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2.
J Am Nutr Assoc ; 41(3): 325-332, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-33734035

RESUMO

OBJECTIVE: This study evaluated whether the consumption of a cereal bar combining different phytoestrogens could contribute to the reduction of climacteric symptoms in women. METHODS: This is a clinical, prospective, randomized, simple-blind trial. Forty-eight women, aged 40-65 years, with climacteric symptoms, from a city in southwestern Paraná, Brazil. Participants were randomly assigned into two groups; Phytoestrogens group (PHY = 24), which received for 90-day period a cereal bar containing 80.73 milligrams of soybean and flaxseed phytoestrogens, and the placebo group (PLA = 24), which consumed rice flakes biscuit. Clinical, sociodemographic and anthropometric data were collected and climacteric symptoms were assessed using the Kupperman Index (KI). RESULTS: Forty-three women were analyzed (PHY = 21 and PLA = 22). There were significant reductions in the overall KI score in both groups at the end of the intervention period (p < 0.05). However, the comparison between the groups using linear regression models presented expressively better symptom improvement in the PHY group -6.43 over time (95% CI: -11.6; -1.26; p < 0.05) KI points, with perimenopausal -15.15 (95% CI: -28.95; -1.35) and postmenopausal women -19.34 (95% CI: -33.68; -4.99) showed considerably greater reductions in symptoms at the end of the intervention period compared to premenopausal women. There was also significant reduction in symptoms of hot flushes, paresthesia, sexual complaints, insomnia and melancholy. CONCLUSION: The consumption of a cereal bar containing phytoestrogens was able to improve the symptoms of climacteric syndrome.


Assuntos
Climatério , Isoflavonas , Grão Comestível , Feminino , Humanos , Isoflavonas/farmacologia , Fitoestrógenos/uso terapêutico , Poliésteres/farmacologia , Estudos Prospectivos
3.
Curr Microbiol ; 72(2): 133-138, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26507335

RESUMO

The use of sugarcane bagasse hemicellulosic hydrolysates presents an interesting alternative to second generation (2G) ethanol production. Techniques to enhance the fermentation process, e.g., the use of immobilized cells, is one of the key factors for efficient production. Here, the effect of two important parameters (cell concentration in immobilized system and stirring rate) on the 2G ethanol production using the wild Brazilian yeast S. shehatae UFMG-HM 52.2 immobilized in calcium alginate matrix are presented. A 2(2) full factorial design of experiments was carried out to evaluate the effect of cell concentrations in sodium alginate solution for immobilized bead production (3.0, 6.0, and 9.0 g/L) and stirring rate (150, 200, and 250 rpm) for 2G ethanol production. Statistical analysis showed that the use of both variables at low levels enhanced ethanol yield (YP/S). Under these process conditions, YP/S of 0.31 g/g and ethanol productivity (Qp) of 0.12 g/L h were achieved. Results showed the potential of this immobilized yeast in 2G ethanol production from C5 sugars and demonstrate the importance of adequate cell concentration in immobilized systems, a finding that stands to increase bioprocesses yields and productivity.


Assuntos
Reatores Biológicos/microbiologia , Células Imobilizadas/metabolismo , Etanol/metabolismo , Glicosídeo Hidrolases/metabolismo , Saccharomycetales/metabolismo , Biotecnologia/métodos , Brasil
4.
Rev. bras. pesqui. méd. biol ; Braz. j. med. biol. res;47(6): 452-460, 06/2014. tab, graf
Artigo em Inglês | LILACS | ID: lil-709442

RESUMO

It has been previously shown that dextran sulfate administered to diabetic rats accumulates in the liver and kidney, and this could be due to a malfunction of the lysosomal digestive pathway. The aim of the present study was to evaluate the expression and activities of lysosomal enzymes that act upon proteins and sulfated polysaccharides in the livers of diabetic rats. Diabetes mellitus was induced by streptozotocin in 26 male Wistar rats (12 weeks old), while 26 age-matched controls received only vehicle. The livers were removed on either the 10th or the 30th day of the disease, weighed, and used to evaluate the activity, expression, and localization of lysosomal enzymes. A 50-60% decrease in the specific activities of cysteine proteases, especially cathepsin B, was observed in streptozotocin-induced diabetes mellitus. Expression (mRNA) of cathepsins B and L was also decreased on the 10th, but not on the 30th day. Sulfatase decreased 30% on the 30th day, while glycosidases did not vary (or presented a transitory and slight decrease). There were no apparent changes in liver morphology, and immunohistochemistry revealed the presence of cathepsin B in hepatocyte granules. The decrease in sulfatase could be responsible for the dextran sulfate build-up in the diabetic liver, since the action of sulfatase precedes glycosidases in the digestive pathway of sulfated polysaccharides. Our findings suggest that the decreased activities of cathepsins resulted from decreased expression of their genes, and not from general lysosomal failure, because the levels of glycosidases were normal in the diabetic liver.


Assuntos
Animais , Masculino , Catepsina B/metabolismo , Diabetes Mellitus Experimental/enzimologia , Fígado/enzimologia , Lisossomos/enzimologia , Albuminas/análise , Western Blotting , Glicemia/efeitos dos fármacos , Catepsina L/metabolismo , Creatinina/urina , Cisteína Proteases/metabolismo , Sulfato de Dextrana/farmacologia , Diabetes Mellitus Experimental/induzido quimicamente , Expressão Gênica/efeitos dos fármacos , Glucuronidase/metabolismo , Hexosaminidases/metabolismo , Imuno-Histoquímica , Rim/metabolismo , Ratos Wistar , Reação em Cadeia da Polimerase em Tempo Real , RNA , Sulfatases/metabolismo
5.
Braz J Med Biol Res ; 47(6): 452-60, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24820066

RESUMO

It has been previously shown that dextran sulfate administered to diabetic rats accumulates in the liver and kidney, and this could be due to a malfunction of the lysosomal digestive pathway. The aim of the present study was to evaluate the expression and activities of lysosomal enzymes that act upon proteins and sulfated polysaccharides in the livers of diabetic rats. Diabetes mellitus was induced by streptozotocin in 26 male Wistar rats (12 weeks old), while 26 age-matched controls received only vehicle. The livers were removed on either the 10th or the 30th day of the disease, weighed, and used to evaluate the activity, expression, and localization of lysosomal enzymes. A 50-60% decrease in the specific activities of cysteine proteases, especially cathepsin B, was observed in streptozotocin-induced diabetes mellitus. Expression (mRNA) of cathepsins B and L was also decreased on the 10th, but not on the 30th day. Sulfatase decreased 30% on the 30th day, while glycosidases did not vary (or presented a transitory and slight decrease). There were no apparent changes in liver morphology, and immunohistochemistry revealed the presence of cathepsin B in hepatocyte granules. The decrease in sulfatase could be responsible for the dextran sulfate build-up in the diabetic liver, since the action of sulfatase precedes glycosidases in the digestive pathway of sulfated polysaccharides. Our findings suggest that the decreased activities of cathepsins resulted from decreased expression of their genes, and not from general lysosomal failure, because the levels of glycosidases were normal in the diabetic liver.


Assuntos
Catepsina B/metabolismo , Diabetes Mellitus Experimental/enzimologia , Fígado/enzimologia , Lisossomos/enzimologia , Albuminas/análise , Animais , Glicemia/efeitos dos fármacos , Western Blotting , Catepsina L/metabolismo , Creatinina/urina , Cisteína Proteases/metabolismo , Sulfato de Dextrana/farmacologia , Diabetes Mellitus Experimental/induzido quimicamente , Expressão Gênica/efeitos dos fármacos , Glucuronidase/metabolismo , Hexosaminidases/metabolismo , Imuno-Histoquímica , Rim/metabolismo , Masculino , RNA/isolamento & purificação , Ratos Wistar , Reação em Cadeia da Polimerase em Tempo Real , Sulfatases/metabolismo
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