Fol. Biol. 2015, 61, 104-109

https://doi.org/10.14712/fb2015061030104

Anthocyanin-Rich Diet in Chemically Induced Colitis in Mice

Katarína Janšáková1, J. Bábíčková1,2, B. Filová3, E. Lengyelová1, M. Havrlentová4,5, J. Kraic4,5, P. Celec1,2,6,7, Ľ. Tóthová1,2

1Institute of Molecular Biomedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia
2Center for Molecular Medicine, Slovak Academy of Sciences, Bratislava, Slovakia
3Institute of Medical Physics, Biophysics, Informatics and Telemedicine, Faculty of Medicine, Comenius University, Bratislava, Slovakia
4Department of Biotechnologies, Faculty of Natural Sciences, University of SS. Cyril and Methodius, Trnava, Slovakia
5National Agricultural and Food Centre – Research Institute of Plant Production, Piešťany, Slovakia
6Department of Molecular Biology, Faculty of Natural Sciences, Comenius University, Bratislava, Slovakia
7Institute of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava, Slovakia

Received February 2015
Accepted April 2015

References

1. Albuquerque, A., Magro, F., Rodrigues, S., Lopes, S., Pereira, P., Melo, R. B., Madureira, M. Macedo, G. (2011) Liver abscess of the caudate lobe due to Staphylococcus aureus in an ulcerative colitis patient: first case report. J. Crohns Colitis 5, 360-363. <https://doi.org/10.1016/j.crohns.2011.02.012>
2. Angelberger, S., Vogelsang, H., Novacek, G., Miehsler, W., Dejaco, C., Gangl, A., Reinisch, W. (2009) Public awareness of Crohn’s disease and ulcerative colitis: a national survey. J. Crohns Colitis 3, 157-161. <https://doi.org/10.1016/j.crohns.2009.01.003>
3. Benzie, I. F., Strain, J. J. (1996) The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal. Biochem. 239, 70-76. <https://doi.org/10.1006/abio.1996.0292>
4. Bi, X., Zhang, J., Chen, C., Zhang, D., Li, P., Ma, F. (2014) Anthocyanin contributes more to hydrogen peroxide scavenging than other phenolics in apple peel. Food Chem. 152, 205-209. <https://doi.org/10.1016/j.foodchem.2013.11.088>
5. Bosaeus, I. (2004) Fibre effects on intestinal functions (diarrhoea, constipation and irritable bowel syndrome). Clinical Nutrition Supplements 1, 33-38. <https://doi.org/10.1016/j.clnu.2004.09.006>
6. Bruckner, M., Westphal, S., Domschke, W., Kucharzik, T., Lugering, A. (2012) Green tea polyphenol epigallocatechin- 3-gallate shows therapeutic antioxidative effects in a murine model of colitis. J. Crohns Colitis 6, 226-235. <https://doi.org/10.1016/j.crohns.2011.08.012>
7. Chan, K. W., Iqbal, S., Khong, N. M. H., Ooi, D.-J., Ismail, M. (2014) Antioxidant activity of phenolics-saponins rich fraction prepared from defatted kenaf seed meal. LWT – Food Science and Technology 56, 181-186. <https://doi.org/10.1016/j.lwt.2013.10.028>
8. Erel, O. (2004) A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin. Biochem. 37, 277-285. <https://doi.org/10.1016/j.clinbiochem.2003.11.015>
9. Gardlik, R., Palffy, R., Celec, P. (2012) Recombinant probiotic therapy in experimental colitis in mice. Folia Biol. (Praha) 58, 238-245.
10. Gardlik, R., Wagnerova, A., Celec, P. (2014) Effects of bacteria- mediated reprogramming and antibiotic pretreatment on the course of colitis in mice. Mol. Med. Rep. 10, 983-988. <https://doi.org/10.3892/mmr.2014.2244>
11. Grace, M. H., Ribnicky, D. M., Kuhn, P., Poulev, A., Logendra, S., Yousef, G. G., Raskin, I., Lila, M. A. (2009) Hypoglycemic activity of a novel anthocyanin-rich formulation from lowbush blueberry, Vaccinium angustifolium Aiton. Phytomedicine 16, 406-415. <https://doi.org/10.1016/j.phymed.2009.02.018>
12. Khoo, H. E., Azlan, A., Nurulhuda, M. H., Ismail, A., Abas, F., Hamid, M., Roowi, S. (2013) Antioxidative and cardioprotective properties of anthocyanins from defatted dabai extracts. Evid. Based Complement. Alternat. Med. 2013, 434057. <https://doi.org/10.1155/2013/434057>
13. Koek, G. H., Verleden, G. M., Evenepoel, P., Rutgeerts, P. (2002) Activity related increase of exhaled nitric oxide in Crohn’s disease and ulcerative colitis: a manifestation of systemic involvement? Respir. Med. 96, 530-535. <https://doi.org/10.1053/rmed.2002.1312>
14. Larrosa, M., Gonzalez-Sarrias, A., Yanez-Gascon, M. J., Selma, M. V., Azorin-Ortuno, M., Toti, S., Tomas-Barberan, F., Dolara, P., Espin, J. C. (2010) Anti-inflammatory properties of a pomegranate extract and its metabolite urolithin-A in a colitis rat model and the effect of colon inflammation on phenolic metabolism. J. Nutr. Biochem. 21, 717-725. <https://doi.org/10.1016/j.jnutbio.2009.04.012>
15. Liang, N.-N., Zhu, B.-Q., Han, S., Wang, J.-H., Pan, Q.-H., Reeves, M. J., Duan, C.-Q., He, F. (2014) Regional characteristics of anthocyanin and flavonol compounds from grapes of four Vitis vinifera varieties in five wine regions of China. Food Res. Int. 64, 264-274. <https://doi.org/10.1016/j.foodres.2014.06.048>
16. Mandalari, G., Bisignano, C., Genovese, T., Mazzon, E., Wickham, M. S., Paterniti, I. , Cuzzocrea, S. (2011) Natural almond skin reduced oxidative stress and inflammation in an experimental model of inflammatory bowel disease. Int. Immunopharmacol. 11, 915-924. <https://doi.org/10.1016/j.intimp.2011.02.003>
17. Marin, M., Maria Giner, R., Rios, J. L. , Recio, M. C. (2013) Intestinal anti-inflammatory activity of ellagic acid in the acute and chronic dextrane sulfate sodium models of mice colitis. J. Ethnopharmacol. 150, 925-934. <https://doi.org/10.1016/j.jep.2013.09.030>
18. Norberto, S., Silva, S., Meireles, M., Faria, A., Pintado, M., Calhau, C. (2013) Blueberry anthocyanins in health promotion: a metabolic overview. J. Funct. Foods 5, 1518-1528. <https://doi.org/10.1016/j.jff.2013.08.015>
19. Omata, Y., Ogawa, Y., Saito, Y., Yoshida, Y., Niki, E. (2009) Assessment of the antioxidant capacity of a fermented grain food product, Antioxidant Biofactor (AOB), by using pyranine and pyrogallol red as a combined probe. Food Chem. 114, 429-433. <https://doi.org/10.1016/j.foodchem.2008.09.066>
20. Orsi, P. R., Seito, L. N. , Di Stasi, L. C. (2014) Hymenaea stigonocarpa Mart. ex Hayne: a tropical medicinal plant with intestinal anti-inflammatory activity in TNBS model of intestinal inflammation in rats. J. Ethnopharmacol. 151, 380-385. <https://doi.org/10.1016/j.jep.2013.10.056>
21. Parmar, A. R., Trivedi, P. P., Jena, G. B. (2014) Dextran sulfate sodium-induced ulcerative colitis leads to testicular toxicity in mice: role of inflammation, oxidative stress and DNA damage. Reprod. Toxicol. 49C, 171-184. <https://doi.org/10.1016/j.reprotox.2014.08.004>
22. Philippe, D., Brahmbhatt, V., Foata, F., Saudan, Y., Serrant, P., Blum, S., Benyacoub, J., Vidal, K. (2012) Anti-inflammatory effects of Lacto-Wolfberry in a mouse model of experimental colitis. World J. Gastroenterol. 18, 5351-5359. <https://doi.org/10.3748/wjg.v18.i38.5351>
23. Rana, S. V., Sharma, S., Kaur, J., Prasad, K. K., Sinha, S. K., Kochhar, R., Malik, A., Morya, R. K. (2014) Relationship of cytokines, oxidative stress and GI motility with bacterial overgrowth in ulcerative colitis patients. J. Crohns Colitis 8, 859-865. <https://doi.org/10.1016/j.crohns.2014.01.007>
24. Roessner, A., Kuester, D., Malfertheiner, P., Schneider-Stock, R. (2008) Oxidative stress in ulcerative colitis-associated carcinogenesis. Pathol. Res. Pract. 204, 511-524. <https://doi.org/10.1016/j.prp.2008.04.011>
25. Sancho, R. A. S., Pastore, G. M. (2012) Evaluation of the effects of anthocyanins in type 2 diabetes. Food Res. Int. 46, 378-386. <https://doi.org/10.1016/j.foodres.2011.11.021>
26. Shigeshiro, M., Tanabe, S., Suzuki, T. (2013) Dietary polyphenols modulate intestinal barrier defects and inflammation in a murine model of colitis. J. Funct. Foods 5, 949-955. <https://doi.org/10.1016/j.jff.2013.02.008>
27. Sundaram, U., Hassanain, H., Suntres, Z., Yu, J. G., Cooke, H. J., Guzman, J., Christofi, F. L. (2003) Rabbit chronic ileitis leads to up-regulation of adenosine A1/A3 gene products, oxidative stress, and immune modulation. Biochem. Pharmacol. 65, 1529-1538. <https://doi.org/10.1016/S0006-2952(03)00067-4>
28. Thompson-Chagoyan, O. C., Maldonado, J., Gil, A. (2005) Aetiology of inflammatory bowel disease (IBD): role of intestinal microbiota and gut-associated lymphoid tissue immune response. Clin. Nutr. 24, 339-352. <https://doi.org/10.1016/j.clnu.2005.02.009>
29. Tothova, L., Hodosy, J., Mucska, I., Celec, P. (2013) Salivary markers of oxidative stress in patients with obstructive sleep apnea treated with continuous positive airway pressure. Sleep Breath 18, 563-570. <https://doi.org/10.1007/s11325-013-0919-z>
30. Tüzün, A., Erdil, A., Inal, V., Aydin, A., Bagci, S., Yesilova, Z., Sayal, A., Karaeren, N., Dagalp, K. (2002) Oxidative stress and antioxidant capacity in patients with inflammatory bowel disease. Clin. Biochem. 35, 569-572. <https://doi.org/10.1016/S0009-9120(02)00361-2>
31. Witaicenis, A., Seito, L. N., da Silveira Chagas, A., de Almeida, L. D., Jr., Luchini, A. C., Rodrigues-Orsi, P., Cestari, S. H. , Di Stasi, L. C. (2014) Antioxidant and intestinal anti-inflammatory effects of plant-derived coumarin derivatives. Phytomedicine 21, 240-246. <https://doi.org/10.1016/j.phymed.2013.09.001>
32. Witko-Sarsat, V., Friedlander, M., Capeillere-Blandin, C., Nguyen-Khoa, T., Nguyen, A. T., Zingraff, J., Jungers, P., Descamps-Latscha, B. (1996) Advanced oxidation protein products as a novel marker of oxidative stress in uremia. Kidney Int. 49, 1304-1313. <https://doi.org/10.1038/ki.1996.186>
33. Wu, L. H., Xu, Z. L., Dong, D., He, S. A., Yu, H. (2011) Protective effect of anthocyanins extract from blueberry on TNBS-induced IBD model of mice. Evid. Based Complement. Alternat. Med. 2011, 525462.
34. Xiao, X., Kim, J., Sun, Q., Kim, D., Park, C. S., Lu, T. S., Park, Y. (2015) Preventive effects of cranberry products on experimental colitis induced by dextran sulphate sodium in mice. Food Chem. 167, 438-446. <https://doi.org/10.1016/j.foodchem.2014.07.006>
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