Specific pathogen free, Balb/c female mice (age, 6–8 weeks) were provided by the Laboratory Animal Center of China Medical University (Shenyang, China). The mice were housed under standard conditions (25°C and 12-h light-dark cycle, 5 mice per 80 cm² cage) for at least one week prior to the start of the experiments. Throughout, the mice were fed with standard pellet diet ad libitum with the exception of when they were fasted for 24 h with free access to drinking for the colitis induction. The experimental settings involving mice were approved by the local authority for Animal Care and Use. The present study was performed in compliance with the animal welfare legislations of China Medical University (Shenyang, China). All efforts were made to minimize animals’ suffering and to reduce the number of animals used.

SM powder for injection (Lot no. 20090612; permission code of State Food and Drug Administration: Z10970093) was purchased from the Second Chinese Medicine Factory of Harbin Pharm Group Co. Ltd., (Harbin, China). It was extracted from 1,500 g dried root of SM with boiled distilled water and ethanol. Filtration and lyophilization were also used to obtain 40 g brownish powder. The dried powder contained 8% sodium Danshensu (C₉H₉O₅Na) and 16% protocatechuic aldehyde (C₇H₆O₃) determined by colorimetric methods (13). In total, 5% TNBS was purchased from Sigma-Aldrich Trading Co., Ltd. (Shanghai, China). A myeloperoxidase activity test kit was purchased from the Nanjing Jiancheng Bioengineering Institute (Nanjing, China). Rabbit anti-Foxp3 antibody was purchased from Santa Cruz Biotechnology Inc. (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA). UltraSensitve^™ S-P kit was purchased from Maixin-Bio. Co. Ltd. (Fuzhou, China). RNAsimple Total RNA kit, TIANScript RT kit and SYBR-Green mastermix were purchased from Tiangen Biotech. Co. Ltd. (Beijing, China).

Colitis was induced by intrarectal injection of TNBS as described previously (14,15). Briefly, subsequent to adaptively being housed for seven days, the mice were fasted for 24 h with free access to water. The mice were administered intrarectally with a single dose of TNBS 100 mg/kg (1% TNBS in 30% ethanol solution) subsequent to being anesthetized by 5% chloral hydrate [3 ml/kg, intraperitoneal (i.p.)]. The mice were held in a vertical position for 30 sec to ensure that TNBS was distributed evenly within the entire colon and cecum.

Mice with colitis were divided into five groups (n=5 per group) randomly. The drugs were administered by i.p injection daily following the induction of colitis. The drugs used for each group were as follows: Group A, none; group B, sterile normal saline 10 ml/kg; group C, 2% of 10 ml/kg SM normal saline (as 25 times for human); group D, 4% SM normal saline 10 ml/kg (as 50 times for human); and group E, 6% SM normal saline 10 ml/kg (as 75 times for human). The normal mice were also studied as group N when required.

The mice were sacrificed by 10% chloral hydrate (3 ml/kg; i.p.) seven days later following a colonic instillation of TNBS. The entire colon was dissected and the colon content was removed by gently rinsing with cold phosphate-buffered saline. Colon sections of ~0.5 cm were obtained from the distal, transversal and proximal segments of the colon. The colon specimens were fixed in 4% paraformaldehyde for 24 h and 5 μM paraffin-embedded sections were stained with hematoxylin and eosin for routine histological examination. The colon tissues for myeloperoxidase activity analysis were enclosed in sterile tubes and immediately frozen into liquid nitrogen. The specimens were stored at −80°C until the testing was performed. The myeloperoxidase activity assay was performed according to the manufacturer’s instructions of the test kit, as described in a previous study (16). Briefly, the colon tissue homogenate was mixed with reagents and incubated for the reactions. The absorbance of reaction products was measured at 460 nm (1 cm optical path). Myeloperoxidase activity was expressed in units/g of tissue. One unit corresponded to the activity required to degrade 1 μmol of hydrogen peroxide at 37°C.

The spleen specimens were packaged in RNase-free tubes and immediately placed in liquid nitrogen. The specimens were stored at −80°C for the analysis of Foxp3 mRNA by qPCR. The frozen spleen tissue was divided into three sections and the RNAsimple Total RNA kit was used for the extraction of the total RNA. All the procedures were conducted according to the instructions of the RNAsimple Total RNA kit. The RNA concentration was determined by ultraviolet spectroscopy and the integrity was assessed by denaturing agarose gel electrophoresis. The TIANScript RT kit was used for the reverse transcription of total RNA, 1.5 μg total RNA was transcribed into cDNA in a 14.5 μl reaction, containing 1 μl oligo (dT)₁₅, 1 μl random primers, 2 μl dNTP (2.5 mM each) and ddH₂O was added to make the volume up to 14.5 μl, and were incubated at 70°C for 5 min and 0°C for 2 min. The product was mixed with 4 μl 5X First-Strand Buffer (Tiangen Biotech. Co. Ltd.), 0.5 μl RNasin (Tiangen Biotech. Co. Ltd.) and 1 μl (200 U) TIANScript M-MLV (Tiangen Biotech. Co. Ltd.) and then incubated at 42°C for 50 min and 95°C for 5 min to give 20 μl cDNA. The product of 1 μl cDNA mixed with 0.5 μl forward and 0.5 μl reverse primers, 10 μl SYBR-Green mastermix and 8 μl ddH₂O were used for the real-time fluorescent qPCR in the Exicycler^™96 (Bioneer Corporation, Daejeon, Korea). An initial denaturation/activation step at 95°C for 10 min was followed by 40 cycles at 95°C for 10 sec, 60°C for 20 sec and 72°C for 30 sec and finally held at 4°C for 5 min. The primers used are shown in Table I.

Triplicates were run for each sample. The specificity of the amplification products was controlled by a melting curve analysis. The mean expression of Foxp3 mRNA was normalized with housekeeping gene β-actin in the same samples. The relative quantification was performed using the comparative threshold cycle (2^−ΔΔct) method (relative gene expression). The expression of Foxp3 mRNA measured in the normal mice was considered the unit value, and the results obtained were reported as the relative levels with respect to the unit value.

Spleen specimens were packaged in sterile tubes and immediately frozen in liquid nitrogen. The specimens were stored at −80°C for western blot analysis of Foxp3 protein. Briefly, the spleen tissue was lysed in ice-cold radio immunoprecipitation assay buffer [150 mM sodium chloride, 1.0% Triton X-100, 0.5% sodium deoxycholate, 0.1% sodium dodecyl sulphate, 50 mM Tris, (pH 8.0) and 1.0% henylmethylsulfonyl fluoride]. The quantity of protein was determined by a bicinchoninic acid assay (Boster Biological Technology Ltd., Wuhan, China) and 30 μg protein were loaded in each lane for electrophoresis. Following electrophoresis, proteins were transferred to a polyvinylidene difluoride membrane. The primary antibody was rabbit anti-Foxp3 (1:500 dilution) and sheep anti-rabbit IgG conjugated to horseradish peroxidase (Boster Biological Technology Ltd.) was used as the secondary antibody. The reactions were developed with the electrochemiluminescence solution (Boster Biological Technology Ltd.). Blots were stripped and analyzed for β-actin, as an internal loading control, using a rabbit anti-β-actin (1:5,000 dilution). The optical density of the bands was measured by Image-Pro Plus 6.0 (Media Cybernatics Manufacturing, Warrendale, PA, USA), the value obtained was reported as the relative level with respect to β-actin in the same sample, and the value obtained from the normal mouse was considered the unit value.

All the data are presented as the mean ± standard deviation and the differences between groups were analyzed with a parametric test (t test). Software SPSS version 13.0 (SPSS, Inc., Chicago, IL, USA) was used for the analysis when appropriate and P<0.05 was considered to indicate a statistically significant difference.

Mucosal erosion, ulceration, infiltration of inflammatory cells and granulomas were observed in the colon. The enteropathy of treated groups D and E was significantly relieved compared with groups A and B (Fig. 1).

Myeloperoxidase is an enzyme contained mainly in polymorphonuclear leucocytes, the myeloperoxidase activity is correlated with the number of inflammatory cells infiltrated in a given tissue (17). The myeloperoxidase activity in the treated groups C (3.16±0.32), D (2.65±0.24) and E (1.91±0.24 units/g) were significantly decreased compared with group A (3.80±0.39) and B (3.84±0.35 units/g). Furthermore, the activity in group N (1.37±0.15 units/g) was lower than in any other group. The difference was not significant between groups A and B (P>0.05, Fig. 2).

The relative levels of Foxp3 mRNA in treated groups C (1.75±0.05), D (1.96±0.06) and E (2.05±0.07) were increased significantly compared with groups A (1.57±0.07) and B (1.56±0.05). In addition, the difference was not significant between group A and B, but the levels in group N were lower than in any other group (P<0.05, Fig. 3).

The relative levels of Foxp3 optical density values in treated groups C, D and E were (1.95 ± 0.03), (2.13 ± 0.02) and (2.22 ± 0.08), respectively, which were increased significantly compared with group A (1.55 ± 0.02) and B (1.57 ± 0.04), but the difference was not significant between group A and B (Fig. 4 and 5).