Inhaled hydrogen sulfide protects against lipopolysaccharide-induced acute lung injury in mice
© Faller et al.; licensee BioMed Central Ltd. 2012
Received: 24 September 2012
Accepted: 24 September 2012
Published: 1 October 2012
Local pulmonary and systemic infections can lead to acute lung injury (ALI). The resulting lung damage can evoke lung failure and multiple organ dysfunction associated with increased mortality. Hydrogen sulfide (H2S) appears to represent a new therapeutic approach to ALI. The gas has been shown to mediate potent anti-inflammatory and organ protective effects in vivo. This study was designed to define its potentially protective role in sepsis-induced lung injury.
C57BL/6 N mice received lipopolysaccharide (LPS) intranasally in the absence or presence of 80 parts per million H2S. After 6 h, acute lung injury was determined by comparative histology. Bronchoalveolar lavage (BAL) fluid was analyzed for total protein content and differential cell counting. BAL and serum were further analyzed for interleukin-1β, macrophage inflammatory protein-2, and/or myeloperoxidase glycoprotein levels by enzyme-linked immunosorbent assays. Differences between groups were analyzed by one way analysis of variance.
Histological analysis revealed that LPS instillation led to increased alveolar wall thickening, cellular infiltration, and to an elevated ALI score. In the presence of H2S these changes were not observed despite LPS treatment. Moreover, neutrophil influx, and pro-inflammatory cytokine release were enhanced in BAL fluid of LPS-treated mice, but comparable to control levels in H2S treated mice. In addition, myeloperoxidase levels were increased in serum after LPS challenge and this was prevented by H2S inhalation.
Inhalation of hydrogen sulfide protects against LPS-induced acute lung injury by attenuating pro-inflammatory responses.
KeywordsAcute lung injury Hydrogen sulfide Sepsis Lipopolysaccharide Inflammation
Acute lung injury (ALI), and the acute respiratory distress syndrome (ARDS), are two major challenges in clinical practice and both are responsible for high rates of morbidity and mortality amongst intensive care patients [1–3]. A variety of stimuli can initiate ALI, such as mechanical ventilation, hyperoxia, ischemia/reperfusion, transfusion, or polytrauma . Sepsis reflects one of the most important causes of ALI . The underlying strong inflammatory response in sepsis-induced ALI is characterized by the transmigration of immune-competent cells (mostly neutrophils) into the lung interstitium and the alveolar space, and the release of numerous pro-inflammatory cytokines, e.g., interleukin-1β (IL-1β) and macrophage inflammatory protein-2 (MIP-2). As a consequence of the inflammatory process, alveolar structures change, endothelial and alveolar permeability increase and alveolar fluid clearance decreases, thus critically impairing lung function . Currently available treatment options have failed to significantly decrease sepsis related mortality. Therefore, alternative strategies are urgently needed to improve supportive care.
In this respect, hydrogen sulfide (H2S) has come to be a focus of interest. H2S belongs to the group of gaseous transmitters, along with nitric oxide and carbon monoxide. It is present in the blood and organs of humans and mammals in low micromolar extracellular concentrations. Endogenous H2S has been shown to be involved in a series of physiological processes, e.g., inflammation, vasodilatation, neuromodulation, pain perception, as well as in organ protective pathways (reviewed in ). Moreover, exogenous application of gaseous H2S and H2S donors in different animal disease models like ventilator-induced lung injury , ischemia/reperfusion injury , or oleic acid-induced ALI [9, 10], succeeded in exerting organ-protective effects. The underlying mechanism may be explained by the ability of H2S to inhibit the activation and transmigration of neutrophil cells and to attenuate the release of pro-inflammatory cytokines.
The aims of the present study were to mimic sepsis-induced ALI by intranasal administration of the endotoxin lipopolysaccharide (LPS) and to examine the role of continuously inhaled H2S in this injury model.
Animals and experimental setting
All animal experiments were performed in accordance with the guidelines of the local animal care commission (Ethics Committee University of Freiburg, Freiburg, Germany, permission No. G-07/25) and in conformance with the journals’ requirements for human and animal trials. C57BL/6 N mice weighing 22.4 g (± 0.3 g) were randomly assigned into four experimental groups: (1) intranasal (i.n.) application of endotoxin-free phosphate buffered saline (70 μl) + spontaneous breathing of room air (PBS + air), (2) PBS treatment + spontaneous breathing of air supplemented with 80 parts per million (ppm) hydrogen sulfide (H2S, Air Liquide, Kornwestheim, Germany) (PBS + H2S), (3) i.n. application of lipopolysaccharide (70 μl dissolved in PBS, LPS; 0,25 ng E.coli 055:B5; Sigma-Aldrich Chemie GmbH, Munich, Germany) + spontaneous breathing of air (LPS + air), (4) LPS treatment + spontaneous inhalation of 80 ppm H2S (LPS + H2S). Spontaneous breathing of the respective gas mixture started 1 h prior to PBS or LPS instillation. Instillation of PBS or LPS was conducted under short isoflurane anesthesia. Afterwards, mice were again placed in a sealed plexiglass chamber and subjected to either breathe room air or H2S for another 6 h. H2S concentration was continuously monitored using a portable gas monitor (MX6 iBrid, Industrial Scientific Corporation, Oakdale, PA).
Tissue sampling and bronchoalveolar lavage
At the end of each experiment all mice were sacrificed by an intraperitoneal, overdosed injection of ketamine (180 mg/kg) and acepromazine (1.8 mg/kg) and additional bleeding. Bronchoalveolar lavage fluid, lung tissue samples, and blood samples were gained and analyzed as described recently .
BAL aliquots were analyzed using interleukin-1β (IL-1β) and macrophage inflammatory protein-2 (MIP-2) ELISA kits (R&D Systems GmbH, Wiesbaden, Germany) according to the manufacturers’ instructions. Serum samples were tested using ELISA kits for myeloperoxidase (MPO) glycoprotein (HK210 ELISA, Hycult biotech GmbH, Beutelsbach, Germany) and IL-1β according to the manufacturers’ instructions.
The left lung was prepared, conserved, and cut into 12 μm thick cryosections for hematoxylin and eosin (H + E) staining as previously described . From each lung, four representative photos were taken (magnification x200). Five high power fields (HPF) were randomly assigned to each photo. Subsequently, alveolar wall thickness and cellular infiltration were analyzed by Axiovision software (AxioVS40LE, Zeiss, Jena, Germany). For each HPF, the degree of lung damage was determined using a modified ALI score as described earlier : In brief, (a) thickness of the alveolar walls, (b) infiltration or aggregation of inflammatory cells, and (c) hemorrhage were rated in a blinded fashion. Each item was graded according to the following point scale: 0: minimal damage, 1: mild damage, 2: moderate damage, 3: severe damage, 4: maximal damage. The degree of ALI was assessed by the sum of scores for each HPF, ranging from 0 to 12. The average of the sum of each field score per lung was compared among groups.
Experiments were performed with 6–8 mice per group. Group size was defined on the basis of expected neutrophil cell numbers in BAL fluid by power calculations prior to the study. Graphs represent means ± standard error of means (SEM). Data were further analyzed for normal variation prior to one way analysis of variance (ANOVA), followed by the Student-Newman-Keuls posthoc test. In cases of a failed normality test, Kruskal-Wallis ANOVA on Ranks was performed followed by Dunn`s posthoc test. P < 0.05 was considered significant.
Results and discussion
In this study, we clearly demonstrate, that inhalation of H2S in low dose prevents the development of acute lung injury. Furthermore, we show that H2S treatment substantially reduces local as well as systemic inflammation.
Hydrogen sulfide prevents lung damage in LPS-induced ALI
These results add important information to the role of exogenous H2S in sepsis. Conflicting data exist in models of cecal ligation and puncture demonstrating aggravation [12–20] as well as substantial reduction of the resulting lung injury in response to application of H2S donors [21, 22]. It is likely that the route of administration, dosage, timing, and the purity of H2S donors may be accountable for the inconsistent data. This study is the first to show that inhalation of H2S clearly prevents lung damage due to local LPS-induced injury, underlining the therapeutic potential of this gas under septic conditions. Our findings are further supported by a recent publication by Tokuda et al. . Here, in contrast to our study, LPS was applied systemically. The study found inhalation of 80 ppm H2S substantially increased survival. Although the authors did not analyze histopathological changes in the lung, the data suggest an organ-protective effect of H2S inhalation. Moreover, we have shown recently that inhalation of H2S in low dosage (80 ppm) ameliorated lung pathology in ventilator-induced lung injury . In a related model, Francis et al. demonstrated, that inhalation of 60 ppm was sufficient to exert a series of lung protective effects . These data suggest that application of lower concentrations as we used can achieve lung protection. Although we did not detect any toxic side effects of H2S inhalation in our model (data not shown), future studies in this direction are needed to minimize H2S exposure.
Hydrogen sulfide mediates lung protection by inhibition of the inflammatory response
In our model, inhalation of hydrogen sulfide substantially reduced LPS-induced acute lung injury. The observed protection appears to be mediated by the anti-inflammatory effects of H2S, i.e., inhibition of neutrophil transmigration and pro-inflammatory cytokine release. Therefore, H2S application displays organ protective properties.
SF conducted the study and wrote the manuscript; KKZ helped to conduct the study and analyzed the data; KMS helped to conduct the study; HE helped to analyze the data and critically revised the manuscript; RS helped to design and conduct the study and to analyze the data; HB helped to analyze the data and to write the manuscript; SGS helped to conduct the study; AH designed and conducted the study, analyzed the data and wrote the manuscript. All authors read and approved the final manuscript.
This study was supported by a grant from the German Research Foundation (DFG, Bonn, Germany) to Alexander Hoetzel (DFG HO 2464/3-1).
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