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Introduction

Sepsis is a systemic response to invasive microbial infection or severe tissue damage, resulting in tissue necrosis, multi-organ failure and death (1). After being triggered by overwhelming initial stimuli, neutrophils and macrophages can produce excessive pro-inflammatory mediators, leading to a dysregulated immune response that characterizes sepsis (2). The dominant causes of acute kidney injury (AKI) in hospitalized patients are sepsis and septic shock (3). Lipopolysaccharide (LPS), known as the major component of the outer membrane of Gram-negative bacteria, is a potent activator for acute inflammatory response in sepsis (4), and LPS signaling is initiated by activation of Toll-like receptor 4 (TLR4) (5). Therefore, the blockade of TLR4 signaling has been considered as a promising therapeutic approach for sepsis (6,7) and draws intensive attention from scientists and clinicians worldwide. However, a recent randomized double-blind controlled trial revealed that the application of a specific TLR4 antagonist failed to reduce sepsis-induced mortality (8). Thus, the further identification of critical mediators and molecular targets in sepsis is required. The developmetn of effective therapeutic approaches is urgenly required.

Reportedly, following bacterial infection, the massive recruitment and activation of neutrophils are presented with the extracellular release of neutrophil elastase (NE). NE is a serine protease that propagates persistent neutrophilic inflammation by accelerating pro-inflammatory cytokine production (9,10). By using mouse models of ischemic AKI, Zager et al observed a marked increase in renal cortical/isolated proximal tubule NE mRNA levels and a decrease in NE protein levels (11). Their study suggested that the downregulated protein expression of renal NE correlated with the upregulation of endogenous α-1-antitrypsin, which has protease inhibitor activity (11). From this previous study, it can be postulated that the blockade of NE toxicity may exert renoprotective effects. Sivelestat, a specific NE inhibitor, has been demonstrated to mitigate lung injury, such as pulmonary fibrosis (12) and acute lung injury (13). Of note, Suda et al found that sivelestat improved the survival of animals with sepsis (14). However, they only focused on the beneficial effects of sivelestat in attenuating lung damage. Apart from lung damage, sepsis often leads to impaired function in other vital organs, including the kidneys (15), liver (16) and heart (17). In order to fully evaluate the potential therapeutic effects of a drug or an agent in sepsis, assessing its effects on multiple organs is mandatory.

In the present study, we examined the effects of sivelestat on sepsis-associated AKI in a rat model of sepsis induced by cecal ligation and puncture (CLP) and also explored the underlying mechanisms.

Materials and methods

Animals and ethics

Male Sprague-Dawley rats (weighing 200–250 g) were obtained from the Changsheng Biotech Co., Ltd. (Beijing, China) and housed under specific pathogen-free conditions at a constant temperature of 20–22°C and humidity of 50–60% with a 12-h light/dark cycle, and were allowed free access to food and water. All animal experiments were performed in accordance with the Guidelines for the Care and Use of Laboratory Animals and were approved by the Institutional Animal Care and Use Committee of China Medical University, Shenyang, China.

CLP procedure and animal grouping

CLP procedure was performed to initiate sepsis in rats according to previously published protocols (18). In short, the rats were first anaesthetized by the intraperitoneal (i.p.) administration of 10% chloral hydrate (350 mg/kg; Sinopharm, Beijing, China), and a ventral midline incision (1.5 cm in length) was made on the rats. The caecum was exposed, ligated, punctured with a gauge needle 3 times, and then placed back into the abdomen. Rats that underwent sham operation (the caecum was exposed by a ventral midline incision, but was not ligated or punctured) were used as the controls. Thereafter, the abdominal incision was closed in layers with 3-0 surgical sutures, and the rats were allowed to recover from the anaesthesia. These rats were randomly divided into 6 groups (n=8/group) as follows: i) group 1: the sham-operated group (Sham); ii) group 2: the sham-operated group administered the low dose of sivelestat (Sham + L-sivelestat); iii) group 3: the sham-operated group administered the high dose of sivelestat (Sham + H-sivelestat); iv) group 4: the rats with sepsis who were not treated (Sepsis); v) group 5: the rats with sepsis who were administered the low dose of sivelestat (Sepsis + L-sivelestat); and vi) group 6: the rats with sepsis who were administered the high dose of sivelestat (Sepsis + H-sivelestat). The rats in groups 2 and 3, and 5 and 6, rats were administered an i.p. injection of 50 or 100 mg/kg body weight sivelestat (Ono Pharmaceutical Co., Osaka, Japan) immediately after the sham-operation or the initiation of sepsis. The rats in groups 1 and 4 received an infusion of normal saline (vehicle) into the intraperitoneal cavity. The doses of sivelestat used in our study were selected based on our preliminary experiments (data not shown) and a previous study (12). Blood samples from each rat were obtained at 6 and 24 h post-surgery, and the rat kidneys were rapidly removed at 24 h post-surgery after sacrifice (by an overdose of anesthetics) and immediately frozen in liquid nitrogen or fixed in 10% formaldehyde (Sinopharm) for use in subsequent experiments.

In order to determine whether sivelestat affects animal survival, the mortalities were measured in another set of rats treated with or without sivelestat up to 108 h after the procedure (n=10/group). In addition, the mean arterial pressure (MAP) in these rats was assessed using a non-invasive blood pressure monitoring system at 24 h according to the manufacturer's instructions (ALC-NIBP, Alcott Biotech Co., Ltd., Shanghai, China).

Measurement of serum biochemical parameters

Serum samples were centrifuged at 1,000 rpm for 20 min, and then subjected to the detection of blood urea nitrogen (BUN), neutrophil gelatinase-associated lipocalin (NGAL) levels, tumor necrosis factor α (TNF-α) and interleukin-1β (IL-1β) levels and NE levels in the serum and renal tissues using commercially available kits (Boster, Uscn Life Science, Inc., Wuhan, China) according to the manufacturer's instructions.

Glomerular filtration rate (GFR) and fractional excretion of sodium (FENa) assessments

The rats that underwent CLP or sham surgery were anaesthetized at 24 h and subjected to the following assessments. GFR was determined by measuring the inulin clearance. In brief, inulin (Sigma-Aldrich, St. Louis, MO, USA) was dissolved in normal saline to a concentration of 5 mg/ml, and then administered through the femoral vein at a dose of 1 ml/h/100 g body weight. Following equilibration, the urinary bladder was cannulated to collect a 30-min urine sample. In addition, a blood sample (1 ml) was collected at the midpoint of the urine collection period. Ten minutes later, urine and blood samples were collected again. Inulin concentrations in the urine and plasma were determined using the anthrone method, while sodium and creatinine concentrations were determined using commercial assay kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China), respectively. The values of GFR and FENa were calculated through standard formulas, as previously described (19–21): GFR = [(urine inulin) x (volume of urine collected)]/[(plasma inulin) x (time of collection)], and expressed as ml/min/100 g body weight; FENa = 100 x [(urine sodium x plasma creatinine)/(plasma sodium x urine creatinine)].

Hematoxylin and eosin (H&E) staining and immunohisto-chemistry

The formaldehyde-fixed kidney tissues were embedded in paraffin, cut into 5-µm-thick sections, and then deparaffinized in xylene and hydrated in graded ethanol. For the morphological examination, these slices were stained with hematoxylin (Solarbio, Beijing, China) and eosin (Sinopharm). For immunohistochemistry, these sections were heated in citrate buffer at 100°C for 10 min to retrieve the antigen and then treated with 3% hydrogen peroxide (both from Sinopharm) at room temperature for 15 min to block the endogenous peroxidase activity. After being blocked with normal goat serum at room temperature for 15 min, these sections were incubated with rabbit polyclonal antibodies against high-mobility group box 1 (HMGB1; 1:100 dilution, bs-0664R), inducible nitric oxide (NO) synthase (iNOS; 1:100 dilution, bs-0162R) (both from Bioss, Beijing, China) and a mouse monoclonal antibody against ED-1 (1:50 dilution, sc-59103; Santa Cruz Biotechnology, Santa Cruz, CA, USA) at 4°C overnight. These sections were then incubated with biotin-labeled goat anti-rabbit IgG (1:200 dilution, A0277) or anti-mouse IgG (1:200 dilution, A0286) at 37°C for 30 min, and treated with horseradish peroxidase (HRP)-conjugated streptavidin (all from Beyotime, Shanghai, China) for an additional 30 min. Finally, the tissue sections visualized with 3,3′-diaminobenzidine (DAB) and counterstained with hematoxylin (both from Solarbio), and evaluated under a light microscope (Olympus, Tokyo, Japan).

Western blot analysis

Total protein samples were extracted from the kidney tissues using RIPA buffer (Beyotime) and the protein concentrations were evaluated by bicinchoninic acid assay. An equivalent amount of each protein sample (40 µg) was loaded and separated through sodium dodecyl sulphate (SDS)-polyacrylamide gel electrophoresis (PAGE) and transferred onto polyvinylidene difluoride membranes (PVDF; Millipore, Bedford, MA, USA). The membranes were then blocked with 5% non-fat milk, and incubated overnight at 4°C with rabbit polyclonal antibodies against NE (1:500 dilution, bs-6982R), HMGB1 (1:500 dilution, bs-0664R), iNOS (1:500 dilution, bs-0162R), serine/threonine kinase (Akt; 1:500 dilution, bs-6951R) and phosphorylated Akt (p-Akt; 1:500 dilution, bs-0876R). All primary antibodies were purchased from Bioss. Thereafter, the membranes were incubated with HRP-conjugated secondary antibodies (1:5000 dilution, A0208; Beyotime) at 37°C for 45 min and visualized using an enhanced chemiluminescence (ECL) system (Seven Sea Pharmtech Co., Ltd., Shanghai, China). The protein expression levels were expressed as a ratio to the endogenous control, β-actin.

Statistical analysis

All data are presented as the means ± standard deviation (SD), and analyzed using GraphPad Prism version 6.0 or SPSS version 20.0. One-way analysis of variance (ANOVA) was performed on data obtained from the same time point, whilst two-way ANOVA was performed on data from different time points. The Bonferroni test was utilized for post hoc comparisons between different groups. A P-value <0.05 was considered to indicate a statistically significant difference. Survival data were analyzed by the Kaplan-Meier curve and log-rank (Mantel-Cox) test.

Results

Sivelestat decreases NE expression in rats with sepsis

We first evaluated whether the NE levels were affected by the CLP procedure using an ELISA kit and western blot analysis. Our results revealed that the administration of sivelestat alone generated no changes in comparison with the sham-operated rats (Fig. 1). The serum NE level was significantly increased at both 6 and 24 h post-CLP surgery, whereas decreased after sivelestat treatment (Fig. 1A). In addition, renal NE expression was significantly enhanced at 24 h post-CLP surgery, whereas it was suppressed by treatment with sivelestat (Fig. 1B and C). The higher dose of sivelestat was more effective than the lower dose.

Figure 1 Sivelestat suppresses serum and kidney neutrophil elastase (NE) expression in septic rats. NE levels in (A) rat serum at 6 and 24 h and (B) kidney tissues at 24 h post-cecal ligation and puncture (CLP) surgery assessed using an ELISA kit (n=8 rats per group). (C) NE protein expression was detected by western blot analysis in rat kidney tissues at 24 h post-CLP procedure (n=5). β-actin was used as an endogenous control. Data are expressed as the means ± SD. No significant differences were observed in the sham-operated rats. ***P<0.001 compared with the sham-operated (Sham) group; †P<0.05, †††P<0.001 compared with the sepsis group at the same time point.

Sivelestat promotes the survival and preserves the kidney function of rats with sepsis

Another set of rats (10 per group) was subjected to survival analysis for 108 h. As indicated in Fig. 2A, no sham-operated rats treated with 50 or 100 mg/kg sivelestat or the vehicle died during the whole experimental period. All rats in the sepsis group were dead at 108 h post-CLP surgery, while 4 and 6 septic rats survived for 108 h when treated with 50 (P=0.062 vs. sepsis group) and 100 mg/kg sivelestat (P<0.01 vs. sepsis group), respectively (Fig. 2A). As compared with the sham-operated group (104±5.8 mmHg), CLP induced a reduction in MAP (89±7.2 mmHg) (P<0.001), which was restored by sivelestat (Fig. 2B). Morphological changes in the rat kidneys were determined by H&E staining and the parameters related to renal function were detected using commercial kits. Pathological alterations in the rat kidneys were characterized by the loss of the brush border, tubular cell flattening and tubular lumen dilation, while the administration of sivelestat partly reversed these changes (Fig. 2C). In addition, sivelestat did not affect the serum BUN levels, NGAL levels, inulin clearance and FENa in the rats that underwent sham surgery (P>0.05; Fig. 2D–G). However, CLP-induced a significant upregulation in serum BUN and NGAL levels in the rats and this effect was suppressed by sivelestat, with the higher dose being more effective (Fig. 2D and E). Additionally, the decreased inulin clearance (indicating reduced GFR) in the rats with sepsis was partly reversed by sivelestat (Fig. 2F). The CLP-induced increase in FENa (indicating tubular dysfunction) was slightly reduced by sivelestat, but failed to reach statistical significance (Fig. 2G). Collectively, the administration of sivelestat protected the rats against sepsis induced by multiple bacterial infection. Since the lower dose of sivelestat did not induce mortality, kidney distortion or renal dysfunction in the sham-operated rats, this group was excluded from the following mechanism experiments.

Figure 2 Effects of sivelestat on kidney function in rats that underwent sham or cecal ligation and puncture (CLP) surgery. (A) Kaplan-Meier survival plots for all experimental rats (n=10 rats per group). ††P<0.01, compared with the sepsis group (log-rank test). (B) Rat mean arterial pressure (MAP) was detected at 24 h post-surgery (n=8–10 rats per group). (C) Representatives of hematoxylin and eosin (H&E) staining of rat kidney tissues. (D) Serum levels of blood urea nitrogen (BUN), (E) neutrophil gelatinase-associated lipocalin (NGAL) were determined at 6 and 24 h post-surgery using commercially available kits (n=8 rats per group). (F) Inulin clearance and (G) FENa were determined at 24 h post-surgery (n=8 rats per group). Data are expressed as the means ± SD. ***P<0.001 compared with the sham-operated (Sham) group; †P<0.05, ††P<0.01, †††P<0.001 compared with the sepsis group at the same time point. Scale bars, 50 µm.

Sivelestat suppresses the release of pro-inflammatory mediators and macrophage infiltration induced by CLP in rats

The overproduction of pro-inflammatory mediators in response to bacterial infection is one of the major characteristics of sepsis (22). Therefore, the serum levels of TNF-α and IL-1β were assessed in this study. We found that the levels of these two pro-inflammatory cytokines were significantly increased at 6 and 24 h post-CLP procedure (Fig. 3A). Although sivelestat alone generated no changes in the serum levels of TNF-α and IL-1β as compared to the sham-operated group (P>0.05), a marked inhibitory effect of sivelestat on these two pro-inflammatory cytokines in the rats with sepsis rats was observed (Fig. 3A). Immunohistochemistry was also performed in the renal tissues to detect the ED-1-positive macrophages (a marker of macrophage infiltration) at 24 h after the surgical procedures (Fig. 3B). As indicated in Fig. 3C, the number of renal ED-1-positive cells was increased from 1.63±1.92 to 13.38±5.29 per 0.095 mm2 after CLP surgery, but was decreased by the administration of sivelestat (9.13±2.64 by L-sivelestat; 5.38±1.77 by H-sivelestat). Unlike TNF-α and IL-1β that are released immediately in response to bacterial infection, HMGB1 is a late pro-inflammatory mediator (23). We therefore wished to determine whether sivelestat can reduce HMGB1 expression by detecting its renal expression at 24 h after the sham or CLP procedure using immunohistochemical staining and western blot analysis. A weak nuclear expression of HMGB1 was observed in a few renal parenchymal cells in the control kidney tissues (Fig. 3B). However, the number of HMGB1-positive cells was significantly increased after the CLP procedure, whereas it was decreased by treatment with sivelestat at different doses (Fig. 3B). The results from western blot analysis confirmed the immunohistochemical results (Fig. 3D). The above-mentioned results indicate an anti-inflammatory effect of sivelestat in a model of sepsis-related AKI.

Figure 3 Sivelestat inhibits cecal ligation and puncture (CLP)-induced macrophage infiltration and pro-inflammation mediator release in rats. (A) Serum concentrations of tumor necrosis factor α (TNF-α) and interleukin-1β (IL-1β) were determined using the respective ELISA kits at 6 and 24 h after sham or CLP surgery (n=8 rats per group). (B) Macrophage infiltration in rat kidney tissues was assessed with specific antibody against ED-1 at 24 h after sham or CLP surgery (upper panels), and (C) the ED-1 positive cells were counted under a light microscope. (B) Representative images of immunohistochemical staining for high-mobility group box 1 (HMGB1) in rat kidney tissues at 24 h post-surgery (lower panels). (D) Renal HMGB1 protein expression was detected by western blot analysis (n=5). β-actin was used as an endogenous control. Data are expressed as the means ± SD. ***P<0.001 compared with the sham-operated (Sham) group; †P<0.05, †††P<0.001 compared with the sepsis group at the same time point. Scale bars, 20 µm.

Sivelestat inhibits renal iNOS expression in septic rats

The polymicrobial infection induced-overproduction of pro-inflammatory mediators can accelerate the release of powerful secondary mediators, such as NO (24). Given the fact that the production of NO is predominantly mediated by iNOS (25), we evaluated renal iNOS protein expression by using immunohistochemical staining and western blot analysis. We found that iNOS was expressed in the cytoplasm of renal tubule epithelial cells (Fig. 4A). As compared with the normal kidney tissues, the more intense expression of iNOS was observed in the septic kidney tissues (Fig. 4A). However, the upregulation of iNOS expression was significantly inhibited by treatment with sivelestat (Fig. 4A). These results were confirmed by western blot analysis (Fig. 4B).

Figure 4 Sivelestat inhibits cecal ligation and puncture (CLP)-induced nitric oxide synthase (iNOS) upregulation in rat kidney tissues. (A) Representative images of immunohistochemical staining fir iNOS in rat kidney tissues at 24 h post-CLP procedure. (B) Renal iNOS protein expression was detected by western blot analysis (n=5). β-actin was used as an endogenous control. Data are expressed as the means ± SD. ***P<0.001 compared with the sham-operated (Sham) group; †P<0.05, †††P<0.001 compared with the sepsis group. Scale bars, 20 µm.

Sivelestat inhibits the activation of the Akt signaling pathway in the kidney tissues of rats with sepsis

The activation of the Akt pathway was assessed by western blot analysis of the Akt phosphorylation product, p-Akt in the rat kidney tissues at 24 h post-surgery. We noted that total Akt protein expression in the kidney tissues remained unaltered in the different experimental groups (Fig. 5). Treatment with sivelestat alone had no significant effect on renal p-Akt expression in the rats subjected to sham operation (Fig. 5). However, a marked increase in the phosphorylation levels of Akt was observed in the septic renal tissues. The high phosphorylation levels of Akt induced by sepsis were suppressed after low-dose sivelestat treatment and the levels almost returned to normal after high-dose sivelestat treatment (Fig. 5). Our data thus suggest that the administration of sivelestat suppresses the CLP-induced activation of Akt in rat kidneys.

Figure 5 Sivelestat inhibits the cecal ligation and puncture (CLP)-induced activation of the phosphatidylinositol 3-kinase (PI3K)/Akt pathway activation in rat kidney tissues. (A) Representative blots for total Akt and phospho-Akt (p-Akt) in rat kidney tissues at 24 h post-CLP procedure (n=5). β-actin was used as an endogenous control. (B) Protein expression levels of total Akt and p-Akt were normalized as ratios to β-actin. Data are expressed as the means ± SD. ***P<0.001 compared with the sham-operated (Sham) group; †P<0.05, †††P<0.001 compared with the sepsis group.

Discussion

Despite improvements in the supportive care of patients with sepsis, current therapeutic approaches are relatively ineffective due to the protean nature of septic AKI (3,26). A variety of animal models have been established to investigate the specific molecular events occurring in sepsis (27). The most frequently used model is the rodent model of CLP, in which sepsis originates from a polymicrobial infection (18,28). While Hirche et al found that the absence of NE increased the mortality of mice to Pseudomonas aeruginosa infection (29), Suda et al found that the inhibition of NE improved the survival rate of rats that uderwent CLP (14). These earlier findings suggest that NE mediates innate host protection against bacterial infection; however, its on-going and excessive activation may have adverse effects. Our present study showed that sivelestat improved the survival of rats with sepsis and preserved their kidney functions, revealing the therapeutic role of sivelestat in sepsis-associated renal injury.

Sivelestat is a specific NE inhibitor first synthesized by Kawabata et al in 1991 (30), and has been reported to attenuate pulmonary inflammation and fibrosis in animal models (12,31). Its effects on lung and cardiovascular diseases have been examined in several clinical trials (32–34). Of note, apart from the therapeutic effects of sivelestat in the lungs, it has also been demonstrated to have potential to reduce inflammation-related lesions in the liver (35) and pancreas (36) in preclinical disease models. Our study demonstrated that treatment with sivelestat alleviated the dysregulation in BUN and NGAL levels in the rats with sepsis. The CLP surgery-induced decrease in GFR and tubular function were partly restored by sivelestat, indicating a protective role of this NE inhibitor in sepsis-related kidney injury.

We then focused on the anti-inflammatory effects of sivelestat in septic AKI. Ischemia/reperfusion injury, bacterial infection or the nephrotoxic agent-induced aberrant infiltration of immune cells, such as neutrophils, macrophages and lymphocytes are considered to contribute to the pathogenesis of AKI (37). Pro-inflammatory mediators, such as TNF-α and IL-1β are released early in response to bacterial infection and can be acutely toxic (38). Therapeutic agents being able to reduce the release of TNF-α and/or IL-1β in murine septic models are suggested to ameliorate sepsis (39–41). The study by Suda et al revealed that sivelestat suppressed the aberrant release of TNF-α (not statistically significant) and IL-1β (statistically significant) in septic lungs (14). In this study, we found that abnormal macrophage infiltration and TNF-α/IL-1β release were reduced by sivelestat. In contrast to other sepsis-associated cytokines, HMGB1 is a late pro-inflammatory cytokine released from monocytes and/or apoptotic cells after the onset of sepsis that further amplifies the inflammatory process (42). The neutralization of HMGB1 can therapeutically reverse lethality in experimental sepsis (38,43). In this study, we demonstrated that the administration of sivelestat markedly reduced the CLP-induced upregulation of renal HMGB1. Such results were supported by an earlier study showing that sivelestat treatment reduced LPS-induced pulmonary HMGB1 upregulation in rats (44). Of note, most clinical trials targeting TNF (45) or IL-1 (46) in sepsis have failed. Therefore, further clinical studies examining the anti-inflammatory effects of sivelestat in sepsis are urgently required.

The polymicrobial infection-induced overproduction of pro-inflammatory mediators can accelerate the release of powerful secondary mediators, such as reactive nitrogen/oxygen species (47). The activation of iNOS during sepsis results in increased NO levels that causes tubular injury through the local generation of reactive nitrogen species, and the selective inhibition of iNOS has been suggested as a potential novel treatment for sepsis-induced AKI (24). In this study, we found that sivelestat was able to reduce CLP-induced renal iNOS overexpression in rats. Although previous studies have indicated an inhibitory effect of sivelestat on iNOS (48,49), as far as we know, our study was the first to show such an effect in septic kidneys.

Previous studies searching for novel anti-inflammatory agents have suggested a critical role of phosphatidylinositol 3-kinase (PI3K)/Akt signaling in sepsis. It is worth noting that the phosphorylation of Akt referring to PI3K/Akt pathway activation is enhanced in the lungs (50) and liver (51), but is weakened in the heart (52) after the CLP procedure or LPS challenge. Consequently, both the blockade and activation of PI3K/Akt signaling transduction have been shown to improve outcome in septic shock. Of note, a previous study by Sadhu et al showed that the inactivation of the PI3K/Akt pathway with a pharmaceutical inhibitor blocked TNF1α-stimulated NE exocytosis (53). Since sivelestat can suppress IL-1β-stimulated Akt phosphorylation in hepatocytes (54), we explored whether sivelestat also has an inhibitory effect on PI3K/Akt signaling transduction in septic kidneys in this study. We found that CLP-enhanced renal Akt phosphorylation was decreased by sivelestat. Moreover, the LPS induction of the phosphorylation of Akt is responsible for nuclear factor-κB (NF-κB) activation in human renal mesangial cells (55), and the inhibitory effects of sivelestat on NF-κB signals have been previously reported (36). It is likely that Akt signals are involved in the regulatory effects of sivelestat on the NF-κB pathway. Further in vitro experiments are thus being carried out by our group to study the underlying mechanisms.

In conclusion, in this study, we demonstrate that the administration of the NE inhibitor, sivelestat, mitigates CLP-induced kidney injury, reduces inflammation, and suppresses the activation of the Akt signaling pathway. Our study suggests that sivelestat has potential to attenuate sepsis-induced kidney injury.

Acknowledgments

This study was supported by grants from the National Natural Science Foundation of China (no. 81471847), the Natural Science Foundation of Liaoning Province (no. 2014021003), and the Science and Technology Project of Shenyang City (no. F14-158-9-40).

References