BACKGROUND Luminal anionic sulphide may contribute to epithelial damage in ulcerative colitis. Thiol methyltransferase (TMT) governs sulphide detoxification by the colonic mucosa and circulating erythrocytes.
AIMS To measure levels of TMT activity in erythrocytes of surgically treated cases of colitis or in rectal biopsies of defined groups of colitis.
PATIENTS Venepuncture blood was obtained from 37 blood donors and 27 subjects who had previously undergone a proctocolectomy for colitis: 18 for ulcerative colitis and nine for Crohn's colitis. Rectal biopsies from 122 cases were obtained: 47 without mucosal disease, 33 post-colon resection for cancer, 14 with moderate to severe ulcerative colitis, 15 with quiescent ulcerative colitis, seven with acute Crohn's colitis, and six with radiation proctitis.
METHODS TMT activity was measured by high performance liquid chromatography with radioactive detection to measure 14C methylmercaptoethanol formation, the reaction product of cell extracts incubated with mercaptoethanol and 14C S-adenosylmethionine.
RESULTS Erythrocyte TMT activity of surgically treated cases of colitis was significantly elevated (p<0.001) compared with control cases. TMT activity of rectal biopsies was significantly decreased (p<0.02) in acute but not quiescent ulcerative colitis, Crohn's colitis, or radiation colitis.
CONCLUSIONS Erythrocyte TMT activity was persistently elevated after proctocolectomy for Crohn's disease and ulcerative colitis. No primary defect of TMT activity was found in any case of unoperated colitis but mucosal activity was diminished with disease progression of ulcerative colitis. Studies of genetic control of TMT activity of erythrocytes in inflammatory bowel disease appear worthwhile.
- thiol methyltransferase
- hydrogen sulphide
- ulcerative colitis
- Crohn's disease
Abbreviations used in this paper
- Crohn's disease
- thiol methyltransferase
- ulcerative colitis
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Bacterially produced hydrogen sulphide may play an intermediary role in the pathogenesis of ulcerative colitis (UC). In support are observations of increased rates of sulphide production from stool samples of colitis sufferers1 ,2 compared with control cases and increased luminal levels of sulphide in colitis,3 ,4 although rectal dialysis, a poor reflector of luminal sulphide production, did not show elevated levels of sulphide in colitis.5 Hydrogen sulphide impairs fatty acid oxidation in colonocytes,6 ,7 the chief energy substrate of these cells, and with increasing concentration also diminishes glucose oxidation.8 Decreasing the formation of sulphide in the colon by therapy with sulphasalazine,4 ,9 bismuth salts,9-11 or by decreasing sulphur amino acid intake12 produced treatment benefit for microscopic and UC patients. A low sulphate diet in patients with UC reduced bacterial sulphide formation.13
Despite evidence in support of sulphide in the causation of colitis, sulphide instilled in fractionated doses into the colon did not produce colitis14 although sulphide enhanced epithelial cell turnover in colonic biopsies.15 In contrast, continuous infusion of sulphide produced mucosal damage.16 Sulphide enhanced the oxidative burst of activated immune cells17and stimulated release of nitric oxide from nitric oxide carriers18 thus placing sulphide in an intermediary category as a damaging agent to the colonic mucosa.
Protection against cellular damage by sulphide results from methylation of sulphide to less toxic methyl derivatives.19Methylation is governed by a supply of the methyl donating agent S-adenosylmethionine (SAM),20 availability of ATP, and the activity of the methylating enzyme thiol methyltransferase (TMT) which is greater in the colonic mucosa than in the liver.21Circulating red blood cell activity of TMT is elevated in cases of UC compared with controls.22 ,23 Levels of TMT activity in rectal biopsies of UC have been reported as normal.24 The aim of the present study was to measure TMT activity in erythrocytes of cases who had undergone proctocolectomy for colitis and who were off medication for colitis and therefore free of bias from medication. TMT activity was also measured in rectal biopsies in defined groups of colitis where disease activity was carefully documented. The present results were compared with those previously reported.
Patients and methods
Approval to conduct the study was obtained from the Ethics of Human Research Committee of the Queen Elizabeth Hospital and University of Adelaide.
For measurement of TMT activity in erythrocytes, patients were recruited from the Ileostomy Association of South Australia and blood samples for comparative purposes were obtained from the Blood Transfusion Services of South Australia, although these subjects did not have a proctocolectomy. Venepuncture samples were obtained in the non-fasting state during the morning and collected in lithium heparin. All UC patients had a total proctocolectomy with a Brooke's type terminal ileostomy and none was receiving steroids or sulphasalazine. None of the subjects had smoked for at least 10 years. There were 18 patients, 11 females and seven male, aged 36–86 years (mean 60.4 (SEM 3.4)) who had undergone their operation 2–50 (mean 18.4 (SEM 2.9) years ago. There were nine patients, six females and three males, who had a proctocolectomy and Brooke's ileostomy for Crohn's colitis, aged 21–80 (54.8 (6.7)) years, with their operation 6–37 (16.6 (3.7)) years ago. Three of the patients had small bowel resections of less than 30 cm and none was receiving sulphasalazine or steroids or had active Crohn's disease. There were 37 control cases, 18 females and 19 males, aged 39–68 (52.8 (1.1)) years and none was receiving steroids or sulphasalazine.
For measurement of TMT activity in the colonic mucosa, biopsies in all cases were obtained at colonoscopy 10–15 cm from the anal verge by means of Pauldrach biopsy forceps. Four biopsies with a combined wet weight of 17–29 mg were pooled for measurement of enzyme activity. Six groups of patients were studied and all had complete colonoscopies (table 1). Ages between the various colitis groups were not significantly different but ages between the control groups (benign and malignant) were significantly different (p<0.001, Student'st test) from the colitis groups. However, there are no reports to suggest that mucosal TMT activity varies with age. There was no significant difference in the sex distribution in any group. Benign conditions were either haemorrhoids, irritable bowel syndrome, or cases who requested colonoscopy to exclude bowel cancer. Cases of treated colonic cancers had resections more than 12 months previously and were undergoing surveillance colonoscopies. All cases of acute colitis histologically based on the Truelove and Richards criteria25 had moderate to severe colitis and all biopsies were taken from the involved area of mucosa. The proximal extent of the disease varied but all had rectosigmoid involvement. Cases of quiescent colitis were clinically and histologically in remission. Cases of Crohn's colitis had active disease. All acute colitis cases were receiving steroids and sulphasalazine and quiescent cases sulphasalazine or mesalazine only. Cases of mild to moderate radiation proctitis were men who had received radiation therapy for carcinoma of the prostate at least three years previously.
To compare TMT levels of mucosal biopsies with levels of isolated colonocytes, tissues were collected, as previously described,6 from the same colonic resections and biopsies taken adjacent to where mucosal strips were obtained to prepare isolated colonic epithelial cells. Such a comparison was done because biopsies as a composite tissue may have different TMT activity than isolated colonocytes.
Erythrocyte membranes were prepared using a modification of the method of Pazmino and Weinshilboum.26 Blood (20 ml) collected into lithium heparin was centrifuged at 800g for 10 minutes. Plasma was removed and an equal volume of normal saline added. Following gentle mixing, recentrifugation at 800 g, the procedure was repeated. After removal of plasma, ice cold distilled water (20 ml) was added and the mixture centrifuged at 13 000g (4°C) for 10 minutes. The supernatant was discarded and the pellet washed carefully with 3 ml Tris HCl buffer, pH 7.4. After the final wash, 6 ml of Tris buffer were added before recentrifugation. The pellet was reconstituted with 120 ml of Tris buffer before storage at −80°C. Prior to assay the mixture was sonicated on ice for about 10 seconds until homogeneous.
Colonocytes were prepared as described previously6 from resected segments of colon uninvolved with pathological change. Dithiothreitol was omitted in the preparation. Colonocytes, after isolation, were washed twice in 0.1 ml dipotassium hydrogen orthophosphate /1 mM EDTA (pH 7.4) then ground finely in liquid nitrogen using a mortar and pestle.
Colonic mucosal biopsies which had been collected into preweighed tubes were kept on ice prior to isolating microsomes. The biopsy weight was calculated and 300 μl of 0.25 M sucrose added. This mixture was homogenised on ice and removed prior to washing the vessel with a further 200 μl of 0.25 M sucrose. This mixture was centrifuged at 12 000 g (4°C) for 15 minutes. The supernatant was removed to another tube which was centrifuged at 105 000 g (4°C) for one hour. The supernatant was removed and the pellet reconstituted in 200 μl Tris buffer prior to freezing at −80°C. The mixture was sonicated as above.
TMT assays were performed on the supernatant fraction of biopsies, colonocyte suspensions, or entire suspensions of erythrocyte membranes. Prior to assay protein concentrations of samples were determined according to the method of Lowry and colleagues.27 TMT activity was determined by a modification of the method of Pazmino and Weinshilboum26 as outlined in detail previously.28 The HPLC system was not changed28 but the mobile phase was altered to 20% methanol/80% distilled water with 1.75 ml/l dibutylamine in 20% phosphoric acid, pH 3. This mobile phase eluted unused 14C SAM as a large peak prior to 14C methylmercaptoethanol and there appeared to be no problems with increased background radioactivity.
TMT activity was calculated as pmol of mercaptoethanol formed. The peak area (μV-seconds) was converted to disintegrations per minute (dpm) after determining a conversion factor by injecting a known amount of14C SAM and relating area to dpm. The specific activity of SAM was then used to calculate pmol of methylmercaptoethanol formed and results expressed as pmol/hour/mg protein.
Analysis of variance (ANOVA) and Wald's test were applied in comparing results of multiple groups of patients. The Student'st test for unpaired samples was also used to test the null hypothesis between groups and p values <0.05 were considered significantly different.
The within assay coefficient of variation of TMT activity was 7% and between assay was 6.4%, with a minimal detection rate of 2 pmol/hour/mg protein, as previously described.25Comparison of TMT activity in isolated colonic epithelial cells with rectal biopsy samples of the same tissue specimen revealed a mean (SEM) value of 277.9 (59.5) (n=11) for isolated cells compared with 293.35 (55.7) (n=11) for biopsies. A linear relationship was found between the two tissue samples (fig 1) with a correlation coefficient of 0.92 (p<0.001) between the two modes of tissue sampling. These results indicate that biopsy values closely reflect TMT activity of isolated colonocytes.
Values of TMT activity of erythrocyte membranes (fig 2) varied in healthy subjects with an intact colon (13–222 pmol/hour/mg; mean (SEM) 120.00 (9.6) (n=37)). Values in colectomised cases of UC varied between 130 and 334.0 pmol/hour/mg (mean (SEM) 201.7 (15.4) (n=8)) and colectomised cases of Crohn's disease between 111.0 and 319 pmol/hour/mg (237.8 (22.9) (n=9)). Values in inflammatory bowel disease were significantly increased (p<0.001) compared with healthy cases that had an intact colon.
Values of TMT activity in rectal biopsies (fig 3) were much higher than in erythrocyte membranes, in agreement with previous findings.25 Mean values for healthy controls were 379.7 (SEM 32.9) (n=46), control colon cancer cases 363 (44.5) (n=33), acute UC 227 (33.7) (n=14), quiescent UC 301.8 (33.2) (n=15), active Crohn's disease 429 (63.2) (n=7), and active radiation proctitis 406.7 (118.7) pmol/hour/mg protein (n=6). Analysis of variance (ANOVA) using STATA (Stata Statistical Software: release 5, 1997, Stata Corporation Texas, USA) detected no difference between the five groups of benign, malignant, acute UC, quiescent UC, and Crohn's disease (F5,115=1.53, p=0.186). Using Wald's test after ANOVA a difference was found comparing the benign group with the two UC groups together (p=0.026). Values for active UC compared with healthy controls were significantly different (p<0.02; Student's test for unpaired samples) but no other values were significantly different from healthy controls or cancer control cases.
TMT activity in the colonic mucosa has been reported as low21 or high,29 ,30 with more recent studies28 intermediary to these values. The method we used to assay TMT activity has previously been validated with regard to reproducibility and coefficient of variance.28 As the activity of TMT may vary along the length of the intestinal tract29 ,30 a fixed region for biopsy was chosen in which colitis usually manifests. Also of concern was whether biopsies, a composite tissue of immune and epithelial cells, would yield TMT activities reflective of isolated epithelial cells.28 This was found to be the case in healthy mucosa but remains untested in the inflamed mucosa. Immune cells are tolerant of high levels (>1.5 mM) of hydrogen sulphide31 and may have considerable TMT activity. Apart from such a drawback, the methodology of the assay was carefully applied.28
TMT activity of erythrocyte membranes in unoperated cases of UC has been found to be elevated in both active and quiescent colitis, the increase being significant in active UC but not Crohn's disease.22 ,23 Current observations in operated cases of colitis replicated elevated TMT activity in erythrocyte membranes seen in unoperated cases of colitis22 ,23 suggesting that factors causing elevation of TMT activity are present irrespective of the presence of the colon. One possible factor in unoperated cases could be a high intake of protein observed in UC32 and particularly foods rich in sulphur amino acids such as meat.33 ,34 Sulphur amino acids can be a source of sulphur via endogenous sulphate production (unpublished observation) for sulphate reducing bacteria to produce sulphide,1 colonic levels of which are elevated in colitis patients.2-4 The foregoing explanation subsumes that TMT activity in erythrocytes is inducible. Other explanations could be that genetically programmed activity of TMT in erythrocytes may be different in colitis than in control cases. TMT activity of erythrocytes in non-colitis patients has a strong genetic relation35 which requires further study in cases of colitis.
Mucosal detoxification processes of sulphation and glutathione transferase activity19 are diminished in UC, particularly in active disease. Loss of sulphation was detected by noting diminished sulphation of paracetamol in rectal dialysate in vivo36 or in vitro by isolated colonocytes.37 The diminished glutathione transferase activity was observed in human UC38 as well as in experimental animal colitis.39 Mucosal detoxification by methylation as now observed was diminished in moderate to severe UC but not quiescent colitis suggesting that the primary process of methylation was not impaired in our cases of UC. The state of TMT activity does not however entirely reflect the capacity to methylate as the process is dependent on a supply of SAM which in the assay was exogenously provided. In UC levels of endogenous SAM are low in colonocytes40 and methylation of DNA, which is also dependent on endogenous SAM, is low in the mucosa of UC.41 The potential for sulphide to cause mucosal metabolic damage is most likely to occur later in the development of the disease process of UC when production rates of sulphide may exceed the capacity of epithelial cells to detoxify the amount of sulphide produced in the colon.
Several lines of research19 ,42 suggest that bacterial metabolism of sulphur may be a component of the disease process of UC. The activity of TMT in the colonic mucosa remains robust in early colitis without significant change from control cases, but a persistently elevated TMT activity in erythrocytes, shown in this and other studies, supports the view that other factors regulate TMT activity irrespective of the presence of the colon. Studies of genetic control of TMT activity in erythrocytes of colitis would be a worthwhile avenue of exploration.
The authors are indebted to Dr A Cummins, Mr J Moore, and Professor I Roberts-Thomson for study of their patients and to the chairman, committee, and members of the Ileostomy Association of South Australia for their cheerful cooperation in the study. Supported by a grant from the National Health and Medical Research Council of Australia.
Abbreviations used in this paper
- Crohn's disease
- thiol methyltransferase
- ulcerative colitis
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