunderink R, Dal Nogare A, Nasraway S, Berman S, Cooney R, Levy H, Baughman R, Rumbak M, Light RB, Poole L, Allred R, Constant J, Pennington J, Porter S: Double-blind randomised controlled trial of monoclonal antibody to human tumour necrosis factor in treatment of septic shock. NORASEPT II Study Group. Lancet 1998, 351:929–33.
Fisher CJ Jr, Dhainaut JF, Opal SM, Pribble JP, Balk RA, Slotman GJ, Iberti TJ, Rackow EC, Shapiro MJ, Greenman RL: Recombinant human interleukin 1 receptor antagonist in the treatment of patients with sepsis syndrome. Results from a randomized, double-blind, placebo-controlled trial. Phase III rhIL-1ra Sepsis Syndrome Study Group. JAMA 1994, 271:1836–43.
Wang H, Bloom O, Zhang M, Vishnubhakat JM, Ombrellino M, Che J, Frazier A, Yang H, Ivanova S, Borovikova L, Manogue KR, Faist E, Abraham E, Andersson J, Andersson U, Molina PE, Abumrad NN, Sama A, Tracey KJ: HMG-1 as a late mediator of endotoxin lethality in mice. Science 1999, 285:248–51.
Wang H, Vishnubhakat JM, Bloom O, Zhang M, Ombrellino M, Sama A, Tracey KJ: Proinflammatory cytokines (tumor necrosis factor and interleukin 1) stimulate release of high mobility group protein-1 by pituicytes. Surgery 1999, 126:389–92.
Andersson U, Wang H, Palmblad K, Aveberger AC, Bloom O, Erlandsson-Harris H, Janson A, Kokkola R, Zhang M, Yang H, Tracey KJ: High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes. J Exp Med 2000, 192:565–70.
Ulloa L, Ochani M, Yang H, Tanovic M, Halperin D, Yang R, Czura CJ, Fink MP, Tracey KJ: Ethyl pyruvate prevents lethality in mice with established lethal sepsis and systemic inflammation. Proc Natl Acad Sci USA 2002, 99:12351–12356.
Yang R, Gallo DJ, Baust JJ, Uchiyama T, Watkins SK, Delude RL, Fink MP: Ethyl pyruvate modulates inflammatory gene expression in mice subjected to hemorrhagic shock. Am J Physiol Gastrointest Liver Physiol 2002, 283:G212-G221.
Sims CA, Wattanasirichaigoon S, Menconi MJ, Ajami AM, Fink MP: Ringer's ethyl pyruvate solution ameliorates ischemia/reperfusion-induced intestinal mucosal injury in rats. Crit Care Med 2001, 29:1513–1518.
Harada T, Moore BA, Yang R, Cruz RJ Jr, Delude RL, Fink MP: Ethyl pyruvate ameliorates ileus induced by bowel manipulation in mice. Surgery 2005, 138:530–537.
Neff TA, Guo RF, Neff SB, Sarma JV, Speyer CL, Gao H, Bernacki KD, Huber-Lang M, McGuire S, Hoesel LM, Riedemann NC, Beck-Schimmer B, Zetoune FS, Ward PA: Relationship of acute lung inflammatory injury to Fas/FasL system. Am J Pathol 2005, 166:685–94.
Szarka RoderickJ, Nandi Wang, Lyle Gordon, Nation PN, Smith RichardH: A murine model of pulmonary damage induced by lipopolysaccharide via intranasal instillation. J Immunol Methods 1997, 202:49–57.
Rittirsch D, Flierl MA, Day DE, Nadeau BA, McGuire SR, Hoesel LM, Ipaktchi K, Zetoune FS, Sarma JV, Leng L, Huber-Lang MS, Neff TA, Bucala R, Ward PA: Acute lung injury induced by lipopolysaccharide is independent of complement activation. J Immunol 2008, 180:7664–72.
Bhatia M, Moochhala S: Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome. J Pathol 2004, 202:145–156.
Agouridakis P, Kyriakou D, Alexandrakis MG, Prekates A, Perisinakis K, Karkavitsas N, Bouros D: The predictive role of serum and bronchoalveolar lavage cytokines and adhesion molecules for acute respiratory distress syndrome development and outcome. Respir Res 2002, 3:25–33.
Gupta S, Feng L, Yoshimura T, Redick J, Fu SM, Rose CE Jr: Intra-alveolar macrophage-inflammatory peptide 2 induces rapid neutrophil localization in the lung. Am J Respir Cell Mol Biol 1996, 15:656–63.
Nijsten MW, Hack CE, Helle M, ten Duis HJ, Klasen HJ, Aarden LA: Interleukin-6 and its relation to the humoral immune response and clinical parameters in burned patients. Surgery 1991, 109:761–7.
Meduri GU, Kohler G, Headley S, Tolley E, Stentz F, Postlethwaite A: Inflammatory cytokines in the BAL of patients with ARDS. Persistent elevation over time predicts poor outcome. Chest 1995, 108:1303–14.
Ulloa L, Fink M, Tracey KJ: Ethyl pyruvate protects against lethal systemic inflammation by preventing HMGB1 release. Ann N Y Acad Sci 2003, 987:319–321.
Abraham E, Arcaroli J, Carmody A, Wang H, Tracey KJ: HMG-1 as a mediator of acute lung inflammation. J Immunol 2000, 165:2950–4.
Fink MP: Ethyl pyruvate: a novel anti-inflammatory agent. Crit Care Med 2003, 31:S51-S56.
Yang R, Uchiyama T, Alber SM, Han X, Watkins SK, Delude RL, Fink MP: Ethyl pyruvate ameliorates distant organ injury in a murine model of acute necrotizing pancreatitis. Crit Care Med 2004, 32:1453–1459.
Venkataraman R, Kellum JA, Song M, Fink MP: Resuscitation with Ringer's ethyl pyruvate solution prolongs survival and modulates plasma cytokine and nitrite/nitrate concentrations in a rat model of lipopolysaccharide-induced shock. Shock 2002, 18:507–512.
Sappington PL, Han X, Yang R, Delude RL, Fink MP: Ethyl pyruvate ameliorates intestinal epithelial barrier dysfunction in endotoxemic mice and immunostimulated Caco-2 enterocytic monolayers. J Pharmacol Exp Ther 2003, 304:464–476.
Han Y, Englert JA, Yang R, Delude RL, Fink MP: Ethyl pyruvate inhibits nuclear factor-kappaB-dependent signaling by directly targeting p65. J Pharmacol Exp Ther 2005, 312:1097–1105.
We would like to thank Dr Zhouxiong for technical assistance, and Mrs Rengui Jie, Mr Gao Yang and Mr Zhangxiao Shi for assistance with the animal experiments and HMGB1 measurement. This study was supported by grants from the Science and Technology Department of Shan Dong Province.
The authors declare that they have no competing interests.
SGH designed the study, performed the analyses and wrote the manuscript. LDJ and XW helped to interpret the data and write the manuscript. JCQ helped with the statistics and writing. LY helped with the animal experiment and writing. WAH helped with the cytokine measurements, animal experiments and writing. DL performed experimental measurements and helped to write the manuscript.
About this article
Cite this article
Shang, GH., Lin, DJ., Xiao, W. et al. Ethyl pyruvate reduces mortality in an endotoxin-induced severe acute lung injury mouse model. Respir Res 10, 91 (2009). https://doi.org/10.1186/1465-9921-10-91
- Acute Lung Injury
- Ethyl Pyruvate
- Permeability Index
- Intestinal Mucosal Injury
- Bronchial Alveolar Lavage Fluid