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Proinflammatory mediators are important in the pathogenesis of IBD, which are regulated by activation of NF-κB. The aim of this study was to investigate whether melatonin reduces inflammatory injury and inhibits proinflammatory molecule and NF-κB in rats with colitis. Rat colitis model was established by TNBS enema. NF-κB p65, TNF-α, ICAM-1, and IκBαin colon tissue were examined by immunohistochemistry, EMSA, RT-PCR, and Western blot analysis. Expression of proinflammatory molecule and activation of NF-κB were upregulated and IκB level decreased in rats with colitis. Melatonin reduces colonic inflammatory injury through downregulating proinflammatory molecule mediated by NF-κB inhibition and blockade of IκBα degradation.
Ulcerative colitis (UC), a major inflammatory bowel disease (IBD), is a chronic intestinal inflammatory disease which afflicts more and more people in China . Although exact etiology and pathogenesis remain obscure, there is substantial evidence that proinflammatory cytokines and adhesion molecules including tumor necrosis factor-α (TNF-α) and intercellular adhesion molecule-1 (ICAM-1) exhibit a key role in the inflammatory process [2, 3, 4]. And many studies have shown increased production of TNF-α and ICAM-1 in intertinal mucosa, serum, lamina propria mononuclear cells (LPMC), and peripheral blood mononuclear cells (PBMC) in patients with UC, which is thought to be an important factor in the pathophysiology of intestinal inflammation in UC [5, 6, 7]. At present, medical treatment of UC relies mainly on traditional drugs: aminosalicylates, corticosteroids, and immunosuppressants. These drugs including glucocorticoids and aminosalicylates reduce inflammatory injury and attenuate the expression of some proinflammatory molecules but their side effects and systemic action are so hard that they disturb the life quality of patients severely, particularly during long-term treatment. And so, it is very important to find an optimal therapy for UC.
Recent studies have unequivocally shown that the expressions of TNF-α and ICAM-1 are regulated by the transcription factor nuclear factor kappa B(NF-κB); NF-κB play a central role in immune and inflammatory responses and may be a good target for therapy [8, 9]. NF-κB is mostly composed of RelA (p65) and NF-κB1(p50); these NF-κB dimers are kept in an inactive cytoplasmic complex by inhibitory proteins, the inhibitor protein kappa B(IκB) family, in resting cells. NF-κB can be activated within minutes by a variety of stimuli, including inflammatory molecules such as TNF-α and IL-1, growth factors, bacterial lipopolysaccharide (LPS), and oxidative stress, which induce site-specific phosphorylation of IκB and consecutive rapid dissociation of the complex accompanied by proteolytic degradation of IκB. The released NF-κB proteins subsequently transmigrate from cytoplasm into the nucleus where they can induce gene transcription by binding to specific promoter elements [10, 11, 12]. Activated NF-κB has been demonstrated in colonic epithelial cells and macrophages of patients with IBD [13, 14], and also NF-κB p65 antisense oligonucleotide treatment was reported to have much benefit in experimental colitis, although toxicity effects must be carefully analyzed [15, 16]. The above data predict that NF-κB is a new and more effective therapy target.
Melatonin, mainly produced in the pineal gland, play an important physiological role in immunoregulation, inflammatory responses, and oxidative stress. Gastrointestinal tract is a rich source of extrapineal melatonin. And melatonin release may have a direct effect on many gastrointestinal tissues but may also well influence the digestive tract indirectly . Some previous data have shown that melatonin can alleviate colonic injury in experimental colitis induced by both dextran sulfate sodium and dinitrobenzene sulfonic acid in rats [18, 19], but the mechanism of action of exogenous melatonin against inflammatory injury is not apparent. These therapeutic effects of melatonin rely at least partially on immunomodulatory function, for example, inhibiting the action of macrophages in inflammatory tissues . Meanwhile, other studies have demonstrated that melatonin exerts an antioxidant and scavenger effect on free radicals to reduce the severity of colitis .
In this study we investigated if melatonin reduces inflammation in 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis through an inhibitory effect on proinflammatory molecule expression and the transcription factor NF-κB.
Healthy adult Sprague-Dawlay (SD) rats of both sexes, weighing 250 ± 30g, were obtained from the Experimental Animal Center of Wuhan University (Wuhan, China). Animals were housed under specific pathogen-free conditions and allowed access to standard rat chow and water. Before the experiments, they were acclimatized to the surroundings for one week. The study protocol was in accordance with the guidelines for animal research and was approved by the Ethical and Research Committee of the hospital.
Rat model of colitis induced with 2,4,6-trinitro- benzene sulfonic acid (TNBS, Sigma Co, Shanghai, China) enema was described in the literature . The experimental animals were randomly divided into six groups of 10 each: normal group, model group, 5-aminosalicylic acid(5-ASA) group, and melatonin treatment group that were treated with saline, TNBS/40% ethanol(150mg/kg), 5-aminosalicylic acid(100mg/kg), and melatonin (Sigma Co) at doses of 2.5, 5.0, 10.0mg/kg enema, respectively (once a day, from the 24hours after colitis was established to the end of experiment). At the end of a 4-week period, the animals were sacrificed and the colon samples were collected.
Colon tissues were fixed in 4% paraformaldehyde, dehydrated, and paraffin embedded. Four-micrometer sections were cut transversely and stained with hemotoxylin and eosin. Colon macroscopic and histological damage indices were evaluated by an independent pathologist blindly as reported previously [20, 22]. At the same time, colon samples from the same sites were also obtained and frozen immediately in liquid nitrogen for subsequent determination.
Sections of colon tissues were kept in an oven at 4°C overnight and were deparaffinized in xylene and rehydrated. Endogenous peroxidase activity was blocked with 1% hydrogen peroxide for 20minutes. And microwave oven-based antigen retrieval was performed. Slides were probed with either anti-RelA (1:50, rat monoclonal, Santa Cruz Biotechnology), anti-TNF-α (1:100, rat polyclonal, Santa Cruz Biotechnology), or anti-ICAM-1 (1:100, rat monoclonal, Santa Cruz Biotechnology). Sections were washed three times with PBS for 10minutes each and incubated with biotin-labeled antirat IgG for 1hour at room temperature, respectively. After three washes with PBS for 10minutes each, the slides were developed in 0.05% freshly prepared diaminobenzedine solution for several minutes and then counterstained with hematoxylin. Incubation with PBS instead of the primary antibody served as a negative control. In specimens containing positive cells, the positive cells were counted in ten randomly selected fields under high-power microscope (400-fold magnification) for each sample, and the average was expressed as the density of positive cells.
Nuclear protein extracts were prepared as described previously . Fresh colon samples were homogenized in 400μL of hypotonic lysis buffer A (10mmol/L HEPES pH 7.9, 10mmol/L KCl, 0.1mmol/L EDTA, 0.1mmol/L EGTA, 1mmol/L DTT, and 1mmol/L PMSF). Homogenized tissues were incubated on ice for 5minutes, NP-40 was added to a final concentration of 5g/L, and samples were vigorously mixed and centrifuged. The cytoplasmic proteins were removed and the pellet nuclei were resuspended in 50μL buffer C (20mmol/L HEPES pH 7.9, 0.4mol/L NaCl, 1mmol/L EDTA, 1mmol/L EGTA, 1mmol/L DTT, and 1mmol/L PMSF). After 30-minute agitation at 4°C, the samples were centrifuged and supernatants, containing nuclear proteins, were transferred to a fresh vial. The protein concentrations of nuclear extracts were determined by Bradford protein assay. Nuclear protein extracts of colon tissues were analyzed by EMSA for NF-κB nuclear translocation as previously described [23, 24]. EMSA binding reaction mixture contained 8μg protein of nuclear extracts, 2μg of poly (deoxyinosinic-deoxycytidylic acid) (Sigma Co), and [32P]-labeled double-stranded oligonucleotide containing the binding motif of NF-κB probe (4000cpm) in binding buffer (10mmol/L HEPES pH 7.9, 50mmol/L NaCl, 1mmol/L EDTA, 1mmol/L DTT, 100mL/L glycerol, and 0.2g/L albumin). The sequence of the double-stranded oligomer used for EMSA was 5′-AGTTGAGGGGACTTTCCCAGGC-3′. The reaction was incubated for 30minutes at room temperature before separation on a 50g/L acrylamide gel, followed by autoradiography. For supershift experiments, 2μg of rat monoclonal antibodies against the p65 subunit (Santa Cruz Biotechnology) of NF-κB was incubated with the nuclear extracts 10 minutes before the addition of the [32P]-labeled probe and then analyzed as described.
Colon samples were snap frozen in liquid nitrogen at the time of removal and later mechanically homogenized (20%w/v) in lysis buffer consisting of 20mM HEPES, pH 7.4, 0.1mM EDTA, 12.5mM MgCl2, 150mM NaCl, 0.1% Nonidet P40, 0.2mM phenylmethylsulfonyl fluoride, 1mM dithiothreitol, and 1μg/mL concentration of each of pepstatin, leupeptin, and aprotinin. The homogenates were transferred to Eppendorf tubes, sonicated for 10seconds and then centrifuged at 14 000rpm for 10minutes. Protein concentrations of samples were assessed using the method of Bradford protein assay, and all samples were adjusted to an equal protein content before analysis. Samples (20μg of total protein) were separated on a 12% denaturing polyacrylamide gel. Separated proteins were transferred to a nitrocellulose membrane (20V, 90minutes; transfer buffer 25mM Tris, 190mM glycine, 20% methanol, 0.5% sodium dodecyl sulfate) by an electroblotter (Bio-ram). The membrane was placed into blocking buffer (5% nonfat milk in 20mMTris/HCl, pH7.6, 140mM NaCl, 0.5% Tween 20) for one hour at room temperature. Blocking buffer was decanted and the membrane was incubated with the primary antibody anti-IκBα (1:500 diluted in blocking buffer, Sigma Co) on a shaker at 4°C overnight. After being washed (in 20mMTris/HCl, pH7.6, 140mM NaCl, 0.1% Tween 20), the membrane was incubated with a peroxidase-conjugated secondary antibody, which was diluted in 5% nonfat milk in wash buffer (one hour; room temperature; gentle shaking). Being washed, the membrane was exposed to sensitive film several minutes after incubation in Western blotting luminol reagent (Cell Signal Corp). The bands were quantified by densitometry.
The mRNA expressions of TNF-α and ICAM-1 were assessed using RT-PCR standardized by coamplifying housekeeping gene β-actin, which served as an internal control. Total RNA from colon tissues was isolated using trizol reagent (Sigma Co) by the single-step method and was reversely transcribed into cDNA. The resulting cDNA was used as a template for subsequent polymerase chain reaction (PCR). The rat-specific primers (sense and antisense primers) for TNF-α, ICAM-1, and β-actin were 5′-CATGATCCGAGATGTGGAACTGGC-3′ and 5′-CTGGCTCAGCCACTCCAGC-3′ (TNF-α, 315 bp); 5′-AGGTATCCATCCATCCCACA-3′ and 5′-AGTGTCTCATTCCCACGGA-3′ (ICAM-1388 bp); 5′-ATGGATGACGATATCGCTG-3′ and 5′-ATGAGGTAGTCTGTCAGGT-3′ (β-actin, 568 bp), respectively. Amplification was performed in 30 cycles with initial incubation at 95°C for 3minutes and final extension at 72°C for 7minutes, each cycle of which consisted of denaturation for 30seconds at 95°C, annealing for 45seconds at 55°C, and extension for 1minute at 72°C. PCR products were separated on 15g/L agarose gels containing 0.5g/L of ethidium bromide and visualized by UV transillumination. HPIAS-1000 software analysis system was used to determine the relative absorbance of mRNA expression.
Colon samples were weighed and homogenized in a solution prepared from the assay kit (Nanjing Jiancheng Bioengineering Co Ltd, China), and homogenates of 5% were obtained and used for MPO assay. MPO can catalyze the redox reaction of H2O2 and 3,3,5,5-tetramethylbenzidine and produce yellow-colored compounds through whose absorbance at 460nm MPO activity was calculated and expressed as U/g wet tissue. One unit of MPO activity was defined as the quantity of enzyme that degraded 1μmol H2O2 at 37°C per g wet tissue.
All statistical analyses were performed with SPSS10.0 statistical package from Microsoft Windows. Student t test and one-way analysis of variance (ANOVA) were used to compare continuous variables among groups. Data were finally expressed as mean ± standard error of the mean. P values less than .05 were considered statistically significant.
Pronounced pathological changes of colonic mucosa similar to that in human IBD were observed in rats with colitis induced by TNBS enema. Most animals inflicted with TNBS enema had disease limited to the rectum and rectosigmiod, some had disease extending beyond the sigmoid or had a total colitis. The mucosa was hyperemic, edematous, and granular, and some small punctate ulcers were visible. There was an inflammatory infiltrate of neutrophils, lymphocytes, and macrophages. Eosinophils and mast cells were also present in increased numbers. The colon mucosal macroscopic and histological injury indices, and MPO activity were significantly increased in these experimental animals compared with normal controls. Administration with melatonin enema at different dosages could effectively reduce the severity of mucosa injury and alleviate the colitis symptoms. And the parameter of mucosa injury was significantly decreased in a dose-dependent manner in rats treated by melatonin compared with that in model control animals (P < .01, Table 1).
The protein expressions of TNF-α and t ICAM-1 in colon tissues were significantly increased in rats inflicted with TNBS enema compared with those of the normal controls. The positive cells of TNF-α and ICAM-1 were with brown-yellow cytoplasma or nuclear membrane and predominantly located within the mucosa and mucosa lamina propria; positive staining of RelA was mainly observed in the cytoplasm, and nuclear staining for RelA was also detected (Figures (Figures1,1, ,2,2, and and3). RelA,3). RelA, TNF-α, and ICAM-1 protein expression decreased dose dependently in rats with melatonin treatment. Effect of 10mg/kg melatonin was similar to that of 5-aminosalicylic acid (100mg/kg). And similar results were obtained with NF-κB protein expression (Table 2).
RT-PCR analysis revealed increased mRNA levels for TNF-α and ICAM-1 in colon tissues of the model group; melatonin could reduce molecule mRNA expression dose dependently; 5-aminosalicylic acid reduced the expression of molecule mRNAs, too. These results are in accord with immunohistochemical analysis of molecule expression (Figure 4).
NF-κB-DNA binding activity was analyzed by EMSA analysis. Increased NF-κB DNA binding activity and the RelA/NF-κB complexes were detected in model animals. Supershift analysis with antibodies specific for RelA (p65) and a competitive study with a 50-fold excess of unlabeled oligonucleotide showed that the antibody specific for RelA which recognizes RelA/NF-κB heterodimer, unlabeled oligonucleotide diminished the intensity of RelA/NF-κB complexes and indicated that complex was the NF-κB binding-specific band. And the NF-κB-DNA binding activity was inhibited dose dependently when animals were treated with melatonin and 5-aminosalicylic acid; the inhibition effect of melatonin was most obvious at a concentration of 10mg/kg (Figure 5).
Western blot analysis of protein extracts of colon tissues showed that IκBα expression was weak in samples from rats without treatment, while it was stronger in the rats with melatonin and 5-aminosalicylic acid treatment. But there was no significant difference in the extent of IκBα expression in colon tissues of rats with melatonin treatment and normal controls (Figure 6).
The incidence and prevalence of IBD increase in China, and medical treatment of theirs is sometimes unsatisfactory at present. Our studies have demonstrated that melatonin given by intrarectal administration reduced rats colitis induced by TNBS and elucidated the molecule mechanism of melatonin inhibitory inflammatory responses in TNBS-induced colitis by inhibition of NF-κB activation firstly.
Ulcerative colitis is characterized by chronic inflammation of colon of unknown etiology, and infiltration and persistence of inflammatory cells within tissues are hallmarks of inflammation [25, 26, 27, 28]. Both TNF-α and ICAM-1 have been suggested to be important mediators involved in the initiation and perpetuation of intestinal inflammation in ulcerative colitis, and the activities of TNF-α and ICAM-1 are often used as sensitive indicators for evaluating the colitis severity [29, 30]. We confirmed that colon tissue obtained from rats with TNBS-induced colitis exhibited significantly more TNF-α and ICAM-1 expressions than normal controls, which supported the idea that proinflammatory molecules participate in the occurrence and development of ulcerative colitis. At the same time, we found that melatonin inhibited protein expression of TNF-α and ICAM-1 dose dependently. In addition, our results showed that melatonin could attenuate the colitis symptoms such as rectal bleeding and occult blood and reduce the frequency and severity of mucosa damage dramatically. These significant protective effects may be partly due to its effect on inhibition of expression of proinflammatory molecule including TNF-α and ICAM-1.
In order to elucidate the mechanism of action of melatonin on proinflammatory molecule, we investigated the mRNA expression of TNF-α and ICAM-1 in colon tissues of rats and determined the influence of melatonin treatment on proinflammatory molecule mRNA production. We found that the mRNA expressions were in accord with the results of immunohistochemistry detection; RT-PCR analysis revealed increased mRNA levels for TNF-α and ICAM-1 in colon tissues of the model group. Similarly, melatonin had a dose-dependent effect in decreasing mRNA expression of proinflammatory molecule. This prompted us to investigate the regulation of proinflammatory molecule gene transcription in the process of inflammatory responses. The important candidate is transcription factor NF-κB, which positively regulates the transcription of genes involved in immune and inflammatory responses.
Activation of NF-κB may be a pivotal event in proinflammatory signal transduction. Moreover, it has been shown that NF-κB activation is increased in the colonic mucosa of IBD patients [13, 14]. In most resting cells, transcription factor members of the Rel-NF-κB are bound to cytoplasmic inhibitory factors IκBs and are released on activation-induced degradation of their cytoplasmic inhibitors by the proteasome/ubiquitin complex [31, 32, 33]. NF-κB p65 hetero- or homodimers migrate to the nucleus and regulate transcriptional activity by binding to specific DNA sequences in promoter/enhancer regions of inflammation genes. Genes regulated by NF-κB include those encoding IL-2, IL-6, IL-8, the IL-2 receptor, the IL-12 P40 subunit, VCAM-1, ICAM-1, TNF-α, and so forth [8, 9, 31, 32, 33]. And studies have also shown that the ICAM-1 and TNF-α gene promoters have binding sites for NF-κB ; the heightened activation of NF-κB could be a major regulator of proinflammatory molecule secretion in IBD. We therefore investigated the effect of melatonin on transcription factor NF-κB and our results have shown that melatonin inhibited nuclear translocation of NF-κB and mRNA expression controlled by it in rats with TNBS-induced colitis. Translocation into the nucleus and binding to target DNA sequences are important events for NF-κB to control transcription process, which relies on phosphorylation of IκB, mediated by IκB kinases (IKK-α, β), followed by its degradation by the proteasome [8, 11]. We further determine if melatonin interferes with IκB levels by Western bolt experiments. We found that protein concentration of IκBα in rats treated with melatonin was higher compared with that in rats without treatment, which indicated that the inhibitory effect of melatonin on NF-κB activation was mediated by stabilization of IκBα levels. We also found that IκBα protein levels were not significantly different in colon tissues from rats with melatonin treatment and normal controls; this suggested that the effect of melatonin on IκBα was probably mainly due to blocking its degradation. Taken together, these data obtained in this study provide evidence that melatonin downregulates inflammatory responses through inhibition of NF-κB.
Previous studies have reported that glucocorticoids and salicylates inhibit the activation of NF-κB/Rel through IκB pathway; Weber et al  identified that sulfasalazine as a direct inhibitor of IKK-α and IKK-β blocks IκB degradation, then suppresses NF-κB activation, which contributes to the antiinflammatory and immunosuppressive effects in IBD. Other investigators  demonstrated that increased IκBα synthesis was present in glucocorticoid-treated patients with Crohn's disease and thus attenuated NF-κB activation. In our study, melatonin may stabilize IκBα against degradation, which is probably associated with IκBα phosphorylation, so it will be important and interesting to define in which step melatonin affects IκB degradation process, and this will be a focus of future investigations.
To date, medical treatment of UC is limited to aminosalicylates, corticosteroids, and immunosuppressants. Although a variety of new therapies have been tested with variable success, none is ideal [37, 38, 39]. In our experimental model of colitis, melatonin treatment reduced colonic lesions and improved colitis symptoms through suppressing NF-κB activation. In conclusion, because of its significant antiinflammatory properties, melatonin could be considered as the novel therapeutic alternative for the treatment of IBD. Further studies are needed to determine how melatonin combines with the established drugs such as sulfasalazine and corticosteroids in clinic.
The first author is employed in Xianning University now.