Multi-glycoside of Tripterygium wilfordii Hook. f. attenuates glomerulosclerosis in a rat model of diabetic nephropathy by exerting anti-microinflammatory effects without affecting hyperglycemia.

Multi-glycoside of Tripterygium wilfordii Hook. f. (GTW) has been proven to be clinically effective in relieving microinflammation in patients with early diabetic nephropathy (DN). However, the therapeutic mechanisms involved in vivo remain unclear. In the process of early DN, microinflammation and activation of p38 mitogen‑activated protein kinase (MAPK) and canonical nuclear factor (NF)-κB signaling pathways are the important mechanisms by which hyperglycemia contributes to glomerulosclerosis (GS). Therefore, this study aimed to examine the ameliorative effects of GTW on GS, and then to clarify its anti‑microinflammatory mechanisms by inhibiting p38 MAPK and NF-κB signaling activities in the kidney. All rats were divided into 4 groups: the sham group, the sham + GTW group, the vehicle group and the GTW group. The suitable dose of GTW and vehicle were daily administered for 8 weeks after the induction of DN by unilateral nephrectomy combined with intraperitoneal injections of streptozotocin (STZ). The general status of the rats, biochemical parameters, renal histological changes and macrophages in glomeruli, as well as expression of the key proteins in the p38 MAPK and canonical NF-κB signaling pathways and inflammatory cytokines including tumor necrosis factor (TNF)-α, interleukin (IL)-1β and transforming growth factor (TGF)-β1 in the kidney were examined, respectively. The results revealed that, GTW improved the general cond-ition and biochemical parameters of the rats, but did not lower blood glucose; GTW attenuated GS and suppressed glomerular microinflammation including the infiltration of ED1+ cells in glomeruli and the protein overexpression of TNF-α, IL-1β and TGF-β1 in the kidney; GTW inhibited the protein overexpression of key signaling molecules of p38 MAPK and canonical NF-κB pathways in the kidney including phosphorylated p38 MAPK, phosphorylated inhibitor protein IκB and NF-κB (p65). On the whole, we expounded that GTW, as a natural regulator in vivo, alleviates GS without affecting hyperglycemia, by exerting anti-microinflammatory effects, including reducing macrophage infiltration in glomeruli, suppressing TNF-α, IL-1β and TGF-β1 overexpression in the kidney and inhibiting p38 MAPK and NF-κB signaling activities.

Introduction

In recent years, accumulating evidence in both the clinic and in experimental animal models have shown that microinflammation characterized by inflammatory cell proliferation, inflammatory cytokine overexpression and subsequent extracellular matrix (ECM) expansion in glomeruli is a common pathway for the progression of diabetic nephropathy (DN). Anti-microinflammatory strategies may thus offer approaches of great interest for early DN patients (1,2). Utimura et al (3) reported that mycophenolate mofetil (MMF), an anti-inflammatory drug, inhibited glomerular macrophage infiltration and improved glomerulosclerosis (GS) in streptozotocin (STZ)-induced and uninephrectomized diabetic rats. Correspondingly, pentoxifylline (PTF), which possesses significant anti-inflammatory properties, has recently been proven to reduce urinary protein excretion in diabetic subjects, both with normal renal function and with renal insufficiency. Moreover, these beneficial effects are related to a reduction in the concentration of tumor necrosis factor (TNF)-α, one of the most important pro-inflammatory cytokines (4,5). Therefore, these findings also indicate that inhibition of microinflammation may be a therapeutic target and a pharmacological mechanism for protecting glomerular lesions in DN.

It is well-known that microinflammation is regulated by inflammation-associated signaling pathways. The p38 mitogen-activated protein kinase (MAPK) signaling pathway becomes activated by inflammation stress-related signals including pro-inflammatory cytokines such as TNF-α, interleukin (IL)-1, IL-6 and IL-18 through phosphorylation mediated by upstream kinases. In turn, phosphorylated p38 MAPK (p-p38 MAPK), as an important active p38 MAPK signaling molecule, enters the nucleus, as well as controls the expression of a variety of downstream inflammatory factors and inflammatory mediators, which lead to the promotion of renal inflammatory response that exacerbates glomerular damage (2,6). For these reasons, by modulating the expression of p-p38 MAPK, transforming growth factor (TGF)-β and nuclear factor (NF)-κB, it is possible to block inflammatory signaling pathway reactions and ameliorate relevant inflammatory injuries in the kidney.

Multi-glycoside of Tripterygium wilfordii Hook. f. (GTW) is a stable glycoside extracted from Tripterygium wilfordii Hook. f. (TWHF), also known as 'Lei Gong Teng' (the local name in China), which is a natural anti-inflammatory phytomedicine used for various autoimmune and inflammatory diseases in Eastern and Southern China, America, Korea and Japan (7–9). GTW, as a Chinese traditional patented medicine, has been approved by the China State Food and Drug Administration (Z32021007) for the routine treatment of glomerulonephritis and rheumatoid arthritis (10,11). For the past 30 years, GTW at the dose of 60 mg/day has been proven to be clinically effective in reducing proteinuria and hematuria by suppressing renal microinflammation, GS and podocyte injury in several types of human chronic kidney disease (CKD) (12–14). In addition, a single central study in China found that a large oral dose of GTW (120 mg/day) reduced proteinuria and alleviated renal dysfunction in 65 DN patients at early and mid-term stages (15). More importantly, the therapeutic mechanisms of GTW and its main bioactive component, triptolide, may act by reducing macrophage proliferation in glomeruli (16–18). Despite this, its pharmacological mechanistic link in vivo between anti-microinflammatory effects and the protection against GS related to diabetes remains to be elucidated.

Hence, in this study, we examined the ameliorative effects of GTW on GS, using a modified STZ-induced DN rat model. We then clarified the anti-microinflammatory mechanisms in vivo of GTW by inhibiting the activation of inflammatory signaling pathways and the overexpression of inflammatory factors in the kidney. These results may provide a novel and effective therapeutic method for early stage DN patients.

Materials and methods

GTW quantity control

GTW purchased from Jiangsu Meitong Pharmaceutical Co., Ltd. (Taizhou, China) was composed of extracts from TWHF. One tablet contained 10 mg of GTW. The extraction method and productive process of GTW are both subjected to strict quality control, and the main components are subjected to standardization (19). In addition, GTW is not only manufactured as granules after dynamic cycle extraction and concentration by evaporating and spray drying, but is also monitored for the absence of contaminants (heavy metals, pesticides, hormone and mycotoxins) prior to formulation. In this study, GTW (batch no. 150206) was dissolved in distilled water (GTW suspension) and stored at 4°C before use.

The quality of GTW was examined with fingerprint analysis by high-performance liquid chromatography (HPLC) in Jiangsu Province Academy of Chinese Medicine (Nanjing, China). As shown in Fig. 1, the known bioactive components including triptolide (C20H24O6; CAS, 38748-32-2), triptonide (C20H22O6; CAS, 38647-11-9), wilforgine (C41H47NO19; CAS, 37239-47-7), wilforine (C43H49O18; CAS, 11088-09-8), tripterine (C29H38O4; CAS, 34157-83-0) and wilforlide A (C30H46O3; CAS, 84104-71-2) (20,21) (Fig. 1A) in 5 batches exhibited high stability.

Figure 1

(A) Chromatograms of mixed standards and (B) samples of Tripterygium wilfordii Hook. f. (GTW).

Animals, drugs and reagents

All experiments were performed using male Sprague-Dawley (SD) rats weighing from 180 to 200 g, purchased from the Animal Center of Nanjing Military District General Hospital (Nanjing, China). The surgical procedures and experimental protocol were approved by the Animal Ethics Committee of Nanjing University Medical School. STZ was purchased from Sigma-Aldrich (St. Louis, MO, USA). Antibodies against TGF-β1, TNF-α, IL-1β and horseradish peroxidase (HRP)-labeled IgG were purchased from Abcam (Cambridge, UK). Antibodies against p38 MAPK, p-p38 MAPK, p-IκB and NF-κB (p65) were purchased from Cell Signaling Technology, Inc. (Beverly, MA, USA). The antibody against glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was obtained from Bioworld Technology, Inc. (Louis Park, MN, USA).

Experimental protocol

The experimental procedure is illustrated in Fig. 2. The DN model was established as described in our previous study (22). Twenty rats were divided into 4 groups: the sham group (sham operation + distilled water), the sham + GTW group (sham operation + GTW), the vehicle group (DN + distilled water) and the GTW group (DN + GTW). In the clinic, GTW at a dose of 60 mg/day is used to treat a patient weighing 60 kg (11,15), which is equivalent to 50 mg/kg/day in rats. Following the second injection of STZ, the GTW suspension was administered to the rats in the 2 GTW-treated groups by gastric gavage once a day for 8 weeks, while rats in the vehicle and sham group were treated with 2 ml distilled water. Eight weeks after administration, all rats were anesthetized and sacrificed through cardiac puncture. Blood samples and kidneys were collected for detection of various indicators.

Figure 2

Experimental procedure.

General status and biochemical parameters of the rats

Energy level, diet, water intake, fur color and activities of the rats in each group were observed daily. Body weight (BW), blood glucose (BG) and urinary albumin (UAlb) of the rats were detected respectively before and every 2 weeks after modeling. The right kidney of rats in each group was removed and weighed after cardiac puncture. At the end of week 8 after drug-intervention, the rats were anesthetized and blood samples (2 ml) were drawn from the heart. Indices including serum creatinine (Scr), blood urea nitrogen (BUN), serum alanine transaminase (ALT) and serum aspartate transaminase (AST) were detected.

Renal histomorphometry

Periodic acid-Schiff (PAS) staining, Masson staining and electron microscopic assessment were performed as previously described (22). Cell numbers, ECM and collagen rates in the glomerulus were calculated with Image-Pro Plus 6.0 software (Media Cybernetics, Inc., Rockville, MD, USA). The results were confirmed by a professional pathologist.

Immunohistochemistry

Macrophages were detected in 4-µm thick paraffin-embedded renal sections. For immunostaining of macrophages, monoclonal anti-ED1 antibody (AbD Serotec, Oxford, UK) was used. Quantitative analysis of ED1+ cells was performed in a blinded fashion and expressed as cells/glomerular cross section (gcs). The results were also confirmed by the pathologist professional.

Semi-quantitative western blot analysis

Western blot analysis was performed as previously described (22). Renal tissues from the rats were isolated with phosphate-buffered saline (PBS) including protease inhibitors (PI) and sequentially solubilized with 1% Triton X-100, RIPA buffer (0.1% SDS, 1% sodium deoxycholate, 1% Triton X-100, 0.15 mol/l NaCl and 0.01 mol/l ethylenediaminetetraacetic acid (EDTA) in 0.025 mol/l Tris-HCl, pH 7.2) with PI, and separated into Triton X-100-soluble (T), RIPA-soluble (R) and RIPA-insoluble (S) fractions. The RIPAI-insoluble fraction was solubilized with SDS-PAGE sample buffer (2% SDS, 10% glycerol, and 5% 2-mercaproethanol in 0.0625 mol/l Tris-HCl, pH 6.8) (Sfractions). Equal amounts of theses equentially solubilized fractions were subjected to SDS-PAGE with 7.5 or 10% acrylamide gel, and transferred onto a PVDF membrane (Bio-Rad, Hercules, CA, USA) by electrophoretic trans-blotting for 30 min using Trans-Blot SD (Bio-Rad). After blocking with BSA, the strips of membrane were exposed to anti-p38 MAPK, p-p38 MAPK, IκB, p-IκB, NF-κB (p65), TGF-β1, TNF-α, IL-1β and GAPDH antibodies, respectively. They were washed and incubated with peroxidase-conjugated secondary antibodies for 1 h at room temperature. The bands were visualized by employing analkaline phosphatase chromogen kit (5-bromo-4-chloro-3-indolil phosphate p-toluidine salt/nitro blue tetrazolium; Biosynth AG, Staad, Switzerland). The density of the positive bands was quantitated by Densitograph (ATTO, Tokyo, Japan). This procedure was carried out 3 times. The ratio of the densitometric signal of the molecules examined to that of GAPDH was determined. Data are shown as ratios relative to control findings and expressed as mean ± SE. of 3 independent experiments.

Statistical analysis

The differences among groups were analyzed by one-way analysis of variance (ANOVA), and LSD method was used for multiple comparison. Qualitative data were analyzed using Fisher's exact test as indicated. P<0.05 was considered statistically significant.

Results

GTW improves the general condition and biochemical parameters of the rats, but does not lower BG

During the experiment, the rats in the vehicle group showed increased diet, water intake and urine volume, low activity, dull fur and BW loss at different degrees. BW of rats in the vehicle group increased slowly from week 2. After GTW-intervention, BW of rats in the GTW group increased gradually. At the end of week 6 and 8, BW of rats in the GTW group was obviously higher than that in the vehicle group, and the differences were statistically significant (Fig. 3A). After sacrifice, we found that renal appearance in the sham and sham + GTW groups was moderated and crimson, while the kidneys in the vehicle group were swollen and pale. The kidneys of rats treated with GTW were significantly ameliorated, with less swelling and ischemia (Fig. 3B). In addition, kidney weight (KW) of rats in the vehicle group was obviously higher than that in the sham group. While KW of rats in the GTW group declined, and the differences were statistically significant compared with the vehicle group, but they were still higher than that in the sham group (Fig. 3C).

Figure 3

Effects of Tripterygium wilfordii Hook. f. (GTW) on changes in (A) body weight (BW), (B) renal appearance and (C) kidney weight (KW) in the 4 groups: (a) the sham group, (b) the sham + GTW group, (c) the vehicle group and (d) the GTW group. Data are expressed as mean ± SE. **P<0.01 vs. the sham group; #P<0.05, ##P<0.01 vs. the vehicle group at every 2 weeks or week 8 after drug-intervention.

Next, we investigated the effects of GTW on BG and UAlb in the 4 rat groups. During the entire course, BG of rats in the sham and sham + GTW groups remained at low levels, while it increased in the rats of the vehicle group after two injections of STZ for 72 h, and remained at a high level (random BG, 20.3±1.72 mmol/l) by the consecutive intervention with Novolin N. Moreover, notably, BG of rats in the GTW group also remained high, and the differences were statistically significant compared with the sham group (Fig. 4A). The level of UAlb in each group was low before modeling, but rapidly increased 2 weeks after modeling, and constantly increased with the extension of time in the vehicle group. At the end of week 8, UAlb in the vehicle group reached an abnormal level (41.82±2.61 mg/l), which was significantly higher than that in the sham and sham + GTW groups. After GTW-intervention, the level of UAlb was significantly decreased in the GTW group at week 8, and the difference was statistically significant compared with the vehicle group (Fig. 4B).

Figure 4

Effects of Tripterygium wilfordii Hook. f. (GTW) on changes in (A) blood glucose (BG) and (B) urinary albumin (UAlb) in the 4 groups. Data are expressed as mean ± SE. **P<0.01 vs. the sham group; ##P<0.01 vs. the vehicle group at every 2 weeks.

Thirdly, we examined the effects of GTW on blood biochemical parameters including Scr, BUN, ALT and AST in the 4 rat groups. At the end of week 8 after GTW-intervention, serum ALT and AST in each group had no obvious changes, but Scr and BUN in the vehicle group were increased, and the differences were statistically significant respectively compared with the sham and sham + GTW groups. After GTW treatment, the levels of Scr and BUN were decreased, but the differences were not statistically significant compared with the vehicle group (Fig. 5).

Figure 5

Effects of Tripterygium wilfordii Hook. f. (GTW) on changes in (A) serum creatinine (Scr), (B) blood urea nitrogen (BUN), (C) serum alanine transaminase (ALT) and (D) serum aspartate transaminase (AST) in the 4 groups. Data are expressed as mean ± SE. **P<0.01 vs. the sham group; ##P<0.01 vs. the vehicle group at week 8 after drug-intervention.

GTW attenuates GS

We observed glomerular morphological changes by light microscopy in the 4 rat groups. In the sham and sham + GTW groups, glomerular capillary loops were well-opened and tubular epithelial cells were arranged in order. Mesangial tissues had hyperplasia in the vehicle group including glomerular mild-hypertrophy, capillary loop area reduction, glomerular cell proliferation, ECM expansion and collagen deposition. With GTW treatment, the injurious glomerular morphological changes were obviously attenuated. When compared with the sham group, cell numbers, rate of ECM and collagen area in glomerulus were significantly increased in the vehicle group respectively, but decreased in the GTW group. However, no significant differences in glomerular morphological changes were found between the sham and sham + GTW groups (Fig. 6A–E). We measured podocytic morphological characteristics and glomerular basement membrane (GBM) thickness by electron microscopy in the 4 rat groups. Unexpectedly, the injurious morphological changes in podocytes and GBM including foot process effacement and GBM thicking in the vehicle group were significantly alleviated in the GTW group (Fig. 6F).

Figure 6

Effects of Tripterygium wilfordii Hook. f. (GTW) on the glomerular morphological changes in the 4 groups. (A) Light microscopy, periodic acid-Schiff (PAS) (magnification, ×400). (B) Light microscopy, Masson staining (magnification, ×400). (C) The number of glomerular cells. (D) The rate of extracellular matrix (ECM)/glomerular area. (E) The rate of collagen/glomerular area. (F) Electron microscopy, ×1,700. The arrows in (F-c) indicate foot process effacement and glomerular basement membrane (GBM) thicking respectively. The arrows in (F-d) indicate the recovered foot process and GBM respectively. (a) Sham group, (b) sham + GTW group, (c) vehicle group and (d) GTW group. Data are expressed as mean ± SE. **P<0.01 vs. the sham group; ##P<0.01 vs. the vehicle group at week 8 after drug-intervention.

GTW suppresses glomerular microinflammation

We determined the number of ED1+ cells, a marker of total macrophages in glomeruli. By means of immunohistochemical staining, the number of ED1+ cells in glomeruli was increased notably in the vehicle group, while the number declined significantly in the GTW group (Fig. 7A and B). No obvious infiltrated macrophages in the glomeruli were detected in the sham and sham + GTW groups. We further investigated the protein expression of inflammatory cytokines in the kidney including TNF-α and IL-1β in 4 rat groups. Western blot analysis of renal tissues revealed that the protein expression of TNF-α and IL-1β was markedly upregulated in the vehicle group. Compared with the vehicle group, the protein overexpression of TNF-α and IL-1β in the kidney was significantly reduced in the GTW group (Fig. 7C–E).

Figure 7

Effects of Tripterygium wilfordii Hook. f. (GTW) on the infiltration of ED1+ cells in glomeruli and the protein expression of tumor necrosis factor (TNF)-α and interleukin (IL)-1β in the kidney in the 4 groups. (A and B) Immunohistochemical analysis and numbers of infiltrative ED1+ cells. (a) Sham group, (b) sham + GTW group, (c) vehicle group and (d) GTW group. (C–E) Western blot analysis and quantitative analysis of TNF-α and IL-1β protein expression. Data are expressed as mean ± SE. **P<0.01 vs. the sham group; #P<0.05, ##P<0.01 vs. the vehicle group at week 8 after drug-intervention.

GTW inhibits activation of p38 MAPK and canonical NF-κB signaling pathways in the kidney

Semi-quantitative western blot analysis showed that the expression level of p-p38 MAPK, p-IκB, NF-κB (p65) and TGF-β1 at the protein levels in the vehicle group was significantly higher than those in the sham group. Compared with the vehicle group, the protein overexpression of p-p38 MAPK, p-IκB, NF-κB (p65) and TGF-β1 was significantly reduced in the GTW group (Fig. 8).

Figure 8

Effects of Tripterygium wilfordii Hook. f. (GTW) on the protein expression of p-p38 mitogen-activated protein kinase (MAPK), p38 MAPK, p-IκB, IκB, nuclear factor (NF)-κB (p65) and transforming growth factor (TGF)-β1 in the kidney in the 4 rat groups. (A) Western blot analysis of p-p38 MAPK, p38 MAPK, p-IκB, IκB, NF-κB (p65) and TGF-β1 protein expression. (B–E) Quantitative analysis of p-p38 MAPK, p-IκB, NF-κB (p65) and TGF-β1 protein expression. Data are expressed as mean ± SE. *P<0.05 vs. the sham group; **P<0.01 vs. the sham group; ##P<0.01 vs. the vehicle group at week 8 after drug-intervention.

Discussion

In the present study, we demonstrated that GTW, a natural anti-inflammatory phytomedicine, can improve GS and glomerular microinflammation in vivo. Nevertheless, GTW had no effect on hyperglycemia in these DN model rats. To clarify the therapeutic effects of phytomedicines on renal damage related with diabetes in vivo, it is necessary to establish an appropriate animal model that simulates human DN patients. In this study, we used a modified DN rat model by unilateral nephrectomy combined with STZ intraperitoneal injections with low doses of 35 mg/kg BW at a 72-h interval. Our results showed that these DN model rats not only had stable hyperglycemia and a certain degree of UAlb, but also had typical GS characteristics. Therefore, we believed that this DN rat model was conducive to discovering novel therapeutic phytomedicines for human DN.

It has been reported that microinflammation plays a pivotal role in promoting glomerular injury in several studies of human and experimental DN induced by STZ injection (23). During microinflammation in renal parenchyma, macrophages can be attracted/activated directly by mechanical stress and may produce pro-inflammatory cytokines such as TNF-α, IL-1, IL-6 and IL-18, thus recruiting additional inflammatory cells that contribute to the propagation of inflammation and GS (24). Hence, to investigate whether the anti-microinflammatory effects of GTW could be related to the improvement of GS in vivo, we examined the number of infiltrated ED1+ cells in glomeruli, a marker of total macrophages, and the protein expression of TNF-α and IL-1β in the kidney, representative inflammatory cytokines, at the end of week 8 after two STZ injections in the GTW and vehicle groups, respectively. Our results showed that macrophage infiltration, affecting almost exclusively glomeruli, was evident at the end of week 8 after modeling in the vehicle group. Furthermore, the intensity of macrophage infiltration in glomeruli and the levels of inflammatory cytokine expression in the kidney were strongly correlated with the injurious characteristics of GS in these DN model rats. In addition to these, GTW suppressed glomerular microinflammation together with the amelioration of GS. Consequently, GTW, as an anti-inflammatory phytomedicine, can alleviate GS in vivo, which is possibly connected with anti-microinflammatory action.

To the best of our knowledge, the therapeutic action in DN animal models of various anti-inflammatory agents such as thiazolidinediones, 1,25-dihydroxyvitamin D3, cilostazol, curcumin (23) and Huangkui capsule (22) are directly related to controlling activation of intracellular signaling pathways associated with renal microinflammation, in which p38 MAPK, Janus kinase/signal transducers and activators of transcription (JAK/STAT) and NF-κB-dependent pathways occupy the key positions in DN at the early stage. Thus, we proposed that regulating the activation of p38 MAPK and/or canonical NF-κB pathways in this DN rat model are the successful means with which to identify anti-inflammatory mechanisms of GTW on attenuating GS in vivo. Our data clearly indicated that enhanced protein expression of p-p38 MAPK, p-IκB, NF-κB (p65) and TGF-β1 in the kidney were obviously detected in these DN model rats, concomitant with deterioration of GS induced by microinflammation. These results indicated that the p38 MAPK and canonical NF-κB pathways were activated in this DN rat model, and there is a strong causality between key signaling molecular overexpression and GS in vivo. More importantly, we also found that GTW simultaneously downregulated the protein overexpression of p-p38 MAPK, p-IκB, NF-κB (p65) and TGF-β1 in the kidney of these DN model rats. For these reasons, we suggest that GTW in vivo can attenuate GS by inhibiting p38 MAPK pathway activation and the release of NF-κB dimer p50/p65 in the canonical NF-κB pathway. Here, unfortunately, we could not assess whether GTW in vivo directly blocks the p38 MAPK signaling pathway based upon this DN rat model, without the signaling inhibitors. Further detailed analyses in vitro of p38 MAPK signaling molecules are needed to address this hypothesis.

Finally, we need to discuss three additional points. First, GTW, a natural anti-inflammatory phytomedicine, did not affect hyperglycemia in this DN rat model induced by STZ injection. We unavoidably think of the cause-and-effect of the relationship among hyperglycemia, microinflammation and GS. Some studies have shown that activation of the immune system and microinflammation are both involved in the pathogenesis of GS in DN and of course play an important role in vivo (25). Thus, we firmly believe that GTW has renoprotective action similar to other CKD models such as the anti-Thy1.1 glomerulonephritis rat model (26) and the adriamycin-induced GS rat model (27), completely independent of affecting hyperglycemia. Second, GTW has been proven clinically effective in suppressing microinflammation in various CKDs; however, its clinical application is often limited by side effects to the liver (28). To exclude the side effects of GTW on hepatic damage in this DN rat model, we compared the levels of serum ALT and AST in the 4 rat groups. Our results revealed that serum ALT and AST in the groups had no obvious changes, especially between the sham and sham + GTW groups (Fig. 5), thereby indicate that GTW at the suitable dose of 50 mg/kg BW daily had no negative effect on liver function in these DN model rats. Third, although GTW affected the activation of the p38 MAPK and canonical NF-κB pathways in vivo, we could not draw a clear conclusion regarding the key molecular mechanisms of p38 MAPK and NF-κB pathways in this DN rat model. It may be worth pursing whether p38 MAPK at the upstream controls NF-κB transcriptional activation both in vivo and in vitro since NF-κB is activated by a wide variety of stimuli such as cytokines, oxygen radicals, bacterial products and metabolic abnormalities, which are related with p38 MAPK activation (29). A diabetic knockout mouse (30) and a special test of NF-κB (p65) DNA-binding activity (31) in the kidney should be necessary in future studies to clarify this point.

In conclusion, in the present study, we demonstrated that GTW, as a natural regulator in vivo, alleviated GS without affecting hyperglycemia using modified DN model rats, by exerting anti-microinflammatory effects, including reducing macrophage infiltration in glomeruli, suppressing TNF-α, IL-1β and TGF-β1 overexpression in the kidney and inhibiting p38 MAPK and NF-κB signaling activities. To the best of our knowledge, the findings of this study provide the first evidence in vivo that GTW directly contributes to the prevention of DN by exerting anti-microinflammatory effects.