RESUMO
Neste trabalho foi realizado estudo comparativo dos níveis de corticóides fecais (CF) de chimpanzé (Pan troglodytes) e orangotango(Pongo pygmaeus). Foram analisadas amostras coletadas em duas fases distintas, relacionadas com a introdução de técnicas de enriquecimento ambiental, a saber: Base (antes da introdução) e Habituação(imediatamente após). Realizamos as validações do conjunto comercial para radioimunoensaio ImmunuChem Double Antibody Corticosterone da MP Biomedicals, para mensuração de CF. A validação laboratorial dos conjuntos diagnósticos para uso em extrato fecal de primatas foi realizada pelo método de paralelismo, no qual, para cada espécie, concentrações conhecidas de corticosterona foram adicionadas a um pool de extratos fecais, sendo estas amostras analisadas em seguida. As inclinações das curvas obtidas nestes ensaios e da curva padrão do ensaio foram então comparadas. Os resultados obtidos para chimpanzé e orangotango, foram respectivamente, Y=17,23+1,31*X;R...
A comparative study of fecal corticoids (FC) concentrations was carried out with chimpanzees (Pan troglodytes) e orangutans (Pongo pygmaeus). Fecal samples were collected before (Basal) and just after (Habituation)enrichment introduction and analyzed. We performed biochemical and physiological validations of the ImmunuChem Double Antibody Corticosterone kit for radioimmunoassay from MP Biomedicals for quantifying FC concentrations. To establish the biochemical validity of our assay we performed parallelism assays in which pooled fecal extracts from both species were spiked with known quantities of corticosterone standard and the slopes of the curves obtained with these samples and the standard curves of the kits were compared. The correlation coefficients were R
Assuntos
Animais , Corticosteroides/análise , Fezes , Imunoensaio/métodos , Pan troglodytes , Pongo pygmaeusRESUMO
INTRODUCTION: A hypercoagulable state has been recognized in patients with inflammatory bowel disease. OBJECTIVE: The aim of this study was to determine the frequency of single and combined thrombophilic abnormalities in patients from northern Portugal with Crohn's disease or ulcerative colitis, without a history of thrombosis. METHODS A cross-sectional study involving 116 patients (42 with ulcerative colitis, 74 with Crohn's disease), and 141 randomly chosen asymptomatic blood donors was carried out. Prothrombotic variables and genetic abnormalities were assessed. RESULTS: The prevalence of single prothrombotic abnormalities (only one alteration) in inflammatory bowel disease patients was higher than in the reference population (26% and 18%, respectively; P < 0.02). The allelic frequency of genetic polymorphisms was higher in Crohn's disease and ulcerative colitis for MTHFR C677T, ACE Del and PAI-1 4G (P < 0.001) than in the reference population. The prevalence of combined thrombophilic abnormalities (at least two alterations) in both Crohn's disease and ulcerative colitis was also higher (22% and 21%, respectively) than in the reference population (9%; P < 0.01). These differences were not related to age or gender; however, in Crohn's disease the frequency of two or more abnormalities was related to disease activity (odds ratio 3.0 [1.3-6.7]). CONCLUSION: Higher prevalences of single and combined thrombophilic defects were found in inflammatory bowel disease patients, factors that could be involved in the disease pathogenesis.
Assuntos
Colite Ulcerativa/genética , Doença de Crohn/genética , Polimorfismo Genético , Trombofilia/genética , Adolescente , Adulto , Idoso , Estudos de Casos e Controles , Distribuição de Qui-Quadrado , Colite Ulcerativa/sangue , Doença de Crohn/sangue , Estudos Transversais , Fator V/genética , Feminino , Frequência do Gene , Humanos , Masculino , Metilenotetra-Hidrofolato Redutase (NADPH2)/genética , Pessoa de Meia-Idade , Peptidil Dipeptidase A/genética , Inibidor 1 de Ativador de Plasminogênio/genética , Protrombina/genética , Estatísticas não ParamétricasRESUMO
We report the case of a boy with hereditary spherocytosis who presented with mild microcytic hypochromic anemia and recurrent leg ulcers that had been present since childhood. Chronic natural killer (NK) cell and B-cell lymphocytosis was detected 1 year after therapeutic splenectomy during investigation of recurrent episodes of neutropenia and persistent lymphocytosis. NK cells proved to be abnormal at immunophenotyping studies, and B-cells were polyclonal and displayed a normal immunophenotype. Genotypic analysis of T-cell receptor (TCR)-beta and TCR-gamma genes showed a germ-line pattern. The clinical course of this patient was characterized by multiple pulmonary infections and amygdalitis. We discuss the potential roles of persistent immune stimulation due to chronic hemolysis and severe leg ulcers and of splenectomy in the origin of NK cell lymphocytosis and the relationship between NK cells and recurrent infections, relapsing neutropenia, and polyclonal B-cell response.
