|Stricture of ileo-anal J pouch anastomosis increased the intensity of pouchitis in an experimental rat model.|
|Jump to Full Text|
|PMID: 23018348 Owner: NLM Status: MEDLINE|
|BACKGROUND: Pouchitis appears to be the most common complication after restorative proctocolectomy.
MATERIAL/METHODS: In experimental models we investigated the correlation between the width of anastomosis and the frequency of pouchitis. Twenty-three Wistar rats underwent restorative proctocolectomy under pentobarbital anesthesia. Normal width anastomosis was performed in 11 animals (Group I). In the remaining 12 animals (Group II) the diameter of anastomosis was reduced by 50%. All animals were sacrificed and the pouch mucosa was histologically (Moskowitz score) and immunohistochemically (IL-1, IL-6, IL-10, IL-12 expression) examined.
RESULTS: Morphological assessment of pouchitis symptoms based on Moskowitz scale revealed considerably more severe inflammation (p=0.0079) in the animals from Group II than in the rats from Group I. The expressions of investigated cytokines, assessed qualitatively in histopathological examination, were higher in rats with narrow anastomosis in comparison with animals with normal anastomosis.
CONCLUSIONS: The stricture of anastomosis increases the intensity of pouchitis and stimulates the production of interleukins. It seems that anastomotic stricture plays an important role in the development of pouchitis.
|Tomasz Banasiewicz; Jarosław Walkowiak; Sławomira Drzymała-Czyż; Maciej Borejsza-Wysocki; Przemysław Majewski; Maciej Biczysko; Zoran Stojcev; Karl-Heinz Herzig; Michał Drews|
Related Documents :
|23988878 - Effect and mechanism of propofol on myocardial ischemia reperfusion injury in type 2 di...
2562548 - The neurobehavioral consequences of n-methyl-d-aspartate (n-mda) administration in rats.
7413688 - Task-dependent development of tolerance to scopolamine.
8450978 - A neurochemical and behavioral investigation of the involvement of nucleus accumbens do...
16055288 - Antidiabetic activities of aqueous and ethanolic extracts of piper betle leaves in rats.
23558988 - Malnutrition affects the pressor response to microinjection of l-glutamate into the rvl...
|Type: Journal Article; Research Support, Non-U.S. Gov't|
|Title: Medical science monitor : international medical journal of experimental and clinical research Volume: 18 ISSN: 1643-3750 ISO Abbreviation: Med. Sci. Monit. Publication Date: 2012 Oct|
|Created Date: 2012-09-28 Completed Date: 2013-02-19 Revised Date: 2013-07-11|
Medline Journal Info:
|Nlm Unique ID: 9609063 Medline TA: Med Sci Monit Country: Poland|
|Languages: eng Pagination: BR409-13 Citation Subset: IM|
|Department of General Surgery, Gastroenterological Oncological Surgery and Plastic Surgery, K. Marcinkowski University of Medical Sciences, Poznan, Poland. firstname.lastname@example.org|
|APA/MLA Format Download EndNote Download BibTex|
Anastomosis, Surgical / adverse effects
Colonic Pouches / adverse effects*
Disease Models, Animal
Ileum / pathology*, surgery*
Interleukins / metabolism
Pouchitis / etiology*, pathology
Journal ID (nlm-ta): Med Sci Monit
Journal ID (iso-abbrev): Med. Sci. Monit
Journal ID (publisher-id): Medical Science Monitor
Publisher: International Scientific Literature, Inc.
© Med Sci Monit, 2012
Received Day: 11 Month: 2 Year: 2012
Accepted Day: 10 Month: 4 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 01 Month: 10 Year: 2012
Volume: 18 Issue: 10
First Page: BR409 Last Page: BR413
PubMed Id: 23018348
Publisher Id: 883481
|Stricture of ileo-anal J pouch anastomosis increased the intensity of pouchitis in an experimental rat model|
1Department of General Surgery, Gastroenterological Oncological Surgery and Plastic Surgery, K. Marcinkowski University of Medical Sciences, Poznan, Poland
2I Chair of Pediatrics, Department of Gastroenterology and Metabolism, K. Marcinkowski University of Medical Sciences, Poznan, Poland
3Department of Clinical Pathomorphology K. Marcinkowski University of Medical Sciences, Poznan, Poland
4Unit of General, Vascular and Oncological Surgery, Regional Hospital Slupsk
5Department of Oncological Surgery Medical University Gdansk, Gdansk, Poland
6Institute of Biomedicine, Division of Physiology and Biocenter Oulu, University of Oulu, Oulu, Finland
|Correspondence: Tomasz Banasiewicz, Department of General, Gastroenterological and Endocrinological Surgery, Przybyszewskiego 49 St., 60-355 Poznan, Poland, e-mail: email@example.com
Restorative proctocolectomy involves the removal of the large intestine with the preservation of the anal sphincter and the performance of ileoanal anastomosis. One of the aims of this procedure is to create an ileal reservoir. Small intestinal mucosa, which forms the intestinal pouch, undergoes several adaptive processes aimed at taking over some of the functions of the removed large intestine. Apart from adaptive changes, a significant number of patients may experience a certain type of inflammation. Its frequency is estimated at 23–60% of patients who underwent restorative proctocolectomy [1,2]. However, the data vary considerably depending on the source. Several potential etiopathological causes of pouchitis might be listed, including static fecal residue in the pouch in patients and experimental models . This phenomenon has also been explained by the overgrowth of bacteria, but the latest research does not confirm this theory . Patients with pouchitis symptoms have been found to develop anastomotic stricture [4,5]. It has been observed that endoscopic dilatation of the stricture decreases the clinical symptoms and improves comfort . Whether the anastomotic stricture is the cause of pouchitis or the result of an inflammatory condition which induces fibrosis is an issue that still raises many doubts and is widely discussed.
All animal studies were approved by the Local Ethics Committee. All surgical procedures were conducted by a qualified surgeon in accordance with the guidelines of the European Community Council directives 86/609/EEC and with the agreements of the Local Ethics Committee (42/2006).
Adult male Wistar rats in good general condition (300–350 gms) were housed individually in stainless steel metabolic cages under controlled temperature (21–23°C) on 12: 12-h light-dark cycle and fed with standard laboratory diet and water ad libitum.
In all examined animals, feeding was stopped 24 hours before surgery. After an intraperitoneal injection of pentobarbital anesthesia (pentobarbital sodium, 50 mg/kg body wt) the skin of the abdomen was sterilized and draped with gauze and a 3–4 cm midline laparotomy was performed. The total proctocolectomy was performed by resecting the colon and ligating the mesentery with 4-0 silk. The intestinal segment was excised from 0.1 cm proximal to the ileocecal junction. The rectum was resected at the level of the pelvic floor, with a 0.5 cm rectal stump. Small intestinal contents were washed with 0.9% warm saline and a 2 cm ileal J-pouch was created by the duplication of the distal end of the small intestine by a single-layer interrupted 6-0 Prolene suture. The pouch anal anastomosis was performed with a single layer interrupted 6-0 Prolene suture. The sufficiency of the anastomosis was controlled by injection of 3–5 ml of 0.9% warm saline through the anus. Two different techniques of anastomosis were applied. In Group I (11 cases) “normal” width anastomosis was performed, assuming 75% of the diameter of the distal part of small intestine to be “normal”. In Group II (12 cases) the diameter of anastomosis was reduced by 50% in comparison to Group I (Figure 1).
The peritoneal cavity was irrigated with 0.9% warm saline. The abdominal incision was closed with a running 2-0 silk suture and the skin with a single-layer interrupted 3-0 silk suture. Intraoperative mortality was not observed and the median time of surgery was 75 minutes. Water was provided immediately after surgery and feeding was restarted 24 hours later.
After 9 weeks of postoperative follow-up, all animals were sacrificed by decapitation. There were no signs of other diseases or malignancy in the abdominal cavity. The intestinal reservoir was resected, opened and rinsed free of intestinal contents. The internal diameter of anastomosis in both groups was measured. The external muscle layer was removed by blunt dissection. The mucosa specimens with an area of 0.5 cm2 were fixed in formalin for further histological and immunohistochemical evaluations.
Each time the histopathological examination was performed by 2 independent histopathologists and every time the examined section was found to be inflamed according to Moskowitz scale and positive for villi atrophy according to Laumonier scale. Histological classification of inflammation suggested by Moskowitz objectively presents the microscopic assessment of acute and prolonged inflammation and ascribes certain points, which we sum up, to particular features. The inflammation is diagnosed when the coefficient of inflammation amounts to ≥4 . Villi atrophy development was assessed in accordance to Laumonier 4-stage scale .
Based on hematoxylin & eosin preparations, paraffin blocks containing sections with the most characteristic changes were selected for further immunohistochemical tests. To demonstrate the expression of the investigated markers (IL-1 alpha, IL-6, IL-10, IL-12), the streptavidin-biotin-peroxidase method was employed using an LSAB kit manufactured by DAKO. The antigen was located using DAB-3.3 (DAKO) as a chromogen, which is a substrate for peroxidase. The preparations were then stained with hematoxylin and – following dehydration – closed with a glass cover. Appropriate positive and negative controls were used.
Values are expressed as ranges and medians. The differences in the anastomosis diameter, intensity of pouchitis and interleukin expression between the 2 selected groups of animals were calculated with the use of the Mann-Whitney U test. The level of significance was set at p<0.05.
Higher postoperative mortality (5 cases) was found in Group II as compared with Group I (2 cases), but the difference did not reach the level of significance. The mean diameter of anastomosis in Group I was 4.2 mm and in Group II was 2.3 mm; the differences were statistically significant (p=0.0086). Morphological assessment of pouchitis symptoms based on Moskowitz scale revealed considerably more severe inflammation (p=0.0079) in the rats from Group II than in the rats from Group I. No significant differences related to intestinal villi atrophy were observed. The expressions of investigated cytokines, assessed qualitatively in histopathological examination, were higher in rats with narrow anastomosis in comparison with animals with normal anastomosis. The differences in IL-10 were statistically significant (p=0.0115) and differences in IL-1, IL-6, IL-12 showed no statistical significance. Detailed data related to all investigated animals are presented in Table 1.
Clinical research on pouchitis is limited by the number of patients, their biological and clinical differences, and their willingness to participate in the follow-up examinations, which are often invasive and have to be performed within particular time periods. Thus, appropriate experimental models are needed in order to enable the better understanding of mechanisms of pouchitis and, consequently, its more effective treatment. It is also believed that pouchitis is a natural model of IBD, with a defined onset time within mucosa .
Pig models have long been used in research on restorative proctocolectomy for the assessment of inflammatory manifestations, bacteria colonization or post-operative peristalsis in the digestive tract [10,11]. These models allow for the reconstruction of surgical procedures in humans but they are relatively rarely used due to their sizes and related costs, as well as other restrictions,. Rat models are used much more frequently [12,13], in which either idiopathic pouchitis is assessed  or it is chemically induced, most frequently with the use of 5% dextran sulfate sodium (DSS) , iodoacetamide or dinitrobenzene sulfonic acid (DNBS) . The rat experimental models of pouchitis pose a vast array of surgical difficulties related to the necessity of the performance of a low anastomosis. Some trials aimed at technical modifications have already been described, which allow for simplification of surgical procedures and the avoidance of a low anastomosis. One of them is to create a U-shaped ileal pouch (analogous to a classical proctocolectomy) and anastomose it to the intestine anterior to the ileocecal valve (without colectomy being performed) .
Clinical observations reveal that anastomotic stricture is one of the most significant problems of restorative proctocolectomy patients, and its endoscopic dilatation decreases the clinical symptoms as well as improving comfort . Presently, more accurate data is available that allows for more precise definition of anastomotic stricture. It is now assumed that an 8 mm diameter is a critical anastomotic stricture after restorative proctocolectomy . There is still a lack of data about the correlations between the diameter of the anastomosis and the occurrence and the severity of pouchitis. Therefore, the model of anastomotic stricture, which is described in our research, was regarded as provisional and based on the team’s previous experiences. The starting point was a standard performance of anastomosis, whose diameter corresponded to 75% of the diameter of the distal part of the small intestine in the part slightly above the pouch. In analogy to clinical data, the stricture was assumed to have an anastomotic diameter equal to 50% or less of the normal diameter.
On the basis of our research it has been concluded that the group of patients with narrow anastomosis presented more severe pouchitis assessed in accordance to the Moskowitz histological classification. Anastomotic stricture leads to static fecal residue, which is one of the potential causes of pouchitis in clinical  and experimental  models. In the examined sections, no divergences related to the atrophy of intestinal villi, in accordance with Laumonier classification, were observed. Atrophy of intestinal villi is a long-term process indicating the continuing restructuring of the mucosa of the small intestinal reservoir. In restorative proctocolectomy patients this process may last several years . Thus, in our research the time for observation might have been insufficient to note the increased atrophy of intestinal villi and potential differences among the groups.
In the present study we also evaluated the expression of several interleukins in the mucosa of the intestinal reservoir. Interleukins known for their pro-inflammatory properties, such as IL-1 [20,21], IL-6  and IL-12 , as well as anti-inflammatory IL-10 [24,25], were assessed. The expression of assessed cytokines was higher in rats with narrow anastomosis. However, in cases of pro-inflammatory cytokines (IL-1, IL-6, IL-12), these differences were statistically insignificant. Obviously, the procedure itself was the factor that greatly influenced the activity of assessed interleukins. The phenomenon of increased activity of pro-inflammatory (IL-6) and anti-inflammatory (IL-10) interleukins was observed in peritoneal cavity exudates in patients with anastomotic leakage after partial resection of the large intestine . The increased level of IL-6 and IL-10 was noted even in cases of non-complicated large intestine partial resection.
The increased level of IL-10 is of particular interest. Despite its known anti-inflammatory properties, the role of this interleukin in the development of pouchitis has not been thoroughly examined. There is some evidence supporting its anti-inflammatory activity in pouchitis , yet it has also been noted that its level was similar in patients with pouchitis and healthy subjects . It seems that significantly higher levels of IL-10 activity in rats with narrow anastomosis may be related to higher inflammatory reaction, which is a non-specific stimulus to IL-10 and, to a smaller extent, to pro-inflammatory interleukins.
Narrow anastomosis significantly influences the intensity of inflammatory changes within the pouch mucosa and stimulates the production of interleukins, in particular the anti-inflammatory IL-10. Obtained results suggest that recommendations in pouchitis should take into consideration the assessment of the anastomosis width and its dilatation in justified cases.
fn8-medscimonit-18-10-br409Source of support: Project N 312 275538 (Ministry of Scientific Research and Information Technology, Poland)
|1.||Hoda KM,Collins JF,Knigge KL,Deveney KE. Predictors of Pouchitis after Ileal Pouch-Anal Anastomosis: A Retrospective ReviewDis Colon RectumYear: 2008515546018266037|
|2.||Pardi DS,Shen B. Endoscopy in the management of patients after ileal pouch surgery for ulcerative colitisEndoscopyYear: 20084065293318464195|
|3.||Lisowska A,Banasiewicz T,Marciniak R,et al. Chronic pouchitis is not related to small intestine bacterial overgrowthInflamm Bowel DisYear: 20081481102418452204|
|4.||Banasiewicz T,Marciniak R,Kaczmarek E,et al. The diameter of the ileal J-pouch-anal anastomosis as an important risk factor of pouchitis – clinical observationsMed Sci MonitYear: 2011172CR919621278694|
|5.||Dolinsky D,Levine MS,Rubesin SE,et al. Utility of contrast enema for detecting anastomotic strictures after total proctocolectomy and ileal pouch-anal anastomosisAm J RoentgenolYear: 20071891252917579147|
|6.||Shen B,Fazio VW,Remzi FH,et al. Endoscopic balloon dilation of ileal pouch stricturesAm J GastroenterolYear: 2004991223404715571580|
|7.||Moskowitz RL,Shepherd NA,Nicholls RJ. An assessment of inflammation in the reservoir after restorative proctocolectomy with ileoanal reservoirInt J Colorectal DisYear: 19861167743039030|
|8.||Fenoglio-Preiser CM,Lentz PE,Listrom MB,et al. Gastrointestinal Pathology EdRaven PressNew YorkYear: 1989|
|9.||Wu H,Shen B. Pouchitis: lessons for inflammatory bowel diseaseCurr Opin GastroenterolYear: 20092543142219349860|
|10.||Schmitz-Winnenthal FH,Kadmon M,Schwab E,et al. Functional outcome after restorative proctocolectomy in pigs: comparing a novel transverse ileal pouch to the J-pouch and straight ileoanal anastomosisJ Gastrointest SurgYear: 20091322616818791770|
|11.||Luukkonen P,Jarvinen H,Lehtola A,Sipponen P. Mucosal alterations in pelvic ileal reservoirs. A histological and ultrastructural evaluation in an experimental modelAnn Chir GynaecolYear: 198877391963223733|
|12.||Koyama K,Sasaki I,Naito H,et al. Induction of epithelial Na+ channel in rat ileum after proctocolectomyAm J PhysiolYear: 19992764 Pt 1G9758410198342|
|13.||Babu M,Purhonen AK,Bansiewicz T,et al. Effect of total colectomy and PYY infusion on food intake and body weight in ratsRegul PeptYear: 20051311–3293315996768|
|14.||Lichtman SN,Wang J,Hummel B,et al. A rat model of ileal pouch-rectal anastomosisInflamm Bowel DisYear: 199843187959741020|
|15.||Atila K,Terzi C,Canda AE,et al. Partially hydrolyzed guar gum attenuates the severity of pouchitis in a rat model of ileal J pouch-anal anastomosisDig Dis SciYear: 20095435222918594969|
|16.||Shibolet O,Karmeli F,Eliakim R,et al. Variable response to probiotics in two models of experimental colitis in ratsInflamm Bowel DisYear: 20028639940612454615|
|17.||Shebani KO,Stucchi AF,McClung JP,et al. Role of stasis and oxidative stress in ileal pouch inflammationJ Surg ResYear: 2000901677510781377|
|18.||Majewski P,Marciniak R,Banasiewicz T,et al. Ultrastructural changes in the small intestinal epithelium after total resection of the colonPol J PatolYear: 199647310514|
|19.||Ludwiczek O,Vannier E,Borggraefe I,et al. Imbalance between interleukin-1 agonists and antagonists: relationship to severity of inflammatory bowel diseaseClin Exp ImmunolYear: 200413823232915498044|
|20.||Dionne S,Laberge S,Deslandres C,Seidman EG. Modulation of cytokine release from colonic explants by bacterial antigens in inflammatory bowel diseaseClin Exp ImmunolYear: 200313311081412823284|
|21.||Maeda S,Hikiba Y,Shibata W,et al. Essential roles of high-mobility group box 1 in the development of murine colitis and colitis-associated cancerBiochem Biophys Res CommunYear: 2007360239440017599806|
|22.||Melgar S,Karlsson A,Michaëlsson E. Acute colitis induced by dextran sulfate sodium progresses to chronicity in C57BL/6 but not in BALB/c mice: correlation between symptoms and inflammationAm J Physiol Gastrointest Liver PhysiolYear: 20052886G13283815637179|
|23.||Strauch UG,Grunwald N,Obermeier F,et al. Loss of CD103(+) intestinal dendritic cells during colonic inflammationWorld J GastroenterolYear: 2010161212920039445|
|24.||Uğraş B,Giriş M,Erbil Y,et al. Early prediction of anastomotic leakage after colorectal surgery by measuring peritoneal cytokines: prospective studyInt J SurgYear: 200861283518037067|
|25.||Celinski K,Dworzanski T,Korolczuk A,et al. Activated and inactivated PPARs-γ modulate experimentally induced colitis in ratsMed Sci MonitYear: 2011174BR1162421455100|
|26.||Ulisse S,Gionchetti P,D’Alo S,et al. Expression of cytokines, inducible nitric oxide synthase, and matrix metalloproteinases in pouchitis: effects of probiotic treatmentAm J GastroenterolYear: 200196926919911569697|
|27.||Bulois P,Tremaine WJ,Maunoury V,et al. Pouchitis is associated with mucosal imbalance between interleukin-8 and interleukin-10Inflamm Bowel DisYear: 2000631576410961587|
Keywords: proctocolectomy, experimental model, anastomotic stricture, pouchitis.
Previous Document: Intrascleral outflow after deep sclerectomy with absorbable and non-absorbable implants in the rabbi...
Next Document: Probing the use of fluorescence spectroscopy as a novel diagnostic tool in patients with rheumatoid ...