A total of 30 male C57BL6 mice (age, 8 weeks; weight, 18–20 g) were purchased from Wuhan University (Wuhan, China) and housed at the Experimental Animal Center of Wuhan University. The mice were maintained at 25°C under a 12-h light/dark cycle, with ad libitum access to food and water. The purified natural product AM was obtained from Shanghai Yuanye Biotechnology Co., Ltd. (Shanghai, China). In order to establish a murine model of UUO, the mice were anesthetized with 1.5 % sodium pentobarbital (50 mg/kg; Shanghai Haling Biological Technology Co., Ltd., Shanghai, China) and a left lateral incision was made on the back of the mice to expose the kidney. The left ureter was ligated with 4–0 silk sutures at the junction between the renal pelvis and ureter and the ligature position was consistent. Following completion, the incision was closed in layers. Sham-group mice received the same incision and closure procedures without ligation. UUO mice were treated by intraperitoneal injection of AM (100, 200, and 400 mg/kg/day) (n=6 per group). Mice in the sham were administered equal volumes of sterile saline (n=6 per group). Mice were sacrificed by cervical dislocation following anesthetization on day 7 post-surgery, and the obstructed kidneys were harvested. Kidney samples were fixed in 4% buffered paraformaldehyde (Guge Biotechnology Co., Ltd., Wuhan, China) and were subsequently embedded in paraffin (Guge Biotechnology Co., Ltd.) for histological and immunohistochemical examination. The remaining kidneys were snap-frozen in liquid nitrogen and stored at −80°C for protein extraction.

NRK-52E cells were obtained from Boster Bioengineering Co., Ltd. (Wuhan, China) and cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum (GE Healthcare Life Sciences, Logan, UT, USA) at 37°C in a humidified atmosphere containing 5% CO₂. A total of 1.5×10⁶ cells/ml cells were transferred to 6-well plates and were divided into the following five treatment groups: Control; 5 ng/ml TGF-β1 (R&D Systems, Minneapolis, MN, USA); 5 ng/ml TGF-β1 + 10 µg/ml AM; 5 ng/ml TGF-β1 + 20 µg/ml AM; and 5 ng/ml TGF-β1 + 40 µg/ml AM.

Kidney sections (5-µm) were prepared using a microtome (RM3225; Leica Geosystems, Milton Keynes, UK). The tissue sections were placed on slides, deparaffinized in xylene (Boster Bioengineering Co., Ltd.) and hydrated in graded ethanol prior to treatment with 3% hydrogen peroxide solution (Guge Biotechnology Co., Ltd.) for 15 min at room temperature. Following three washes with phosphate-buffered saline (PBS), the antigens were retrieved by boiling the tissue sections in Tris-ethylenediaminetetraacetic acid (EDTA) buffer (12.1 g Tris base; 3.7 g EDTA; 500 ml H₂O; Boster Bioengineering Co., Ltd.) for 15 min in a microwave oven on high power. Following cooling, the tissue sections were washed three times with PBS and incubated with the following primary antibodies at 37°C for 1 h: Mouse anti-α-SMA monoclonal antibody (1:100; BM0002; Boster Bioengineering Co., Ltd.), mouse anti-E-cadherin monoclonal antibody (1:50; 610181; BD Biosciences, Franklin Lakes, NJ, USA), rabbit anti-collagen I polyclonal antibody (1:200; BA0326; Boster Bioengineering Co., Ltd.), and rabbit anti-FN polyclonal antibody (1:200; ab2413; Abcam, Cambridge, UK). Subsequently, the tissue sections were washed three times with PBS and incubated with horseradish peroxidase (HRP)-conjugated goat anti-rabbit/mouse polyclonal secondary antibody (1:100; BA1003; Boster Bioengineering Co., Ltd.) for 10 min at 37°C. The sections were treated with 3,3′-diaminobenzidine (Beyotime Institute of Biotechnology, Shanghai, China) to develop a color reaction, and the reaction was subsequently terminated by washing twice with distilled water. The tissue sections were finally counterstained with hematoxylin (Guge Biotechnology Co., Ltd.).

Cells were fixed in 4% paraformaldehyde for 30 min at room temperature and subsequently permeabilized with 0.1% Triton X-100 (Boster Bioengineering Co., Ltd.) in PBS for 5 min prior to rinsing three times with PBS for 5 min. Following blocking in 5% bovine serum albumin (BSA; Guge Biotechnology Co., Ltd.) and 1% Triton X-100/PBS for 30 min at room temperature, the cells were incubated with primary antibodies targeting α-SMA (1:100), E-cadherin (1:50) and FN (1:200) overnight at 4°C. The cells were then cultured with cyanine 3-goat anti-mouse immunoglobulin G (IgG; 1:100; GB21303) and fluorescein isothiocyanate-goat anti-rabbit IgG (1:100; GB22303; both Boster Bioengineering Co., Ltd.) for 1 h. The cell nuclei were stained with 4′6′-diamino-2-phenylindole dihydrochloride (Beyotime Institute of Biotechnology).

Total RNA was isolated from renal cortex samples and NRK-52E cells using TRIzol^® reagent (Invitrogen; Thermo Fisher Scientific, Inc., Waltham, MA, USA), according to the manufacturer's protocol. RNA underwent purification with DNase (Qiagen, Inc., Valencia, CA, USA), after which the concentration of RNA was measured using a spectrophotometer (Nanodrop™ 2000; Thermo Fisher Scientific, Inc.) at 260 nm, and the purity was assessed by determining the absorbance ratio at A260/A280. Subsequently, RNA (20 µl) was reverse transcribed into cDNA using the RevertAid First Strand cDNA Synthesis kit (cat. no. K1622; Thermo Fisher Scientific, Inc.). qPCR was performed using the iQ SYBR Green Supermix reagent (Bio-Rad Laboratories, Inc., Hercules, CA, USA) and 7.5 µM each of forward and reverse primers on an T100 thermal cycler (Bio-Rad Laboratories, Inc.). Primer sequences for the renal cortex samples were as follows: E-cadherin forward, 5′-GTCAAACGGCATCTAAAGC-3′, and reverse, 5′-CAAAGACCTCCTGGATAAACT-3′; α-SMA, forward 5′-ACTGGGACGACATGGAAAAG-3′, and reverse, 5′-CATCTCCAGAGTCCAGCACA-3′; collagen I forward, 5′-GAGCGGAGAGTACTGGATCG-3′, and reverse, 5′-TACTCGAACGGGAATCCATC-3′; and FN forward, 5′-CCATTGCAAATCGCTGCCAT-3′, and reverse, 5′-AACATTTCTCAGCTATTGGCTT-3′. In the NRK-52E cells, the primer sequences were as follows: E-cadherin forward, 5′-AACGAGGGCATTCTGAAAACA-3′, and reverse, 5′-CACTGTCACGTGCAGAATGTACTG-3′; α-SMA forward, 5′-GACCCTGAAGTATCCGATAGAACA-3′, and reverse, 5′-CACGCGAAGCTCGTTATAGAAG-3′; and FN forward, 5′-CATGGCTTTAGGCGAACCA-3′, and reverse, 5′-CATCTACATTCGGCAGGTATGG-3′ (Sangon Biotech Co., Ltd., Shanghai, China). In both cases, GAPDH was used as the reference gene and had the following primer sequences: Forward 5′-AGTGGCAAAGTGGAGATT-3′ and reverse, 5′-GTGGAGTCATACTGGAACA-3′ (Sangon Biotech Co., Ltd.). The PCR cycling conditions were as follows: Predenaturation at 95°C for 10 min, 40 cycles at 95°C for 15 sec, 60°C for 1 min and 72°C for 20 sec, and a final extension at 60°C for 5 min. The specificity of the qPCR was confirmed by 1% agarose gel electrophoresis and melting curve analysis. The relative mRNA expression levels were determined using the 2^−ΔΔCq method (13).

Kidney and cell culture samples were resuspended in 0.4 ml sodium dodecyl sulfate (SDS) lysis buffer containing 50 mM Tris-HCl (pH 7.4), 150 mM NaCl, 0.1% SDS, 1% sodium deoxycholate, 1% Triton X-100, 1 mM phenylmethylsulfonyl fluoride, 1 mM EDTA and 5 µg/ml leupeptin (Beyotime Institute of Biotechnology). Protein concentration was determined using a BCA protein assay kit (cat. no. p0012s; Beyotime Institute of Biotechnology) and 30 µg total protein/well was subsequently loaded and separated by 10% SDS-polyacrylamide gel electrophoresis. The gels were electroblotted onto polyvinylidene difluoride membranes (EMD Millipore, Billerica, MA, USA) and blocked with 5% milk for 1 h prior to incubation with rabbit anti-Smad2/3 (1:1,000; sc-11769) and anti-TFG-β1 (1:1,000; sc-146) polyclonal antibodies (both Santa Cruz Biotechnology, Inc., Dallas, TX, USA), and rabbit anti-GAPDH monoclonal antibody (1:1,000; 5174; Cell Signaling Technology, Inc., Danvers, MA, USA), overnight at 4°C. Following washing three times with Tris-buffered saline containing Tween-20, the membranes were incubated with HRP-conjugated goat anti-rabbit/mouse polyclonal secondary antibody (1:100; G1201; Guge Biotechnology Co., Ltd.) for 1 h at room temperature. Bound antibodies were detected using an enhanced chemiluminescence system (RPN998; GE Healthcare Life Sciences, Chalfont, UK). Band signals were detected using an Odyssey Infrared Imaging system Model 9120 (LI-COR Biotechnology, Lincoln, NE, USA), and band intensities were analyzed using Quantity-One software (Bio-Rad Laboratories, Inc.). Relative protein expression levels were normalized to GAPDH and compared with a control.

SPSS 17.0 software (SPSS, Inc., Chicago, IL, USA) was used for statistical analysis. Data were analyzed using one-way analysis of variance and Fisher's least significant difference t-test was used for multiple comparisons of two sample means. Data were presented as the mean ± standard deviation. P<0.05 was considered to indicate a statistically significant difference.

The effects of AM on the expression levels of α-SMA, E-cadherin, and ECM were investigated during obstructive nephropathy, which is a well-characterized and widely-used model of renal interstitial fibrosis. Immunohistochemistry staining demonstrated that the protein expression of α-SMA, collagen I, and FN in the renal interstitium were significantly elevated in the mouse kidney following obstructive injury, whereas E-cadherin protein expression decreased. AM markedly reversed the changes in the expression levels of the markers (Fig. 1).

The mRNA expression levels of α-SMA significantly increased in the UUO group (P<0.05), whereas E-cadherin expression levels significantly decreased (P<0.05). As compared with the UUO group, downregulated α-SMA, collagen I, and FN mRNA expression levels were detected in the AM groups, whereas E-cadherin mRNA expression levels were upregulated. The difference between the AM and UUO groups was determined to be significant (P<0.05), and the three AM treatment groups were significantly different from the UUO group (P<0.05; Fig. 2). These data suggest that AM may be a potent agent for the reversal of renal tubular EMT in UUO mice.

Immunofluorescence analysis of the TGF-β1-stimulated NRK-52E cells demonstrated that the protein expression of α-SMA and FN increased, whereas E-cadherin protein expression decreased. AM administration markedly decreased α-SMA protein expression and increased E-cadherin protein expression (Fig. 3), in a dose-dependent manner; therefore, the greatest AM concentration (40 µg/ml) markedly inhibited these changes. These results were concordant with the RT-qPCR analysis, which demonstrated reduced α-SMA expression levels and increased E-cadherin expression levels following AM administration, as compared with the results following TGF-β1 treatment without AM intervention (P<0.05; Fig. 4).

Western blot analysis demonstrated that ureteral obstruction markedly increased the protein expression levels of TGF-β1 and the phosphorylation of Smad2/3 in the UUO group, as compared with the sham group (P<0.05; Fig. 5A and B). As compared with the UUO group, the AM treatment groups exhibited significantly reduced renal TGF-β1 and phosphorylated Smad2/3 expression levels (P<0.05). Furthermore, western blot analysis demonstrated that Smad2/3 protein expression levels were significantly increased in the TGF-β1-stimulated NRK-52E cells, as compared with the control group (P<0.05). Treatment with AM significantly downregulated p-Smad2/3 protein expression levels (Fig. 5C and D). These data suggested that AM may effectively inhibit the expression and phosphorylation of the Smad2/3 protein in NRK-52E cells.