Perfil das citocinas de ratos alimentados com dieta de camarão

Autores

  • Elizabeth Lage BORGES Universidade Federal de Minas Gerais
  • Dirce Ribeiro de OLIVEIRA Universidade Federal de Minas Gerais
  • Lucíola da Silva BARCELOS Universidade Federal de Minas Gerais
  • Jorge Luiz PESQUERO Universidade Federal de Minas Gerais

Palavras-chave:

Citocinas, Dieta, Eosinófilos, Interleucinas

Resumo

Objetivo
Estudos mostraram que a dieta suplementada com camarão reduziu a resistência cicatricial na pele de ratos. Nesse contexto, o objetivo do presente estudo foi avaliar o perfil das citocinas de ratos que receberam dieta adicionada com camarão.

Métodos
Foram comparados um grupo controle e um grupo experimental, que receberam uma dieta enriquecida com camarão (33%) durante nove dias. As duas dietas continham quantidades semelhantes de proteínas, lipídeos, e carboidratos. Os níveis séricos de citocinas foram avaliados por ELISA, assim como um segmento de jejuno foi obtido para exame histológico da morfologia e infiltrado de eosinófilos.

Resultados
A dieta adicionada com camarão diminuiu os níveis séricos de IL-4 (14,4±1,9 versus 18,11±2,6pg/mL, p<0,05) e IL-10 (5,0±0,98 versus 7,5±1,2pg/mL, p<0,05 e aumentou os níveis séricos de IL-6 (3,2±0,4 versus 17,8±2,3pg/mL, p<0,001) quando comparada com os animais controle. Morfologicamente, a dieta adicionada com camarão causou uma desorganização da arquitetura da mucosa intestinal, juntamente com uma abundância de eosinófilos nas vilosidades jejunais.

Conclusão
Os dados sugerem que a ingestão de dieta adicionada com camarão leva a um aumento significativo da citocina IL-6, juntamente com uma diminuição da citocina imunomoduladora IL-10 no soro de ratos e um infiltrado de eosinófilos no jejuno. O padrão inflamatório das citocinas e o aspecto histológico do jejuno são compatíveis com alergia alimentar.

Referências

Cribbs RK, Harding PA, Luquette MH, Besner GE. Endogenous production of heparin-like EGF-like growth factor during murine partial-thickness burn wound healing. J Burn Care Rehabil. 2002; 23(2): 116-25.

Crowe MJ, Doestschman T, Greenhalgh DG. Delayed wound healing in immunudeficient TGF-beta 1 knockout mice. J Invest Dermatol. 2000; 115(1):3-11.

Dammeier J, Beer HD, Brauchle M, Werner S. Dexamethasone is a novel potent inducer of connective tissue growth factor expression: implications for glucocorticoid therapy. J Biol Chem. 1998; 273(29):18185-90. doi: 10.1074/jbc.273.29.18185.

Danilenko DM, Ring BD, Lu JZ, Tarpley JE, Chang D, Liu N, et al. New differentiation factor upregulates epidermal migration and integrin expression in excisional wounds. J Clin Invest. 1995; 95(2):842-51.

Danilenko DM, Ring BD, Tarpley JE, Morris B, Van GY, Morawiecki A, et al. Growth factoring porcine full and partial thickness burn repair. Differing targets and effects of keratinocyte growth factor, platelet derived growth factor-BB, epidermal growth factor, and neu differentiation factor. Am J Pathol. 1995; 147(5):1261-77.

Diehl S, Rincón M. The two faces of IL-6 on Th1/Th2 differentiation. Mol Immunol. 2002; 39(9):531-6.

Bundoc VG, Keane-Myers A. IL-10 confers protection from mast cell degranulation in a mouse model of allergic conjunctivitis. Exp Eye Res. 2007; 85(4):575-9.

Koulis A, Robinson DS. The anti-inflammatory effects of interleukin-10 in allergic disease. Clin Exp Allergy. 2000; 30(6):747-50.

Tournoy KG, Kips JC, Pauwels RA. Endogenous interleukin-10 suppresses. Allergy. 2000; 30(6): 775-83.

Knippels LMJ, Wijk FW, Penninks AH. Food allergy: what do we learn from animal models? Curr Opin Allerg Clin Immunol. 2004; 4(3):205-9.

Ogawa T, Miura S, Tsuzuki Y, Ogino T, Teramoto K, Inamura T, et al. Chronic allergy to dietary ovalbumin induces lymphocyte migration to rat small intestinal mucosa that is inhibited by MAdCAM-1. Am J Physiol Gastrointest Liver Physiol. 2004; 286(5):G702-10.

Borges EL, Pereira FKS, Alvarez-Leite JI, Alberti LR, Ferreira MAND, Petroianu A. Shrimp diet and skin healing strength in rats. Rev Nutr. 2007; 20(3):257-63. doi: 10.1590/S141552732007000300004.

Lowry OH, Rosenbrough NJ, Farr AL, Randal AL. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193(1):265-75.

Ahern DJ, Robinson DS. Regulatory T cells as a target for induction of immune tolerance in allergy. Curr Opin Allergy Clin Immunol. 2005; 5(6):531-6.

Doganci A, Eigenbrod T, Krug N, De Sanctis GT, Hausding M, Erpenbeck VJ, et al. The IL-6RD chain controls lung CD4+CD25+ Treg development and function during allergic airway inflammation in vivo. J Clin Invest. 2005; 115(2):313-25.

Sato Y, Ohshima T, Kondo T. Regulatory role of endogenous interleukin-10 in cutaneous inflammatory response of murine wound healing. Biochem Biophys Res Commun. 1999; 265(1):194-9.

Zubaidi A, Buie WD, Hart DA, Sigalet D. Temporal expression of cytokines in rat cutaneous, fascial, and intestinal wounds: a comparative study. Dig Dis Sci. 2010; 55(6):1581-8.

Prigione I, Morandi F, Tosca MA, Silvestri M, Pistoia V, Ciprandi G, et al. Interferon-gamma and IL-10 may protect from allergic polysensitization in children: preliminary evidence. Allergy. 2010; 65(6):740-2.

Chuang YH, Yang YH, Wu SJ, Chiang BL. Gene therapy for allergic diseases. Curr Gen Ther. 2009; 9(3):185-91.

Tay SS, Plain KM, Bishop GA. Role of IL-4 and Th2 responses in allograft rejection on tolerance. Curr Opin Organ Transplant. 2009; 14(1):16-22.

Werner S, Grose R. Regulation of wound healing by growth factors and cytokines. Physiol Rev. 2003; 83(3):835-70.

Hübner G, Brauchle M, Smola H, Madlener M, Fassler R, Werner S. Differential regulation of pro-inflammatory cytokines during wound healing in normal and glucocorticoid-treated mice. Cytokine. 1996; 8(7):548-56.

Feiken E, Romer J, Eriksen J, Lund LR. Neutrophils express tumor necrosis factor-alpha during mouse skin wound healing. J Invest Dermatol. 1995; 105(1): 120-3.

Gallucci RM, Simeonova PP, Matheson JM, Kommineni C, Guriel JL, Sugawara T, et al. Impaired cutaneous wound healing in interleukin-6-deficient and immunosuppressed mice. FASEB J. 14(15): 2525-31.

Sato M, Sawamura D, Ina S, Yaguchi T, Hanada K, Hashimoto I. In vivo introduction of the interleukin 6 gene into human keratinocytes: induction of epidermal proliferation by the fully spliced form of interleukin 6, but not by the alternatively spliced

form. Arch Dermatol Res. 1999; 291(7-8):400-4. doi: 10.1007/s004030050429.

Moore KW, De Waal Malefyt R, Coffman RL, O’Garra A. Interleukin-10 and interleukin-10 receptor. Annu Rev Immunol. 2001; 19:683-765.

Downloads

Publicado

19-04-2023

Como Citar

Lage BORGES, E. ., Ribeiro de OLIVEIRA, D., da Silva BARCELOS, L. ., & PESQUERO, J. L. . (2023). Perfil das citocinas de ratos alimentados com dieta de camarão. Revista De Nutrição, 26(1). Recuperado de https://seer.sis.puc-campinas.edu.br/nutricao/article/view/8386

Edição

Seção

ARTIGOS ORIGINAIS