Resveratrol alleviates intestinal mucosal barrier dysfunction in dextran sulfate sodium-induced colitis mice by enhancing autophagy

Hang-Hai Pan, Xin-Xin Zhou, Ying-Yu Ma, Wen-Sheng Pan, Fei Zhao, Mo-Sang Yu, Jing-Quan Liu

Abstract

Key words: Resveratrol; Ulcerative colitis; Autophagy; Intestinal mucosal barrier;Dextran sulfate sodium-induced colitis; Intestinal inflammation

INTRODUCTION

Inflammatory bowel disease (IBD) is a chronic intestinal inflammatory condition involving the gastrointestinal tract, comprising ulcerative colitis (UC) and Crohn’s disease. UC is characterized by abdominal pain, diarrhoea, and haematochezia. The incidence of UC is rising with changes in dietary habits and the rhythm of life[1,2]. UC is often persistent or recurrent in patients and increases the risk of colorectal cancer[3]. Currently, drugs such as 5-aminosalicylic acid (5-ASA), corticosteroids and immunosuppressants are used, but the effect of these drugs is poor, and the long-term use of these drugs may cause severe adverse reactions, resulting in great psychological and economic burdens on the patients[4,5]. Therefore, effective and safe drugs against UC are urgently needed.

The initiating event and pathogenesis of UC currently remain elusive. Recent work has highlighted the importance of intestinal mucosal barrier dysfunction in disease pathophysiology[6]. Many studies have shown that the destruction of the intestinal mucosal barrier plays an important role in the deterioration of IBD, especially in UC patients[7-9]. Protecting the integrity of the intestinal mucosal barrier is thought to be a potential clinical treatment approach for UC.

Resveratrol (3,4′,5-Trihydroxy-trans-stilbene), a natural plant polyphenol found in grapes, is the principal biologically active component in red wine. Resveratrol has antiinflammatory and immunoregulatory functions, with the advantages of low price and few side effects[10-12]. So far, very few clinical studies have indicated that resveratrol can alleviate clinical colitis activity and improve quality of life and in patients with active UC[13,14]. Although these limited studies show that resveratrol may ameliorate inflammation in UC, the mechanism remains unclear. Intestinal epithelial cells (IECs) are reported to act as the first line of defence in the intestinal mucosal barrier. The IECs tight junctions may play an important role in intestinal mucosal barrier. Occludin and ZO-1 are important tight junction proteins that play a significant role in maintaining the integrity of the intestinal mucosal barrier. Thus, we focused on whether resveratrol can alleviate intestinal mucosal barrier injury and inflammation. In addition, the mechanism underlying the anti-inflammatory effect of resveratrol in colitis was explored.

Autophagy is a cellular recycling process involving self-degradation and the reconstruction of damaged organelles and proteins[15]. Recent studies have shown that impaired autophagy is related to intestinal mucosal damage in mice with colitis, and stimulation of autophagy can prevent intestinal mucosal inflammation and ameliorates murine colitis in mice[16]. Furthermore, the regulatory effect of resveratrol on autophagy in inflammatory diseases has gradually attracted attention[17,18]. In the present study, we evaluated the effect of resveratrol on dextran sulfate sodium (DSS)-induced colitis in mice and explore the mechanism of resveratrol on protecting the integrity of the intestinal mucosal barrier and anti-inflammation.

MATERIALS AND METHODS

Chemicals and reagents

Resveratrol (3,4′,5-Trihydroxy-trans-stilbene; C14H12O3; Molecular Weight: 228.24 g/moL; Figure 1A) and 5-Aminosalicylic acid (5-ASA; C7H7NO3; Molecular Weight: 153.14 g/moL; Figure 1B) were purchased from Sigma Chemical (United States). The purity was checkedviaHPLC analysis and exceeded 99%. Dextran Sulfate Sodium (DSS, Molecular Weight: 36000-50000) was purchased from MP Biomedicals (United States).

Animals

Male C57BL/6 mice aged 5 wk and weighing 17-19 g were purchased from Shanghai SLAC Laboratory Animal Co., Ltd. Animals were housed in mouse cages at a controlled temperature (21 ± 2 °C) with a pre-set 12-h light/dark cycle. The mice were fed a standard laboratory diet and normal drinking water. The normal diet included crude proteins ≥ 20%, crude fat ≥ 6%, crude fibre ≤ 5%, crude ash ≤ 8%, lysine 1.32%, calcium 1%-1.8%, and phosphorus 0.6%-1.2%, respectively. The animals were acclimated to the experimental conditions for one week before the experiment. According to the guidelines for the care and use of laboratory animals, all the procedures for the treatment and execution of mice were approved by the Animal Care and Use Committee of Zhejiang Chinese Medical University.

Experimental design

DSS-induced colitis is a widely used model that morphologically and symptomatically resembles UC in humans. In this study, we established DSS-induced chronic colitis model to study UC. Mice were randomly divided into four experimental groups (n= 12 mice/group): Negative control group, DSS model group, resveratrol-treated group and 5-ASA positive-control group. Mice in the negative control group received normal drinking water for 28 d. In the DSS model group, chronic colitis was induced by two cycles of giving drinking water containing 3% DSS for 7 d and normal drinking water for 7 d. Resveratrol treatment group (DSS + RES) mice received two cycles of DSS by drinking water, and treatment of resveratrol 100 mg/kg per day by gavage for two cycles followed by DSS at the same time (Figure 1C). 5-ASA, the first-line therapy for UC, was used as a positive control to evaluate the efficacy of resveratrol. Mice in the positive-control group (DSS + 5-ASA) were treated with two cycles of DSS, and 5-ASA 200 mg/kg per day for 28 d at the same time. Body mass was detected every 5 d, and body mass loss was calculated as (detected body mass-initial mass) /initial mass. All animals were euthanized with carbon dioxide and sacrificed at humane end points.

Figure 1 Chemical structures of resveratrol and 5-aminosalicylic acid, and timeline of in vivo experiment. A: The chemical structures of resveratrol; B: The chemical structures of 5-aminosalicylic acid; and C: Timeline of in vivo experiment. Dextran sulfate sodium (DSS) group was induced by two cycles of intake of drinking water containing 3% DSS for 7 d and normal drinking water for 7 d. Other groups were also treated by two cycles, first received DSS by drinking water for 7 d, followed by treatment of 5-aminosalicylic acid or resveratrol by gavage for 7 d. DSS: Dextran sulfate sodium; 5-ASA: 5-aminosalicylic acid; RES: Resveratrol.

Clinical evaluation of colitis

To assess the severity of colitis, the disease activity index (DAI) was calculated daily based on weight loss, stool consistency and rectal bleeding (Table 1)[19]. Stool consistency (0, normal; 2, loose stool; 4, watery diarrhea); bloody stools (0, normal; 2, slight bleeding; 4, gross bleeding); and body weight loss (0, < 2%; 1, decreased ≥ 2 - < 5%; 2, decreased ≥ 5 - < 10%; 3, decreased ≥ 10 - < 15%; 4, decreased ≥ 15). These values were assessed for each animal, and the sum of the 3 values constituted the DAI. For each parameter, the scores ranged from 0 to 4, resulting in a total DAI score ranging from 0 (unaffected) to 12 (severe colitis).

Inflammatory cytokine assay

Mice were sacrificed, and blood samples (1.0 mL) were collected from the heart. The expression levels of tumour necrosis factor-α (TNF-α, MTA00B, R&D Systems Europe Ltd., Abingdon, England), interleukin (IL)-6 (M6000B, R&D Systems Europe Ltd., Abingdon, England ), and IL-1β (MLB00C, RD Systems Europe Ltd., Abingdon, England) in the plasma were detected using the enzyme-linked immunosorbent assay kits according to the manufacturer’s instructions. The concentration of the cytokines was expressed as pg/mL per mg protein.

Histopathological analysis

Colon length can be used as an indirect marker of inflammation. Thus, when mice were sacrificed, the length of colons from the caecum to the anus was measured. Then, the colon was fixed in 10% formalin, dehydrated at gradient concentrations of ethanol, and embedded in paraffin. Tissue sections (8 µm) were prepared and stained with haematoxylin and eosin (HE), and mucosal damage was evaluated. To evaluate the colonic mucosal damage severity, 9 fields were randomly selected and observed under an inverted fluorescence microscope by two pathologists who were blinded to the experimental groups. Colonic mucosal damage was confirmed by the mean histological score (Table 2)[20]. Each histological score, such as inflammation (0-3), extent (0-3), regeneration (0-4) and crypt damage (0-4), was multiplied by the percentage of compromised tissue (1 point for 25%, 2 points for 26%-50%, 3 points for 51%-75%, and 4 points for 76%-100%). Therefore, the scores of inflammation and extent range from 0 to 12, and the scores of regeneration and crypt damage range from 0 to 16, which reached a maximum score of 56.

Table 1 Assessment of the disease activity index

Table 2 Histological scoring of colitis

Immunohistochemical analysis

The expression of occludin and ZO-1 was detected by immunohistochemical analysis. Briefly, all blocks of colonic tissue were sectioned (3-5 µm). Then, sections were deparaffinized, rehydrated at graded ethanol concentrations and incubated with fresh 3% hydrogen peroxide for 10 min. After being rinsed with phosphate buffer saline (PBS), each tissue section was subjected to antigen retrieval by a suitable antigen retrieval method (boiling in 0.01 M citrate buffer). After endogenous peroxidases were blocked, sections were incubated with anti-occludin antibody (ab222691, 1:200 dilution in PBS, Abcam, United States) and a monoclonal ZO-1 antibody (ab221546, 1:300, Abcam, United States) overnight at 4°C. Subsequently, the sections were incubated for 20 min at room temperature with biotin-labelled secondary antibodies, stained with 3,3-diaminobenzidine, counterstained with haematoxylin, dehydrated and mounted. Primary antibody was replaced by PBS as the negative control. The following criterion was used for semi-quantitative staining: 0 (no staining), 1 (weak staining, light yellow), 2 (moderate staining, yellow brown), and 3 (strong staining, brown). The proportion of stained tumor cells was scored according to the proportion of positively stained tumor cells as follows: 0 (< 5%); 1 (6-25%); 2 (26-50%); and 3 (> 51%). A composite score was obtained by the staining intensity score multiplied the proportion scores. The total score ≤ 4 was defined as low expression, and > 5 was regarded as high expression.

Western blotting analysis

Briefly, proteins were extracted using radioimmunoprecipitation assay buffer, separated by sodium dodecyl sulphate-polyacrylamide gel (5%-10%) electrophoresis, and then transferred to polyvinylidene difluoride membranes (Millipore, Billerica, MA, United States). These membranes were washed with PBS and blocked with Trisbuffered saline-Tween with 5% skim milk (232100, BD, Bioscience, United States). Primary β-actin (3700S, 1:1000, Cell Signal Technology, United States), LC3B (3868T, 1:1000, Cell Signal Technology, United States) and Beclin-1 (3495T, 1:1000, Cell Signal Technology, United States) antibodies were applied, followed by horseradish peroxidase-conjugated secondary antibodies. Then, an enhanced chemiluminescence detection system (Thermo Fisher Scientific, United States) was used to detect antibody binding. Meanwhile, β-actin was used as a negative control.

Reverse transcription-polymerase chain reaction analysis

Total ribonucleic acid was extracted from tissue specimens using TRIzol reagent, and messenger ribonucleic acid (mRNA) was reverse transcribed to complementary deoxyribonucleic acid with a QuantiTect reverse transcription kit (205311, Qiagen, German) according to the manufacturer’s instructions. Quantitative polymerase chain reaction (qPCR) was performed using a SuperScript III Platinum SYBR green one-step qPCR kit (11732088, Thermo Fisher). The qPCR primer sequences were as follows: actin: 5’-CAT CCG TAA AGA CCT CTA TGC CAA C-3’ (forward) and 5’-ATG GAG CCA CCG ATC CAC A-3’ (reverse); Beclin: 5’-ATG GAG GGG TCT AAG GCG TC-3’ (forward) and 5’-TGG GCT GTG GTA AGT AAT GGA-3’ (reverse); LC3B: 5’-TCA AGT CCA ACT ACC GAG TCC-3’ (forward) and 5’-TCA GAG GTT TCC CAT CCA AG-3’ (reverse). Relative messenger ribonucleic acid expression levels were calculated based on the computerized tomography values and normalized using actin expression. All experiments were performed in triplicate on a Roche LightCycler 480 platform.

Transmission electron microscopy

First, colon tissues were fixed with glutaraldehyde and osmium teroxid, then dehydrated in ethanol, passed through propylene oxide, and embedded in Spurr resin. Fifty nanometres thick sections were cut by an ultramicrotome, and the sections were subsequently post-stained with 4% uranyl acetate for 10 min and Reynold's lead citrate for 1.5 min. The structure of the IECs and autolysosomes were observed by transmission electron microscopy (HITACHI H-7650).

Statistical analysis

All statistical analyses were performed using Statistical Package for the Social Sciences software (version 13.0; Statistic Package for Social Science Inc., Chicago, IL, United States). Continuous variables were presented as the mean and standard deviation and analysed using one-way Anova or Kruskal-Wallis test. All values were expressed as the mean ± standard deviation. All statistical analyses were conducted with α = 0.05, andP< 0.05 was considered significant.

RESULTS

Clinical activity of DSS-induced colitis mice

DSS-induced colitis was evaluated, and the clinical course was monitored and scored for the presence of bloody stool, watery diarrhoea and weight loss. During this experiment, three mice in the DSS group died, and one of the mice died on the 13thday, and the other two died on the 14thday; one mouse in the DSS + 5-ASA group died on the 13thday, and no mice in the DSS + RES group died. In comparison with those in the negative control group, mice in the DSS group showed progressively increased DAI score. However, the DSS + RES group showed 1.72-fold decrease in DAI score compared with the DSS group (P< 0.05, Figure 2A), which indicated that resveratrol may have a favourable effect on colitis.

Figure 2 Clinical evaluation of dextran sulfate sodium-induced chronic colitis by disease activity index, body mass loss and colon length (n = 12 for the control group, n = 9 for disease activity index group, n = 11 for dextran sulfate sodium + 5-aminosalicylic acid group, n = 12 for dextran sulfate sodium + resveratrol treatment group). A: The disease activity index score was reduced in the resveratrol treated group compared with the dextran sulfate sodium group (aP < 0.05); B and C: Resveratrol treatment increased the body mass and colon length of dextran sulfate sodium-induced colitis mice. Body mass loss was calculated as (detected body mass - initial mass)/initial mass. DSS: Dextran sulfate sodium; 5-ASA: 5-aminosalicylic acid; RES: Resveratrol.

Effects of resveratrol on body mass and colon length in DSS-induced colitis mice

Body mass could be decreased by DSS-induced inflammation; therefore, we studied the effect of resveratrol on body mass in DSS-induced colitis mice. The body mass was measured every 5 d, and the results showed that DSS-treated mice exhibited a statistically significant decrease. Resveratrol and 5-ASA treatment increased the body mass of DSS-induced colitis mice, but the difference was not significant (Figure 2B). We also measured the colon length of DSS-induced colitis mice and found that the colon length of the resveratrol-treated group was longer than that of the DSS group, but the difference was also not significant (Figure 2C).

Resveratrol ameliorates the production of inflammatory cytokines in DSS-induced colitis mice

The enzyme-linked immunosorbent assay results demonstrated that the protein expression levels of the inflammatory cytokines TNF-α, IL-6, and IL-1β were higher in the DSS-induced colitis group than in the control group (P< 0.05, Figure 3). Furthermore, the levels of TNF-α and IL-6 in the 5-ASA-treatment group were lower than those in the DSS-induced colitis group (P< 0.05). However, the levels of TNF-α, IL-6 and IL-1β showed 1.42, 3.81, and 1.65-fold decrease in the resveratrol group compared with the DSS group (P< 0.05), and level of IL-1β also showed a 1.57-fold decrease in the resveratrol group compared with that in the DSS + 5-ASA group (P< 0.05).

Figure 3 Inflammatory cytokine expression in the dextran sulfate sodium-induced chronic colitis determined by enzyme-linked immunosorbent assay. The levels of interleukin-1β, interleukin-6 and tumor necrosis factor-α were decreased in the resveratrol treatment group compared with the dextran sulfate sodium group. aP < 0.05. TNF: Tumor necrosis factor; DSS: Dextran sulfate sodium; 5-ASA: 5-aminosalicylic acid; RES: Resveratrol.

Resveratrol alleviates intestinal mucosal barrier injury in DSS-induced colitis mice as determined by histopathology

We also assessed colon damage by histologic examination. DSS group showed significant colonic mucosal damages, crypt depletion, infiltration of inflammatory cells into the mucosa and submucosa, loss of epithelial barrier. The colon damage and intestinal inflammation in mice treated with resveratrol and 5-ASA were less severe than that in DSS-induced colitis mice (Figure 4A). Consistent with the histologic damage, the histological scores of colitis mice treated with resveratrol were significantly lower than those of DSS-induced colitis mice (P< 0.05, Figure 4B), while the histological scores of 5-ASA-treated colitis mice were not significantly different from those of mice in the DSS group. These results indicate that resveratrol may alleviate intestinal mucosal barrier dysfunction in DSS-induced colitis mice more effectively than 5-ASA.

Resveratrol increases the production of ZO-1 and occludin in the colons of DSStreated mice

The tight junction proteins occludin and ZO-1 have been reported to play an important role in maintaining the integrity of the intestinal mucosal epithelial barrier. In the present study, we found that the expression levels of occludin and ZO-1 were higher in the resveratrol-treated DSS group than in the 5-ASA and DSS groups (Figure 5 and Table 3).

Table 3 ZO-1 and occludin expressions in colitis

Resveratrol may reduce inflammation by the enhancement of autophagy in DSSinduced colitis

To explore whether the inhibition of colitis by resveratrol treatment is mediated by autophagy activation, we examined the mRNA and protein levels of LC3B and Beclin-1. As determined by real-time PCR, a substantial increase in the mRNA expression level of LC3B and Beclin-1 was observed in the DSS + RES group compared with the DSS group, suggesting that resveratrol increases the mRNA levels of LC3B and Beclin-1 in the colons of DSS-treated mice (P< 0.05, Figure 6A). Consistent with the mRNA level analysis, the western blot results also showed that resveratrol treatment induced significant increases in the LC3-II/I ratio and Beclin-1 level in DSS-induced colitis mice (P< 0.05, Figure 6B and C). However, the difference in the mRNA levels of LC3B and Beclin-1 was not significant between the 5-ASA-treated colitis group and the DSS group (P> 0.05).

The transmission electron microscopy results showed that IECs in the control group had normal organelle structure with a normal endoplasmic reticulum and mitochondria (Figure 7A). However, in the DSS-induced colitis group, the organelle structure was markedly damaged, with swollen mitochondria, disrupted mitochondrial inner ridges and dilated rough endoplasmic reticulum (Figure 7B). Inflammation induced by the 5-ASA treatment and autophagosomes were rare (Figure 7C). Additionally, resveratrol administration increased the number of autophagosomes and improved the condition of the endoplasmic reticulum and mitochondria, which indicated that resveratrol promoted the progression of autophagy (Figure 7D).

DISCUSSION

UC is a recurrent chronic inflammation of the colon. DSS-induced colitis models, including acute and chronic colitis models, are most commonly used in UC. Acute colitis model is usually induced by administering DSS for 7 d. In this study, a chronic colitis model was successfully established by the administration of two cycles of DSS treatment. Each cycle involved the administration of 3% DSS for 7 d followed by normal drinking water for 7 d[21]. Mice in the chronic colitis group developed clinical symptoms, such as bloody stool and weight loss; the mice also showed pathological features similar to UC patients, such as shortened colon length, intestinal mucosa congestion, oedema and erosion, ulceration, crypt damage, and the infiltration of inflammatory cells into the mucosa and submucosa; the histological scores of colitis and serum inflammation indices (TNF-α, IL-6, IL-1β) in the DSS group increased. The chronic colitis model induced by administering repeated cycles of DSS more closely resembled human UC than the acute colitis model did.

Figure 4 Histological staining showed colitis induced dysfunction. A: Dextran sulfate sodium group showed significant colonic mucosal damages, crypt depletion, infiltration of inflammatory cells into the mucosa and submucosa, loss of epithelial barrier. Resveratrol treatment group and 5-aminosalicylic acid could alleviate colitis-induced intestinal mucosal barrier dysfunction; and B: The histological score of resveratrol treatment group was lower than the dextran sulfate sodium group. aP < 0.05. DSS: Dextran sulfate sodium; 5-ASA: 5-aminosalicylic acid; RES: Resveratrol.

In recent years, the role of intestinal mucosal barrier dysfunction in the pathogenesis of UC has attracted wide attention. IECs are the first-line defence in the intestinal mucosal barrier[22]. The IECs tight junctions are key epithelial intracellular junctions[23,24]. Occludin and ZO-1 are important tight junction proteins that play a significant role in maintaining the integrity of the intestinal mucosal barrier. The integrity of the intestinal mucosal barrier prevents and defends against the invasion of inflammatory factors and bacteria and further mitigates intestinal inflammation. Resveratrol is a well-known phytophenol with pleiotropic properties and has antioxidative and anti-inflammatory activity. Recently, resveratrol has also been shown to alleviate intestinal inflammation[25-27]. Consistent with these studies, our results also showed that resveratrol can reduce intestinal inflammation and alleviate intestinal mucosal barrier dysfunction in DSS-induced colitis mice. Resveratrol significantly increased levels of tight junction proteins (occludin and ZO-1) and reduced histological colonic mucosa injury scores, even than 5-ASA did. Resveratrol also decreased serum inflammation indices (TNF-α, IL-6, and IL-1β), although there was no significant difference between resveratrol and 5-ASA treatment. These results showed that both resveratrol and 5-ASA alleviated intestinal inflammation, and resveratrol performed better at maintaining the integrity of the intestinal mucosal epithelial barrier than 5-ASA.

Figure 5 Immunohistochemical staining of ZO-1 and occludin. Expressions of ZO-1 and occludin were higher in resveratrol treatment than in the dextran sulfate sodium group and 5-aminosalicylic acid treated group. Negative control: antibody was replaced by phosphate buffer saline. DSS: Dextran sulfate sodium; 5-ASA: 5-aminosalicylic acid; RES: Resveratrol.

Autophagy is a cellular self-protective mechanism stimulated by both internal and external adverse environmental factors. In this process, degenerated proteins, aged and damaged organelles, even pathogenic microorganisms, are recycledviaautophagic degradation to maintain cellular metabolic balance and homeostasis[15,28,29]. Autophagy can be activated when an organ is stimulated by adverse factors. Saito M and others found a reduced LC3-II/I ratio, expression of adhesion proteins and IECs adhesion, and a damaged mucosal epithelial barrier when IECs were exposed to TNFα and treated with autophagy inhibitors[30]. In this study, we found that resveratrol alleviated the intestinal mucosal barrier dysfunction and reduced the intestinal inflammatory response by enhancing autophagy in experimental chronic colitis(two cycles of DSS treatment for 28 d), as the expression of LC3B and Beclin-1, and the number of autophagosomes in resveratrol-treated group were increased when compared to that in the chronic colitis model group and the negative control group.

A previous study conducted by Zhanget al[31]reported that DSS-inducing increased the autophagy in acute colitis models(DSS treatment for 7 d), and curcumin and resveratrol could protect against colitis by reducing autophagy rather than enhancing autophagy[31]. We speculated that this inconsistency may be caused by the different colitis models used in the two studies. The acute colitis model resembles the early stage of human UC, while the chronic colitis model resembles the advanced stage of UC. Our previous study showed that autophagy was dynamic in the progression of colitis. It was activated in IECs by inflammatory factors in the early stage of a rat model of sepsis-induced acute colitis,and decreased as the disease progressed, thereby reducing the removal of oxidative stress products and the damaged organelles and other substances in cells, which lead to the destruction of the intestinal mucosal barrier and the aggravation of intestinal inflammation[32]. We believe that the chronic colitis mouse model is a better tool to explore the pathogenesis and drug effects of ulcerative colitis.

However, there are still many limitations in the present study. The detailed autophagy involved in resveratrol-induced protection of intestinal mucosal barrier was unclear as we did not study the effect of autophagy inhibitors on colitis treated by resveratrol. On the other hand, we only investigated the effect of resveratrol on animals, therefore, further research is still needed for clinical application.

Figure 6 Expression levels of Beclin-1 and LC3B in dextran sulfate sodium induced chronic colitis. A: A substantial increase in the messenger ribonucleic acid expression level of LC3B and Beclin-1 was observed in the dextran sulfate sodium (DSS) + resveratrol treatment group compared with the DSS group (P < 0.05); B and C: The Western blotting showed that resveratrol treatment induced significant increases in the LC3-II/I ratio and Beclin-1 level in DSS-induced colitis mice; Mean grey level of Beclin-1 and LC3B protein level was increased in DSS + resveratrol treatment group. aP < 0.05. DSS: Dextran sulfate sodium; 5-ASA: 5-aminosalicylic acid; mRNA: Messenger ribonucleic acid; RES: Resveratrol.

Figure 7 Structures of the intestinal epithelial cells and autolysosomes observed by transmission electron microscopy. A: Control group showed normal organelle structure; B: Dextran sulfate sodium induced colitis group showed mitochondrial swelling and ruptures of internal cristae, along with distention of the rough endoplasmic reticulum; C: 5-aminosalicylic acid group revealed that mitochondrial swelling was not obvious, and mitochondrial cristae showed blurred appearance; and D: Resveratrol treatment group showed that organelle structure was basically normal, and autophagosome could be observed. ER: Endoplasmic reticulum, M: Mitochondria.

ARTICLE HIGHLIGHTS

Research conclusions

Resveratrol treatment reduces the expression of inflammatory factors, increases the expression of tight junction proteins and alleviates UC intestinal mucosal barrier dysfunction; this effect is achievedviathe regulation of autophagy in intestinal epithelial cells.

Research perspectives

This work suggests that resveratrol may be useful as a new approach to treat UC by enhancing autophagy. Further study of the functionary mechanism will help us to understand the role of resveratrol in colitis and provide a theoretical basis for future clinical application.