RESUMEN
In spite of the many studies examining alcohol consumption, recent reviews have indicated that binge drinking has not been extensively studied. Furthermore, it is becoming increasingly clear that sleep is associated with many physiological functions and to drug addictions. The present study aimed to evaluate the relationship between alcohol binge drinking and insomnia in college students of health sciences. All first-year health sciences students (n=286) were evaluated in a cross-sectional study. Envelopes containing the Insomnia Severity Index (ISI), the Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST), and questions capturing sociodemographic data were distributed and collected in classes. It was found that most non-drinkers were female (70.6%), although there were no sex-related differences in the number of binge drinkers (more than 5 drinks on each occasion at least once a week), allowing statistical comparison. The Mann-Whitney U test indicated that the ISI scores were significantly greater in female than male binge drinkers (P=0.014). Moderate or severe insomnia was reported by 23% of the sample, with alcohol being the most frequently associated substance. A specialized intervention was suggested by ASSIST: brief for marijuana (19.2%) and tobacco (23.3%) use, and moderate (31.5%) or intensive (1.4%) for alcohol consumers. The data highlighted the need to pay attention to the habits of college students beyond obtaining scientific information. New data suggesting the influence of genetics on insomnia may be of importance when performing additional studies on the sex differences in alcohol binge drinking.
Asunto(s)
Consumo Excesivo de Bebidas Alcohólicas , Trastornos del Inicio y del Mantenimiento del Sueño , Consumo de Bebidas Alcohólicas/epidemiología , Consumo Excesivo de Bebidas Alcohólicas/epidemiología , Brasil/epidemiología , Estudios Transversales , Femenino , Humanos , Masculino , Trastornos del Inicio y del Mantenimiento del Sueño/epidemiología , Estudiantes , UniversidadesRESUMEN
In spite of the many studies examining alcohol consumption, recent reviews have indicated that binge drinking has not been extensively studied. Furthermore, it is becoming increasingly clear that sleep is associated with many physiological functions and to drug addictions. The present study aimed to evaluate the relationship between alcohol binge drinking and insomnia in college students of health sciences. All first-year health sciences students (n=286) were evaluated in a cross-sectional study. Envelopes containing the Insomnia Severity Index (ISI), the Alcohol, Smoking, and Substance Involvement Screening Test (ASSIST), and questions capturing sociodemographic data were distributed and collected in classes. It was found that most non-drinkers were female (70.6%), although there were no sex-related differences in the number of binge drinkers (more than 5 drinks on each occasion at least once a week), allowing statistical comparison. The Mann-Whitney U test indicated that the ISI scores were significantly greater in female than male binge drinkers (P=0.014). Moderate or severe insomnia was reported by 23% of the sample, with alcohol being the most frequently associated substance. A specialized intervention was suggested by ASSIST: brief for marijuana (19.2%) and tobacco (23.3%) use, and moderate (31.5%) or intensive (1.4%) for alcohol consumers. The data highlighted the need to pay attention to the habits of college students beyond obtaining scientific information. New data suggesting the influence of genetics on insomnia may be of importance when performing additional studies on the sex differences in alcohol binge drinking.
Asunto(s)
Humanos , Masculino , Femenino , Consumo Excesivo de Bebidas Alcohólicas/epidemiología , Trastornos del Inicio y del Mantenimiento del Sueño/epidemiología , Estudiantes , Universidades , Brasil/epidemiología , Consumo de Bebidas Alcohólicas/epidemiología , Estudios TransversalesRESUMEN
Frozen fish can be stored in freezers for about a year. Glaciation, a stage that occurs after freezing, confers protection and prevents fish oxidation. Studies with fish showed fraud in relation to the glaciation process. In this context, the present research aimed to analyze the amount of glaciation in 81 samples of frozen tilapia fillets of 3 brands, as well as the real price, labeling, packaging integrity, weight and conservation status of these products in 3 supermarket chains in São Carlos-SP, in order to identify frauds. In relation to glaciation, 100% of the samples were in agreement with the current regulatory laws, which stablishes the maximum icing in 20% of the total fish weight, as well as the real prices of each brand and the labels. There were irregularities with the net weights reported on the packages, where 95% of the samples were incompatible with the true weight of the products and only 4.05% were with the effective weights described in the labels. 37.5% of marketing freezers had temperatures above -18C, which determines the irregularity of the merchant establishment. However, although the glaciation was respected by the three brands, the net weight characterized fraud by the fillet production companies.
O pescado congelado pode ser armazenado em freezers durante aproximadamente um ano. O glaciamento, etapa que ocorre após congelamento, confere proteção e evita a oxidação do pescado. Diversos estudos realizados com pescados,demonstraram fraudes em relação ao processo de glaciamento. Neste contexto, o presente trabalho objetivou analisar a quantidade de glaciamento em 81 amostras de filés de tilápia congelados de três marcas, assim como, os preços reais,rotulagem, integridade do pescado e da embalagem, peso líquido e modo de conservação, em três redes de supermercados da cidade de São Carlos-SP. Em relação ao glaciamento, 100% das amostras estavam de acordo com a normativa vigente, que estabelece o máximo de glacê em 20% do peso total do pescado, assim como os preços reais decada marca e os rótulos. Houve irregularidades com os pesos líquidos informados nas embalagens, em que 95% das amostras estavam incompatíveis com o peso verdadeiro dos produtos e apenas 4,05% estavam com os pesos efetivos iguais ou superiores ao peso líquido descrito na embalagem. Das gôndolas verificadas com termômetro infravermelho externo, nas três redes de supermercados, 37,5% estavam com temperaturas superiores a -18°C, o que determina irregularidade do estabelecimento comercializador. Contudo, apesar do glaciamento ter sido respeitado pelas três marcas, o peso líquido caracterizava fraude das empresas de produção dos filés.
Asunto(s)
Alimentos Congelados/análisis , Alimentos Congelados/normas , Comercio/normas , Fraude , Glaseantes , Control y Fiscalización de Alimentos y Bebidas , Inocuidad de los Alimentos , Fecha de Caducidad de Productos , TilapiaRESUMEN
Frozen fish can be stored in freezers for about a year. Glaciation, a stage that occurs after freezing, confers protection and prevents fish oxidation. Studies with fish showed fraud in relation to the glaciation process. In this context, the present research aimed to analyze the amount of glaciation in 81 samples of frozen tilapia fillets of 3 brands, as well as the real price, labeling, packaging integrity, weight and conservation status of these products in 3 supermarket chains in São Carlos-SP, in order to identify frauds. In relation to glaciation, 100% of the samples were in agreement with the current regulatory laws, which stablishes the maximum icing in 20% of the total fish weight, as well as the real prices of each brand and the labels. There were irregularities with the net weights reported on the packages, where 95% of the samples were incompatible with the true weight of the products and only 4.05% were with the effective weights described in the labels. 37.5% of marketing freezers had temperatures above -18°C, which determines the irregularity of the merchant establishment. However, although the glaciation was respected by the three brands, the net weight characterized fraud by the fillet production companies.
RESUMEN
Frozen fish can be stored in freezers for about a year. Glaciation, a stage that occurs after freezing, confers protection and prevents fish oxidation. Studies with fish showed fraud in relation to the glaciation process. In this context, the present research aimed to analyze the amount of glaciation in 81 samples of frozen tilapia fillets of 3 brands, as well as the real price, labeling, packaging integrity, weight and conservation status of these products in 3 supermarket chains in São Carlos-SP, in order to identify frauds. In relation to glaciation, 100% of the samples were in agreement with the current regulatory laws, which stablishes the maximum icing in 20% of the total fish weight, as well as the real prices of each brand and the labels. There were irregularities with the net weights reported on the packages, where 95% of the samples were incompatible with the true weight of the products and only 4.05% were with the effective weights described in the labels. 37.5% of marketing freezers had temperatures above -18C, which determines the irregularity of the merchant establishment. However, although the glaciation was respected by the three brands, the net weight characterized fraud by the fillet production companies.(AU)
O pescado congelado pode ser armazenado em freezers durante aproximadamente um ano. O glaciamento, etapa que ocorre após congelamento, confere proteção e evita a oxidação do pescado. Diversos estudos realizados com pescados,demonstraram fraudes em relação ao processo de glaciamento. Neste contexto, o presente trabalho objetivou analisar a quantidade de glaciamento em 81 amostras de filés de tilápia congelados de três marcas, assim como, os preços reais,rotulagem, integridade do pescado e da embalagem, peso líquido e modo de conservação, em três redes de supermercados da cidade de São Carlos-SP. Em relação ao glaciamento, 100% das amostras estavam de acordo com a normativa vigente, que estabelece o máximo de glacê em 20% do peso total do pescado, assim como os preços reais decada marca e os rótulos. Houve irregularidades com os pesos líquidos informados nas embalagens, em que 95% das amostras estavam incompatíveis com o peso verdadeiro dos produtos e apenas 4,05% estavam com os pesos efetivos iguais ou superiores ao peso líquido descrito na embalagem. Das gôndolas verificadas com termômetro infravermelho externo, nas três redes de supermercados, 37,5% estavam com temperaturas superiores a -18°C, o que determina irregularidade do estabelecimento comercializador. Contudo, apesar do glaciamento ter sido respeitado pelas três marcas, o peso líquido caracterizava fraude das empresas de produção dos filés.(AU)
Asunto(s)
Alimentos Congelados/análisis , Alimentos Congelados/normas , Fraude , Glaseantes , Comercio/normas , Tilapia , Fecha de Caducidad de Productos , Control y Fiscalización de Alimentos y Bebidas , Inocuidad de los AlimentosRESUMEN
The aims of the this study were a) to verify whether the performance decrease induced by nonfunctional overreaching (NFOR) is linked to high concentrations of cytokines in serum, skeletal muscles and liver; b) to verify muscle myostatin adaptation to NFOR; c) to verify the effects of chronic glucose supplementation on the parameters mentioned above. Mice were divided into control (C), trained (TR), overtrained (OTR) and supplemented overtrained (OTR + S). The incremental load test (ILT) and exhaustive test (ET) were used to measure performances before and after exercise protocols. 24 h after ET, muscles and liver were removed and stored at -80°C for subsequent measurements. Total blood was collected from decapitation for subsequent determination of cytokine concentrations. Generally, OTR and OTR + S presented higher contents of IL-6, TNF-alpha, GLUT-4 and myostatin in muscle samples compared to C and TR. Glucose supplementation attenuated the high contents of IL-6, TNF-alpha and IL-15 in liver, and of IL-6 in serum. In summary, NFOR led to low-grade chronic inflammation and myostatin upregulation.
Asunto(s)
Glucosa/administración & dosificación , Inflamación/metabolismo , Movimiento/fisiología , Miostatina/metabolismo , Condicionamiento Físico Animal/fisiología , Animales , Biomarcadores/metabolismo , Enfermedad Crónica , Transportador de Glucosa de Tipo 4/metabolismo , Inflamación/etiología , Interleucina-6/metabolismo , Hígado/metabolismo , Masculino , Ratones , Músculo Esquelético/metabolismo , Condicionamiento Físico Animal/efectos adversos , Factor de Necrosis Tumoral alfa/metabolismo , Regulación hacia ArribaRESUMEN
The objective of this research was to evaluate the interference of ethanol consumption by female rats with cytokines involved in the sepsis process and its correlation with mortality, the main outcome of sepsis. Female Wistar rats in estrus phase were evaluated in three experiments. Experiment 1 (n=40) was performed to determine survival rates. Experiment 2 (n=69) was designed for biochemical analysis, measurement of cytokine and estrogen levels before and after sepsis, and experiment 3 (n=10) was performed to evaluate bacterial growth by colony counts of peritoneal fluid. In all experiments, treated animals were exposed to a 10% ethanol/water solution (v/v) as the single drinking source, while untreated animals were given tap water. After 4 weeks, sepsis was induced in the rats by ip injection of feces. In experiment 1, mortality in ethanol-exposed animals was delayed compared with those that drank water (48 h; P=0.0001). Experiment 2 showed increased tumor necrosis factor alpha (TNF-α) and decreased interleukin-6 (IL-6) and macrophage migration inhibitory factor in septic animals exposed to ethanol compared to septic animals not exposed. Sepsis also increased TNF-α and IL-6 levels in both ethanol- and water-exposed groups. Biochemical analysis showed higher creatinine, alanine aminotransferase and aspartate aminotransferase and decreased glucose levels in septic animals that were exposed to ethanol. In experiment 3, septic animals exposed to ethanol showed decreased numbers of colony-forming units than septic animals exposed to water. These results suggest that ethanol consumption delays the mortality of female rats in estrus phase after sepsis induction. Female characteristics, most probably sex hormones, may be involved in cytokine expression.
RESUMEN
The objective of this research was to evaluate the interference of ethanol consumption by female rats with cytokines involved in the sepsis process and its correlation with mortality, the main outcome of sepsis. Female Wistar rats in estrus phase were evaluated in three experiments. Experiment 1 (n=40) was performed to determine survival rates. Experiment 2 (n=69) was designed for biochemical analysis, measurement of cytokine and estrogen levels before and after sepsis, and experiment 3 (n=10) was performed to evaluate bacterial growth by colony counts of peritoneal fluid. In all experiments, treated animals were exposed to a 10% ethanol/water solution (v/v) as the single drinking source, while untreated animals were given tap water. After 4 weeks, sepsis was induced in the rats by ip injection of feces. In experiment 1, mortality in ethanol-exposed animals was delayed compared with those that drank water (48 h; P=0.0001). Experiment 2 showed increased tumor necrosis factor alpha (TNF-α) and decreased interleukin-6 (IL-6) and macrophage migration inhibitory factor in septic animals exposed to ethanol compared to septic animals not exposed. Sepsis also increased TNF-α and IL-6 levels in both ethanol- and water-exposed groups. Biochemical analysis showed higher creatinine, alanine aminotransferase and aspartate aminotransferase and decreased glucose levels in septic animals that were exposed to ethanol. In experiment 3, septic animals exposed to ethanol showed decreased numbers of colony-forming units than septic animals exposed to water. These results suggest that ethanol consumption delays the mortality of female rats in estrus phase after sepsis induction. Female characteristics, most probably sex hormones, may be involved in cytokine expression.
RESUMEN
The objective of the study was to evaluate the frequency and clinical characteristics of ocular complications and their risk factors, as well as autologous serum tears (AST) for the treatment of dry eye in these patients. Data from the files of 124 patients who had undergone allogeneic haematopoietic progenitor cell transplantation (HPCT) were evaluated. In addition, 33 HPCT patients were examined and their data were compared with controls. Analysis of tears and AST was performed. Dry eye manifestation occurred in 32% of patients and was positively correlated with age over 27 years (P = 0.05), peripheral blood progenitor cell transplant (P = 0.002), chronic graft-versus-host disease (P = 0.0027), and chronic or acute myeloid leukaemia (P = 0.001). Dry mouth and Schirmer test < 5 mm were predictive factors for dry eye in HPCT patients (P = 0.002 and odds ratio 3.9 and P = 0.007, odds ratio = 5.9, respectively). Microbiological analysis revealed that six of 11 AST samples were contaminated after 30 days of use. The present study supports the role of potential risk factors for ocular complications and key elements to detect alterations in the tear film from HPCT patients. In addition, AST contamination must be considered after longer periods of use.
Asunto(s)
Síndromes de Ojo Seco , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Soluciones Oftálmicas/uso terapéutico , Suero , Adolescente , Adulto , Factores de Edad , Niño , Síndromes de Ojo Seco/tratamiento farmacológico , Síndromes de Ojo Seco/etiología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Soluciones Oftálmicas/química , Soluciones Oftálmicas/aislamiento & purificación , Factores de RiesgoRESUMEN
AIMS/HYPOTHESIS: To assess the involvement of the AGE-specific receptor (AGER, also known as RAGE) axis and nuclear factor kappa-B (NFKB, also known as NF-kappaB) activation in the development of lacrimal gland and tear film dysfunction in diabetes, the present study evaluated: (1) lacrimal gland and tear film alterations in diabetic rats; and (2) the expression of AGE, AGER and NFKB in ocular tissues of normoglycaemic and diabetic rats. MATERIALS AND METHODS: Diabetes was induced in male Wistar rats with intravenous streptozotocin. Tear secretion parameters were measured and NFKB expression was evaluated in lacrimal glands of control and diabetic rats by western blot. Immunohistochemistry with confocal microscopy was used to assess AGE, AGER and NFKB expression in lacrimal glands of both groups. RESULTS: Lacrimal gland weight and tear film volume were lower in diabetic than in control rats (p=0.01 and 0.02, respectively). IL1B and TNF concentrations in tears were higher in diabetic than in control rats (p=0.007 and 0.02, respectively). NFKB protein was identified in rat cornea, conjunctiva and lacrimal glands. AGE, AGER and NFKB expression were greater in lacrimal glands of diabetic than in those of control rats. CONCLUSIONS/INTERPRETATION: Diabetes induces significant alterations in rat lacrimal gland structure and secretion. The higher expression of AGE, AGER and NFKB in lacrimal glands of diabetic rats suggests that these factors are involved in signalling and in subsequent inflammatory alterations related to dry eye in diabetes mellitus.
Asunto(s)
Diabetes Mellitus Experimental/metabolismo , Productos Finales de Glicación Avanzada/análisis , Aparato Lagrimal/metabolismo , FN-kappa B/metabolismo , Receptores Inmunológicos/metabolismo , Animales , Western Blotting , Conjuntiva/metabolismo , Conjuntiva/fisiopatología , Córnea/metabolismo , Córnea/fisiopatología , Diabetes Mellitus Experimental/genética , Diabetes Mellitus Experimental/fisiopatología , Síndromes de Ojo Seco/fisiopatología , Expresión Génica , Productos Finales de Glicación Avanzada/genética , Productos Finales de Glicación Avanzada/metabolismo , Inmunohistoquímica , Interleucina-1/metabolismo , Aparato Lagrimal/fisiopatología , Masculino , FN-kappa B/genética , Ratas , Ratas Wistar , Receptor para Productos Finales de Glicación Avanzada , Receptores Inmunológicos/genética , Lágrimas/metabolismo , Factor de Necrosis Tumoral alfa/metabolismoRESUMEN
AIMS: To determine the pattern and the genetic basis of resistance to terbinafine, a drug extensively used for the treatment of fungal infections in humans. METHODS AND RESULTS: Four resistant mutants from Aspergillus nidulans isolated after irradiation with ultraviolet light were crossed with the master strain F (MSF). Genetic analysis revealed that a single gene, located on chromosome IV, is responsible for resistance to terbinafine and that the alleles responsible for this resistance in these mutants are of a codominant or dominant nature at high terbinafine concentrations. Furthermore, the interaction of this mutation with another one identified on chromosome II causes the double mutant to be highly resistant. CONCLUSIONS: Periodic surveillance of antimycotic susceptibility would be an important measure in detecting the emergence and spread of resistance. Mutation in a single gene could be responsible for resistance to terbinafine and a genic interaction may be responsible for a higher level of antimycotic resistance. SIGNIFICANCE AND IMPACT OF THE STUDY: The understanding of the mechanisms that lead to changes in the sensitivity of a fungus to a given antifungal agent is important both in order to define strategies for the use of such agent and to guide the development of new antifungal agents.
Asunto(s)
Antifúngicos/farmacología , Aspergillus nidulans/efectos de los fármacos , Farmacorresistencia Fúngica/genética , Proteínas Fúngicas/genética , Naftalenos/farmacología , Aspergillus nidulans/genética , Mapeo Cromosómico , Pruebas de Sensibilidad Microbiana , Mutación , Terbinafina , Rayos UltravioletaRESUMEN
Shc protein phosphorylation has been extensively characterized as the initial step that activates a complex mitogenic pathway through its association with Grb2. In the present study, we investigated the adrenergic control of insulin-induced Shc phosphorylation and Shc-Grb2 association, and the modulating effect of streptozotocin-induced diabetes mellitus on Shc phosphorylation and Shc/Grb2 association. Acute treatment with epinephrine, which leads to a normoglycemic insulin-resistant state, does not affect insulin-induced Shc tyrosine phosphorylation or Shc-Grb2 association in liver, muscle, or fat. By contrast, a significant increase in insulin-induced Shc phosphorylation is observed in liver and muscle of rats treated with streptozotocin. The association of Shc/Grb2 is also increased in both tissues following insulin treatment. These data suggest that while epinephrine preserves the insulin-induced phosphorylation of Shc and the mitogenic pathway stimulated by Shc-Grb2 association, treatment with streptozotocin leads to a tissue-specific increase in the activity of the initial step that ultimately results in the activation of the Shc/Grb2 mitogenic pathway.
Asunto(s)
Proteínas Adaptadoras Transductoras de Señales , Proteínas Adaptadoras del Transporte Vesicular , Tejido Adiposo/metabolismo , Agonistas Adrenérgicos/farmacología , Diabetes Mellitus Experimental/metabolismo , Epinefrina/farmacología , Insulina/fisiología , Hígado/metabolismo , Músculo Esquelético/metabolismo , Proteínas/metabolismo , Tirosina/metabolismo , Dominios Homologos src/genética , Animales , Proteína Adaptadora GRB2 , Fosforilación , Ratas , Receptor de Insulina/metabolismo , Proteínas Adaptadoras de la Señalización Shc , Proteína Transformadora 1 que Contiene Dominios de Homología 2 de SrcRESUMEN
A survey on the prevalence of Dirofilaria immitis and Dipetalonema reconditum was conducted in 1,519 dogs from Maceió and two coastal areas in the State of Alagoas, Northeast Brazil, from 1995 to 1999, by testing for microfilariae in blood. All blood samples were from exclusively domiciled dogs with a known history, showing that the infections were autochthonous, confirming transmission of canine filariasis in these areas. In Greater Metropolitan Maceió, 15 (1.3%) microfilaremic dogs were detected with D. immitis and 15 (1,3%) with D. reconditum. In the southern coastal area there was an estimated prevalence of 12.7% for D. immitis. D. immitis and D. reconditum microfilaria were 298.1 micrometer and 249.2 micrometer long and 7.3 micrometer and 4.4 micrometer wide, respectively. A Witness immunotest that detects D. immitis antigen was used to confirm parasitological results and reveal occult dirofilariasis cases. Of the total 6,579 females examined, 8 (0.1%) Culex quinquefasciatus were observed to be naturally infected with D. immitis larvae. These results proved dirofilariasis transmission in Maceió and demonstrated D. reconditum in the same geographic area.
Asunto(s)
Infecciones por Dipetalonema/veterinaria , Dirofilariasis/parasitología , Enfermedades de los Perros/parasitología , Animales , Antígenos Helmínticos/sangre , Brasil/epidemiología , Dipetalonema/aislamiento & purificación , Infecciones por Dipetalonema/epidemiología , Infecciones por Dipetalonema/parasitología , Dirofilaria immitis/aislamiento & purificación , Dirofilariasis/epidemiología , Enfermedades de los Perros/epidemiología , Perros , Femenino , Masculino , PrevalenciaRESUMEN
The periodicity of Wuchereria bancrofti microfilariae (mff) in peripheral blood was analysed in 42 microfilaraemics living in Maceió, in Alagoas state, north-eastern Brazil. Nine blood samples were collected from each subject, over a 24-h period, and two quantitative (60-microliter) thick smears were prepared from each sample. Although all the subjects had detectable microfilaraemias from 23.00 hours to 06.00 hours, no mff could be detected in most (71.4%) of the smears prepared from samples collected at 15.00 hours. Samples collected during the day, at 15.00 hours, contained 170 times fewer mff/microliter than those collected at 01.00 hours, when microfilaraemias were generally most intense. For diagnosis of bancroftian filariasis in Maceió, blood samples should be collected between 22.00 and 03.00 hours, when microfilarial counts will be at least 90% of the peak counts. The circadian variation observed was independent of the subject's gender and microfilarial density. Mathematical analysis, using a simple harmonic-wave model, indicated a periodicity index of 127.6 and that maximum microfilarial densities occurred at 00.51 hours, confirming the nocturnal pattern of microfilaraemia in the study area.
Asunto(s)
Filariasis Linfática/sangre , Wuchereria bancrofti/aislamiento & purificación , Adolescente , Adulto , Algoritmos , Animales , Brasil , Ritmo Circadiano , Filariasis Linfática/diagnóstico , Reacciones Falso Negativas , Femenino , Humanos , Masculino , Persona de Mediana Edad , Sensibilidad y EspecificidadRESUMEN
Two cases of GVHD with severe dry eyes are reported where conventional therapy failed to control ocular signs and symptoms. Autologous serum tears, however, resulted in a beneficial clinical effect with marked attenuation of the symptoms. This therapy proved to be safe during 10 months of treatment. Bone Marrow Transplantation (2000).
Asunto(s)
Sangre , Enfermedad Injerto contra Huésped/complicaciones , Soluciones Oftálmicas , Xeroftalmia/terapia , Adulto , Estudios de Evaluación como Asunto , Ojo/patología , Femenino , Humanos , Leucemia Mieloide de Fase Crónica/terapia , Síndrome de Sjögren/etiología , Xeroftalmia/etiología , Xeroftalmia/patologíaRESUMEN
De 2.007 amostras de sangue examinadas de cäes da cidade de Maceió-AL, foram detectados 62 (3,1 por cento) animais positivos para a presença de microfilária (mf). Em 11 cäes, escolhidos aleatoriamente, foi colhido sangue venoso para a identificaçäo específica de Dirofilaria immitis. Para tal, foram utilizadas a motilidade, o tamanho, a morfologia das mf e a presença de antígenos solúveis do parasito, sendo encontrados cinco animais portadores de D. immitis. Mosquitos da espécies Culex quinquefasciatus foram alimentados com sangue de um cäo portador de D. immitis. O desenvolvimento de formas larvárias foi obsevado nos títulos de Malpighi, confirmando a ocorrência da dirofilariose canina por D. immitis na cidade de Maceió-AL
Asunto(s)
Animales , Masculino , Femenino , Culex , Dirofilaria immitis , Dirofilariasis , PerrosRESUMEN
PURPOSE: Insulin has been acknowledged as a mediator of several physiological events in lacrimal and salivary glands. We investigated the presence of insulin receptors and of insulin-induced autophosphorylation of the insulin receptor and activation of elements involved in the early steps of insulin signaling in lacrimal and salivary glands of rats. METHODS: Lacrimal and salivary glands of Wistar rats were removed and processed for immunohistochemistry using anti-insulin receptor and anti-IGF-1 receptor antibodies. The activation of insulin receptors following insulin treatment, and the involvement of insulin receptor substrates-1 and -2, Shc, JAK-2 and STAT-1, were analyzed by immunoprecipitation, followed by SDS-PAGE and immunoblotting of rat lacrimal and salivary glands after exposure to insulin. RESULTS: Insulin and IGF-1 receptors were present in rat lacrimal and salivary glands and were located predominantly in the cytoplasm and plasma membrane. Functional studies demonstrated that insulin induced a dose-dependent phosphorylation of the insulin receptor, IGF-1R, insulin receptor substrates-1 and -2, Shc, and STAT-1. In rats with streptozotocin-induced diabetes mellitus there was a significant reduction in insulin-induced insulin receptor and STAT-1 phosphorylation in the lacrimal gland but not in the salivary gland; there was no influence on Shc phosphorylation in either tissue. CONCLUSIONS: The present results indicate that insulin and IGF-1 receptors are expressed in lacrimal and salivary glands, and that insulin can induce the phosphorylation of its receptor and activate elements involved in the early steps of insulin signaling in both tissues.
Asunto(s)
Proteínas Adaptadoras Transductoras de Señales , Proteínas Adaptadoras del Transporte Vesicular , Insulina/fisiología , Aparato Lagrimal/metabolismo , Proteínas Proto-Oncogénicas , Receptor IGF Tipo 1/metabolismo , Receptor de Insulina/metabolismo , Glándulas Salivales/metabolismo , Transducción de Señal , Animales , Proteínas de Unión al ADN/metabolismo , Diabetes Mellitus Experimental/metabolismo , Relación Dosis-Respuesta a Droga , Electroforesis en Gel de Poliacrilamida , Immunoblotting , Insulina/farmacología , Proteínas Sustrato del Receptor de Insulina , Péptidos y Proteínas de Señalización Intracelular , Janus Quinasa 2 , Aparato Lagrimal/efectos de los fármacos , Masculino , Fosfoproteínas/metabolismo , Fosforilación , Pruebas de Precipitina , Proteínas Tirosina Quinasas/metabolismo , Proteínas/metabolismo , Ratas , Ratas Wistar , Factor de Transcripción STAT1 , Glándulas Salivales/efectos de los fármacos , Proteínas Adaptadoras de la Señalización Shc , Proteína Transformadora 1 que Contiene Dominios de Homología 2 de Src , Transactivadores/metabolismo , Tirosina/metabolismoRESUMEN
In order to assess the present status of lymphatic filariasis in Alagoas State, Brazil, hemoscopic surveys were carried out in the human population of the three different physiographic regions of the State. Blood samples were collected by thick smear technique taken after 10:00 p.m. From a total of 101 cities of the State, 10 were randomly selected, Bancroftian filariasis was only found in Maceió, the capital of Alagoas State. In a cross-sectional survey conducted among the general population of 4 neighborhoods in the city, 10,973 individuals were examined, 226 were microfilaraemic with prevalence in the city neighborhoods ranging from 0 to 5.4%. Prevalence rates and microfilariae density were significantly higher in males. Among the examined inhabitants born out of Maceió, microfilariae carriers had lived a significantly longer time in endemic areas than the amicrofilaraemic subjects. Based on the data obtained in the present study, measures to avoid expansion of bancroftian filariasis in the region were established.
Asunto(s)
Filariasis/epidemiología , Wuchereria bancrofti , Adolescente , Adulto , Animales , Brasil , Niño , Femenino , Humanos , Masculino , Persona de Mediana Edad , Salud UrbanaRESUMEN
De 2.007 amostras de sangue examinadas de cães da cidade de Maceió-AL, foram detectados 62 (3,1%) animais positivos para a presença de microfilárias (mf). Em 11 cães, escolhidos aleatoriamente, foi colhido sangue venoso para a identificação específica de Dirofilaria immitis. Para tal, foram utilizadas a motilidade, o tamanho, a morfologia das mf e a presença de antígenos solúveis do parasito, sendo encontrados cinco animais portadores de D. immitis. Mosquitos da espécie Culex quinquefasciatus foram alimentados com sangue de um cão portador de D. immitis. O desenvolvimento de formas larvárias foi observado nos túbulos de Malpighi, confirmando a ocorrência da dirofilariose canina causada por D. immitis na cidade de Maceió-AL.
RESUMEN
Insulin stimulates rapid tyrosine phosphorylation of the protein Shc, which subsequently binds to Grb2, resulting in the activation of a complex mitogenic signaling network. In this study, we examined the levels of Shc protein, its phosphorylation state and Shc-Grb2 association in liver, muscle and adipose tissue before and after insulin administration in three animal models of insulin resistance (chronic dexamethasone treatment, 72-h starvation and aging). There were no differences in Shc protein expression between tissues from control and insulin resistant animals. In fasted hypoinsulinemic rats, there was a decrease in insulin-induced Shc phosphorylation in liver and adipose tissue. However, a significant increase in Shc phosphorylation was observed in liver and muscle from dexamethasone-treated hyperinsulinemic rats and in liver, muscle and adipose tissue of hyperinsulinemic 20-month-old rats. Alterations in Shc phosphorylation correlated well with the level of Shc-Grb2 association. These results indicate that Shc tyrosyl phosphorylation and Shc-Grb2 association are regulated in the different types of insulin resistance and that this regulation is apparently related to the animals' plasma insulin levels. The Shc-Grb2 association is directly related to the insulin-induced tyrosyl phosphorylation of Shc.