Neurokinin-1 receptor, a new modulator of lymphangiogenesis in obese-asthma phenotype

Aims Obesity and asthma are widely prevalent and associated disorders. Recent studies of our group revealed that Substance P (SP) is involved in pathophysiology of obese-asthma phenotype in mice through its selective NK1 receptor (NK1-R). Lymphangiogenesis is impaired in asthma and obesity, and SP activates contractile and inflammatory pathways in lymphatics. Our aim was to study whether NK1-R expression was involved in lymphangiogenesis on visceral (VAT) and subcutaneous (SAT) adipose tissues and in the lungs, in obese-allergen sensitized mice. Main methods Diet-induced obese and ovalbumin (OVA)-sensitized Balb/c mice were treated with a selective NK1-R antagonist (CJ 12,255, Pfizer Inc., USA) or placebo. Lymphatic structures (LYVE-1 +) and NK1-R expression were analyzed by immunohistochemistry. A semi-quantitative score methodology was used for NK1-R expression. Key findings Obesity and allergen-sensitization together increased the number of LYVE-1 + lymphatics in VAT and decreased it in SAT and lungs. NK1-R was mainly expressed on adipocyte membranes of VAT, blood vessel areas of SAT, and in lung epithelium. Obesity and allergen-sensitization combined increased the expression of NK1-R in VAT, SAT and lungs. NK1-R antagonist treatment reversed the effects observed in lymphangiogenesis in those tissues. Significance The obese-asthma phenotype in mice is accompanied by increased expression of NK1-R on adipose tissues and lung epithelium, reflecting that SP released during inflammation may act directly on these tissues. Blocking NK1-R affects lymphangiogenesis, implying a role of SP, with opposite physiological consequences in VAT, and in SAT and lungs. Our results provide a clue for a novel SP role in the obese-asthma phenotype.

O Estudo da personagem em "O Meu mundo não é deste reino": desconstruir para reconstruir

A arte na actualidade, nomeadamente a literatura, caracteriza-se pela recorrência a temas de feição neobarroca e pós-moderna, como a vulnerabilidade humana1, o sentimento de culpa, a invasão da interioridade, a perda da identidade, com recurso a formas que têm a ver com a fragmentação discursiva. Na narrativa de João de Melo, O meu mundo não é deste reino, o processo de desconstrução identitária, seja através do deslocamento do sujeito a partir de um centro para a periferia, seja através da construção de identidades parcelares, imperfeitas, monstruosas, fragmentadas, é usado com o intuito último de reafirmar o Homem e a condição humana.

Neurokinin-1 receptor, a new modulator of lymphangiogenesis in obese-asthma phenotype

Aims: Obesity and asthma are widely prevalent and associated disorders. Recent studies of our group revealed that Substance P (SP) is involved in pathophysiology of obese-asthma phenotype in mice through its selective NK1 receptor (NK1-R). Lymphangiogenesis is impaired in asthma and obesity, and SP activates contractile and inflammatory pathways in lymphatics. Our aim was to study whether NK1-R expression was involved in lymphangiogenesis on visceral (VAT) and subcutaneous (SAT) adipose tissues and in the lungs, in obeseallergen sensitized mice. Main methods: Diet-induced obese and ovalbumin (OVA)-sensitized Balb/c mice were treated with a selective NK1-R antagonist (CJ 12,255, Pfizer Inc., USA) or placebo. Lymphatic structures (LYVE-1+) and NK1-R expression were analyzed by immunohistochemistry. A semi-quantitative score methodology was used for NK1-R expression. Key findings: Obesity and allergen-sensitization together increased the number of LYVE-1+ lymphatics in VAT and decreased it in SAT and lungs. NK1-R was mainly expressed on adipocyte membranes of VAT, blood vessel areas of SAT, and in lung epithelium. Obesity and allergen-sensitization combined increased the expression of NK1-R in VAT, SAT and lungs. NK1-R antagonist treatment reversed the effects observed in lymphangiogenesis in those tissues. Significance: The obese-asthma phenotype in mice is accompanied by increased expression of NK1-R on adipose tissues and lung epithelium, reflecting that SP released during inflammation may act directly on these tissues. Blocking NK1-R affects lymphangiogenesis, implying a role of SP, with opposite physiological consequences in VAT, and in SAT and lungs. Our results provide a clue for a novel SP role in the obese-asthma phenotype.

Processo de internacionalização das filiais portuguesas de construção civil para Angola: alguns estudos de caso (Mota-Engil, Soares da Costa e Conduril)

Dissertação apresentada no Instituto Superior de Contabilidade e Administração do Instituto Politécnico do Porto para obtenção do Grau de Mestre em Empreendedorismo e Internacionalização Orientador: Professor Doutor José de Freitas Santos

The importance of physical education classes in pre-school children

The purpose of this study was to analyse differences between total physical activity (TPA) and moderate-to-vigorous PA (MVPA) of pre-school children during daily school hours when they attended the physical education class (PED) and school days without PE class (NPED) and to assess the contribution of PE classes to TPA in school hours. The sample was composed of 193 pre-school healthy children (96 girls) aged from three to five years old and was conducted between February and December of 2008. Children wore accelerometers for at least four consecutive days during school hours. Data were analysed with specific software, age-specific counts-per-minute cut-off points and a 5 s epoch were used. Independent and general linear model repeated measures were used to assess differences between gender and differences between different days within each gender, respectively. Boys engaged more MVPA than girls (P < 0.05). During PED, pre-school children engaged significantly more in TPA and MVPA than during NPED (P < 0.05). PE class contributed, on average, 27.7% for the TPA and 32.8% of daily MVPA during PED in both gender. The results of this study suggest that structured PA such as a PE class increased the daily TPA and MVPA level of pre-school children.

Estudo comparativo do conceito de Mulligan e a aplicação de kinesio taping na epicondilite lateral

Introdução: A epicondilite lateral (EL) é uma das lesões mais comuns que afeta o membro superior, caracterizada pela dor lateral do cotovelo. Na literatura são descritas diferentes opções de tratamento para a EL mas sem existir consenso sobre a estratégia de intervenção com maior eficácia. A mobilização com movimento (MWM) e aplicação de kinesio taping (KT) tem apresentado bons resultados na melhoria da dor e funcionalidade e no aumento de força de preensão. No entanto, não existe estudos a comparar a efectividade das duas técnicas. Objetivo(s): Analisar e comparar os efeitos da técnica mobilização com movimento (MWM) em relação à aplicação de kinesio taping (KT), na dor, na força de preensão e na funcionalidade em indivíduos com EL. Métodos: Foram incluídos 39 participantes com EL, divididos em três grupos, um grupo de controlo (GC) e dois grupos experimentais, sendo um grupo submetido a uma das técnicas do conceito de Mulligan (GEM) e um grupo submetido a uma aplicação de KT (GEKT). Foram avaliadas a intensidade da dor através da Escala Visual Analógica (EVA), a força de preensão isométrica através de um dinamómetro digital e a funcionalidade através do questionário Patient-Rated Tennis Elbow Evaluation (PRTEE). Resultados: Observaram-se diferenças significativas entre o momento inicial e o momento final de intervenção em todos os grupos em estudo (p≤0,018). Ao analisar a EVA, a força de preensão e o questionário PRTEE, os grupos experimentais obtiveram melhores resultados relativamente ao GC (p<0,001). Comparando os dois grupos experimentais, o GEM apresentou melhores resultados na dor (p=0,012) e na funcionalidade (p=0,001). Conclusão: Ambas as técnicas estudadas promovem melhorias na sintomatologia em indivíduos com EL. Contudo, os resultados sugerem que a aplicação da técnica de Mulligan produz um maior efeito na diminuição da dor e no aumento da funcionalidade, comparativamente à aplicação de KT.