El efecto de la adición de gluten de trigo y maíz a la dieta de ratas sobre los parámetros autoinmunes e histopatológicos en el intestino y el hígado

  • Recep Gümüş Sivas Cumhuriyet University, Faculty of Veterinary Medicine, Department of Animal Nutrition and Nutritional Diseases. Sivas, Türkiye
  • Kübra Asena Terim Kapakin Ataturk University, Faculty of Veterinary Medicine, Department of Veterinary Pathology. Erzurum, Türkiye
  • Esra Manavoğlu Kirman Ataturk University, Faculty of Veterinary Medicine, Department of Veterinary Pathology. Erzurum, Türkiye
  • İsmail Bolat Ataturk University, Faculty of Veterinary Medicine, Department of Veterinary Pathology. Erzurum, Türkiye
  • Aybuke İmik Selçuk University, Faculty of Health Sciences, Department of Nutrition and Dietetics. Konya, Türkiye
  • Nazlı Ercan Sivas Cumhuriyet University, Faculty of Veterinary Medicine, Department of Biochemistry, Sivas, Türkiye
Palabras clave: Autoimmune, gluten, histopatología, intestino, hígado

Resumen

Este estudio investigó el efecto histopatológico e inmunohistoquímico en los tejidos del intestino y el hígado con la adición de harina de soja (SBM), harina de gluten de trigo (WGM) y harina de gluten de maíz (CGM) a la dieta de ratas. En el estudio se utilizaron un total de 24 ratas macho (Wistar albino) de veinte días de edad promedio. Las ratas se dividieron aleatoriamente en 3 grupos con 8 animales en cada grupo (grupos Control, Trigo y Maíz). La dieta proporcionada a los tres grupos contenía proteínas, que eran SBM, WGM y CGM en los grupos Control, Trigo y Maíz, respectivamente. En el estudio, el grupo alimentado con SBM se utilizó como grupo Control. Las ratas fueron alimentadas con una dieta que contenía 22% de proteína cruda y 2.598 kcal·kg-1 de energía metabólica durante todo el período experimental. La prueba de alimentación continuó durante un período de 50 días. Se observaron cambios degenerativos de diversa gravedad en las células epiteliales intestinales y atrofia de las vellosidades. De manera similar, en los hepatocitos se determinaron los cambios degenerativos, especialmente la degeneración vacuolar o hidrópica. Se determinó que el nivel de CD4 aumentó de manera estadísticamente significativa en los grupos de trigo y maíz en comparación con el grupo de control (P<0,01) en el tejido intestinal. Además, se determinó que el nivel de IgA aumentó estadísticamente de manera significativa en el tejido hepático de los grupos Trigo y Maíz. (P<0,05). Como resultado, se observó que los parámetros histopatológico e inmunohistoquímico de los tejidos del intestino y del hígado de las ratas alimentadas con dietas que contenían un alto contenido de WGM y CGM se vieron afectados de forma limitada.

Descargas

La descarga de datos todavía no está disponible.

Citas

Biesiekierski JR. What is gluten? J. Gastroenterol. Hepatol. [Internet]. 2017; 32(51):78–81. doi: https://doi.org/f9st3c

Wieser H. Chemistry of gluten proteins. Food Microbiol. [Internet]. 2007; 24(2):115–119. doi: https://doi.org/cb957r

Sharma N, Bhatia S, Chunduri V, Kaur S, Sharma S, Kapoor P, Garg M. Pathogenesis of celiac disease and other gluten related disorders in wheat and strategies for mitigating them. Front. Nutr. [Internet]. 2020; 7(6):1–26. doi: https://doi.org/mjr2

Wang Y, Zhang Z, He R, Mintah BK, Dabbour M, Qu W, Ma H. Proteolysis efficiency and structural traits of corn gluten meal: Impact of different frequency modes of a low–power density ultrasound. Food Chem. [Internet]. 2021; 344:128609. doi: https://doi.org/mjr4

Fevzioglu M, Hamaker BR, Campanella OH. Gliadin and zein show similar and improved rheological behavior when mixed with high molecular weight glutenin. J. Cereal Sci. [Internet]. 2012; 55(3):265–271. doi: https://doi.org/fzvggr

Woldemariam KY, Yuan J, Wan Z, Yu Q, Cao Y, Mao H, Sun B. Celiac disease and immunogenic wheat gluten peptides and the association of gliadin peptides with HLA DQ2 and HLA DQ8. Food Rev. Int. [Internet]. 2022; 38(7):1553–1576. doi: https://doi.org/mjr5

Cabanillas B. Gluten–related disorders: Celiac disease, wheat allergy, and nonceliac gluten sensitivity. Crit. Rev. Food Sci. Nutr. [Internet]. 2020; 60(15):2606–2621. doi: https://doi.org/gh2dmv

Freitag TL, Podojil JR, Pearson RM, Fokta FJ, Sahl C, Messing M, Getts DR. Gliadin nanoparticles induce immune tolerance to gliadin in mouse models of celiac disease. Gastroenterol. [Internet]. 2020; 158(6):1667–1681. doi: https://doi.org/gg9g8r

Novacek G, Miehsler W, Wrba F, Ferenci P, Penner E, Vogelsang H. Prevalence and clinical importance of hypertransaminasaemia in coeliac disease. Eur. J. Gastroenterol. Hepatol. [Internet]. 1999; 11(3):283–288. doi: https://doi.org/cr8bsn

Iskender H, Dokumacioglu E, Terim–Kapakin KA, Yenice G, Mohtare B, Bolat I, Hayirli A. Effects of oleanolic acid on inflammation and metabolism in diabetic rats. Biotech. Histochem. [Internet]. 2022; 97(4):269–276. doi: https://doi.org/mjr6

Kapakin KAT, Gümüş R, İmik H, Kapakin S, Sağlam YS. Effects of ascorbic and α–lipoic acid on secretion of HSP–70 and apoptosis in liver and kidneys of broilers exposed to heat stress. Ankara Univ. Vet. Fak. Derg. [Internet]. 2012; 59(4):279–287. doi: https://doi.org/mjr8

Kapakin KAT, Sahin M, Buyuk F, Kapakin S, Gursan N, Saglam YS. Respiratory tract infection induced experimentally by Ornithobacterium rhinotracheale in quails: effects on heat shock proteins and apoptosis. Revue Méd. Vét. 2013; 164(3):132–140.

Imik H, Kapakin KAT, Karabulutlu O, Gumus R, Çomakli S, Ozkaraca M. The effects of dietary wheat and corn glutens on the histopathological and immunohistochemical structure of the ovarian tissue and serum and ovarian tissue LH and FSH levels and lipid profiles in rats. Braz. Arch. Biol. Technol. [Internet]. 2023; 66:e23210726. doi: https://doi.org/mjsc

IBM Corp. Released 2011. IBM SPSS Statistics for Windows, Version 20.0. Armonk, NY, USA: IBM Corp. 2011.

Fasano A. Clinical presentation of celiac disease in the pediatric population. Gastroenterol. [Internet]. 2005; 128:68–73. doi: https://doi.org/bvs6x7

Collin P, Syrjänen J, Partanen J, Pasternack A, Kaukinen K, Mustonen J. Celiac disease and HLA DQ in patients with IgA nephropathy. Am. J. Gastroenterol. [Internet]. 2002; 97(10):2572–2576. doi: https://doi.org/bshvj7

Sollid LM, Jabri B. Triggers and drivers of autoimmunity: lessons from coeliac disease. Nat. Rev. Immunol. [Internet]. 2013; 13(4):294–302. https://doi.org/grhbfv

Matsumoto I, Uchida K, Nakashima K, Hiyoshi S, Chambers JK, Tsujimoto H, Nakayama, H. IgA antibodies against gliadin and tissue transglutaminase in dogs with chronic enteritis and intestinal T–cell lymphoma. Vet. Pathol. [Internet]. 2018; 55(1):98–107. doi: https://doi.org/mjsx

Marsh MN. Gluten, major histocompatibility complex, and the small intestine. A molecular and immunobiologic approach to the spectrum of gluten sensitivity (‘celiac sprue’). Gastroenterol. [Internet]. 1992; 102:330–354. doi: https://doi.org/gpmqpv

Sollid LM. Coeliac disease: dissecting a complex inflammatory disorder. Nat. Rev. Immunol. [Internet]. 2002; 2(9):647–655. doi: https://doi.org/fwrjn8

Lähdeaho ML, Mäki M, Laurila K, Huhtala H, Kaukinen K. Small–bowel mucosal changes and antibody responses after low–and moderate–dose gluten challenge in celiac disease. BMC Gastroenterol. [Internet]. 2011; 11(129):1–9. doi: https://doi.org/djd6hs

Štěpánková R, Tlaskalova–Hogenova H, Šinkora J, Jodl J, Frič P. Changes in jejunal mucosa after long–term feeding of germfree rats with gluten. Scan. J. Gastroenterol. [Internet]. 1996; 31(6):551–557. doi: https://doi.org/czb3ng

Albenayan W, Alruwaili N, Pauli JR, King A, Migliore M, Zaghloul I. Development and validation of a gliadin ınduced ıntestinal enteropathy rat model of non–celiac gluten sensitivity. J. Pharm. Pharmacol. Res. [Internet]. 2021; 5(4):205–217. doi: https://doi.org/mjs4

Rubio‐Tapia A, Murray JA. The liver in celiac disease. Hepatol. [Internet]. 2007;46(5):1650–1658. doi: https://doi.org/d8w88m

Sharma BC, Bhasin DK, Nada R. Association of celiac disease with non‐cirrhotic portal fibrosis. J. Gastroenterol. Hepatol. [Internet]. 2006; 21(1):332–334. doi: https://doi.org/c2m7nv

Kim JV, Wu GY. Celiac disease and elevated liver enzymes: A review. J. Clin. Transl. Hepatol. [Internet]. 2021; 9(1):116–124. doi: https://doi.org/mjs5

Rubio‐Tapia A, Murray JA. Liver involvement in celiac disease. Minerva Med. 2008; 99(6):595–604. Cited in: PubMed; PMID 19034257.

Molberg Ø, Mcadam SN, Körner R, Quarsten H, Kristiansen C, Madsen L, Sollid LM. Tissue transglutaminase selectively modifies gliadin peptides that are recognized by gut–derived T cells in celiac disease. Nat. Med. [Internet]. 1998; 4:713–717. doi: https://doi.org/ftkqwt

Bengi G, Duran Y. [Analysis of liver function tests in patients newly diagnosed with celiac disease]. Turk J. Gastroenterol. [Internet]. 2019; 18(3):95–100. Turkish. doi: https://doi.org/mjs6

Zanini B, Baschè R, Ferraresi A, Pigozzi MG, Ricci C, Lanzarotto F, Lanzini, A. Factors that contribute to hypertransaminasemia in patients with celiac disease or functional gastrointestinal syndromes. Clin. Gastroenterol. Hepatol. [Internet]. 2014; 12(5):804–810. doi: https://doi.org/f2rgg4

Hoffmanová I, Sánchez D, Hábová V, Anděl M, Tučková L, Tlaskalová–Hogenová H. Serological markers of enterocyte damage and apoptosis in patients with celiac disease, autoimmune diabetes mellitus and diabetes mellitus type 2. Physiol. Res. [Internet]. 2015;64(4):537–546. doi: https://doi.org/mjs7

Spadoni I, Zagato E, Bertocchi A, Paolinelli R, Hot E, Di Sabatino A, Rescigno M. A gut–vascular barrier controls the systemic dissemination of bacteria. Sci. [Internet]. 2015; 350(6262):830–834. doi: https://doi.org/f3ptnf

Drastich P, Honsová E, Lodererová A, Jarešová M, Pekáriková A, Hoffmanová I, Sánchez D. Celiac disease markers in patients with liver diseases: A single center large scale screening study. World J. Gastroenterol. [Internet]. 2012; 18(43):6255–6262. doi: https://doi.org/f4fn3h

Sjöberg K, Lindgren S, Eriksson S. Frequent occurrence of non–specific gliadin antibodies in chronic liver disease endomysial but not gliadin antibodies predict coeliac disease in patients with chronic liver disease. Scand. J. Gastroenterol. [Internet]. 1997; 32(11):1162–1167. doi: https://doi.org/ff2gcc

Green PHR, Cellier C. Celiac disease. N. Engl. J. Med. [Internet]. 2007; 357(17):1731–1743. doi: https://doi.org/csbng2

Björck S, Lindehammer SR, Fex M, Agardh D. Serum cytokine pattern in young children with screening detected coeliac disease. Clin. Exp. Immunol. [Internet]. 2015; 179(2):230–235. doi: https://doi.org/f25bw8

Kelly DL, Demyanovich HK, Rodriguez KM, Čiháková D, Talor MV, McMahon RP, Eaton WW. Randomized controlled trial of a gluten–free diet in patients with schizophrenia positive for antigliadin antibodies (AGA IgG): a pilot feasibility study. J. Psychiatry Neurosci. [Internet]. 2019; 44(4):269–276. doi: https://doi.org/gg892m

Vojdani A. Detection of IgE, IgG, IgA and IgM antibodies against raw and processed food antigens. Nutr. Metab. [Internet]. 2009; 6(1):1–17. doi: https://doi.org/b7cg6w

Iskender H, Dokumacıoglu E, Hayirli A, Terim Kapakin KA, Bolat I, Manavoglu Kirman E. Effects of oleanolic acid administration on renal NF–κB/IL–18/IL–6 and YKL–40/KIM–1 pathways in experimental diabetic rats. Iran J. Basic Med. Sci. [Internet]. 2023; 26(10):1–6. doi: https://doi.org/mjs8

Himmerich H, Patsalos O, Lichtblau N, Ibrahim MA, Dalton B. Cytokine research in depression: principles, challenges, and open questions. Front. Psychiatry. [Internet]. 2019; 10(30):1–16. doi: https://doi.org/ggxb38

Halstensen TS, Brandtzaeg P. Activated T lymphocytes in the celiac lesion: non‐proliferative activation (CD25) of CD4+ α/β cells in the lamina propria but proliferation (Ki‐67) of α/β and γ/δ cells in the epithelium. Eur. J. Immunol. [Internet]. 1993; 23(2):505–510. doi: https://doi.org/cksgvv

Brandtzaeg P, Halstensen TS, Kett K, Krajči P, Kvale D, Rognum TO, Sollid LM. Immunobiology and immunopathology of human gut mucosa: humoral immunity and intraepithelial lymphocytes. Gastroenterol. [Internet]. 1989; 97:1562–1584. doi: https://doi.org/mjs9

Nilsen EM, Lundin KE, Krajci P, Scott H, Sollid LM, Brandtzaeg P. Gluten specific, HLA–DQ restricted T cells from coeliac mucosa produce cytokines with Th1 or Th0 profile dominated by interferon gamma. Gut. [Internet]. 1995; 37(6):766–776. doi: https://doi.org/fpz6c8

Risnes LF, Eggesbø LM, Christophersen A, Sollid LM. Response to: “Some considerations about γδ and CD8+ T–cell responses in blood after gluten challenge in treated celiac disease”. Mucosal Immunol. [Internet]. 2021; 14(5):1216–1217. doi: https://doi.org/gkhf8s

Leonard MM, Silvester JA, Leffler D, Fasano A, Kelly CP, Lewis SK, Smithson G. Evaluating responses to gluten challenge: a randomized, double–blind, 2–dose gluten challenge trial. Gastroenterol. [Internet]. 2021; 160(3):720–733. doi: https://doi.org/mjtb

Gümüş R, Uslu S, Aydoğdu U, İmik A, Ekici M. Investigation of the effects of glutens on serum ınterleukin–1 beta and tumor necrosis factor–alpha levels and the ımmunohistochemical distribution of CD3 and CD8 receptors in the small intestine in male rats. Braz. Arch. Biol. Technol. [Internet]. 2021; 64:e21210256. doi: https://doi.org/mjtc

Publicado
2024-03-11
Cómo citar
1.
Gümüş R, Terim Kapakin KA, Kirman EM, Bolat İsmail, İmik A, Ercan N. El efecto de la adición de gluten de trigo y maíz a la dieta de ratas sobre los parámetros autoinmunes e histopatológicos en el intestino y el hígado. Rev. Cient. FCV-LUZ [Internet]. 11 de marzo de 2024 [citado 29 de abril de 2024];34(1):9. Disponible en: https://www.produccioncientificaluz.org/index.php/cientifica/article/view/41706
Sección
Medicina Veterinaria