Differences in MUC2 Gene Expression Based on the Clinical Severity of Colitis and the Degree of Histopathological Damage to the Colonic Mucosa in Colitis-induced Rat

Authors

  • Saptino Miro Department of Internal Medicine, Faculty of Medicine, Universitas Andalas, Padang, Indonesia
  • Arni Amir Department of Physiology, Faculty of Medicine, Universitas Andalas, Padang, Indonesia
  • Nasrul Zubir Department of Internal Medicine, Faculty of Medicine, Universitas Andalas, Padang, Indonesia
  • Andani Eka Putra Department of Microbiology, Faculty of Medicine, Universitas Andalas, Padang, Indonesia

DOI:

https://doi.org/10.3889/oamjms.2022.8963

Keywords:

Disease activity index, Dextran sodium sulfate, Histopathology, Inflammatory bowel disease, MUC2

Abstract

BACKGROUND: Inflammatory bowel disease (IBD), such as Crohn’s disease (CD) and ulcerative colitis (UC), is characterized by intestinal inflammation and epithelial damage. Impaired mucosal cell barrier function mainly associated with thinning of the mucin layer may be the initial events underlying injury and inflammation in UC. Impaired expression of specific mucins is closely associated with IBD. MUC2 is a gene that produces mucin, which is predominant in the colon in humans and rats.

METHODS: This study is an experimental study with a posttest-only design. The sample comprised 16 colitis-induced rats. Induction of colitis was done by giving a solution of dextran sodium sulfate (DSS) 2.5% 1 mL/day orally for 7 days. MUC2 gene expression was measured by rtPCR. The clinical severity of colitis was classified based on the disease activity index (DAI) score. The degree of histopathological damage was classified based on the score of colonic histology observations. The statistical analysis was done by the Shapiro–Wilk normality test and continued with an independent samples t-test.

RESULTS: There were differences in MUC2 gene expression in mild and moderate colitis (1.81 vs. 2.99) but the difference was not significant (p > 0.05). MUC2 gene expression also differed in mild and severe histopathological damage degrees (2.32 vs. 2.1) but the difference was not significant (p > 0.05).

CONCLUSION: It was concluded in this study that MUC2 gene expression did not have significant differences based on the clinical severity of colitis and the degree of histopathological damage to the colonic mucosa in colitis-induced rats.

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References

Neurath MF. Cytokines in inflammatory bowel disease. Nat Publ Gr. 2014;14(5) 329-42. DOI: https://doi.org/10.1038/nri3661

Matsuoka K, Kobayashi T, Ueno F, Matsui T, Hirai F, Inoue N, et al. Evidence-based clinical practice guidelines for inflammatory bowel disease. J Gastroenterol. 2018;53:305-53. https://doi.org/10.1007/s00535-018-1439-1 PMid:29429045 DOI: https://doi.org/10.1007/s00535-018-1439-1

Ng WK, Wong SH, Ng SC. Changing epidemiological trends of inflammatory bowel disease in Asia. Intest Res. 2016;14(2):111-9. https://doi.org/10.5217/ir.2016.14.2.111 PMid:27175111 DOI: https://doi.org/10.5217/ir.2016.14.2.111

Jairath V, Feagan BG. Global burden of inflammatory bowel disease. Lancet Gastroenterol Hepatol. 2020;5(1):2-3. https://doi.org/10.1016/s2468-1253(19)30358-9 PMid:31648974 DOI: https://doi.org/10.1016/S2468-1253(19)30358-9

Blumberg RS, Snapper SC. Inflammatory bowel disease: Immunologic considerations and therapeutic implications. In: Greenberger NJ, Blumberg RS, BuRakoff R, editors. Current Diagnosis and Treatment Gastroenterology, Hepatology, and Endoscopy. 3rd ed. New York: McGraw-Hill Education; 2016. p. 14-25.

Friedman S, Blumberg RS. Inflammatory bowel disease. In: Longo DL, Fauci AS, editors. Harrison’s Gastroenterology and Hepatology. 2nd ed. New York: McGraw-Hill Education; 2013. p. 179-203.

Lukic J, Strahinic I, Jovcic B, Filipic B, Topisirovic L, Kojic M, et al. Different roles for lactococcal aggregation factor and mucin binding protein in adhesion to gastrointestinal mucosa. Appl Environ Microbiol. 2012;78(22):7993-8000. https://doi.org/10.1128/aem.02141-12 PMid:22961901 DOI: https://doi.org/10.1128/AEM.02141-12

La Fata G, Weber P, Mohajeri MH. Probiotics and the gut immune system: Indirect regulation. Probiotics Antimicrob Prot. 2018;10:11-21. https://doi.org/10.1007/s12602-017-9322-6 DOI: https://doi.org/10.1007/s12602-017-9322-6

Dharmani P, Leung P, Chadee K. Tumor necrosis factor-α _and Muc2 mucin play major roles in disease onset and progression in dextran sodium sulphate-induced colitis. PLoS One. 2011;6(9):25058. https://doi.org/10.1371/journal.pone.0025058 PMid:21949848 DOI: https://doi.org/10.1371/journal.pone.0025058

Ananthakrishnan AN, Xavier RJ, Podolsky DK. Inflammatory bowel disease: Pathogenesis. In: Podolsky DK, Camilleri M, Fitz JG, Kalloo AN, Shanahan F, Wang TC, editors. Yamada’s Textbook of Gastroenterology. 6th ed. United Kingdom: John Wiley and Sons Ltd.; 2016. p. 1364-77. https://doi.org/10.1002/9781118512074 DOI: https://doi.org/10.1002/9781118512074

Wenzel UA, Magnusson MK, Rydstrom A, Jonstrand C, Hengst J, Johansson M, et al. Spontaneous colitis in Muc2- deficient mice reflects clinical and cellular features of active ulcerative colitis. PLoS One. 2014;9(6):100217. https://doi.org/10.1371/journal.pone.0100217 PMid:24945909 DOI: https://doi.org/10.1371/journal.pone.0100217

Van der Sluis M, Koning B, De Bruijn A, Velcich A, Meijerink J, Van Goudoever J, et al. Muc2-deficient mice spontaneously develop colitis, indicating that Muc2 is critical for colonic protection. Gastroenterology. 2006;131(1):117-29. https://doi.org/10.1053/j.gastro.2006.04.020 PMid:16831596 DOI: https://doi.org/10.1053/j.gastro.2006.04.020

Petersson J, Schreiber O, Hansson GC, Gendler SJ, Velcich A, Lundberg JO, et al. Importance and regulation of the colonic mucus barrier in a mouse model of colitis. Am J Physiol Gastrointest Liver Physiol. 2011;300(2):327-33. https://doi.org/10.1152/ajpgi.00422.2010 PMid:21109593 DOI: https://doi.org/10.1152/ajpgi.00422.2010

Renes IB, Boshuizen JA, Van Nispen D, Bulsing NP, Buller HA, Dekker J, et al. Alterations in Muc2 biosynthesis and secretion during dextran sulfate sodium-induced colitis. Am J Physiol. Gastrointest Liver Physiol. 2002;282(2):382-9. https://doi.org/10.1152/ajpgi.00229.2001 PMid:11804861 DOI: https://doi.org/10.1152/ajpgi.00229.2001

Xu X, Lin S, Yang Y, Gong X, Tong J, Li K, et al. Histological and ultrastructural changes of the colon in dextran sodium sulfateinduced mouse colitis. Exp Ther Med. 2020;20(3):1987-94. https://doi.org/10.3892/etm.2020.8946 PMid:32782508 DOI: https://doi.org/10.3892/etm.2020.8946

Allenspach KA, Mochel JP, Du Y, Priestnall SL, Moore F, Slayter M, et al, Correlating gastrointestinal histopathologic changes to clinical disease activity in dogs with idiopathic inflammatory bowel disease. Vet Pathol. 2019;56(3):435-43. https://doi.org/10.1177/0300985818813090 PMid:30563436 DOI: https://doi.org/10.1177/0300985818813090

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Published

2022-04-10

How to Cite

1.
Miro S, Amir A, Zubir N, Putra AE. Differences in MUC2 Gene Expression Based on the Clinical Severity of Colitis and the Degree of Histopathological Damage to the Colonic Mucosa in Colitis-induced Rat. Open Access Maced J Med Sci [Internet]. 2022 Apr. 10 [cited 2024 Apr. 25];10(B):1170-5. Available from: https://oamjms.eu/index.php/mjms/article/view/8963

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