Introduction
Diabetic nephropathy (DN) is a primary complication of diabetes mellitus. Oxidative stress has been suggested to have an important role in DN (1). The loss of resident renal tubular epithelial cells via apoptosis has been demonstrated in experimental DN, and renal tubular epithelial cell apoptosis has been demonstrated to be associated with the progression of albuminuria (2). Normal cellular metabolism may produce reactive oxygen species (ROS), and it has previously been revealed that a number of environmental factors, including exposure to chemical agents, may induce oxidative stress (3). The physiological levels of ROS have important roles in intracellular signal transduction, follicle development, ovulation and gene expression (4,5). Furthermore, excessive ROS production may result in oxidative stress. According to previous studies, it has been suggested that the suppression of high glucose (HG)-induced apoptosis in tubular cells is a predominant cause of renal injury in patients with diabetes (6,7). The hyperglycemia-induced production of ROS has an important role in the progression of DN (8). It has been revealed that HG-induced renal tubular epithelial cellular apoptosis is significantly decreased following the administration of N-acetylcysteine and ascorbic acid antioxidants (9,10). Numerous studies have demonstrated that HG induces the apoptosis of renal tubular epithelial cells via an oxidant-dependent mechanism. Therefore, the inhibition of oxidative stress may serve as a potential therapeutic target for the treatment of DN.
A previous study demonstrated that the intake of naturally grown fresh vegetables and fruits attenuates the progression of diabetes and associated complications (11). For example, anthocyanins, the largest group of water-soluble pigments, belong to a family of phenolic flavonoid compounds that affect the pigment of numerous plants. Anthocyanins have been demonstrated to exhibit marked antioxidative properties in animal models of diabetes mellitus and to exhibit protective effects against hyperglycemia-induced kidney injury (12,13). In the present study, in vivo and in vitro experiments were performed to investigate the regulation of apoptosis metabolism and the antioxidative effects exhibited by anthocyanins [grape seed procyanidin (GSPE) and cyanidin cyanidin-3-O-β-glucoside chloride (C3G)] in db/db mice. Furthermore, the present study aimed to investigate the molecular mechanism underlying this process using HG-stimulated HK-2 cells.
Materials and methods
Animals and treatment
Non-diabetic littermate, 6-8 weeks of age, control male db/m mice and male BKS db/db C57BL6 mice (body weight 40±2.5 g; total no. of mice, 40) were purchased from the Model Animal Research Center of Nanjing University (Nanjing, China). According to the guidelines of the National Institutes of Health (Bethesda, MD, USA), all experimental animals were housed in pathogen-free conditions with clean sawdust bedding. All mice were acclimated for 1 week prior to use and housed in polypropylene cages (30×21×10 cm), with free access to food and water, a 12 h light-dark cycle and a constant temperature of 23±2°C and a humidity of 50–60%. All procedures and experiments involving mice were reviewed and approved by the Ethics Committee of Hebei Medical University (Shijiazhuang, China). At the age of 8 weeks, the mice were divided randomly into 4 groups: Control group (db/m mice; n=10), db/m + GSPE group (db/m mice treated with GSPE; n=10), diabetes group (db/db mice; n=10) and db/db + GSPE group (db/db mice treated with GSPE; n=10). GSPE was dissolved in normal saline and administered to mice (once per day) intraperitoneally. GSPE (30 mg/kg body weight/day; Beijing Solarbio Science and Technology Co., Ltd., Beijing, China; purity ≥95%) was dissolved in normal saline and administered to mice intragastrically for 12 weeks (once per day). The mice in the control group and the diabetes groups were administered the same quantity of normal saline (once per day). At the age of 20 weeks, the mice were placed in individual metabolic cages in order to collect urine samples over a 24-h time period. Prior to blood sample collection, mice fasted for 6 h following the termination of experiments. Plasma and urinary supernatants were frozen and then stored at −80°C for further analysis. Following this, animals were sacrificed and kidneys were subsequently stored for further analysis.
Cell isolation, culture and treatment
HK-2 cells were purchased from the American Type Culture Collection (Manassas, VA, USA), and cultured in Dulbecco's modified Eagle's medium (DMEM)-F12 medium (3:1) supplemented with 5% fetal bovine serum (both Beijing Solarbio Science and Technology Co., Ltd.) 2 mM l-glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin at 37°C in a 95% air-5% CO2 atmosphere. HK-2 cells were grown to 75–85% confluence, washed once with serum-free DMEM-F12, and growth-arrested in serum-free DMEM-F12 at 37°C for 24 h in order to synchronize cell growth. Following this, cells were treated with normal glucose (NG; 5.6 mM), HG (30 mM), NG plus mannitol (24.4 mM) as an osmotic control, HG plus C3G [50 μM (14)], HG plus SB203580 (10 μM), or HG plus PD98059 (50 μM) for 48 h.
Immunohistochemistry analysis
All samples were incubated with 4% paraformaldehyde at room temperature for 12 h and then embedded in paraffin for immunohistochemical analysis used light microscope (magnification, ×400). Paraffin sections were cut into 4-mm sections, deparaffinized using xylene, and rehydrated using gradient alcohol. Internal peroxidase was inactivated using 3% hydrogen peroxide in 100% methanol at room temperature for 30 min. Antigen retrieval was performed via incubation with 10 mM citrate buffer at room temperature for 15 min. To block nonspecific antibody binding, sections were incubated with 10% normal goat serum (Beijing Solarbio Science and Technology Co., Ltd.) in PBS for 30 min at room temperature. The sections were then incubated overnight at 4°C with primary antibodies for thioredoxin interacting protein (TXNIP; 1:300; cat. no. ab86983), B-cell lymphoma-2 (Bcl-2; 1:350; cat. no. ab7973) and Bcl-2-associated X protein (Bax; 1:300; cat. no. ab7977) (all from Abcam, Cambridge, UK). Following washing with PBS, sections were incubated with biotinylated secondary antibodies (SP-9000; 1:4,000; cat. no. 004-2013; ZSGB-BIO; OriGene Technologies, Inc., Beijing, China) and horseradish peroxidase-conjugated streptavidin at 37°C for 2 h. Chromogen detection was performed using 3,3′-diaminobenzidine at room temperature for 2-3 min to produce a brown color, and sections were then counterstained using hematoxylin at room temperature for 1-2 min. Negative controls were not incubated with primary antibodies.
Determination of intracellular and urinary ROS
The intracellular formation of ROS was determined using the fluorescence probe 5-(and 6) chloromethyl-2′,7′-dichlorodihy-drofluorescein diacetate (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA). Following incubation in 6-well plates under the different experimental conditions at room temperature for 48 h, the cells were washed, trypsinized, suspended in PBS, loaded with 10 μM dichlorodihydro-fluorescein diacetate, and incubated at 37°C for 30 min. ROS levels were determined using a flow cytometer (BD Biosciences, Franklin Lakes, NJ, USA). To remove particulates, urine samples were centrifuged at 600 × g for 10 min. The supernatants were removed, and 8-hydroxy-2-deoxyguanosine levels were determined using a competitive in vitro ELISA kit (cat. no. YH8802; Nanjing Jiancheng Bioengineering Institute, Nanjing, China), in accordance with the manufacturer's protocol.
Analysis of mitochondrial membrane potential (MMP)
MMP was investigated using JC-1 (Shanghai Genmed Pharmaceutical Technology, Co., Ltd., Shanghai, China) staining. Cells were seeded in 60 mm culture dishes (2.5×105 cells/well) and incubated with 5 mM JC-1 dye (Shanghai Genmed Pharmaceutical Technology, Co., Ltd.) at 37°C for 15 min. Cells were washed three times with PBS and immediately analyzed using a confocal microscope (magnification, ×400; DM4000B; Leica Microsystems GmbH, Wetzlar, Germany). The MMP loss was quantified via the shift of JC-1 emission from red (~590 nm) to green (~525 nm). Red emission revealed membrane potential-dependent JC-1 aggregates in the mitochondria. Green fluorescence revealed the monomeric form of JC-1 entering the cytoplasm following mitochondrial membrane depolarization. This assay functions on the basis of an electrochemical proton gradient at the mitochondrial inner membrane (15).
Thioredoxin (TRX) activity analysis
TRX activity was determined using the insulin disulfide reduction assay, as previously described (16). Following incubation of the cells in 6-well plates under the different experimental conditions for 48 h, total cellular protein was extracted using a lysis buffer (cat. no. P0013G; Nanjing Jiancheng Bioengineering Institute). A total of 40 μl reaction mixture [200 μl HEPES buffer (1 M, pH 7.6), 40 μl EDTA (0.2 M), 40 μl NADPH (40 mg/ml) and 500 μl insulin (10 mg/ml)] was incubated with cellular protein extracts at 37°C for 15 min following the administration of 10 μl bovine TRX reductase (Sekisui Diagnostics, LLC, Lexington, MA, USA). The reaction was terminated by the administration of 500 μl stop mix (6 M guanidine HCl, 1 mM DTNB in 0.2 M Tris·HCl pH 8.0), and then the absorption at a wavelength of 412 nm was determined by Rayto RT-9600 semi-automatic biochemical analyzer (Rayto Life and Analytical Sciences Co., Ltd., Shenzhen, China).
Apoptosis analysis
The apoptosis of proximal tubular epithelial cells was investigated using a terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay kit (Promega Corp., Madison, WI, USA). The TUNEL assay was performed in accordance with the manufacturer's instructions. Fluorescence images were obtained using a laser-scanning confocal microscope (magnification, ×400; Leica Microsystems GmbH). A total of 6 fields of each cover-slip were randomly selected for counting, and 100 cells were randomly counted from each field of vision. The numbers of apoptotic cells and the total number of cells were counted for all 6 fields of vision. The apoptosis rate was subsequently determined.
Following this, slides were immersed in 4% formaldehyde in PBS at 4°C for 10 min and then incubated in 0.2% Triton X-100 in PBS for 10 min at room temperature. Equilibration Buffer (100 μl; Promega Corp.) was added to the cells at room temperature for 10 min, followed by 50 μl terminal deoxynucleotidyl transferase reaction mix for 60 min at 37°C. Subsequently, slides were immersed in 2X saline-sodium citrate and propidium iodide (PI; 1:10,000), at room temperature for 15 min, was used to stain all cells. Green fluorescence of apoptotic cells on a red background was imaged using fluorescence microscopy. In order to quantify the number of TUNEL-positive (apoptotic) cells, ≥200 cells were counted per group and the percentage of positively-labeled cells was determined.
The number of apoptotic cells in different groups was determined using an Annexin V/PI apoptosis detection kit according to the manufacturer's protocol (MultiSciences Biotech, Co., Ltd., Hangzhou, China). Briefly, the cell pellet was resuspended in 1X binding buffer and incubated with 5 ml Annexin V (conjugated with fluorescein isothiocyanate) and 10 ml PI in the dark at room temperature for 5 min. Cell fluorescence was analyzed using a flow cytometer (BD Biosciences). This assay was used to discriminate between intact cells (Annexin V−/PI−), early apoptotic cells (Annexin V+/PI−) and late apoptotic cells (Annexin V+/PI+).
Western blot analysis
All cells were isolated via scraping in lysis buffer (cat. no. P0013G; Nanjing Jiancheng Bioengineering Institute). The protein concentration was determined using Coomassie Protein assay reagent (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany). A total of 40 μg proteins was loaded in each lane, separated by electrophoresis on a 30% gel, and transferred to polyvinylidene fluoride membranes. Membranes were blocked with 5% dry milk at 37°C for 2 h and incubated overnight at 4°C with primary antibodies. Following washing, the membranes, at room temperature for 45 min, were incubated with goat anti-rabbit or mouse immu-noglobulin G horseradish peroxidase conjugate (1:5,000; cat. nos. SA00001-2 and SA00001-1; ProteinTech Group, Inc., Chicago, IL, USA). In order to perform western blotting analysis, membranes were hybridized with the following primary antibodies: Rabbit Bax (1:1,000; cat. no. ab7977), Bcl-2 (1:1,000; cat. no. ab7973), TXNIP (1:1,000; cat. no. ab86983) (all from Abcam), cleaved caspase-3 (Asp175; 1:1,000; cat. no. 9661; Cell Signaling Technology, Inc., Danvers, MA, USA), caspase-3 (1:1,000; cat. no. 19677-1-AP), thioredoxin 2 (TRX2; 1:1,000; cat. no. 13089-1-AP) (both from ProteinTech Group, Inc.), p-p38 MAPK (Thr180/Tyr182; 1:1,000; cat. no. 4092; Cell Signaling Technology, Inc.), p-ERK1/2 (Thr202/Tyr204; 1:1,000; cat. no. 1150), p38 MAPK (1:1,000; cat. no. 9212), ERK1/2 (1:1,000; cat. no. 1240) (all from Cell Signaling Technology, Inc.), and mouse antibody cytochrome c (cyt c; 1:2,000; cat. no. sc-514435; Santa Cruz Biotechnology, Inc., Dallas, TX, USA). Subsequently, the membranes were incubated with goat anti-rabbit or mouse IgG horseradish peroxidase conjugate, and scanned using the Odyssey Fc System (LI-COR Biosciences, Lincoln, NE, USA). The density of the bands was quantified using LabWorks 4.5 software (UVP, LLC, Phoenix, AZ, USA). Protein expression was quantified via comparison with the internal control, β-actin (1:2,000; cat. no. 60008-1-Lg; ProteinTech Group, Inc.).
Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) analysis
Total RNA was isolated from granulosa cells using TRIzol reagent (Invitrogen; Thermo Fisher Scientific, Inc.), according to the manufacturer's protocol. The first complementary DNA strand was synthesized using PrimeScript RT Master Mix (Takara Biotechnology Co., Ltd., Dalian, China). The primers used for amplification were as follows: Bax sense, 5′-GCTTGCTTCAGGGTTTCATCC A-3′ and antisense, 5′-TGTCCACGGCGGCAATCATC-3′; Bcl-2 sense, 5′-GGCGGAGAACAGGGTACGATAAC-3′ and antisense, 5′-CGGGATGCGGCTGGATGGGG-3′; TXNIP sense, 5′-CCGTTAGGATCCTGGCTTGC-3′ and antisense, 5′-GGCGCCTTGTACTCATATTTGTTTC-3′; 18s rRNA sense, 5′-ACACGGACAGGATTGACAGA-3′ and antisense, 5′-GGACATCTAAGGGCATCACAG-3′. The 18s rRNA was used for normalization. RT-qPCR was performed in a 96-well optical reaction plate using SYBR Premix Ex TaqII (Takara Biotechnology Co., Ltd.). The PCR amplification began with a 5-min denaturation at 95°C, followed by 40 cycles of denaturation at 95°C for 45 sec, annealing at 55°C for 45 sec, and extension at 72°C for 60 sec. The final extension was set for 10 min at 72°C. PCR experiments were performed on an Agilent Mx3000P qPCR System (Agilent Technologies, Inc., Santa Clara, CA, USA). Relative expression levels were determined using the 2−ΔΔCq method (17).
Statistical analysis
All data presented in bar graphs are expressed as mean ± standard deviation. Experiments were performed in triplicate, and data were analyzed using SPSS 15.0 for Windows (SPSS, Inc., Chicago, IL, USA). One-way analysis of variance was followed by Dunnett's test for multiple comparisons. P<0.05 was considered to indicate a statistically significant difference.
Results
Treatment with GSPE reduces the body weight and the fasting blood glucose (FBG), blood urea nitrogen, serum creatinine, triglyceride, ROS and urine albumin excretion (UAE) levels in db/db mice
In order to investigate the role of GSPE in the progression of DN in db/db mice, 8-week-old db/db mice were intragastrically administered 30 mg/kg GSPE (dissolved in water) every second day for 12 weeks. Total body weight and the FBG level of mice at the termination of the experiments were determined, and the results are presented in Fig. 1. The body weight and FBG levels were significantly enhanced in the db/db group compared with the db/m group. Treatment of db/db mice with GSPE suppressed the increase in body weight. However, treatment with GSPE significantly increased the body weight of the db/db + GSPE group compared with the db/db group. All db/db mice exhibited markedly increased blood glucose levels compared with db/m mice. Furthermore, db/db mice treated with GSPE demonstrated significantly decreased blood glucose levels compared with non-treated db/db mice following 12 weeks of treatment. In addition, the exhibited levels of blood urea nitrogen, serum creatinine, were significantly enhanced in the db/db group compared with the db/m group, however, this was significantly attenuated following treatment with GSPE (Table I). These results suggested that GSPE administration significantly stabilized metabolic parameters and preserved the renal function of db/db mice. Furthermore, the levels of ROS [8-Oxo-2′-deoxyguanosine (8-OHdG)] were significantly elevated in the db/db group compared with the control group (Table I). However, this effect was attenuated via GSPE administration in the db/db + GSPE group. There were no significant differences regarding the biochemical and physical characteristics between the control group and control + GSPE group.
Treatment with GSPE suppresses the apoptosis of renal tubular cells in db/db mice
The level of apoptosis of renal tubular cells was determined using the TUNEL assay. The db/db group exhibited enhanced levels of renal tubular cell apoptosis compared with the control group (Fig. 2). This effect was significantly attenuated following treatment with GSPE in the db/db + GSPE group (Fig. 2).
Expression of apoptosis-associated proteins in the kidneys of db/db mice is suppressed following treatment with GSPE
To further investigate the renal protective effects of GSPE administration in db/db mice, apoptosis-associated protein expression levels were determined via western blotting. As demonstrated in Fig. 3A and B, the Bax/Bcl-2 ratio was suppressed and cleaved caspase-3 was markedly increased in db/db mice compared with db/m mice. As revealed in Fig. 3C and D, the expression level of TXNIP was markedly enhanced in db/db mice, and treatment with GSPE markedly suppressed TXNIP expression in db/db mice. This suggests that there is enhanced intrinsic apoptosis in the kidneys of db/db mice compared with db/m mice; however, treatment with GSPE significantly attenuated these effects.
GSPE inhibits the phosphorylation of ERK1/2, p38 MAPK in db/db mice kidneys
The level of cyt c, in addition to the p-ERK1/2/ERK1/2 and p-p38/p38 ratios, was investigated in the kidneys of db/db mice via western blotting. The results revealed that the level of cyt c (Fig. 3E and F), in addition to the p-ERK1/2/ERK1/2 and p-p38/p38 ratios (Fig. 4), were significantly enhanced in db/db mice compared with db/m mice. Furthermore, treatment with GSPE in db/db mice was demonstrated to significantly attenuate these effects.
C3G protects HK-2 cells from HG-induced apoptosis
To investigate whether treatment with C3G protects HK-2 cells from oxidative stress, primary cultured cells were exposed to HG conditions. Annexin V/PI staining of HK-2 cells isolated from C3G-pretreated groups was significantly reduced compared with the HG-treated group (Fig. 5A). In addition, RT-qPCR analysis was performed in order to determine the mRNA expression levels of caspase-3, Bax and Bcl-2 (Fig. 5B). The results suggested that the Bcl-2/Bax and cleaved caspase-3/caspase-3 ratios were significantly suppressed in the HG + C3G group compared with the HG-treated group. Furthermore, the expression of cyt c was demonstrated to be significantly suppressed in the HG group; however, this effect was significantly attenuated following treatment with C3G (Fig. 5C).
Treatment with C3G attenuates the HG-induced enhancement of TXNIP expression, suppression of TRX2 expression, suppression of TRX activity, alteration of MMP, and enhancement of ROS production in HK-2 cells
The authors' previous study demonstrated that TXNIP is involved in the HG-induced apoptosis of mouse mesangial cells, and that knockdown of TXNIP attenuates HG-induced suppression of TRX activity (18). As revealed in Fig. 6A–D, HK-2 cells under HG conditions demonstrated enhanced levels of MMP following treatment with HG for 48 h. The HG-induced increase in MMP in HK-2 cells was significantly attenuated following treatment with C3G. In addition, to investigate whether TXNIP is involved in the protective effect of C3G in HK-2 cells under HG treatment, RT-qPCR analysis and western blotting were performed to determine the expression of TXNIP. Following treatment with HG for 48 h, the expression levels of TXNIP mRNA were significantly increased in the HG group compared with the control group, whereas treatment with C3G was revealed to significantly suppress HG-induced expression of TXNIP in HK-2 cells (Fig. 6E and F). Following this, the effect of C3G treatment on TRX2 expression in HK-2 cells exposed to HG was investigated. As revealed in Fig. 6E, HG exposure did not markedly affect the expression of TRX2; however, the expression of TRX2 was significantly enhanced in the HG + C3G group compared with the HG group. Furthermore, the effect of treatment with C3G on the activity of TRX in HK-2 cells under HG conditions was investigated. Furthermore, following exposure to HG for 48 h, the activity of TRX was significantly suppressed, whereas treatment with C3G under HG conditions significantly attenuated this effect (Fig. 6G).
These results suggest that C3G treatment inhibits ROS production and suppresses MMP in HK-2 cells otherwise induced by HG conditions.
C3G suppresses HG-induced apoptosis via inhibition of p38 MAPK and ERK1/2 phosphorylation
The involvement of p38 MAPK and ERK1/2 in HG-induced apoptosis in renal tubular epithelial cells has previously been demonstrated (19). However, whether C3G is involved in HG-induced apoptosis via p38 MAPK and ERK1/2 associated pathways remains unclear. As demonstrated in Fig. 7A–C, the levels of p-p38 MAPK and p-ERK1/2 were significantly increased following HG exposure, whereas treatment with C3G significantly suppressed the HG-induced increase of p-p38 MAPK and p-ERK1/2 levels. To investigate whether p38 MAPK or ERK1/2 signaling affects HG-induced apoptosis, HK-2 cells were treated with either specific p38 MAPK SB203580 (10 μM) or ERK1/2 PD98059 (50 μM) inhibitors for 0.5 h. Following this, cells were incubated under HG conditions, in the presence of SB203580 or PD98059, for 48 h. Furthermore, the effects of p38 MAPK and ERK1/2 knockdown regarding apoptosis were investigated. HG exposure in HK-2 cells was revealed to significantly enhance cellular apoptosis compared with non-treated cells (Fig. 7D and E). In HK-2 cells, the increase in apoptosis exhibited by HG-treated cells was significantly suppressed following incubation with either SB203580 or PD98059 (Fig. 7D and E). In addition, administration of C3G to HG-treated HK-2 cells significantly attenuated the otherwise enhancement of apoptosis (Fig. 7D and E). In conclusion, these results suggested that HG-induced apoptosis may be attenuated by suppression of p38 MAPK and ERK1/2 phosphorylation in HK-2 cells via treatment with C3G.
Discussion
In the present study, it was demonstrated that treatment with GSPE in db/db mice suppresses kidney cell apoptosis and superoxide production, thus suggesting that GSPE may have a therapeutic effect regarding DN. Furthermore, C3G was demonstrated to suppress HG-induced ROS generation, MMP, cyt c translocation from the mitochondria to the cytoplasm, TXNIP expression, and the phosphorylation of p38 MAPK and ERK. In addition, C3G was demonstrated to upregulate TRX2 expression, stabilize the biological activity of TRX and suppress HK-2 cellular apoptosis in response to hyperglycemia.
The enhancement of ROS production is an important feature of microvascular and macrovascular complications associated with deformity and death in patients with diabetes mellitus type 2 (20,21). Furthermore, ROS levels have an important role in the pathogenesis of DN (1,22). These results suggest that ordinary and catalytic antioxidants may exhibit protective properties against, or suppress the morbidity of, DN, and a combination of methods to suppress excessive production of ROS, and thus increase the elimination of preformed ROS, may serve as a potential therapeutic agent against the development and progression of DN. C3G has been suggested to possess vigorous antioxidant and anti-inflammatory properties (23,24). Recent studies have revealed that C3G is able to suppress 1,3-dichloro-2-propanol-induced ROS generation and suppress the apoptosis of R2C leydig cells (25). In a db/db model of DN, treatment with grape seed procyanidin B2 (GSPB2) was demonstrated to result in a suppression of triglyceride concentration in serum, total cholesterol level, advanced glycation end products and UAE, compared with vehicle-treated diabetic mice (26). Chronic exposure to Diquat significantly enhances granulosa cell damage, whereas treatment with GSPB2 suppresses granulosa cell apoptosis and causes the autophagy process in ICR mice (27). In the present study, the results suggested that db/db mice demonstrated markedly enhanced UAE, total body weight and average glomerular volume at 12 weeks post-development of diabetes (19). In addition, treatment with GSPE in db/db mice attenuated albuminuria and the level of urinary 8-OHdG. Furthermore, the results of the present study demonstrated that GSPE administration suppressed renal cell apoptosis in db/db mice, thus suggesting that GSPE exhibits therapeutic effects on the diabetic kidney. However, Tyagi et al (28) and Li et al (29) suggested that procyanidin B2 leads to apoptosis in PCa cells of human prostate cancer and in endothelial cells of diabetes mellitus. The discrepancy between the results of the present study and previous studies may reflect differences in the chosen cell lines.
Apoptosis contributes to the development of DN (30). Previous studies have suggested that HG-induced cellular apoptosis is an important factor in the development of kidney injury, and ROS results in the apoptosis of renal tubular cells (31,32). A predominant factor of apoptosis is the accumulation of ROS, which enhances intracellular DNA damage and may induce cell apoptosis. C3G has been demonstrated to suppress hyperglycemia-induced liver oxidative damage by enhancing glutathione synthesis via a cyclic adenosine mono-phosphate-protein kinase A-dependent signaling pathway (33). In the present study, cellular apoptosis in db/db mouse kidneys was significantly enhanced; however, this was attenuated by treatment with GSPE. In vitro, it was revealed that treatment with C3G suppressed HG-induced ROS generation, apoptosis, the expression of cleaved caspase-3, the Bax/Bcl-2 ratio, and cyt c translocation from the mitochondria to the cytoplasm in HK-2 cells. Furthermore, the results of the present study demonstrated that C3G treatment reversed the HG-induced alteration in MMP in HK-2 cells. The results suggest that anthocyanins may attenuate diabetic renal injury via suppression of ROS, and may thus protect mitochondrial function. Furthermore, the results suggest that the administration of anthocyanins enhances antioxidant function and decreases oxidative stress, thus suppressing apoptosis.
The TRX system, a predominant thiol antioxidant pathway, regulates the metabolic breakdown of intracellular ROS. TXNIP, first identified as the product of the 1,25-dihydroxyvitamin D-3 inducible gene in HL-cells (additionally termed vitamin D3 upregulated protein 1 or thioredoxin binding protein-2), is the endogenous inhibitor of cellular TRX, inhibiting its antioxidative role by combining with redox-active cysteine residues (34). TRX/TXNIP, a redox-sensitive signaling complex, may regulate cellular redox status and has an important role in the association of redox regulation with the etiopathogenesis of diseases (35). In a recent study, it was demonstrated that TXNIP is upregulated under HG conditions in mouse mesangial cells and renal cells, and that TXNIP knockout may attenuate the HG-induced suppression of TRX activity, and suppress HG-induced apoptosis and ROS generation (10,18). In the present study, it was demonstrated that the administration of anthocyanins significantly suppressed TXNIP expression in the kidneys of db/db mice and in HK-2 cells incubated under HG conditions. Furthermore, the results suggested that C3G treatment enhanced TRX2 expression and attenuated the HG-induced suppression of TRX activity in HK-2 cells. These results suggest that anthocyanins attenuate oxidative stress in diabetic kidneys via regulation of TXNIP and TRX expression.
Increasing studies have suggested that an increase in the activity of p38 MAPK and ERK1/2 contributes to the etiopathogenesis of DN (36,37). Numerous studies have suggested that GSPEs may protect the kidney by suppressing p38 MAPK and ERK1/2 phosphorylation (38,39). In the present study, it was demonstrated that the expression levels of p-p38 MAPK and p-ERK1/2 were significantly suppressed in HK-2 cells following treatment with anthocyanin in vivo and in vitro, thus suggesting that a reduction in the HG-induced phosphorylation of p38 MAPK and ERK1/2 may be a downstream effector of the anthocyanin associated pathway. Furthermore, the present study revealed that treatment with a p38 MAPK inhibitor (SB203580) or ERK inhibitor (PD98059) was able to suppress HG-induced apoptosis, thus suggesting that ROS-MAPK and ROS-ERK is involved in apoptosis.
The present study demonstrated that treatment with anthocyanins suppressed the TXNIP expression-enhanced p38 MAPK and ERK1/2 activity, and suppressed renal cellular apoptosis under diabetic conditions. Therefore, the results suggest that anthocyanins (GSPE and C3G) may serve as potential therapeutic agents for the treatment of DN.