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Introduction

Diabetic nephropathy (DN) is a major cause of end-stage renal failure and is one of the direct causes of mortality in diabetic patients (1,2). In clinical terms, DN patients are commonly characterized by the development of proteinuria, specifically albuminuria, with a subsequent reduction in the glomerular filtration rate (2). Multitude pathological changes in the kidneys contribute to the progressive decline in renal function, including macrophages in filtration, extracellular matrix (ECM) accumulation in multiple renal cells, glomerular and tubular hypertrophy, endothelial dysfunction, mesangial cell expansion and podocyte injury (3). Identification of molecular changes associated with the pathophysiology of DN is imperative for the development of therapeutic strategies.

The loss of size-selective and/or charge-selective properties of the glomerular filtration barrier are reported to be responsible for the observed proteinuria in glomerular diseases. The glomerular filtration barrier is composed of three layers: A glomerular basement membrane (GBM), a fenestrated endothelial layer and podocyte foot processes that are connected by a slit diaphragm. Diaphragm-associated proteins podocin and nephrin (4) are crucial proteins in the complex of molecules that assemble and reinforce the slit diaphragm and serve central roles in maintaining the size-selective barrier (5,6).

Advanced glycation end-products (AGEs) are biochemical end-products of nonenzymatic glycation (7). AGEs have been suggested to serve a vital role in the development of DN due to the fact that drugs that either break the AGE crosslink or inhibit AGE formation have been demonstrated to exhibit a protective effect on experimental DN (8). The structure and function of matrix tissue proteins can be altered by AGE modification, which thus stimulates a variety of cellular responses via a specific cell-surface receptor on glomerular cells (9). Importantly, the specific cellular receptor for AGE (RAGE) that is upregulated and activated by AGE (10), has been demonstrated to serve an important role in the development of DN (11). Therefore, the AGE-RAGE interaction likely serves an important role in the pathogenesis of DN (12–14).

GSPE is derived from grape seeds and possesses potent properties, such as radical scavenging, anti-inflammation, antioxidant, anti-tumor and cardiovascular protection activity (15). Previous studies demonstrate that GSPE can act in the prevention of multiple diseases such as cataracts, gastric ulcer, atherosclerosis, myocardial ischemia-reperfusion and especially diabetes (16–18). However, the function of GSPE on DN has been rarely studied. The aim of the current study was to determine the effect of GSPE on the streptozotocin-induced diabetic rat model and to explore the underlying mechanisms of its activity.

Materials and methods

Ethics statement

The current study was approved by the Animal Ethics Committee of Shandong University (Jinan, Shandong, China).

Animals

A total of 60 male Wistar rats (lot no. SCXL20030004; 6–7 weeks old; weight, 180–200 g) were obtained from the Shandong University Experimental Animal Center (Jinan, Shandong, China). These rats were housed in cages and allowed free access to food and tap water. They were maintained on a 12:12 h dark/light cycle, with a room temperature of 22±1.5°C and a humidity of 55±5%. A total of 24 rats were selected randomly and divided into 2 groups (n=12 in each group), and the control group (C group) was treated with a dosage of 250 mg·kg−1·day−1 GSPE (CT group) (lot no. G050412; Tianjin Jianfeng Natural Product R&D Co., Ltd., Tianjin, China) (14). The remaining 36 rats were injected with a dose of 55 mg·kg−1 STZ (injected into the tail veins). After five days, rats with blood glucose levels higher than 16.7 mmol/l were considered as being diabetic, and six rats were excluded for failure to meet this criterion. One week after STZ injection, the diabetic rats were then divided randomly into 2 groups (n=15 in each group), a diabetic group without any treatment (diabetes mellitus; DM; group), and another diabetic group that was treated with a dosage of 250 mg·kg−1·day−1 GSPE (T group). The GSPE was intragastrically administrated in normal saline solution for 24 weeks. At the end of the experiments, the animals were fasted overnight for 18 h and then anesthetized with intraperitoneal injection of sodium pentobarbitone (60 mg/kg; Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) and sacrificed. Kidneys were perfused with ice-cold PBS and then were stored at −80°C.

Assessment of renal function

At the end of the experiments, the fasting plasma glucose (FPG), 24 h urinary albumin excretion, hemoglobin A1c (HbA1C), urinary creatinine (Ucr), serum creatinine (Scr), Ccr = Ucr/ScrxV (V:ml/min, urine per minute), and the ratio of kidney weight to bodyweight and serum AGEs was measured for each rat. Scr and Ucr were measured using an automatic biochemical analysis instrument (DVI 1650; Bayer AG, Leverkusen, Germany). HbA1C was measured by high-pressure liquid phase methods (ADAMS A1c HA-8180; Arkray, Inc., Kyoto, Japan). The level of AGEs in serum was measured by the enzyme-linked immunosorbent assay (ELISA) method (19) (Hitachi 850; Hitachi, Tokyo, Japan). To collect urine samples, rats were placed in individual metabolic cages for 24 h prior to sacrificing. ELISA (Nephrat II; Exocell, Philadelphia, PA, USA) was used to determine 24 h urinary albumin excretion levels.

Light microscope examination

For the light microscopic examination, the kidneys were immersion-fixed, embedded and two sections (4 µm thickness) were stained with periodic acid-Schiff (PAS) reagent. For electron microscope examination, the renal cortex was cut into small pieces and pre-fixed in glutaraldehyde, post-fixed in buffered sodium tetroxide for 1 h, and then embedded in EPON 812 embedding resin (Electron Microscopy Sciences, Fort Washington, PA, USA). The PAS-positive area present in the mesangial region excluding cellular elements indicated mesangial matrix expansion. By using Leica QWin version 3 image analysis software (Leica Microsystems GmbH, Wetzlar, Germany), the percentage of the PAS-positive area in the glomerulus was analyzed. A total of 10 glomeruli, randomly selected in the two slides from the rats (a minimum of 8 rats in each group), were evaluated by two investigators blinded of the origins of the slides.

Electron microscope examination

For transmission electron microscopic examination, a JEOL JSM 1011 microscope (JEOL, Ltd., Tokyo, Japan), was used to photograph images covering one or two glomerular cross-sections. The images at ×15,000 magnification were used to measure the GBM length and the number of slit pores. To determine the FPW (foot process width), the slit pore length, and the GBM thickness, the images at ×50,000 or ×100,000 magnification were used according to published methods (20–22).

Reverse transcription-polymerase chain reaction (RT-PCR)

The total RNA was extracted from the renal cortex using TRIzol reagent (Thermo Fisher Scientific Inc., Waltham, MA, USA). Primers for RAGE, nephrin, podocin, and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) were designed and synthesized (Huada Gene Center, Beijing, China) based on the published sequence. The primers were as follows: RAGE forward, 5′-GCTCTGACCGAAGCGTGA-3′ and reverse, 5′-CCTTCAGGCTCAACCAACAG-3′, 240 bp product; nephrin forward, 5′-ACCAAGTCCAGTCGCCCAG-3′ and reverse, 5′-ATACCAGCCTCACCCGAGTCCC-3′, 306 bp product; podocin forward, 5′-GTGTCCAAAGCCATCCAGTT-3′ and reverse, 5′-GTCTTTGTGCCTCAGCTTCC-3′, 232 bp product; and GAP DH forward, 5′-GAGGGGCCATCCACAGTCTTCTG-3′ and reverse, 5′-CCCTTCATTGACCTCAACTACATGGT-3′. The Titan One Tube RT-PCR kit (Boehringer-Mannheim, Shanghai, China) was used to amplify a total of 0.5 µg RNA. Agarose gel electrophoresis was used to separate products and ethidium bromide staining was used for visualization. A Tanon-1000 Gel Image System (Tanon, Shanghai, China) was used to digitize bands and GAPDH was used as the control gene based on previous studies (5,23).

Western blotting

Western blot analysis was performed as previously described (24). Renal tissues were homogenized with ice-cold lysis buffer and were centrifuged at 10,000 × g for 15 min at 4°C. Equal amounts (100 µg) of protein were loaded and separated by 10% SDS-PAGE. Separated proteins were then transferred onto nitrocellulose paper (Bio-Rad Laboratories, Inc., Hercules, CA, USA). A sample of total protein from the lysate (20 µg) was separated and blotted. The membranes were incubated with the following primary antibodies: Anti-RAGE (1:250, cat no. MAB1179; R&D Systems, Inc., Indianapolis, IN, USA), anti-nephrin (1:1,000, cat no. ab58968; Abcam, Cambridge, UK), anti-podocin (1:1,000, cat no. sc-21009; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) and anti-β-actin (1:500, cat no. ab8226; Abcam) overnight at 4°C, and then reacted with anti-rabbit IgG horseradish peroxidase-conjugated secondary antibodies (1:5,000, cat no. sc-2004; Santa Cruz Biotechnology, Inc.) at room temperature for 1.5 h. Signal detection was performed via exposure of the blot to enhanced diaminobenzidenecolor reagents (OriGene Technologies, Inc., Rockville, MD, USA) for 5 min. Quantification of the luminosity of each identified protein band was performed using Adobe Photoshop software (AdobePhotoshop 7.0; Adobe Systems, Inc., San Jose, CA, USA).

Immunohistochemical study

Renal tissue sections (4 µm) were subjected to immunohistochemical staining based on the published method with specific antibodies anti-RAGE (1:100, ab37647; Abcam), anti-nephrin (1:500, ab58968; Abcam), and anti-podocin (1:400, H-130, sc-21009; Santa Cruz Biotechnology, Inc.) (25). Color was developed by incubating with diaminobenzidine and counterstaining with hematoxylin. Controls were obtained by replacing the primary antibody with PBS. Semi quantitative analysis of the percentage of positive staining area in the glomeruli and tubules was evaluated using a computer imaging analysis system (Image-Pro Plus software version 4·5; Media Cybernetics, Inc., Rockville, MD, USA). The brown areas were judged as positive.

Statistical analysis

Data were presented as the mean ± standard deviation. One way analysis of variance or the Mann-Whitney U test was performed to compare the differences between groups. P<0.05 was considered to indicate a statistically significant difference.

Results

Changes of renal function and general parameters

There were four treatment groups, the control group (C group) that received no treatment, rats treated with 250·mg·kg−1·day−1 GSPE (CT group), rats that received STZ injection to induce diabetes, however no additional treatment (DM group) and rats that were diabetic but received 250·mg·kg−1·day−1 GSPE (T group). Rats in each group were observed from 1 week to 24 weeks. At the start of the experiment, there were 12 rats in each of the C and CT groups and 15 rats in each of the T and DM groups. At the end of the experiment, there were 10, 10, 8, and 12 surviving rats in the C, CT, DM and T groups, respectively. As presented in Table I, the FPG, HbA1C, 24 h urinary albumin excretion, Ccr and ratio of kidney weight to body weight in the DM group were significantly increased compared with the C group (P<0.01). The diabetic rats treated with GSPE (T group) had markedly reduced Ccr, urinary albumin excretion (P<0.01), and ratio of kidney weight to body weight than that of the DM group. However, no significant differences in FPG and HbA1C were identified between the DM and the T groups.

Table I. General data of the rats.

Table I.

General data of the rats.

Group	n	FPG (mmol/l)	HbA1C (%)	Ccr (ml/min)	Urinary albumin excretion 24 h (mg)	Kidney weight/body weight (×10−3)
C	10	6.98±0.86	5.60±0.73	1.98±0.32	10.22±1.67	3.34±0.18
CT	10	6.60±0.81	5.56±0.71	2.11±0.74	11.37±1.08	3.24±0.18
DM	8	23.04±0.93a	11.41±2.14a	5.11±1.14a	24.96±2.56a	5.48±0.17a
T	12	21.22±1.12a	8.71±3.54a	2.80±1.23b,c	15.15±3.27a,c	4.30±0.17a,c

{ label (or @symbol) needed for fn[@id='tfn1-mmr-16-06-9393'] } Mean ± standard deviation.

a P<0.01

b P<0.05 vs. C group

c P<0.01 vs. DM group. FPG, fasting plasma glucose; HbA_1C, hemoglobin A1c; Ccr, endogenous creatinine clearance rate; C, normal kidney; CT, normal rats treated with grape seed proanthocyanidin extracts (250 mg·kg⁻¹ ·day⁻¹); DM, diabetes mellitus rats; T, diabetes mellitus rats treated with grape seed proanthocyanidin extracts (250 mg·kg⁻¹ ·day⁻¹).

Changes in serum AGE levels

As presented in Table II, animals that were injected with STZ exhibited a significantly higher level of AGEs in serum than that in the C group (P<0.01). Diabetic rats that were treated with GSPE (T group) had significantly lower AGEs than the level in the DM group (P<0.01).

Table II. Alterations in serum AGE levels in rats.

Table II.

Alterations in serum AGE levels in rats.

Group	n	AGEs
C	10	0.0182±0.0005
CT	10	0.0221±0.0063
DM	8	0.0351±0.0021a
T	12	0.0276±0.0054b

{ label (or @symbol) needed for fn[@id='tfn5-mmr-16-06-9393'] } Data are presented as the mean ± standard deviation. All animals injected with streptozotocin exhibited a high level of AGEs in serum compared with C group

a P<0.01). Diabetic rats treated with GSPE (T group) had lower AGEs compared with DM group

b P<0.01). AGEs, advanced glycation end products; C, normal kidney; CT, normal rats treated with grape seed proanthocyanidin extracts (250 mg·kg⁻¹ ·day⁻¹); DM, diabetes mellitus rats; T, diabetes mellitus rats treated with grape seed proanthocyanidin extracts (250 mg·kg⁻¹ ·day⁻¹).

Renal morphological changes

The PAS-staining results in the glomeruli of each group are presented in Fig. 1A. Quantitative analysis of the percentage of the PAS-positive area in the glomeruli is summarized in Fig. 1B. The ECM accumulation was significantly higher in the glomeruli of the DM group than that of the C group (P<0.01), and diabetic rats treated with GSPE (T group) had a significantly lower ECM accumulation in the glomeruli than that of the DM group (P<0.01).

Figure 1. (A) Light microscopic images of renal morphological changes in rats by PAS (PAS, magnification ×400). ECM accumulation in DN rat kidneys by PAS staining. C, normal kidney; CT, normal rats treated with GSPE (250 mg·kg−1·day−1); DM, DM rats; T, DM rats treated with GSPE (250 mg·kg−1·day−1). (B) Analysis of ECM in glomeruli by PAS staining. Higher ECM accumulation was observed in the kidneys of DM group rats compared with that of the C group (**P<0.01 vs. C) Lower ECM accumulation was observed in the kidneys of the T group rats compared with the DM group (∆∆P<0.01 vs. DM). ECM, extracellular matrix; DN, diabetic nephropathy; PAS, periodic acid-Schiff; DM, diabetes mellitus; GSPE, grape seed proanthocyanidin extracts.

Electron microscopic observations

The foot processes of glomeruli were broader and flatter in the DM group than that in the other groups. It was also identified that the mean FPW was significantly greater in diabetic glomeruli as compared with control glomeruli (P<0.01). The mean slit pore length was significantly shorter in diabetic glomeruli than that of the control glomeruli (P<0.01). Additionally, there were significantly fewer slit pores (per 100 µm) of GBM in diabetic glomeruli than in the control glomeruli (P<0.01). The GBM was significantly thicker in diabetic glomeruli as compared with control glomeruli (P<0.01). However, these changes were significantly reversed by GSPE treatment (Fig. 2 and Table III).

Figure 2. Electron microscopic images of renal microstructure changes in rats (magnification, ×15,000). GSPE treatment decreased STZ-induced renal ultrastructural abnormalities. (Original magnification ×15,000.) GSPE, grape seed proanthocyanidin extracts; BM, basement membrane; PC, podocyte; End, endothelial cell; FP, foot processes; Mes, mesangial cell; Go, golgi apparatus; RBC, red blood cell.

Table III. Electron microscopic findings in the four groups.

Table III.

Electron microscopic findings in the four groups.

Parameter	C	DM	T
n	10	8	12
Foot process width (nm)	296.2±10.5	404.5±20.7a	353.9±18.4b
Slit pore length (nm)	32.5±2.6	26.2±3.2a	30.6±3.4b
Number of slit pores (per 100 µm)	256.3±13.2	181.5±12.1a	239.2±13.5b
GBM thickness (nm)	165.8±20.5	270.2±29.8a	190.3±22.3b

{ label (or @symbol) needed for fn[@id='tfn8-mmr-16-06-9393'] } Data are presented as the mean ± standard deviation.

a P<0.01 vs. C group

b P<0.01 vs. DM group. C, normal kidney; CT, normal rats treated with grape seed proanthocyanidin extracts (250 mg·kg⁻¹ ·day⁻¹); DM, diabetes mellitus rats; T, diabetes mellitus rats treated with grape seed proanthocyanidin extracts (250 mg·kg⁻¹ ·day⁻¹); GBM, glomerular basement membrane.

Renal expression of RAGE, nephrin, and podocin by RT-PCR and western blotting

In the kidney cortex of DM rats, the mRNA and protein expression of RAGE were markedly increased compared with the levels in the C group (P<0.01), and GSPE treatment significantly decreased the expression of RAGE (P<0.01) (Figs. 3 and 4). A significantly decreased expression of nephrin mRNA and protein was observed in the DM group as compared with the C group (P<0.05 and P<0.01, respectively), and GSPE treatment significantly increased the mRNA expression and protein level of nephrin (P<0.05 and P<0.01, respectively) (Figs. 3 and 4). However, no significant differences were identified in the mRNA or protein expression of podocin among the four groups (P>0.05) (Figs. 3 and 4).

Figure 3. (A) Expression of renal RAGE, nephrin, and podocin measured byreverse transcription-polymerase chain reaction (B) Renal RAGE was significantly decreased in the kidneys of the T group rats compared with the DM group (∆∆P<0.01 vs. DM) and renal nephrin was significantly increased in the kidneys of T group rats compared with the DM group (∆P<0.05 vs. DM). RAGE, receptor for advanced glycation end-products; DM, diabetes mellitus; C, normal kidney; CT, normal rats treated with grape seed proanthocyanidin extracts (250 mg·kg−1·day−1); DM, DM rats; T, DM rats treated with grape seed proanthocyanidin extracts (250 mg·kg−1·day−1).

Figure 4. (A) Expression of RAGE, nephrin, and podocin by western blotting analysis. (B) Renal RAGE was significantly decreased (∆∆P<0.01 vs. DM) and renal nephrin was significantly increased (∆∆P<0.01 vs. DM) in the kidneys of T group rats compared with the DM group. RAGE, receptor for advanced glycation end-products; DM, diabetes mellitus; C, normal kidney; CT, normal rats treated with grape seed proanthocyanidin extracts (250 mg·kg−1·day−1); DM, DM rats; T, DM rats treated with grape seed proanthocyanidin extracts (250 mg·kg−1·day−1).

Immunohistochemical staining for RAGE, nephrin, and podocin protein in glomeruli

Immunohistochemical staining indicated the localization of signals for RAGE, nephrin and podocin predominantly in the glomeruli. The intensity and area of RAGE staining were significantly increased in the glomeruli of diabetic rats as compared with the C group, and GSPE treatment significantly reversed this effect (Fig. 5A). The intensity and area of nephrin staining were significantly decreased in the glomeruli of diabetic rats compared with the C group, and GSPE treatment also significantly reversed these effects (Fig. 5B). No differences were observed in the intensity and area of podocin staining in the glomeruli for the four groups (Fig. 5C).

Figure 5. Immunohistochemical staining for RAGE, nephrin, and podocin in glomeruli (ABC; magnification, ×400). (A) RAGE protein expression was significantly reduced in the kidneys of T group rats compared with the DM group (∆∆P<0.01 vs. DM; *P<0.01 vs. C). (B) Protein expression of nephrin was significantly increased in the kidneys of T group rats compared with those in the DM group (∆∆P<0.01 vs. DM; *P<0.01 vs. C). (C) Protein expression of podocin were unchanged in the four groups (P>0.05). RAGE, receptor for advanced glycation end-products; C, normal kidney; CT, normal rats treated with grape seed proanthocyanidin extracts (250 mg·kg−1·day−1); DM, DM rats; T, DM rats treated with grape seed proanthocyanidin extracts (250 mg·kg−1·day−1).

Discussion

The incidence of diabetic nephropathy is increasing worldwide, and identification of associated molecular changes is important for prevention and treatment (1,2). Among the three intrinsic cells in the glomerulus, podocytes have special physiological functions and cytobiological traits (26). Podocyte damage occurs in the early stage of DN, and this injury to podocytes can cause proteinuria, and accelerate the development of DN (27). The slit diaphragm bridges adjacent foot processes derived from different podocytes and functions as the ultimate molecular size filter. Nephrin serves an important role in the pathogenesis of proteinuria in DN as a podocyte-associated protein that can comprise the slit diaphragm (28,29). Additionally, proteinuria is closely associated with ultrastructural changes in podocytes in DN. Reduced slit pore length and increased foot process width have been demonstrated in animal models of diabetes in addition to in patients with diabetes (30,31). Berg et al (30) also identified a strong correlation between FPW and urinary albumin excretion inpatients with type 1 diabetes.

In the present study, the HbA1C, 24 h urinary albumin excretion, Ccr, and ratio of kidney weight to body weight in DM group were significantly higher than in the C group. The electron microscopic analysis demonstrated that the foot processes of glomeruli in the DM group were broader and flatter than that of the other groups. In diabetic glomeruli, the FPW was significantly greater, the mean slit pore length was significantly shorter, the number of slit pores (per 100 µm) of GBM was significantly fewer and the GBM was significantly thicker as compared with control glomeruli. Notably, the current study observed that GSPE treatment significantly reversed these morphological changes. Additionally, markedly reduced Ccr, urinary albumin excretion and ratio of kidney weight to body weight were observed in the T group relative to that of the DM group. These results suggested that GSPE can decrease proteinuria and aid in the maintenance podocyte microstructure.

In order to explore the underlying mechanism of GSPE action, the effects on the podocyte-associated molecules nephrin and podocin were examined. The results indicated that expression of nephrin was significantly decreased, however the expression of podocin was unchanged in diabetic rats, which was also observed in a previous study (32). GSPE treatment significantly increased the expression of nephrin in the diabetic rats. These results suggested that the mechanism by which GSPE decreases proteinuria may be associated with the improved expression of nephrin.

AGEs have been documented to serve an important role in stimulating growth factor and cytokine synthesis, which contributes to the pathogenesis of DN (33). RAGE-dependent mechanisms are likely to be responsible for the AGE-induced tissue damage and dysfunction. In vivo study in RAGE-overexpressing diabetic mice observed that interaction between AGEs and their receptor is important in the development of DN (24). AGE-RAGE interactions may lead to diabetic vascular derangement, or trigger and promote the development of renal lesions (24). Additionally, a previous study suggested that, in a mouse model of DN, inactivation of the RAGE gene results in significant suppression of kidney changes, including increased glomerular cell number, advanced glomerulosclerosis, kidney enlargement, mesangial expansion, increased albuminuria, and increased serum creatinine compared with wild-type diabetic mice (34). Importantly, a recent study indicated that blockade of RAGE using a neutralizing antibody prevented the loss of nephrin expression induced by glycated albumin (GA), suggesting the involvement of this receptor in mediating the effect of GA on nephrin expression (35). In the present study, in diabetic rats, markedly higher AGEs and increased expression of RAGE were observed in the DM group relative to the C group.

However, diabetic rats treated with GSPE had lower serum AGEs and decreased expression of RAGE. The inhibition by GSPE of AGEs formation may be associated with the antioxidative activities of GSPE (17). The oxidation system has been documented to serve an important role in the formation of AGEs (8,33,35). GSPE increases the renal antioxidative ability, decreases NO levels and decreases the activity of NOS in kidney and serum (16). GSPE decreased RAGE mRNA and protein expression in diabetic rats in the present study, which also contributed to the improvement of renal function. It has been reported that AGE can activate the RAGE gene through NF-κB and AGEs accumulation (11). Thus, the action of GSPE to decrease RAGE is associated with the GSPE's inhibition of AGE formation. The in vitro experiments suggest at least two possible mechanisms of nephrin alteration in diabetic conditions, the first mediated by GA-RAGE interaction involving the inhibition of nephrin gene transcription, and the second associated with a rapid redistribution and shedding from the cell surface that depends on Ang II stimulation of the cell cytoskeleton (35,36). A previous study indicated that GA inhibited nephrin synthesis through the engagement of the receptor for AGEs, whereas angiotensin II acted on cytoskeleton redistribution, inducing the shedding of nephrin in proteinuric patients with diabetes (37). The results are consistent with an inhibitory effect of GSPE on the AGEs/RAGE system, which results in increased nephrin expression and decreased proteinuria.

In summary, the results demonstrated that GSPE has a protective effect on kidney in STZ-induced diabetic rats by decreasing urinary albumin excretion and reversing renal pathological damage. The underlying mechanism is associated with the decreased expression of the AGEs/RAGE axis and the increased expression of nephrin in DN rats. Based on these results, it is suggested that GSPE may be a promising therapeutic approach for the prevention and treatment of DN.

Acknowledgements

The authors would like to thank Dr Xueqing Gao from the Institute of Medical Science (Jinan, China) for the technical assistance, and Mr David Henry (World International English of Jinan, USA) for revising the paper.

References