O modelo de inflamação crônica associada ao Trypanossoma cruzi no intestino de camundongos como plataforma experimental para compreender mecanismos de plasticidade do sistema nervoso entérico e musculatura lisa intestinal

• Ano de defesa: 2016
• Autor(a) principal: Camila Franca Campos
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal de Minas Gerais; UFMG
• Palavras-chave em Português: Sistema nervosa entérico; Histopatologia; Músculo liso; Doença de Chagas crônica; Plasticidade neuromuscular; Megacólon; Colo/patologia; Plasticidade neuronal; Medicina; Doença de Chagas; Sistema nervoso entérico; Trypanosoma cruzi
• Link de acesso: http://hdl.handle.net/1843/BUOS-AP2RJG

Our group had developed a novel murine model of long-term infection with Trypanosoma cruzi with the aim to elucidate the pathogenesis of megacolon and the associated adaptive and neuromuscular intestinal disorders. Our intent was to produce a chronic stage of the disease since the early treatment should avoid 100% mortality of untreated animals at acute phase. Treatment allowed animals to be kept infected and alive in order to develop the chronic phase of infection with low parasitism. A group of Swiss mice was infected with the Y strain of T. cruzi. At the 11th day after infection, a sub-group was euthanized (acute-phase group) and another sub-group was treated with benznidazole and euthanized 15 months after infection (chronic-phase group). Whole colon samples were used for studying the histopathology of the intestinal smooth muscle and the plasticity of the enteric nerves. In the acute phase, all animals presented inflammatory lesions associated with intense and diffuse parasitism of the muscular and submucosa layers, that were enlarged when compared with the controls. The occurrence of intense degenerative inflammatory changes and increased reticular fibers suggests inflammatory-induced necrosis of muscle cells. In the chronic phase, parasitism was insignificant; however, the architecture of Aüerbach plexuses were focally affected in the inflamed areas and a significant decrease in the number of neurons and in the density of intramuscular nerves bundles were detected. Other changes observed included increased thickness of the colon wall, diffuse muscle cell hypertrophy, and increased collagen deposition. We propose a model for studying the long-term (15 months) pathogenesis of Chagasic megacolon in mice that mimics the human disease, which persists for several years and has not been fully elucidated. The long-term structural changes may represent the basic mechanism for the formation of the Chagasic megacolon.