J Y Oda1,2, M O Belém3, T M Carlos4, R Gouveia4, B F C Luchetti2, N M Moreira5, C L Massocatto6, S M Araújo7, D M G Sant Ana6, N C Buttow6, P Pinge-Filho2, E J A Araújo4. 1. Department of Medicine, Federal University of Mato Grosso do Sul, Três Lagoas, Mato Grosso do Sul, Brazil. 2. Department of Pathological Science, State University of Londrina, Londrina, Paraná, Brazil. 3. Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará, Brazil. 4. Department of Histology, State University of Londrina, Londrina, Paraná, Brazil. 5. Center for Education, Letters and Health, State University of Western Paraná, Foz do Iguaçu, Paraná, Brazil. 6. Department of Morphological Science, State University of Maringá, Maringá, Paraná, Brazil. 7. Department of Basic Health Science, State University of Maringá, Maringá, Paraná, Brazil.
Abstract
BACKGROUND: Experimental and clinical studies have shown that myenteric neuron cell death during infection with Trypanosoma cruzi mainly occurs in the esophagus and colon, resulting in megaesophagus and megacolon, respectively. Evidence suggests that the cyclooxygenase enzyme (COX) is involved in the T. cruzi invasion process. The use of low-dose aspirin (ASA), a COX-1/COX-2 inhibitor, has been shown to reduce infection with T. cruzi. Therefore, in this study, we evaluated the effects of treatment with low-dose ASA on myenteric colonic neurons during murine infection with T. cruzi. METHODS: Swiss mice were assigned into groups treated with either phosphate-buffered saline or low doses of ASA during the acute phase (20 mg/kg ASA) and chronic phase (50 mg/kg ASA) of infection with the Y strain of T. cruzi. Seventy-five days after infection, colon samples were collected to quantify inflammatory foci in histological sections and also general (myosin-V+ ), nitrergic, and VIPergic myenteric neurons in whole mounts. Gastrointestinal transit time was also measured. KEY RESULTS: Aspirin treatment during the acute phase of infection reduced parasitemia (P<.05). Aspirin treatment during the acute or chronic phase of the infection reduced the intensity of inflammatory foci in the colon, protected myenteric neurons from cell death and plastic changes, and recovered the gastrointestinal transit of mice infected with T. cruzi (P<.05). CONCLUSION & INFERENCES: Early and delayed treatment with low-dose ASA can reduce the morphofunctional damage of colonic myenteric neurons caused by murine T. cruzi infection.
BACKGROUND: Experimental and clinical studies have shown that myenteric neuron cell death during infection with Trypanosoma cruzi mainly occurs in the esophagus and colon, resulting in megaesophagus and megacolon, respectively. Evidence suggests that the cyclooxygenase enzyme (COX) is involved in the T. cruzi invasion process. The use of low-dose aspirin (ASA), a COX-1/COX-2 inhibitor, has been shown to reduce infection with T. cruzi. Therefore, in this study, we evaluated the effects of treatment with low-dose ASA on myenteric colonic neurons during murineinfection with T. cruzi. METHODS: Swiss mice were assigned into groups treated with either phosphate-buffered saline or low doses of ASA during the acute phase (20 mg/kg ASA) and chronic phase (50 mg/kg ASA) of infection with the Y strain of T. cruzi. Seventy-five days after infection, colon samples were collected to quantify inflammatory foci in histological sections and also general (myosin-V+ ), nitrergic, and VIPergic myenteric neurons in whole mounts. Gastrointestinal transit time was also measured. KEY RESULTS:Aspirin treatment during the acute phase of infection reduced parasitemia (P<.05). Aspirin treatment during the acute or chronic phase of the infection reduced the intensity of inflammatory foci in the colon, protected myenteric neurons from cell death and plastic changes, and recovered the gastrointestinal transit of mice infected with T. cruzi (P<.05). CONCLUSION & INFERENCES: Early and delayed treatment with low-dose ASA can reduce the morphofunctional damage of colonic myenteric neurons caused by murine T. cruzi infection.
Authors: José Rodrigues do Carmo Neto; Rhanoica Oliveira Guerra; Wellington Francisco Rodrigues; Marcos Vinicius da Silva; Juliana Reis Machado Journal: Oxid Med Cell Longev Date: 2022-09-25 Impact factor: 7.310
Authors: Shankar Suman; Girish Rachakonda; Sammed N Mandape; Shruti S Sakhare; Fernando Villalta; Siddharth Pratap; Maria F Lima; Pius N Nde Journal: PLoS Negl Trop Dis Date: 2018-09-17