Impact of a community-based exercise programme on physical fitness in middle-aged and older patients with type 2 diabetes

AbstractObjectivesPhysical fitness is related to all-cause mortality, quality of life and risk of falls in patients with type 2 diabetes. This study aimed to analyse the impact of a long-term community-based combined exercise program (aerobic+resistance+agility/balance+flexibility) developed with minimum and low-cost material resources on physical fitness in middle-aged and older patients with type 2 diabetes.MethodsThis was a non-experimental pre-post evaluation study. Participants (N=43; 62.92±5.92 years old) were engaged in a community-based supervised exercise programme (consisting of combined aerobic, resistance, agility/balance and flexibility exercises; three sessions per week; 70min per session) of 9 months’ duration. Aerobic fitness (6-Minute Walk Test), muscle strength (30-Second Chair Stand Test), agility/balance (Timed Up and Go Test) and flexibility (Chair Sit and Reach Test) were assessed before (baseline) and after the exercise intervention.ResultsSignificant improvements in the performance of the 6-Minute Walk Test (Δ=8.20%, p<0.001), 30-Second Chair Stand Test (Δ=28.84%, p<0.001), Timed Up and Go Test (Δ=14.31%, p<0.001), and Chair Sit and Reach Test (Δ=102.90%, p<0.001) were identified between baseline and end-exercise intervention time points.ConclusionsA long-term community-based combined exercise programme, developed with low-cost exercise strategies, produced significant benefits in physical fitness in middle-aged and older patients with type 2 diabetes. This supervised group exercise programme significantly improved aerobic fitness, muscle strength, agility/balance and flexibility, assessed with field tests in community settings

Short-Term Effects of Complex Training on Agility with the Ball, Speed, Efficiency of Crossing and Shooting in Youth Soccer Players

Complex training (CXT) is the result of a combination of strength and plyometric exercises in the sam

Finely tuned fiber-based porous structures for bone tissue engineering applications

info:eu-repo/semantics/publishedVersio

Preditores de anormalidades do sistema de conduçao cardíaco e necessidade de marcapasso definitivo após implante por cateter de bioprótese valvar aórtica (Transcatheter Aortic Valve Implantation - TAVI)

O implante por cateter de bioprótese valvar aórtica (do inglês Transcatheter Aortic Valve Implantation - TAVI) vem ganhando espaço e configura-se como opçao terapêutica para pacientes com estenose aórtica grave sintomática e risco cirúrgico elevado ou proibitivo. Apesar da menor manipulaçao e da menor agressividade comparativamente à abordagem cirúrgica tradicional, a incidência de bloqueio atrioventricular avançado é expressiva e resulta em aproximadamente 30% de implantes de marcapasso cardíaco definitivo. A identificaçao de fatores clínicos, eletrocardiográficos, anatômicos e relacionados ao tipo de prótese ou à técnica de liberaçao do dispositivo é fundamental para o desenvolvimento de novas técnicas e materiais, visando a reduzir a taxa de bloqueio atrioventricular avançado após o procedimento de TAVI. Os preditores mais relevantes analisados foram: bloqueio de ramo direito prévio, tipo de prótese (autoexpansível vs. balao expansível), profundidade do implante sobre a via de saída do ventrículo esquerdo, expansao excessiva da prótese, bloqueio atrioventricular total intraprocedimento, bloqueio atrioventricular de 1º grau ao eletrocardiograma de base e sexo masculino

Preditores de anormalidades do sistema de conduçao cardíaco e necessidade de marcapasso definitivo após implante por cateter de bioprótese valvar aórtica (Transcatheter Aortic Valve Implantation - TAVI)

O implante por cateter de bioprótese valvar aórtica (do inglês Transcatheter Aortic Valve Implantation - TAVI) vem ganhando espaço e configura-se como opçao terapêutica para pacientes com estenose aórtica grave sintomática e risco cirúrgico elevado ou proibitivo. Apesar da menor manipulaçao e da menor agressividade comparativamente à abordagem cirúrgica tradicional, a incidência de bloqueio atrioventricular avançado é expressiva e resulta em aproximadamente 30% de implantes de marcapasso cardíaco definitivo. A identificaçao de fatores clínicos, eletrocardiográficos, anatômicos e relacionados ao tipo de prótese ou à técnica de liberaçao do dispositivo é fundamental para o desenvolvimento de novas técnicas e materiais, visando a reduzir a taxa de bloqueio atrioventricular avançado após o procedimento de TAVI. Os preditores mais relevantes analisados foram: bloqueio de ramo direito prévio, tipo de prótese (autoexpansível vs. balao expansível), profundidade do implante sobre a via de saída do ventrículo esquerdo, expansao excessiva da prótese, bloqueio atrioventricular total intraprocedimento, bloqueio atrioventricular de 1º grau ao eletrocardiograma de base e sexo masculino

Optical Properties And Antiangiogenic Activity Of A Chalcone Derivate

Chalcones and their derivatives exhibit numerous pharmacological activities such as antibacterial, antifungal, cytotoxic, antinociceptive and anti-inflammatory. Recently, they have been assessed aiming for novel application in nonlinear optics and in the treatment of immune diseases and cancers. In this study, we investigate the optical properties of synthetic chalcona 1E,4E-1-(4-chlorophenyl)-5-(2,6,6-trimethylcyclohexen-1-yl)penta-1,4-dien-3-one (CAB7β) and its antiangiogenic potential using the chorioallantoic membrane (CAM) with the S180 sarcoma cell line. Experimental and theoretical results show intense absorption in the UVA-UVC region, which is associated with a π → π* transition with intramolecular charge transfer from the trimethyl-cyclohexen-1-yl ring to the chlorophenyl ring. Quantum chemical calculations of the first hyperpolarizability, accounting for both solvent and frequency dispersion effects, are in very good concordance with hyper-Rayleigh scattering measurements. In addition, two-photon absorption allowed band centered at 650 nm was observed. Concerning antiangiogenic activity, CAB7β causes a significant reduction in the total number, junctions, length and caliber of blood vessels stimulated by S180 cells reducing the presence of blood vessels, inflammatory cells and others elements related to angiogenic process. It is found that CAB7β is a versatile compound and a promising candidate for linear and nonlinear optical applications, in therapy against sarcoma and phototherapy

EFICIÃ?NCIA DO MÃ?TODO DE ESPECTROMETRIA DE MASSAS EM DROGAS DE ABUSO

Resumo: com objetivo demonstrar o papel da Espectrometria de Massas como ferramenta à identificação de várias drogas e destacar seus principais efeitos no organismo humano, realizamos uma revisão, por meio de bases de dados online, periódicos científicos e livros, analisando publicações dos últimos 10 anos. Foi alvo deste estudo drogas como cocaína, ecstasy, LSD, maconha e crack. A Espectrometria de Massas é uma técnica fundamental para os testes preliminares de triagem de drogas e essencial para a caracterização destas moléculas. Palavras-chave: Espectrometria de massa. Drogas de abuso. Química Forense

Finely tuned fiber-based porous structures for bone tissue engineering applications

[Excerpt] Scaffolds developed for bone tissue engineering (TE) must possess specific structural properties to allow neo-tissue formation and integration within the material[1]. Several polymeric systems and processing methodologies have been proposed to develop bone TE scaffolds. Nevertheless, the so far proposed strategies do not fulfil all the requirements for effective bone regeneration. Textile technologies have recently emerged as an industrial route for producing more complex fibre-based porous scaffolds[2]. Silk fibroin (SF) from Bombyx mori has already proved to be a good biomaterial for bone TE[3]. SF-based structures are known for the impressive mechanical properties and biocompatibility, which meet the basic requirements for developing bone TE scaffolds[4],[5]. [...]Portuguese Foundation for Science and Technology (FCT) for the project TISSUE2TISSUE (PTDC/CTM/105703/2008); Investigator FCT program IF/00423/2012 and IF/00411/2013

New biotextiles for tissue engineering : development, characterization and in vitro cellular viability

This work proposes biodegradable textile-based structures for tissue engineering applications. We describe the use of two polymers, polybutylene succinate (PBS) proposed as a viable multifilamentand silk fibroin (SF), to produce fibre-based finely tuned porous architectures by weft knitting. PBS is here proposed as a viable extruded multifilament fibre to be processed by a textile-based technology. A comparative study was undertaken using a SF fibre with a similar linear density. The knitted constructs obtained are described in terms of their morphology, mechanical properties, swelling capability, degradation behaviour and cytotoxicity. The weft knitting technology used offers superior control over the scaffold design (e.g. size, shape, porosity and fibre alignment), manufacturing and reproducibility. The presented fibres allow the processing of a very reproducible intra-architectural scaffold geometry which is fully interconnected, thus providing a high surface area for cell attachment and tissue in-growth. The two types of polymer fibre allow the generation of constructs with distinct characteristics in terms of the surface physico-chemistry, mechanical performance and degradation capability, which has an impact on the resulting cell behaviour at the surface of the respective biotextiles. Preliminary cytotoxicity screening showed that both materials can support cell adhesion and proliferation. These results constitute a first validation of the two biotextiles as viable matrices for tissue engineering prior to the development of more complex systems. Given the processing efficacy and versatility of the knitting technology and the interesting structural and surface properties of the proposed polymer fibres it is foreseen that the developed systems could be attractive for the functional engineering of tissues such as skin, ligament, bone or cartilage.The authors are grateful to the Portuguese Foundation for Science and Technology (FCT) under the programs POCTI and/or FEDER (post-doctoral fellowship to Ana L Oliveira, SFRH/BPD/39102/2007), and the project TISSUE2TISSUE (PTDC/CTM/105703/2008), founded by FCT agency

Direct Visualization of Peptide/MHC Complexes at the Surface and in the Intracellular Compartments of Cells Infected In Vivo by Leishmania major

Protozoa and bacteria infect various types of phagocytic cells including macrophages, monocytes, dendritic cells and eosinophils. However, it is not clear which of these cells process and present microbial antigens in vivo and in which cellular compartments parasite peptides are loaded onto Major Histocompatibility Complex molecules. To address these issues, we have infected susceptible BALB/c (H-2d) mice with a recombinant Leishmania major parasite expressing a fluorescent tracer. To directly visualize the antigen presenting cells that present parasite-derived peptides to CD4+ T cells, we have generated a monoclonal antibody that reacts to an antigenic peptide derived from the parasite LACK antigen bound to I-Ad Major Histocompatibility Complex class II molecule. Immunogold electron microscopic analysis of in vivo infected cells showed that intracellular I-Ad/LACK complexes were present in the membrane of amastigote-containing phagosomes in dendritic cells, eosinophils and macrophages/monocytes. In both dendritic cells and macrophages, these complexes were also present in smaller vesicles that did not contain amastigote. The presence of I-Ad/LACK complexes at the surface of dendritic cells, but neither on the plasma membrane of macrophages nor eosinophils was independently confirmed by flow cytometry and by incubating sorted phagocytes with highly sensitive LACK-specific hybridomas. Altogether, our results suggest that peptides derived from Leishmania proteins are loaded onto Major Histocompatibility Complex class II molecules in the phagosomes of infected phagocytes. Although these complexes are transported to the cell surface in dendritic cells, therefore allowing the stimulation of parasite-specific CD4+ T cells, this does not occur in other phagocytic cells. To our knowledge, this is the first study in which Major Histocompatibility Complex class II molecules bound to peptides derived from a parasite protein have been visualized within and at the surface of cells that were infected in vivo