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2.
Acta gastroenterol. latinoam ; 31(3): 115-121, 2001. ilus, graf
Article in Spanish | LILACS | ID: lil-305320

ABSTRACT

INTRODUCTION: The action of non-steroidal anti-inflammatory drugs (NSAIDs) on the Helicobacter Pylori (Hp) infected mucosa is a matter of debate. Some authors consider them to cause additive iatrogeny whilst others attribute a purportedly protective action to them. The development of on experimental animal model could help clarify this phenomenon. OBJECTIVES: 1--To develop an animal model of Hp gastric infection. 2--To evaluate the aggressiveness of NSAIDs in this model. MATERIALS AND METHODS: Male 6 month old BALC/C mice weighing 38 g were studied. Pylori Hp infection was ruled out. On three occasions, in the same week, 18 mice were inoculated intra-gastrically with 0.6 ml of Hp culture broth (brain-heart infusion) containing 1 x 10 8-1 x 10 9 CFU/ml. Another group of mice were inoculated with sterile saline. After two months the mice were killed and their stomachs studied. They were divided into groups: a) 6 Hp negative control mice. b) 8 Hp negative mice with prior intra-peritoneal injection of 25 mg/Kg indomethacin (24 hs.) c) 8 mice inoculated with Hp with indomethacin. d) 8 mice inoculated with Hp, without indomethacin. The stomachs were opened along the greater curvature and photographed macroscopically in order to map the necrotic area. The antrums were biopsied to test for urease and separate antrum and body specimens were send for staining with Warthin-Starry H & B and histopathology. RESULTS: All the mice inoculated with Hp acquired the infection. The necrotic area was larger in Group B: 55.5 +/- 7.87 mm than in Group C: 15 +/- 1.82 mm P < 0.00019. HISTOLOGY: Group A: normal mucosa. Group B: extensive coagulation necrosis and focal erosions. Group C: ulcers with inflammatory infiltrate and smaller necrotic area, presence of Hp on the surface epithelium. Group D: no ulcers, Hp present. CONCLUSION: An animal model of Hp infection was successfully developed Hp infection could play a potentially protective role against indomethacin aggression in the mouse.


Subject(s)
Animals , Male , Anti-Inflammatory Agents, Non-Steroidal , Disease Models, Animal , Gastric Mucosa , Helicobacter Infections , Helicobacter pylori , Indomethacin , Gastric Mucosa , Mice , Mice, Inbred BALB C
3.
Acta gastroenterol. latinoam ; 27(2): 81-2, jun. 1997.
Article in Spanish | LILACS | ID: lil-196649

ABSTRACT

Se presenta un caso de hemorragia intestinal como manifestación inicial de un coriocarcinoma testicular. El diagnóstico de la causa de hemorragia requirió laparatomfa. Lesión metastástica del intestino delgado debe considerarse como causa de hemorragia en paciente con coriocarcinoma testicular.


Subject(s)
Humans , Male , Adult , Choriocarcinoma/complications , Gastrointestinal Hemorrhage/etiology , Testicular Neoplasms/complications , Acute Disease , Choriocarcinoma/pathology , Gastrointestinal Hemorrhage/diagnosis , Intestinal Neoplasms/secondary , Intestine, Small/pathology , Testicular Neoplasms/pathology
4.
Acta physiol. pharmacol. ther. latinoam ; 44(1/2): 11-6, 1994. ilus, tab
Article in English | LILACS | ID: lil-147306

ABSTRACT

En este trabajo hemos la influencia de un ácido graso de cadena corta (acetato) sobre el número de células enterocromafines (EC) conteniendo serotonina (5HT) a dos diferentes pH (pH 6.9, estímulo absortivo y pH 2.9 estímulo secretor) infundido durante una hora en el colon. El número de células EC disminuye significativament con una solución infundida a pH 2.9, especialmente en el ciego. La acción de la pirencepina en prevenir esta reducción demuestra que el mecanismo se efectúa parcialmente a través de receptores colinérgicos. Por parte, se observa una disminución de la liberación de 5HT, a través de un mecanismo colinérgico, como lo indica la inhibición observada con la droga antimuscarínica


Subject(s)
Animals , Male , Rats , Fatty Acids, Volatile/pharmacology , Colon/cytology , Pirenzepine/pharmacology , Serotonin/metabolism , Acetates/pharmacology , Cecum/cytology , Cecum/drug effects , Cecum/metabolism , Enterochromaffin Cells , Enterochromaffin Cells , Colon/drug effects , Colon/metabolism , Hydrogen-Ion Concentration , Infusions, Intravenous , Intestinal Mucosa/cytology , Rats, Sprague-Dawley
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