Oral supplementation with ursolic acid ameliorates sepsis-induced acute kidney injury in a mouse model by inhibiting oxidative stress and inflammatory responses
- Authors:
- Published online on: March 16, 2018 https://doi.org/10.3892/mmr.2018.8767
- Pages: 7142-7148
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Copyright: © Zhang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Acute kidney injury (AKI) is a common problem in critically ill patients, particularly in the intensive care unit (ICU) (1). Sepsis and septic shock are factors that contribute to the development of AKI, and ≥50% mortality of sepsis patients in the ICU is associated with AKI (2). Evidence suggests that patients with non-severe pneumonia with sepsis have a significantly higher incidence of AKI and increased inflammatory responses (3,4). However, the underlying mechanisms are not completely understood. A growing body of evidence has suggested that sepsis-induced oxidative stress and inflammatory responses contributed to sepsis-associated organ dysfunction, including AKI (5–7).
Ursolic acid (UA) as a pentacyclic triterpenoid compound is isolated from many plants, including Ligustrum lucidum, Arctostaphylos uva-ursi and Eriobotrya japonica, which are widely used as Chinese herbal medicines (8). UA is readily absorbed from daily foods, such as Fructus Crataegi (9), Fructus Chaenomelis Lagenariae (10) and Fructus Mume (11). It is generally known that UA exhibits multiple biological activities, such as anti-inflammatory (12), anti-oxidant (13) and anti-tumor properties (14). Emerging evidence has demonstrated that UA has a beneficial effect on hyperglycemia-induced renal injury (15). In addition, UA ameliorates carbon tetrachloride-induced oxidative DNA damage and inflammation in kidneys of rats (16). Previous research has shown that UA exerts protective effects on sepsis-induced organ damage (17,18). However, the beneficial effect and underlying molecular mechanisms of UA in sepsis-induced AKI are not clearly delineated. As sepsis is an acute inflammatory and oxidative stress disorder involved in AKI, inhibiting excessive inflammatory responses and oxidative stress may be an effective therapeutic target.
In the present study, it was hypothesized that UA may ameliorate sepsis-induced AKI via the inhibition of oxidative stress and inflammatory responses. This study may further increase understanding of organ failure prevention and the underlying mechanisms of UA, which may be useful in managing sepsis-induced AKI.
Materials and methods
Experimental animals
Ten-week-old male imprinting control region mice (n=64) were purchased from Charles River Laboratories, Inc., (Wilmington, MA, USA) and were allowed to acclimate to the environment for 1 week. The mice were fed under controlled conditions: Temperature (25±2°C), humidity (55±5%) and 12-h light/dark cycle, and the mice were given free access to food and tap water.
Sepsis was induced in mice undergoing cecal ligation and puncture (CLP) surgery (CLP Group, n=8). Mice were anesthetized with 2% pentobarbital, and a 1- to 2-cm midline incision was made along the linea-alba of the abdominal muscle to isolate and exteriorize the cecum. A total of 75% of the cecum was ligated with a 4-0 silk suture, and the cecum was punctured twice with a 21-gauge needle. A small amount (1 droplet) of feces was gently extruded from the holes to ensure patency. The cecum was then returned to the peritoneal cavity and the abdominal incision was closed with 4-0 silk sutures. After the operation, 1 ml pre-warmed normal saline was administered into the peritoneal cavity. The survival rate was examined over the whole experiment (up to 4 days). For the UA (Aldrich Chemical Co., Milwaukee, WI, USA; high performance liquid chromatography, 98%) treatment groups (2 mg/kg, low-concentration, n=8 or 20 mg/kg, high-concentration, n=8), mice received intraperitoneal administration of UA 2 weeks before CLP surgery. In the sham-operated group (control group, n=8), mice underwent the same procedure but were neither ligated nor punctured, and the mice were intraperitoneally injected with 2 ml PBS. In another experiment, the 96 h survival of CLP mice with or without UA treatment was observed (n=8 in each group).
The animal study was approved by the Animal Care and Use Committee at the Beijing Tsinghua Changgung Hospital (Beijing, China; permit number: TCH-2015-0019).
Serum inflammatory cytokine measurement
The effects of UA on serum cytokine levels were analyzed by ELISA at 24 h after CLP, which was determined to be the optimum measuring time in previous studies (17,19). Serum levels of tumor necrosis factor-α (TNF-α; cat. no. E-EL-M0049), interleukin (IL)-1β (cat. no. E-EL-M0037) and IL-6 (cat. no. E-EL-M0044) were detected using a mouse bioactive ELISA assay, according to the manufacturer's protocol (Elabscience Biotechnology Co., Ltd., Wuhan, China), there were three replicates for each sample tested, n=8 in the control group; n=6 in CLP group (2 mice succumbed within 24 h); n=7 in UA(L)+CLP group (1 mouse succumbed within 24 h); n=8 in UA(H)+CLP group.
Measurement of serum creatinine (Scr) and blood urea nitrogen (BUN)
Blood samples were collected at 24 h after CLP surgery in each group and renal function was monitored by measuring the concentration of BUN (cat. no. C013-2) and Scr (cat. no. C011-1) in serum using an enzymatic kinetic methods and picric acid methods detection kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China), according to the manufacturer's protocol. For BUN and Scr, n=8 in the control group; n=6 in CLP group (2 mice succumbed within 24 h); n=7 in UA(L)+CLP group (1 mouse succumbed within 24 h); n=8 in UA(H)+CLP group.
Measurement of reactive oxygen species (ROS)
The renal tissues were harvested and homogenized in phosphate buffer at 24 h after CLP surgery in each group. ROS (ID: GMS10016.3; Genmed Scientifics, Inc., Shanghai, China) levels were measured using a dichloro-dihydro-fluorescein diacetate (DCFH-DA) assay, according to the manufacturer's protocol. In brief, kidney tissue whole homogenate (100 µl) was added to 1.4 ml 50 mM phosphate buffer in dark-adapted counting vials. After dark adaptation for 1 h at room temperature, the homogenate was incubated with 10 µM DCFH-DA for 20 min at 37°C in the dark for the detection of ROS. The samples were counted every 20 sec for 3 min using a luminometer (Autolumat Plus LB953; Berthold Technologies GmbH, Bad Wildbad, Germany).
Measurement of 8-hydroxy-2′-deoxyguanosine (8-OHdG)
Plasma levels of an oxidative stress marker, 8-OHdG, was measured using a DNA damage ELISA kit (cat. no. ADI-EKS-350; Enzo Life Sciences, Inc., Farmingdale, NY, USA), according to the manufacturer's protocol.
Hematoxylin and eosin staining
Formalin-fixed (4% formalin at room temperature for 24 h) and paraffin-embedded kidney tissues were cut into ~5 µm-thick sections, which were stained with hematoxylin and eosin (cat. no. C0105; Beyotime Institute of Biotechnology, Haimen, China) at room temperature for 1–2 min, and visualized under a light microscope (model DM 2500; Leica Microsystems, Inc., Buffalo Grove, IL, USA).
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
Total RNA was extracted from mouse kidney [n=8 in the control group; n=6 in CLP group (2 mice succumbed within 24 h); n=7 in UA(L)+CLP group (1 mouse succumbed within 24 h); n=8 in UA (H) +CLP group] using TRIzol (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA) and reverse transcribed into cDNA using a SuperScriptIII reverse transcriptase kit (Invitrogen; Thermo Fisher Scientific, Inc.), following the manufacturer's protocol. RT-qPCR was used to determine mRNA expression levels using SYBR-Green Master mix (Invitrogen; Thermo Fisher Scientific, Inc.) on a Stratagene MX3005P system (Agilent Technologies, Inc., Santa Clara, CA, USA). The thermocycling conditions were as follows: 95°C for 10 min followed by 40 cycles of 95°C for 15 sec, 60°C for 30 sec and 72°C for 30 sec. GAPDH served as an internal standard. Relative gene expression was calculated using the 2−ΔΔCq method (20). The following primers were used: Forward, 5′-CACCACCATCAAGGACTCAA-3′ and reverse, 5′-GAGACAGAGGCAACCTGACC-3′ for TNF-α; forward, 5′-TCGCCAGTGAAATGATGGCTTA-3′ and reverse, 5′-GTCCATGGCCACAACAACTGA-3′ for IL-1β; forward, 5′-CGGAGAGGAGACTTCACAGAG-3′ and reverse, 5′-CATTTCCACGATTTCCCAGA-3′ for IL-6; forward, 5′-GGGTGAGAACGGGCCTGGAGGA-3′ and reverse, 5′-GTAGAAGCCCGGTGTGCCGTGA-3′ for superoxide dismutase (SOD)1; forward, 5′-TCGGTAACGTGAGTGTGGCAAT-3′ and reverse, 5′-CGTGTTGGACCGGTGTGCACCGT-3′ for SOD2; forward, 5′-ACAGGGGAGGTGATAGCATT-3′ and reverse, 5′-GACCAAAAGCCTTCATACATCTC-3′ for GAPDH. For PCR, n=8 in the control group; n=6 in CLP group (2 mice death within 24 h); n=7 in UA(L)+CLP group (1 mouse death within 24 h); n=8 in UA(H)+CLP group. The experiment was repeated twice. Three replicates were performed for each sample.
Western blotting
Kidneys were homogenized and lysed in NP-40 buffer (Beyotime Institute of Biotechnology, Haimen, China). Following 5–10 min boiling, homogenates were centrifuged at 10,000 × g at 4°C for 10 min to obtain the supernatant. Protein samples (50 µg) were separated by 10% SDS-PAGE and transferred to polyvinylidene difluoride membranes (EMD Millipore, Billerica, MA, USA). Membranes were blocked with 5% (w/v) non-fat milk powder in Tris-buffered saline containing 0.1% (w/v) Tween 20 for 2 h at room temperature, and subsequently incubated with the following primary antibodies: TNF-α (cat. no. sc-52746), IL-1β (cat. no. sc-515598), IL-6 (cat. no. sc-32296), NF-κB (cat. no. sc-114) and β-actin (cat. no. sc-517582; all from Santa Cruz Biotechnology, Inc., Dallas, TX, USA; all 1: 1,000), at 4°C overnight. After being washed, the membranes were incubated with horseradish peroxidase-conjugated anti IgG (cat. no. sc-516102; 1:10,000; Santa Cruz Biotechnology, Inc.) at room temperature for 2 h. Signal detection was carried out with an enhanced chemiluminescence system (GE Healthcare, Chicago, IL, USA), and protein bands were analyzed with Quantity One® software version 4.5 (Bio-Rad Laboratories, Inc., Hercules, CA, USA). For western blotting, n=8 in the control group; n=6 in CLP group (2 mice succumbed within 24 h); n=7 in UA(L)+CLP group (1 mouse succumbed within 24 h); n=8 in UA(H)+CLP group.
Statistical analysis
Data are presented as the mean ± standard deviation for each group. Statistical analyses were performed by using GraphPad Prism version 6.0 software (GraphPad Software, Inc., La Jolla, CA, USA). Inter-group differences were analyzed by one-way analysis of variance followed by Tukey's multiple comparison post-hoc test. P<0.05 was used to indicate a statistically significant difference.
Results
UA administration improves survival in septic mice
A previous study demonstrated that UA administration improves survival in CLP-induced lung injury septic mice (17). In line with these findings, the present study revealed that UA pretreatment before the induction of sepsis by CLP significantly improved the survival of mice undergoing CLP compared with mice treated with CLP alone. Approximately 90% of mice in the CLP group died at 72 h after undergoing CLP surgery. Administration of UA (20 mg/kg) had a protective effect against lethality induced by CLP (P<0.05), and increased the animal survival rate from 12.5 to 50%. However, a low concentration of UA (2 mg/kg) did not significantly improve the survival of CLP-induced septic mice (Fig. 1).
UA improves sepsis-induced AKI in mice
Previous studies have suggested that UA alleviates sepsis-induced acute lung injury in rodent models (17,18). However, there appears to be no associated reports on sepsis-induced AKI. To determine the role of UA in sepsis-induced AKI in mice, renal histological examination by hematoxylin and eosin staining was implemented. In control mice, relatively intact structures of the kidney tissues were observed. By contrast, glomerular damage and vacuolization were observed in the proximal tubules in the CLP group. Low concentrations of UA (2 mg/kg) had no dramatic improvement in renal tissue damage in septic mice. However, high concentrations of UA (20 mg/kg) ameliorated the renal tissue damage in septic mice (Fig. 2A). It is well known that AKI is a serious complication in septic rats, and BUN and Scr are frequently used as biomarkers in the early stages of the development of AKI (21). In the present study, BUN and Scr levels were measured at 24 h after CLP surgery to evaluate renal function in septic mice. As shown in Fig. 2B and C, BUN and Scr were significantly increased in mice undergoing CLP surgery compared with the control group. Administration of high concentrations of UA significantly reversed the CLP-induced upregulation of BUN and Scr in septic mice (P<0.05). Low concentrations of UA did not significantly reduce the levels of BUN and Scr.
UA restrains CLP-induced oxidative stress damage in septic mice
The effect of UA on CLP-induced ROS in the kidney of septic mice was measured. Treatment with CLP surgery resulted in a significant increase in ROS production compared with the control group (P<0.001), whereas pretreatment with high concentrations of UA significantly inhibited CLP-induced ROS production (P<0.05; Fig. 3A). In addition, plasma 8-OHdG levels, a measure of DNA oxidative damage, were significantly higher in the CLP group compared with the control group (P<0.001), whereas pretreatment with high concentrations of UA significantly reversed CLP-induced 8-OhdG (P<0.05; Fig. 3B). Furthermore, SOD1 and SOD2, as antioxidant enzymes, serve crucial roles in the defense against oxygen-free radicals (22). In the present study, the mRNA expression levels of SOD1 and SOD2 were measured by RT-qPCR in mouse kidney tissue, and the results demonstrated that SOD1 and SOD2 were significantly decreased in the kidney from CLP septic mice compared with that from control animals (P<0.01). High concentrations of UA significantly reversed the CLP-induced downregulation of SOD1 and SOD2 in CLP septic mice (P<0.05; Fig. 3C and D).
UA suppresses inflammatory responses in septic mice
Previous studies have suggested that oxidative stress directly or indirectly elevates inflammatory responses (21,23,24). Therefore, serum TNF-α, IL-1β and IL-6 levels were measured at 24 h after CLP surgery. Serum TNF-α (Fig. 4A), IL-1β (Fig. 4B) and IL-6 (Fig. 4C) levels were significantly increased in the CLP group compared with the control group. However, treatment with high concentrations of UA significantly decreased the levels of these inflammatory cytokines in septic mice (P<0.05). In addition, the mRNA expression levels of TNF-α (Fig. 4D), IL-1β (Fig. 4E) and IL-6 (Fig. 4F) were measured using RT-qPCR in kidney tissues, and the results demonstrated that treatment with high concentrations of UA attenuated the CLP-activated increase in TNF-α, IL-1β and IL-6 expression (P<0.05). As shown in Fig. 5A, B and C, it was found that pretreatment with high concentrations of UA significantly suppressed the CLP-induced increase in TNF-α, IL-1β and IL-6 protein expression in kidney tissues from septic mice (P<0.01). Consequently, we examined whether the upstream NF-κB signal transduction pathway was also involved in CLP-induced AKI. The transcription factor NF-κB is considered to be the primary mediator of the inflammatory response (25), and the inhibition of NF-κB has been shown to alleviate sepsis-associated AKI in rats (5,26). Therefore, the present study evaluated the effect of UA on the nuclear translocation of NF-κB. The results demonstrated that the expression of NF-κB was significantly increased in the CLP group compared with control group (P<0.001). Conversely, the administration of high concentrations of UA significantly reversed the increase in NF-κB expression in the kidney from septic mice (P<0.001; Fig. 5D).
Discussion
The present study used the experimental model of CLP-induced AKI to examine the effects of UA on sepsis-associated kidney injury in mice. First, results demonstrated that UA administration improved survival in septic mice induced by CLP surgery. The treatment of UA revealed protection against AKI induced by CLP surgery, including alleviation of glomerular damage and vacuolization in the proximal tubules. Furthermore, the effects of UA on oxidative stress and inflammation in septic mice were determined. The findings suggested that the high concentrations of UA (20 mg/kg) significantly protected against sepsis-induced AKI by inhibiting oxidative stress and inflammatory cytokines in the kidney from septic mice. It is well known that the concentration of UA is flexible in different experimental research. Consistent with previous reports, the dose of UA in rodent animal model is used at the same magnitude (16).
Mounting evidence has demonstrated that high free-radical concentrations are generated in patients with sepsis syndrome, and the balance between oxidation and anti-oxidation is markedly disturbed (5,27). Increased production of ROS is one of the key features of sepsis, which may cause enhanced AKI (5,21,28). In the present study, the findings revealed that ROS production was significantly increased by CLP surgery, whereas pretreatment with high concentrations of UA significantly inhibited CLP-induced ROS production in the kidney of septic mice, which suggested that UA protects against sepsis-induced AKI by inhibiting oxidative stress damage. A previous study indicated that SOD activity is significantly downregulated in septic patients, which is negatively associated with the severity of sepsis (29). In addition, the levels of the antioxidant SOD notably decreased in septic rats in every region of the brain (30). In the present study, it was found that the mRNA expression levels of SOD1 and SOD2 were significantly decreased in the kidney from septic mice, and high concentrations of UA treatment significantly reversed CLP-induced downregulation of SOD1 and SOD2. These results concur with previous observations that an imbalance exists between oxidants and antioxidants during sepsis (31). The findings of the present study demonstrated an anti-oxidant role for UA in septic mice.
TNF-α, IL-1β and IL-6 may be readily activated by pathological conditions, and are biomarkers of early inflammatory responses, as confirmed in previous studies (32–34). Under septic conditions, the expression of inflammatory cytokines, such as IL-1β, IL-6 and TNF-α, are significantly upregulated in pathological tissues, including lung (17), cerebrum (18,30) and kidney (3,5). Clinical studies have found that the levels of TNF-α and IL-1β are increased in the serum of septic patients (35). Inhibition of TNF-α and IL-1β alleviates the progression of sepsis in animal models (18,28). In the present study, it was demonstrated that serum levels of TNF-α, IL-1β and IL-6 and mRNA and protein expression levels of TNF-α, IL-1β and IL-6 in kidney were significantly increased in septic mice; however, pretreatment with UA attenuated the inflammatory response in septic mice, resulting in the downregulation of TNF-α, IL-6 and IL-1β levels in serum and kidney tissues. Inflammatory signals are known to merge in the activation of the NF-κB signaling pathway, and NF-κB has been shown to serve a critical role in modulating mortality in experimental sepsis (36,37). The results of the present study demonstrated that NF-κB was significantly increased in septic mice. Consistent with several original studies (16,17), the findings of the present study also revealed that UA has anti-inflammatory properties by inhibiting NF-κB expression. Previous studies indicated that targeted knockout of IL-17A protects against sepsis-associated AKI and host defense (38,39). The precise underlying pathogenic mechanism of TNF-α, IL-1β or IL-6 knockout in sepsis-induced AKI will be discussed in future studies. In addition, a more in-depth kinetic analysis of the inflammatory markers in septic mice is to be explored.
To the best of our knowledge, the present study provides evidence for the first time that UA is a novel therapeutic drug that protects against sepsis-induced AKI, and the underlying mechanism was mediated, at least partially, by inhibiting oxidative stress and inflammatory responses. The present study also provides a possible method for therapy sepsis-induced AKI in clinical practice. However, cross-sectional and longitudinal studies are required to determine the proper concentration of UA, which will be performed in future studies.
Acknowledgements
Not applicable.
Funding
No funding was received.
Availability of data and materials
The analyzed data sets generated during the study are available from the corresponding author on reasonable request.
Authors' contributions
Study design: ZW and ZZ; literature research, data acquisition and data analysis: ZZ, RC, ZW and HZ; manuscript preparation and manuscript editing: ZZ and RC; manuscript review: ZW, ZZ, HZ and RC; final approval of the version of the manuscript to be published: ZZ, HZ, RC and ZW; histological examination: RC; establishment of animal model: HZ.
Ethics approval and consent to participate
The animal study was approved by the Animal Care and Use Committee at the Beijing Tsinghua Changgung Hospital (Beijing, China; permit number: TCH-2015-0019).
Consent for publication
Not applicable.
Competing interests
The authors declare they have no competing interests.
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