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1.
Mem. Inst. Oswaldo Cruz ; 107(supl.1): 34-42, Dec. 2012. ilus, graf, tab
Article in English | LILACS | ID: lil-659738

ABSTRACT

The clinical course of leprosy is often interrupted by reactions, which are acute inflammatory episodes that can be classified as type I or type II. Type II reactions can present as cutaneous lesions that resemble erythema multiforme (EM). EM is classically associated with drug allergies or pre-existing viral infections. However, the differential diagnostic criteria of the diverse causative agents remain controversial. The aim of this study was to determine both the clinical relevance and the morphological and immunohistochemical characteristics of the EM-like lesions during the course of type II leprosy reactions. Twenty-seven skin biopsies were taken from typical EM-like lesions of multibacillary patients and reviewed; their histological features were correlated to their clinical aspects. Then, a computer-assisted morphometric analysis was performed to measure the extent of angiogenesis during these acute episodes. The histopathological and immunohistochemical analysis of the EM lesions revealed that they shared the same features that have been previously described for ENL, including immunopositivity in the identical cell-mediated immune markers. Our results point to leprosy as the cause of the EM-like lesions in our patients. Therefore, leprosy should be considered in the differential diagnosis of EM.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Erythema Multiforme/pathology , Leprosy, Lepromatous/pathology , Biopsy , Diagnosis, Differential , Immunohistochemistry
2.
Rev. nutr ; 24(5): 667-677, Sept.-Oct. 2011.
Article in English | LILACS | ID: lil-611643

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate serum levels of appetite-related hormones (peptide YY3-36, total ghrelin, leptin and insulin) before and after consumption of a meal in obese women with and without binge eating episodes and normal weight women. METHODS: Twenty-five women aged 32-50 years were invited to participate in this study, including 9 normal weight women without binge eating episodes (20-25kg/m², group 1), 9 obese women with binge eating episodes (³30kg/m², group 2), and 7 obese women without binge eating episodes (group 3). Four blood samples were collected from each participant, one being 60 minutes before and three being 15, 45 and 90 minutes after a meal. The composition of the meal was 55 percent carbohydrates, 15 percent protein and 30 percent lipids. RESULTS: Group 3 presented increased HOMA-IR (M=2.5, SD=1.04) when compared with group 1 (M=1.5, SD=0.53) and group 2 (M=1.8, SD=0.58), p=0.04. Body mass index (p<0.0001), leptin (p<0.0001) and insulin (p=0.01) were higher in group 3 than in the other groups before and after the meal. Additionally, total ghrelin (p=0.003) and PYY3-36 (p=0.02) levels were lower in group 2 than in the other groups before and after the meal. After adjustment for body mass index, only the lower PYY3-36 level of group 2 remained statistically different from the other groups (p=0.01). CONCLUSION: Our study suggests that lower levels of PYY 3-36 are associated with binge eating in obese women.


OBJETIVO: O objetivo deste estudo foi avaliar, antes e após a refeição, as concentrações séricas de hormônios ligados ao controle do apetite (peptídeo YY3-36, grelina total, leptina e insulina) em mulheres obesas com e sem episódios de compulsão alimentar e compará-las às mulheres de peso normal. MÉTODOS: Vinte e cinco mulheres com idade entre 32 e 50 anos foram convidadas a participar deste estudo, incluindo 9 mulheres com peso normal (20-25kg/m²) sem episódios de compulsão alimentar (grupo 1), 9 mulheres obesas (³30 kg/m²) com episódios de compulsão alimentar (grupo 2) e 7 mulheres obesas sem episódios de compulsão alimentar (grupo 3). Foram coletadas quatro amostras de sangue pós-prandiais a 60 minutos (1 hora antes), bem como 15, 45 e 90 minutos após uma refeição composta de 55 por cento de carboidratos, 15 por cento de proteínas e 30 por cento de lipídeos. RESULTADOS: O maior HOMA-IR foi observado no grupo 3 (M=2,5, DP=1,04) quando comparado ao grupo 1 (M=1,5, DP=0,53) e ao grupo 2 (M=1,8, DP=0,58), p=0,04. O índice de massa corporal (p<0,0001), a leptina (p<0,0001) e a insulina (p=0,01) foram maiores no grupo 3 antes e após a refeição. A grelina total (p=0,003) e o PYY3-36 (p=0,02) foram menores no grupo 2 antes e após a refeição. Após o ajuste do índice de massa corporal, apenas a baixa concentração de PYY3-36 no grupo 2 manteve-se estatisticamente diferente entre os grupos (p=0,01). CONCLUSÃO: Este estudo sugere que níveis baixos do PYY-3-36 estejam associados à compulsão alimentar em mulheres obesas.


Subject(s)
Humans , Female , Adult , Middle Aged , Ghrelin/metabolism , Peptide Hormones/metabolism , Insulin/metabolism , Obesity , Peptide YY , Binge-Eating Disorder
3.
Braz. arch. biol. technol ; 53(3): 575-582, May-June 2010. ilus, graf
Article in English | LILACS | ID: lil-548577

ABSTRACT

This work evaluated the effect of in vitro and in vivo treatment with ASA on the morphology of the red blood cells. Blood samples or Wistar rats were treated with ASA for one hour. Blood samples or animals treated with saline were used as control group. Blood smears were prepared, fixed, stained and the qualitative and quantitative morphology of red blood cells were evaluated under optical microscopy. Data showed that the in vitro treatment for one hour with ASA at higher dose used significantly (p<0.05) modified the perimeter/area ratio of the red blood cells. No morphological alterations were obtained with the in vivo treatment. ASA use at highest doses could interfere on shape of red blood cells.


Este trabalho avaliou o efeito do tratamento in vitro e in vivo com AAS na morfologia dos eritrócitos. Amostras de sangue ou ratos Wistar foram tratadas com AAS por uma hora. Amostras sangüíneas ou animais tratados com salina foram utilizados como grupos controle. Distensões de sangue foram preparadas, fixadas, coradas e a análise morfológica qualitativa e quantitativa dos eritrócitos foi realizada em microscópio óptico. Os dados mostraram que o tratamento in vitro por uma hora com AAS na maior dose utilizada modificou significativamente (p<0.05) a relação perímetro/área dos eritrócitos. Não foram obtidas alterações morfológicas com o tratamento in vivo. O uso do AAS em doses altas poderia interferir na forma dos eritrócitos.

4.
Rio de Janeiro; s.n; 2009. 68 p. ilus, tab.
Thesis in Portuguese | LILACS | ID: lil-576284

ABSTRACT

O comportamento alimentar de uma espécie é determinado por um conjunto de características filogenéticas, ontogenéticas, e epigenéticas, e regulado por fatores internos e externos ao organismo. Os fenômenos naturais que regem a vida no nosso planeta são periódicos em sua maioria, e a oferta de alimentos não é exceção. Cada safra é seguida de uma entressafra, e este ritmo sincroniza diversos outros ritmos, exógenos e endógenos, capazes de determinar a sobrevivência de espécies. Uma das estratégias adaptativas mais primitivas e bem sucedidas na dinâmica oscilatória da natureza, é o acúmulo de reservas. Nossa espécie, nos últimos 50 anos, vive uma situação de grande oferta de alimentos, período este extremamente pequeno, se visto sob a ordem de grandeza da evolução humana. Este fenômeno tem sido determinante na prevalência do depósito de energia e em decorrência, do surgimento da obesidade e suas consequentes patologias. O hipotálamo está intimamente associado à homeostase energética e ao comportamento alimentar. No núcleo arqueado hipotalâmico encontram-se populações neuronais orexigênicas e anorexigênicas, dentre as quais, as que expressam os neuroreceptores POMC, NPY e o substrato de receptor de insulina IRS2. A modificação da expressão destas proteínas tem sido associada à alterações do comportamento alimentar, bem como à impressão e programação metabólica, capazes de induzir obesidade em ratos adultos. A correlação desta circuitaria neuronal com o comportamento alimentar, porém, ainda não está suficientemente compreendida. A detecção do estado de fome-saciedade nos ratos, fundamental no estudo da neurofisiologia relacionada ao comportamento alimentar, vem sendo obtida via de regra, por meio de procedimentos complexos de observação comportamental. O presente estudo contribui para o conhecimento de padrões de alimentação determinados por condições nutricionais, e sua relação com a expressão neurofisiológica hipotalâmica dos neurônios POMC, NPY e IRS2 ...


The feeding behavior of a specie is determined by a group of phylogenetic, ontogenetic, and epigenetic features, and regulated by internal and external factors to the organism. The natura phenomena that govern life in our planet are mainly periodic, and the food stocks is not an exception. Each harvest is followed by a time between harvests, and this rhythm synchronizes other several exogenous and endogenous rhythms, capable of determining the survival of species. One of the most primitive strategies of adaptative evolution of species, and what usually happens regarding the oscillatory dynamics of nature, is the reserve accumulation. Our species, in the last 50 years, has been living a situation of great food offer, such period is exremely small if analysed under the greatness order of the human evolution. This phenomenon has been decisive in the prevalence of the energy deposit and, in consequence, determining the appearance of obesity and its consequent pathologies. The hypothalamus is intimately associated to the energy homeostasis and the feeding behavior. In the arcuate nucleous are orexigenic and anorexigenic neuronal populations, that express the neuroreceptors POMC, NPY and insulin receptor substratum IRS2. The modification of these proteins expression, has been associated to alterations of the feeding behavior, as well as to the metabolic imprinting and programming, capable to induce obesity in adult rats. The correlation of this neuronal circuits with the alimentary behavior, however, it is not yet sufficiently understood. The detection of the hunger-satiation state in the rat, crucial in the neurophysiology studies related to the alimentary behavior, has been obtained through complex procedures of behavioral observation. The present study contributed to the knowledge of certain feeding patterns for nutritional conditions, and its relationship with the neurophysiological expression of POMC, NPY and IRS2 neurons. Using the metabolic programming ...


Subject(s)
Animals , Rats , Feeding Behavior/physiology , Neuropeptide Y/metabolism , Arcuate Nucleus of Hypothalamus/metabolism , Food Deprivation/physiology , Pro-Opiomelanocortin/metabolism , Insulin Receptor Substrate Proteins/metabolism , Satiety Response/physiology , Circadian Rhythm/physiology , Nutritional Status , Obesity/metabolism , Overweight/metabolism
5.
Braz. arch. biol. technol ; 51(spe): 127-133, Dec. 2008. ilus, graf, tab
Article in English | LILACS | ID: lil-508866

ABSTRACT

This work evaluates effects of the sweetener with sucralose on the labeling of blood constituents with technetium- 99m (99mTc), on the morphology of red blood cells (RBC) and on the biodistribution of sodium pertechnetate in Wistar rats. Animals were treated with sweetener for 8 days. Blood samples were withdrawn and the assay of labeling of blood constituents with 99mTc was performed. Blood cells (BC) and plasma (P) were isolated. Aliquots of BC and P were also precipitated, soluble and insoluble fractions separated. The radioactivity in each fraction was counted and percentage of incorporated radioactivity (%ATI) determined. Blood smears were prepared, fixed, stained and the qualitative and quantitative morphology of the RBC was evaluated under optical microscopy. In biodistribution experiments, sodium pertechnetate was administrated, organs and tissues isolated, radioactivity was counted and percentage of incorporated radioactivity per gram (%ATI/g) determined. The data showed no significant alterations in %ATI, morphology of RBC and in %ATI/g in the studied organs.


Neste estudo foram avaliados efeitos do adoçante com sucralose na marcação de constituintes sangüíneos com 99mTc, na morfologia de hemácias e na biodistribuição do pertecnetato de sódio em ratos Wistar. Animais foram tratados com adoçante durante 8 dias. Amostras de sangue foram retiradas e a marcação de constituintes sangüíneos com 99mTc foi realizada. Células sangüíneas (CS) e plasma (P) foram isolados. Alíquotas de CS e P foram precipitadas, fraçõesinsolúvel e solúvel foram separadas. Aradioatividade em cada fração foi contada e o percentual de radioatividade incorporada (%ATI), determinado. Distensões sangüíneas foram preparadas, fixadas, coradas e análise morfológica, qualitativa e quantitativa, de hemácias foi avaliada sob microscopia óptica. Nos experimentos debiodistribuição, pertecnetato de sódio foiadministrado, órgãos e tecidos isolados, a radioatividade contada e o percentual de radioatividade incorporada por grama (%ATI/g), determinada. Os dados sugerem que não houve alterações significativas no %ATI, morfologia de hemácias e no %ATI/g.

6.
Braz. arch. biol. technol ; 51(spe): 135-141, Dec. 2008. ilus, graf, tab
Article in English | LILACS | ID: lil-508867

ABSTRACT

The aim of this work was to evaluate the effect of fenoprofen on the labeling of blood constituents with technetium-99m, on the morphology of red blood cells and on the plasmid DNA. Blood samples from Wistar rats were incubated with fenoprofen and the assay of labeling of blood constituents with technetium-99m (99mTc) was performed. Blood cells, plasma, soluble and insoluble fractions of blood cells and plasma were separated. The radioactivity in each fraction was counted and percentage of incorporated radioactivity ( percentATI) was determined. Blood smears were prepared, fixed, stained and the qualitative and quantitative morphology of the red blood cells (RBC) was evaluated. Plasmid (pBSK) was incubated with fenoprofen with stannous chloride, and agarose gel electrophoresis procedure was carried out to evaluate genotoxic and the protection of this drug against stannous chloride effect on DNA. In conclusion, under the conditions used in this work, our data suggest that fenoprofen would not (i) affect the fixation of the 99mTc on the blood constituents, (ii) alter the RBC membrane and (iii) present genotoxic and redox effects.


O objetivo deste trabalho foi avaliar o efeito do fenoprofeno na marcação de constuintes sanguíneos com tecnécio-99m (99mTc), na morfologia de hemácias e no DNA plasmidial. Amostras de sangue de ratos Wistar foram incubadas com fenoprofeno e a marcação de constituintes sangüíneos com 99mTc foi realizada. Células sangüíneas (CS) e plasma (P) foram isolados. Alíquotas de CS e P foram precipitadas, frações insolúvel e solúvel foram separadas. A radioatividade em cada fração foi contada e o percentual de radioatividade incorporada ( por centoATI), determinada. Distensões sangüíneas foram preparadas, fixadas, coradas e análise morfológica, qualitativa e quantitativa, de hemácias foi realizada sob microscopia óptica. Plasmídios pBSK foram incubados com fenoprofeno na presença e ausência de cloreto estanoso, e o procedimento de eletroforese em gel de agarose realizado para avaliar o efeito genotóxico deste fármaco e seu efeito sobre a ação do cloreto estanoso no DNA. Os resultados obtidos sugerem que, nas condições utilizadas nesse estudo, o fenoprofeno não poderia: (i) afetar a fixação do 99mTc nos constituintes sanguíneos, (ii) alterar a membrana de hemácias e (iii) apresentar efeitos genotóxicos e redox.

7.
Mem. Inst. Oswaldo Cruz ; 96(suppl): 107-112, Sept. 2001. ilus, graf
Article in English | LILACS | ID: lil-295868

ABSTRACT

Mast cells and eosinophils actively participate in tissue repair and are prominent components of Schistosoma mansoni granulomas. Since pentoxifillyne (PTX) is an immunomodulatory and antifibrotic substance, we aimed to characterize, by morphological techniques, the effect of this drug on fibrosis developed inside murine hepatic schistosomal granulomatous reaction, beyond the quantification of eosinophil and mast cell populations. The drug (1 mg/100 g animal weight) was administrated from 35 to 90 days post-infection, when the animals were killed. The intragranulomatous interstitial collagen network was analyzed by confocal laser scanning microscopy, the number of eosinophils and mast cells was quantified and the results were validated by t-student test. Treatment did not interfere on the granuloma evolution but caused a significant decrease in the total and involutive number of hepatic granulomas (p = 0.01 and 0.001, respectivelly), and in the intragranulomatous accumulation of eosinophils (p = 0.0001). Otherwise, the number of mast cells was not significantly altered (p = 0.9); however, it was positively correlated with the number of granulomatous structures (r = 0.955). In conclusion, PTX does not affect development and collagen deposition in S. mansoni murine granuloma, but decreases the intragranulomatous eosinophil accumulation possibly due to its immunomodulatory capability, interfering in cellular recruitment and/or differentiation


Subject(s)
Animals , Male , Mice , Eosinophils/drug effects , Extracellular Matrix/drug effects , Granuloma/parasitology , Liver Diseases, Parasitic/parasitology , Pentoxifylline/pharmacology , Phosphodiesterase Inhibitors/pharmacology , Schistosomiasis mansoni/complications , Collagen/drug effects , Fibrosis/drug therapy , Fibrosis/parasitology , Granuloma/drug therapy , Liver Diseases, Parasitic/drug therapy , Liver/pathology , Mast Cells/drug effects , Pentoxifylline/therapeutic use , Phosphodiesterase Inhibitors/therapeutic use
8.
Mem. Inst. Oswaldo Cruz ; 95(6): 839-42, Nov.-Dec. 2000. tab, ilus
Article in English | LILACS | ID: lil-273438

ABSTRACT

Morphometrics of Brazilian strains (BH, SJ and CMO) of Schistosoma mansoni cercariae were obtained with a computerized image analyzer (IMAGE PRO PLUS, MEDIA CYBERNETICS), considering the following characters: body area, tail, furcae, oral and ventral suckers and distance between them. For statistical analysis, the variance test (one-way Anova) was applied and significant differences of p< 0.05 were considered. All morphometric values in the BH strain were significantly higher (p< 0.05) than in the others. Lower values were obtained in females of SJ strain for all characters, excepting the body area. Only this character showed to be significantly different in males and females of the three strains. Specimens of both sexes in the BH and SJ strains showed significant differences regarding all characters. It was observed that this morphometric analysis permits the characterization of strains and also the sex identification in S. mansoni cercariae. Due to its feasibility, this method can be applied as a tool in laboratories devoid of more complex equipment


Subject(s)
Animals , Male , Female , Mice , Schistosoma mansoni/classification , Analysis of Variance , Brazil , Schistosoma mansoni/physiology , Sex Characteristics
9.
Mem. Inst. Oswaldo Cruz ; 93(supl.1): 309-12, Oct. 1998. tab
Article in English | LILACS | ID: lil-218696

ABSTRACT

A computer software for image (IMAGE PRO PLUS, MEDIA CYBERNETICS) was utilized in male and females adult worms aiming the morphological characterization of Schistosoma mansoni samples isolated from a sylvatic rodent, Nectomys squamipes and humans in Sumidouro, Rio de Janeiro, Brazil and recovered from Mus musculus C3H/He. The following characters for male's testicular lobes were analyzed: number, area, density, larger and shorter diameter, longer and shorter axis and perimeter and extension; for females: area, longer and shorter axis, larger and smaller diameter and perimeter of the eggs and spine; oral and ventral suckers area and distance between them in both sex were determined. By the analysis of variance (one way ANOVA) significant differences (p<0.05) were observed in all studied characters, except for the density of testicular lobes. Significant differences (p<0.05) were detected for all characters in the female worms. Data ratify that sympatric isolates present phenotypic differences and the adult female characters are useful for the proper identification of S. mansoni isolates.


Subject(s)
Humans , Animals , Mice/parasitology , Schistosoma mansoni/anatomy & histology , Brazil
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