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1.
Braz J Med Biol Res ; 49(10): e5310, 2016 Sep 29.
Article in English | MEDLINE | ID: mdl-27706439

ABSTRACT

Although it is well known that physical training ameliorates brain oxidative function after injuries by enhancing the levels of neurotrophic factors and oxidative status, there is little evidence addressing the influence of exercise training itself on brain oxidative damage and data is conflicting. This study investigated the effect of well-established swimming training protocol on lipid peroxidation and components of antioxidant system in the rat brain. Male Wistar rats were randomized into trained (5 days/week, 8 weeks, 30 min; n=8) and non-trained (n=7) groups. Forty-eight hours after the last session of exercise, animals were euthanized and the brain was collected for oxidative stress analysis. Swimming training decreased thiobarbituric acid reactive substances (TBARS) levels (P<0.05) and increased the activity of the antioxidant enzyme superoxide dismutase (SOD) (P<0.05) with no effect on brain non-enzymatic total antioxidant capacity, estimated by FRAP (ferric-reducing antioxidant power) assay (P>0.05). Moreover, the swimming training promoted metabolic adaptations, such as increased maximal workload capacity (P<0.05) and maintenance of body weight. In this context, the reduced TBARS content and increased SOD antioxidant activity induced by 8 weeks of swimming training are key factors in promoting brain resistance. In conclusion, swimming training attenuated oxidative damage and increased enzymatic antioxidant but not non-enzymatic status in the rat brain.


Subject(s)
Antioxidants/metabolism , Brain/metabolism , Exercise Therapy/methods , Oxidative Stress/physiology , Physical Conditioning, Animal/physiology , Swimming/physiology , Animals , Antioxidants/analysis , Body Weight , Lipid Peroxidation/physiology , Male , Malondialdehyde/analysis , Malondialdehyde/metabolism , Random Allocation , Rats, Wistar , Reactive Oxygen Species/metabolism , Reference Values , Reproducibility of Results , Spectrophotometry , Superoxide Dismutase/analysis , Superoxide Dismutase/metabolism , Thiobarbituric Acid Reactive Substances/analysis , Thiobarbituric Acid Reactive Substances/metabolism , Time Factors
2.
Braz. j. med. biol. res ; 49(10): e5310, 2016. graf
Article in English | LILACS | ID: biblio-951650

ABSTRACT

Although it is well known that physical training ameliorates brain oxidative function after injuries by enhancing the levels of neurotrophic factors and oxidative status, there is little evidence addressing the influence of exercise training itself on brain oxidative damage and data is conflicting. This study investigated the effect of well-established swimming training protocol on lipid peroxidation and components of antioxidant system in the rat brain. Male Wistar rats were randomized into trained (5 days/week, 8 weeks, 30 min; n=8) and non-trained (n=7) groups. Forty-eight hours after the last session of exercise, animals were euthanized and the brain was collected for oxidative stress analysis. Swimming training decreased thiobarbituric acid reactive substances (TBARS) levels (P<0.05) and increased the activity of the antioxidant enzyme superoxide dismutase (SOD) (P<0.05) with no effect on brain non-enzymatic total antioxidant capacity, estimated by FRAP (ferric-reducing antioxidant power) assay (P>0.05). Moreover, the swimming training promoted metabolic adaptations, such as increased maximal workload capacity (P<0.05) and maintenance of body weight. In this context, the reduced TBARS content and increased SOD antioxidant activity induced by 8 weeks of swimming training are key factors in promoting brain resistance. In conclusion, swimming training attenuated oxidative damage and increased enzymatic antioxidant but not non-enzymatic status in the rat brain.


Subject(s)
Animals , Male , Physical Conditioning, Animal/physiology , Swimming/physiology , Brain/metabolism , Oxidative Stress/physiology , Exercise Therapy/methods , Antioxidants/metabolism , Reference Values , Spectrophotometry , Superoxide Dismutase/analysis , Time Factors , Body Weight , Lipid Peroxidation/physiology , Random Allocation , Reproducibility of Results , Reactive Oxygen Species/metabolism , Malondialdehyde/analysis , Malondialdehyde/metabolism , Antioxidants/analysis
3.
J Dairy Sci ; 98(7): 4377-83, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25912867

ABSTRACT

Different studies in humans have provided evidence about the health benefits of probiotics. However, most probiotic strains do not maintain good viability in the harsh conditions of the gastrointestinal tract (GIT). In the present study, Latin-style fresh cheese produced with potential probiotic bacteria was tested to evaluate this cheese type as a food carrier for the delivery of viable microorganisms after exposure to simulated GIT conditions. The resistance of 28 lactic acid bacteria (LAB) strains and Listeria monocytogenes upon exposure to acidic conditions (pH 2.5) and bile and pancreatic enzymes (0.3% of bile salts and 0.1% of pancreatin) was evaluated in vitro. When compared with fresh cultures, fresh cheese greatly improved LAB survival to simulated GIT conditions, as no loss of viability was observed in either acidic conditions (pH 2.5) or bile salts and pancreatin environment over a 3-h period. In opposition, L. monocytogenes did not survive after 1h under acidic conditions. These data demonstrated that Latin-style fresh cheese could play an important role in probiotic protection against gastrointestinal juices, enhancing delivery within the gut and thereby maximizing potential health benefits of LAB.


Subject(s)
Cheese/microbiology , Listeria monocytogenes/physiology , Animals , Bile Acids and Salts , Cattle , Drug Resistance, Bacterial , Gastrointestinal Tract , Hydrogen-Ion Concentration , Lactic Acid , Lactobacillaceae/physiology , Pancreas/enzymology , Probiotics
4.
Rural Remote Health ; 14: 2632, 2014.
Article in English | MEDLINE | ID: mdl-24601746

ABSTRACT

INTRODUCTION: Global development processes have been associated with the nutritional transition, where undernutrition is replaced by overnutrition. Income transfer policies in Brazil have targeted hunger, but may not address the need for balanced nutrition. METHODS: Data was collected from government databanks that document the nutritional status of Brazilians applying for social services. This data was analyzed for descriptive statistics. RESULTS: Development and income transfer processes appear to be associated with an increase in overweight children between the years 2008 and 2012. CONCLUSIONS: Income transfer programs need to incorporate educational programs that address the need to budget for balanced nutrition.


Subject(s)
Body Weight , Nutritional Status , Public Assistance/statistics & numerical data , Rural Population/statistics & numerical data , Brazil/epidemiology , Humans , Social Work , Socioeconomic Factors
5.
Rural Remote Health ; 12: 2188, 2012.
Article in English | MEDLINE | ID: mdl-22931053

ABSTRACT

CONTEXT: People living in rural or remote Brazil, as in other sub-tropical or tropical nations, are vulnerable to infections that would not normally occur in urban areas or wealthier nations. Brazil is a geographically extensive nation, historically marked by vast socioeconomic inequalities. Approximately 16% of the population live in rural areas. ISSUE: This clinical case report demonstrates the vulnerability of rural residents who are underserved by Brazil's 'universal' public healthcare system, despite social and economic challenges that increase their risk for disease. Myiasis (especially oral myiasis) is a rare health condition in humans caused by fly larvae. Oral myiasis usually appears in periodontal pockets and open wounds, such as after dental extractions. It is associated with poverty, lack of access to health care, and very poor overall health status. While myiasis has a worldwide distribution, it is particularly associated with the tropical and sub-tropical regions of North and South America. LESSONS LEARNED: This article describes a rare case of myiasis in the upper lip of a rural male patient. The case report demonstrate that rural and remote residents can be socially excluded from the benefits of technology and biomedicine, making them vulnerable to rare infections.


Subject(s)
Antiparasitic Agents/therapeutic use , Ivermectin/therapeutic use , Lip Diseases/drug therapy , Mouth Mucosa , Myiasis/drug therapy , Rural Health Services , Social Isolation , Alzheimer Disease/diagnosis , Anesthesia, Local , Brazil , Emergency Service, Hospital , Health Services Accessibility/standards , Humans , Lip Diseases/parasitology , Lip Diseases/surgery , Male , Malnutrition/therapy , Medically Underserved Area , Middle Aged , Mouth Mucosa/parasitology , Mouth Mucosa/surgery , Myiasis/diagnosis , Myiasis/parasitology , Myiasis/surgery , Practice Guidelines as Topic , Rural Health Services/standards , Social Conditions , Treatment Outcome , Vulnerable Populations
6.
Braz J Med Biol Res ; 38(11): 1585-92, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16258626

ABSTRACT

Lactococcus lactis, the model lactic acid bacterium, is a good candidate for heterologous protein production in both foodstuffs and the digestive tract. We attempted to produce Streptomyces tendae antifungal protein 1 (Afp1) in L. lactis with the objective of constructing a strain able to limit fungal growth. Since Afp1 activity requires disulfide bond (DSB) formation and since intracellular redox conditions are reportedly unfavorable for DSB formation in prokaryotes, Afp1 was produced as a secreted form. An inducible expression-secretion system was used to drive Afp1 secretion by L. lactis; Afp1 was fused or not with LEISSTCDA, a synthetic propeptide (LEISS) that has been described to be a secretion enhancer. Production of Afp1 alone was not achieved, but production of LEISS-Afp1 was confirmed by Western blot and immunodetection with anti-Afp1 antibodies. This protein (molecular mass: 9.8 kDa) is the smallest non-bacteriocin heterologous protein ever reported to be secreted in L. lactis via the Sec-dependent pathway. However, no anti-fungal activity was detected, even in concentrated samples of induced supernatant. This could be due to a too low secretion yield of Afp1 in L. lactis, to the absence of DSB formation, or to an improper DSB formation involving the additional cysteine residue included in LEISS propeptide. This raises questions about size limits, conformation problems, and protein secretion yields in L. lactis.


Subject(s)
Bacterial Proteins/metabolism , Carrier Proteins/metabolism , Lactococcus lactis/metabolism , Antifungal Agents/isolation & purification , Antifungal Agents/metabolism , Antifungal Agents/pharmacology , Aspergillus fumigatus/drug effects , Bacterial Proteins/genetics , Bacterial Proteins/pharmacology , Blotting, Western , Carrier Proteins/genetics , Carrier Proteins/pharmacology , Microbial Sensitivity Tests , Paecilomyces/drug effects , Plasmids/genetics , Trichophyton/drug effects
7.
Braz. j. med. biol. res ; 38(11): 1585-1592, Nov. 2005.
Article in English | LILACS | ID: lil-414712

ABSTRACT

Lactococcus lactis, the model lactic acid bacterium, is a good candidate for heterologous protein production in both foodstuffs and the digestive tract. We attempted to produce Streptomyces tendae antifungal protein 1 (Afp1) in L. lactis with the objective of constructing a strain able to limit fungal growth. Since Afp1 activity requires disulfide bond (DSB) formation and since intracellular redox conditions are reportedly unfavorable for DSB formation in prokaryotes, Afp1 was produced as a secreted form. An inducible expression-secretion system was used to drive Afp1 secretion by L. lactis; Afp1 was fused or not with LEISSTCDA, a synthetic propeptide (LEISS) that has been described to be a secretion enhancer. Production of Afp1 alone was not achieved, but production of LEISS-Afp1 was confirmed by Western blot and immunodetection with anti-Afp1 antibodies. This protein (molecular mass: 9.8 kDa) is the smallest non-bacteriocin heterologous protein ever reported to be secreted in L. lactis via the Sec-dependent pathway. However, no anti-fungal activity was detected, even in concentrated samples of induced supernatant. This could be due to a too low secretion yield of Afp1 in L. lactis, to the absence of DSB formation, or to an improper DSB formation involving the additional cysteine residue included in LEISS propeptide. This raises questions about size limits, conformation problems, and protein secretion yields in L. lactis.


Subject(s)
Lactococcus lactis/metabolism , Bacterial Proteins , Carrier Proteins , Antifungal Agents/isolation & purification , Antifungal Agents/metabolism , Antifungal Agents/pharmacology , Aspergillus fumigatus/drug effects , Blotting, Western , Microbial Sensitivity Tests , Paecilomyces/drug effects , Plasmids/genetics , Bacterial Proteins/genetics , Bacterial Proteins/pharmacology , Carrier Proteins/genetics , Carrier Proteins/pharmacology , Trichophyton/drug effects
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