Introduction
Acute kidney injury (AKI), a common complication observed in critically ill patients admitted to the intensive care unit, is characterized by a sharp and sustained decline in renal function during a short period of time (1,2). The occurrence of AKI was estimated to be 13 million cases worldwide in 2016, and AKI results in ~1.7 million deaths per year (3). Lipopolysaccharide (LPS), an endotoxin from the outer membrane of gram-negative bacteria, has been widely used to induce AKI-associated pathologies, including inflammation and oxidative stress (OS) (4,5). LPS has been reported to mediate both systemic and renal inflammation through signaling by recognition of Toll-like receptor 4, which is present on immune and proximal tubule epithelial cells (2). At present, there are no targeted strategies for the treatment of AKI, and the underlying mechanisms of development are incompletely understood. Therefore, it is necessary to find effective drugs to treat AKI and understand its molecular mechanisms.
Increasing evidence has demonstrated that traditional Chinese medicine may prevent or ameliorate AKI (6-8). Echinacea (Asteraceae) is frequently utilized in North America and Europe to prevent and treat the common cold (9). Root preparations of Echinacea purpurea (E. purpurea) and E. angustifolia have been applied to promote wound healing and treat burns, and are widely used as an ingredient of cosmetic or antimicrobial preservatives, or as a functional food ingredient (10-12). In vitro studies have suggested that Echinacea may act directly on monocytes, natural killer cells, human keratinocytes and macrophages (11,13,14). Additionally, E. purpurea extract has been employed as a prophylactic for treatment of a range of viral infections, particularly for respiratory tract infections in animals and humans (15). Pharmacological studies have emphasized the immunomodulatory activities of cichoric acid, alkamides and polysaccharides from E. purpurea (13,14,16). The immunostimulant effect of E. purpurea appears to be due to polysaccharides surrounding tissue cells that protect against pathogenic invasion (14), suggesting that polysaccharides may serve as the primary active factor associated with the anti-inflammatory effects of E. angustifolia. Aarland et al (17) reported that E. purpurea and E. angustifolia exhibited anti-oxidative, anti-inflammatory and anti-proliferative effects in vitro. Additionally, it was demonstrated that E. purpurea polysaccharide exhibited anti-viral properties in herpes simplex virus type-1 infections (14). Accordingly, the present study hypothesized that E. purpurea polysaccharide (EP) may be used to treat LPS-induced AKI.
Mitogen-activated protein kinases (MAPKs) are a family of serine-threonine protein enzymes that control several physiological processes including cell proliferation, apoptosis, inflammation and OS (18,19). The MAPK signaling pathway primarily encompasses three signaling cascades: Extracellular signal-regulated kinase (ERK), c-Jun-N-terminal kinase (JNK) and p38 (18). A previous study demonstrated that a novel polysaccharide derived from algae extracts inhibited proliferation and induced apoptosis, as well as cell cycle arrest, of breast cancer cells (MCF-7 cells) via the JNK signaling pathway (20). Additionally, Sherif et al (21) revealed that the MAPK signaling pathway was closely associated with the occurrence and development of AKI. For example, the suppression of the MAPK signaling pathway by baicalein (a bioflavonoid) prevented cisplatin-induced AKI (22). Another study demonstrated that polygonatum sibiricum polysaccharides improved gentamicin-mediated AKI in rats via repressing p38 in the MAPK signaling pathway (23). However, whether EP can attenuate LPS-induced AKI via inhibition of the MAPK signaling pathway has not been determined.
The aim of the present study was to investigate the under-lying mechanism by which EP alleviated AKI using in vivo and in vitro models. HBZY-1 cells have been intensively utilized as a cell model in LPS-induced inflammation in accordance with previous studies (24,25). Therefore, HBZY-1 cells were used in the present study to establish an in vitro model to evaluate the role of EP in inflammatory responses mediated by LPS. The current results revealed that LPS-induced AKI was attenuated by EP via inhibition of inflammation, OS and the activation of the MAPK signaling pathway, suggesting that EP may be used as a potential therapeutic for the treatment of AKI.
Materials and methods
Materials
LPS was provided by Shanghai Aladdin Biochemical Technology Co., Ltd. EP was purchased from Nanjing Daosifu Biological Technology Co., Ltd., extracted from Echinacea purpurea Moench with a purity of 90.26%. EP was diluted using DMSO for both the in vivo and in vitro experiments. For the in vivo experiments, C57BL/6 mice were supplied by Liaoning Changsheng Biotechnology Co., Ltd. HBZY-1 cells were obtained from Procell Life Science & Technology Co., Ltd..
Mouse model of LPS-induced AKI
To establish a mouse model of AKI, 8-week-old male C57BL/6 mice (30 mice; weight, 20 g) underwent an acclimatization period for a week (living conditions: 12-h light/dark cycle, 25±1°C, 45-55% humidity and ad libitum access to food and water). Mice were randomly divided into five groups (n=6 per group), including a control group (without treatment), 10 mg/kg EP group, LPS group, LPS+5 mg/kg EP group and LPS+10 mg/kg EP group. Mice were given an intraperitoneal injection of LPS (10 mg/kg) alone or followed by an intravenous injection of EP (5 or 10 mg/kg); the concentrations used were based on previous studies (14,26). After 24 h from injection, mice were anesthetized via intraperitoneal injection of sodium pentobarbital (50 mg/kg). Peripheral blood samples (1-1.5 ml per mouse) were collected from mice with the eyeball removed in the animal experiment room, and mice were euthanized (weight, 22-24 g) using 200 mg/kg sodium pentobarbital. Renal tissues were collected and either fixed in 4% paraformaldehyde at 4°C for 15 min or frozen at −70°C. All animal studies and proto-cols were approved by the Animal Care Committee of Hebei Normal University of Science and Technology (approval no. 201823; 5 September 2018) and performed in accordance with the Committee's guidelines on animal care.
Histopathological evaluation
Fixed renal tissues were embedded in paraffin and cut into 5-µm-thick sections. For hematoxylin and eosin (H&E) staining, the sections were deparaffinized in xylene at room temperature (RT) and stained with hematoxylin (Sangon Biotech Co., Ltd.) for 5 min and eosin (Beijing Solarbio Science & Technology Co., Ltd.) for 3 min, both at RT. For periodic acid-Schiff (PAS) staining, tissues were cut into 5-µm-thick sections. After deparaffinizing the sections as aforementioned, the tissues were stained with periodic acid for 10 min and counterstained with Schiff for 15 min, both at RT, using a PAS staining solution obtained from BaSO Biotech Co., Ltd.. All the sections were observed using a fluorescence microscope (Olympus Corporation; magnification, ×200 for H&E and ×400 for PAS). Inflammation was scored on a scale from 0 to 4: 0, None; 1, rare; 2, common; 3, frequent; and 4, severe (27). PAS-positive cells were quantified using Image Pro-Plus v6.0 (Media Cybernetics, Inc.).
Serum analysis
After 24 h of EP and LPS treatment, blood samples were collected, and the levels of blood urea nitrogen (BUN) and creatinine (Cr) were determined using BUN and Cr detection kits (Nanjing Jiancheng Bioengineering Institute) according to the manufacturer's protocol. BUN levels were measured at a wavelength of 640 nm, while Cr levels at a wavelength of 510 nm using a UV-visible spectrophotometer (Shanghai Yoke Instrument Co., Ltd.).
Immunohistochemistry
Paraffin-embedded 5-µm-thick renal tissue sections were deparaffinized with xylene for 30 min at RT and rehydrated in a descending alcohol series (95, 85 and 75%). After antigen retrieval, sections were incubated with 3% H2O2 at room temperature for 15 min and blocked with goat serum (Beijing Solarbio Science & Technology Co., Ltd.) for 15 min at RT. Sections were incubated with primary antibodies against inducible nitric oxide synthase (iNOS; 1:100; cat. no. 18985-1-AP; ProteinTech Group, Inc.) or cyclo-oxygenase-2 (COX-2; 1:100; cat. no. ab133466; Abcam) overnight at 4°C, and subsequently incubated with a biotin-labeled goat anti-rabbit IgG secondary antibody (1:200; cat. no. A0277; Beyotime Institute of Biotechnology) at 37°C for 30 min. The slides were labeled with horseradish peroxidase enzyme (Beyotime Institute of Biotechnology), stained with DAB (Beijing Solarbio Science & Technology Co., Ltd.) and counterstained with hematoxylin for 3 min at RT. All sections were observed under a fluorescence microscope (Olympus Corporation) at a magnification of ×400 and quantified using Image Pro-Plus v6.0.
LPS-induced HBZY-1 cell model
HBZY-1 cells were cultured in DMEM (Procell Life Science & Technology Co., Ltd.) containing 10% FBS (Biological Industries) at 37°C in a humidified incubator with 5% CO2. Cells (3×103/well) were seeded in a 96-well plate and cultured for 24 h. Cells were pretreated with EP (100 µg/ml), PD98095 (ERK inhibitor; 50 µmol/l; Selleck Chemicals), SP600125 (JNK inhibitor; 10 µmol/l; MedChemExpress) or SB203580 (p38 inhibitor; 10 µmol/l; MedChemExpress) for 1 h and then stimulated with LPS (1 µg/ml) for 24 h, all at 37°C.
Cell viability assay
Cell viability was assessed after treatment with EP and/or LPS using an MTT assay (Sigma-Aldrich; Merck KGaA). MTT (0.5 mg/ml; 100 µl) was added to each well, and cells were cultured at 37°C with 5% CO2 for 4 h. DMSO (150 µl) was added to the cells to solubilize the formazan crystals for 10 min at RT in the dark. The absorbance was measured at 570 nm using a microplate reader (BioTek Instruments, Inc.).
Detection of inflammatory cytokines
The levels of tumor necrosis factor (TNF)-α, interleukin (IL)-1β and IL-6 were evaluated using commercial ELISA kits (Wuhan USCN Business Co., Ltd.), including a TNF-α detection kit (cat. no. SEA133Mu), IL-1β detection kit (cat. no. SEA563Mu) and IL-6 detection kit (cat. no. SEA079Mu). Briefly, renal tissues and cell supernatants by centrifugation (1,000 × g for 20 min at RT) were collected after treatment with EP and/or LPS. The concentrations of the proteins were determined using a bicinchoninic acid (BCA) kit (Beyotime Institute of Biotechnology). Subsequently, samples were analyzed using the corresponding kits according to the manufacturer's protocols, and the absorbance was measured at a wavelength of 450 nm using a microplate reader (BioTek Instruments, Inc.).
Determination of nitric oxide (NO) levels
NO content in renal tissues was detected using a microwell plate method (5) and an NO assay kit (cat. no. A013-2; Nanjing Jiancheng Bioengineering Institute) according to the manufacturer's protocol. The absorbance was measured at a wavelength of 550 nm using a microplate reader (BioTek Instruments, Inc.).
Determination of prostaglandin E2 (PGE2)
The levels of PGE2 in renal tissues were detected using a PGE2 detection kit (cat. no. CEA538Ge; Wuhan USCN Business Co., Ltd.) according to the manufacturer's protocol. The absorbance was measured at a wavelength of 450 nm using a microplate reader (BioTek Instruments, Inc.).
Measurement of reactive oxygen species (ROS) production
The production of ROS was assessed using a ROS detection kit (cat. no. E004; Nanjing Jiancheng Bioengineering Institute). Briefly, kidney tissues or cells after treatment with EP and/or LPS were washed with PBS twice and incubated with dichloro-dihydro-fluorescein diacetate (DCFH-DA; 10 µmol/l) at 37°C for 30 min in the dark. After washing with PBS, ROS generation was observed using a fluorescence microplate reader (Tecan Group, Ltd.).
Biochemical assays
The levels of malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), reduced glutathione (GSH) and oxidized glutathione (GSSG) were measured using specific kits (Nanjing Jiancheng Bioengineering Institute), including MDA detection kit (cat. no. A003-1), SOD detection kit (cat. no. A001-1), CAT detection kit (cat. no. A007-1) and T-GSH/GSSG detection kit (cat. no. A061-1). In addition, the activity of glutathione reductase (GR) was assessed using a GR detection kit (cat. no. BC1160; Beijing Solarbio Science & Technology Co., Ltd.). Briefly, renal tissues and cells after treatment with EP and/or LPS were prepared by centrifugation (tissues at 420 × g for 10 min and cells at 1,500 g for 10 min, both at RT). The concentrations of collected supernatants were determined using a BCA kit. The absorbance of the samples was detected according to the manufacturers' instructions of the aforementioned detection kits using a microplate reader (BioTek Instruments, Inc.).
Western blotting
Kidney tissues and treated cells were lysed using RIPA lysis buffer (Beyotime Institute of Biotechnology). The protein concentrations were quantified using a BCA kit. A total of 20 µg protein/lane was separated via SDS-PAGE (5, 8 or 10% gel) and transferred to a PVDF membrane (Thermo Fisher Scientific, Inc.). After blocking non-specific binding sites with 5% BSA (Biosharp Life Sciences) dissolved in TBS-Tween (0.15% Tween 20) for 1 h at RT, the membranes were incubated with primary antibodies against β-actin (1:2,000 in 5% BSA; cat. no. 60008-1-Ig), iNOS (1:500; cat. no. 18985-1-AP) and COX-2 (1:300; cat. no. 12375-1-AP) from ProteinTech Group, Inc.; phospho-(p-)ERK (Thr202/Tyr204; 1:1,000; cat. no. AF1015) and ERK (1:2,000; cat. no. AF0155) from Affinity Biosciences; and p-JNK (Thr183/Tyr185; 1:1,000; cat. no. 4668), JNK (1:1,000; cat. no. 9252), p-p38 (Thr180/Tyr182; 1:1,000; cat. no. 4511) and p38 (1:1,000; cat. no. 8690) from Cell Signaling Technology, Inc., overnight at 4°C. β-actin was used as the internal reference. Subsequently, membranes were incubated with goat anti-rabbit IgG-HRP (1:5,000; cat. no. SA00001-2; ProteinTech Group, Inc.) or goat anti-mouse IgG-HRP (1:5,000; cat. no. SA00001-1; ProteinTech Group, Inc.), both diluted in 5% BSA, at 37°C for 40 min. The signals were visualized using an enhanced chemiluminescent reagent (cat. no. E002-100; Shanghai Qihai Futai Biological Technology Co., Ltd.) and quantified using Gel-Pro Analyzer v4.0 (Media Cybernetics, Inc.).
Immunofluorescence analysis of HBZY-1 cells
Cells were grown on slides and treated with EP and/or LPS. Subsequently, cells were fixed using 4% paraformaldehyde for 15 min at 4°C, washed three times with PBS (5 min per wash) and incubated with 0.1% Triton X-100 (Beyotime Institute of Biotechnology) for 30 min at RT. After washing three times with PBS, the slides were blocked using goat serum (cat. no. SL038; Beijing Solarbio Science & Technology Co., Ltd.) for 15 min at RT and incubated with primary antibodies against p-ERK (1:200; cat. no. AF1015; Affinity Biosciences), p-JNK (1:200; cat. no. bs-1640R; BIOSS) and p-p38 (1:200; cat. no. bs-0636R; BIOSS) overnight at 4°C. Cells were incubated with a Cy3-labeled goat anti-rabbit IgG secondary antibody (1:200; cat. no. A0516; Beyotime Institute of Biotechnology) for 1 h at RT and counterstained with DAPI (Beyotime Institute of Biotechnology) for 3 min at RT. Cells were visualized using a fluorescence microscope (magnification, ×400).
Statistical analysis
The data are expressed as the mean ± standard deviation. All data analyses were performed using GraphPad Prism version 8.0 (GraphPad Software, Inc.). Comparisons between ≥3 groups were performed using a one-way ANOVA followed by Tukey's post hoc test. P<0.05 was considered to indicate a statistically significant difference.
Results
EP attenuates LPS-induced AKI in mice
The effects of EP on LPS-induced histological changes in the kidney tissues were assessed using H&E and PAS staining. Fig. 1A shows that inflammation was successfully induced by LPS and that the co-administration of EP significantly attenuated this process. As shown in Fig. 1B, the glomerular structure was intact, and no obvious pathological changes were observed in the control and 10 mg/kg EP-treated mice. By contrast, proliferation of mesangial cells, swelling of glomerular epithelial cells, interstitial edema and glycogen deposition were observed in the LPS-treated renal tissues. Pretreatment with EP markedly alleviated LPS-induced glomerular and tubular damage, and significantly decreased the number of PAS-positive cells. Additionally, the levels of BUN in the blood were elevated following LPS treatment for 24 h (Fig. 1C) compared with the control group. Similarly, Cr levels were also increased in LPS-treated mice (Fig. 1D). EP co-administration markedly decreased BUN and Cr levels.
EP represses inflammation in LPS-treated mice
The levels of indices of inflammation were measured to evaluate the effect of EP on the inflammatory response. As shown in Fig. 2A-E, TNF-α, IL-1β, IL-6, NO and PGE2 levels were significantly increased in the LPS-treated kidney tissues compared with in the control mice and were significantly decreased following EP treatment compared with the LPS group. Compared with the control group, the protein expression levels of iNOS and COX-2 were significantly upregulated by LPS treatment; however, pretreatment with EP decreased this upregulation (Fig. 2F). In addition, as shown in Fig. 2G and H, immunohistochemistry results for iNOS and COX-2 revealed that administration of EP decreased LPS-induced upregulation of iNOS and COX-2 in kidney tissues. Additionally, there were few or no iNOS and COX-2-positive cells in the control and EP-treated control mice.
EP decreases OS induced by LPS in mice
To investigate the role of EP in OS, the levels of ROS and MDA, as well as SOD activity, were detected in kidney tissues. DCFH-DA is a fluorescent probe of ROS. As illustrated in Fig. 3A, the fluorescence intensity of the LPS group was significantly higher than that of the control group, indicating that the production of ROS in LPS-treated mice was increased. EP administration significantly decreased ROS generation compared with the LPS group. Furthermore, the LPS-treated group exhibited a significant increase in MDA and GSSG levels, and a significant decrease in SOD, CAT and GR levels, as well as GSH activity, compared with the control mice (Fig. 3B-F). Additionally, compared with in the control group, the ratio of GSH/GSSG was significantly decreased in the LPS-treated group. Administration of EP markedly attenuated these changes.
EP inhibits the activation of the MAPK signaling pathway in LPS-treated kidney tissues
To determine the effects of EP on the MAPK signaling pathway in renal tissues following LPS treatment, the expression levels of p-ERK, ERK, p-JNK, JNK, p-p38 and p38 were measured via western blotting. As shown in Fig. 4, the levels of p-ERK, p-JNK and p-p38 were significantly increased in LPS-treated kidneys compared with in the control group. However, LPS-induced upregulation of p-ERK, p-JNK and p-p38 levels was attenuated by administration of EP (5 or 10 mg/kg). Furthermore, there was no difference in ERK, JNK and p38 levels in the kidney irrespective of treatment.
EP mitigates LPS-mediated HBZY-1 cell damage
To further explore the role of EP in OS and inflammation in vitro, an LPS-treated HBZY-1 cell model was established. As shown in Fig. 5A, compared with the control cells, LPS significantly decreased HBZY-1 cell viability, whereas pretreatment with EP restored the viability of LPS-treated cells. Fig. 5B-G shows that EP decreased OS in LPS-treated cells as demonstrated by the lowered ROS, MDA and GSSG levels, and the elevated SOD, CAT and GR levels, as well as GSH contents, compared with the LPS group. Additionally, LPS treatment resulted in a significant increase in TNF-α, IL-1β, IL-6, NO and PGE2 contents compared with the control cells, while these levels were significantly decreased by co-administration of EP compared with the LPS-treated cells (Fig. 5H).
EP suppresses the MAPK signaling pathway in LPS-treated HBZY-1 cells
The effects of EP on proteins involved in the MAPK signaling pathway in HBZY-1 cells were investigated using western blotting. The expression levels of p-ERK, p-JNK and p-p38 were significantly higher in LPS-treated cells compared with in the control group, and these alterations were significantly attenuated by pretreatment with EP (Fig. 6A). Notably, immunofluorescence analysis revealed that EP markedly blocked nuclear translocation of p-ERK, p-JNK and p-p38 in LPS-treated cells (Fig. 6B). Additionally, cells were treated with EP, PD98095, SP600125 or SB203580 for 1 h and then treated with LPS for 24 h. Cell viability and the indicators associated with OS and inflammation were evaluated. Cell viability was significantly decreased in the LPS group compared with in control cells and was significantly reversed with the administration of EP, PD98095, SP600125 or SB203580 (Fig. 6C). The results presented in Fig. 6D-I confirmed that the treatment with EP, PD98095, SP600125 or SB203580 attenuated OS through the significantly decreased levels of ROS and MDA, and the significantly increased SOD activity, as well as decreasing the inflammatory response as demonstrated by the significantly lower TNF-α, IL-1β and IL-6 levels compared with those in LPS-treated cells. Therefore, EP may exhibit its therapeutic effect in AKI via regulating the MAPK signaling pathway. However, the detailed mechanism requires further study.
Discussion
LPS treatment resulted in renal impairment in the present mouse model of AKI, and EP effectively mitigated the LPS-mediated AKI. BUN and Cr are established biomarkers used for the diagnosis of AKI (28,29). In the present study, there was a prominent decrease in the levels of BUN and Cr following EP administration in LPS-treated kidney tissues, in agreement with a previous study, which demonstrated that AKI was attenuated by podocyte-specific soluble epoxide hydrolase deficiency in mice and that BUN and Cr levels were decreased (30). Furthermore, the current histological analysis revealed that EP decreased LPS-induced AKI.
A previous study highlighted the importance of inflammation in burn-associated AKI (31). The inflammatory response is a complex biological process, which includes the synthesis and release of pro-inflammatory cytokines, such as TNF-α, IL-1β and IL-6 (32). Additionally, LPS induces the release of TNF-α and IL-1β via a Toll-like receptor 4 pathway, resulting in increased OS (33). TNF-α serves an essential role in the development of AKI by activating kidney endothelial TNF receptor 1 (34). A recent study has indicated that IL-1β and IL-6 are important pro-inflammatory indicators in renal diseases (35), which accelerate NO release. Additionally, overproduction of NO generates peroxynitrite ions, directly or indirectly resulting in the damage of target cells and tissues (36). It has been demonstrated that enhanced renal NO levels significantly increase the expression levels of iNOS in glycerol-mediated AKI (37). Yu et al (36) reported that honokiol significantly decreased the expression levels of iNOS in a rat model of renal ischemia/reperfusion injury. COX-2, one of the downstream molecules of NO, was upregulated in mononuclear cells, endothelial cells and macrophages following elevated NO (38). Additionally, PGE2, the product of COX-2, is an essential inflammatory mediator (38). As described by Hwang et al (39), COX-2 and PGE2 serve critical roles in the pathogenesis of kidney inflammation. A previous study indicated that Aloe vera polysaccharides suppressed TNF-α-induced secretion of inflammatory cytokines in HaCaT cells (40). Another study confirmed that EP exhibited anti-inflammatory properties in a rat model of colitis induced by acetic acid (41). Consistent with previous studies (3,42), the anti-inflammatory effect of EP on LPS-induced AKI in the present study was achieved via decreasing the levels of inflammatory indicators in vivo and in vitro. Cellular injury and its associated molecular products serve as vital triggers in inflammation following acute tissue damage (6). Additionally, EP pretreatment in the present study increased cell viability in LPS-mediated HBZY-1 cells, which was similar to a previous study demonstrating that Maerkang Lactarius Deliciosus Gray polysaccharides promoted the proliferation of RAW264.7 cells (43).
OS serves an important role in the occurrence and development of AKI (44). It has been demonstrated that OS is enhanced in LPS-induced models of AKI (45) and that the MAPK signaling pathway is an essential modulator of altered gene transcription in response to increased OS (46). OS can be caused by an imbalance between ROS generation and anti-oxidant defense (47). Excessive ROS production is detrimental to cellular functions; it has been reported that ROS may damage biomolecules such as DNA, RNA, proteins and lipids (3), and may induce the release of inflammatory cytokines through activation of the NF-κB signaling pathway (48). The production of endogenous ROS activates ERK, while exogenous ROS generation results in p38 activation (46). Furthermore, MDA, the end product of unsaturated lipid peroxidation, has been widely utilized as a marker of oxidative damage (48). SOD, CAT, GR and GSH are vital antioxidant indicators modulating oxidative injury (36,49). The anti-oxidative status is closely associated with the ratio of GSH/GSSG (35). In the present study, ROS, MDA and GSSG levels were elevated, while SOD, CAT, GR and GSH activities were lowered in LPS-treated mice and cells. EP administration reversed these levels, similarly to previous studies (4,50).
JNK may be activated by OS, and is considered vital for the regulation of oxidative damage (47). Additionally, p38 is able to participate in the progression and development of inflammation when tissues or cells are impaired (51). Following injury, the majority of inflammatory mediators, including TNF-α, IL-1β and IL-6, are released (52). These molecules can act on JNK and p38, phosphorylating and activating them; subsequently, p-JNK and p-p38 are translocated to the nucleus resulting in a series of responses, such as oxidative injury, apoptosis and inflammatory responses (53-55). Additionally, the ERK signaling pathway is an important signaling pathway, of which the abnormal or dysregulated activation may lead to renal tissue impairment (56). The MAPK signaling pathway has been demonstrated to modulate pro-inflammatory cytokines, such as IL-1β, in AKI (57). A previous study revealed that JNK, ERK and p38 where inactivated by hesperetin, suggesting that hesperetin may be used to inhibit inflammation in cisplatin-induced AKI (58). In the present study, ERK, JNK and p38 were notably activated by LPS in renal tissues and HBZY-1 cells. Notably, EP treatment decreased the expression levels of p-ERK, p-JNK and p-p38. The current findings suggest that EP may attenuate LPS-induced AKI in vivo and in vitro, potentially via inhibiting the activation of the MAPK signaling pathway, similarly to a previous study (5). However, another previous study demonstrated that a novel polysaccharide derived from algae extracts inhibited breast cancer progression via activation of the JNK signaling pathway (20), which is inconsistent with the results of the present study. This may be due to the different sources of polysaccharides, cell types and models. Additionally, the protein kinase B (Akt) signaling pathway serves a critical role in inflammatory and autoimmune diseases (59). A previous study revealed that Terminalia bellirica (Gaertn.) Roxb. extract decreased the inflammatory response and OS via activation of the Akt signaling pathway in an LPS-shock mouse model (60). Zhao et al (61) reported that dexmedetomidine protected against LPS-mediated AKI in rats via inhibiting the activation of the Akt signaling pathway. Additionally, another study demonstrated that water extracts from the roots of E. purpurea containing a polysaccharide with anti-inflamma-tory properties activated the Akt signaling pathway in human acute monocytic leukemia (THP-1) cells (62). Therefore, future studies should further investigate the effects of EP on the Akt signaling pathway in LPS-induced AKI.
A previous study indicated that the absorption of natural bioactive polysaccharides in the body was likely directly via the gut, gut microbiota or Peyer's patches (63). As suggested by Yu et al (64), pumpkin polysaccharides may be metabolized by various enzymes in the liver. Dendrobium aphyllum polysaccharides consist of mannose and glucose (65), and glucose metabolism is strongly involved in regulation of diabetes and immune responses. Possible metabolic pathways involved with polysaccharides include glucose dehydrogenase, glucose-6-phosphatase and glucose transporters (GLUT1 and GLUT2). Notably, the aforementioned studies provide some references for studying the in vivo metabolism of EP; however, the full mechanism of how EP is metabolized in vivo remains unknown. Therefore, the in vivo metabolism of EP, the effect of EP on other possible signaling pathways and the underlying mechanisms in LPS-induced AKI should be further investigated in future studies. The present study illustrated the inhibitory effect of EP on the MAPK signaling pathway, but how EP exerts its function in AKI via this signaling pathway and detailed mechanisms require further research.
In conclusion, the results of the present study clearly indicated that EP attenuated AKI by decreasing inflammation and OS. In addition, EP likely suppressed the activation of the MAPK signaling pathway via decreasing the protein expression levels of p-ERK, p-JNK and p-p38. Therefore, EP may be a potential therapeutic agent for the treatment of AKI, given its anti-inflammatory and anti-oxidative effects.