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1.
Scand J Med Sci Sports ; 26(11): 1360-1372, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27152850

ABSTRACT

Experimental studies have reported that aerobic exercise after asthma induction reduces lung inflammation and remodeling. Nevertheless, no experimental study has analyzed whether regular/moderate aerobic training before the induction of allergic asthma may prevent these inflammatory and remodeling processes. For this purpose, BALB/c mice (n = 96) were assigned into non-trained and trained groups. Trained animals ran on a motorized treadmill at moderate intensity, 30 min/day, 3 times/week, for 8 weeks, and were further randomized into subgroups to undergo ovalbumin sensitization and challenge or receive saline using the same protocol. Aerobic training continued until the last challenge. Twenty-four hours after challenge, compared to non-trained animals, trained mice exhibited: (a) increased systolic output and left ventricular mass on echocardiography; (b) improved lung mechanics; (c) decreased smooth muscle actin expression and collagen fiber content in airways and lung parenchyma; (d) decreased transforming growth factor (TGF)-ß levels in bronchoalveolar lavage fluid (BALF) and blood; (e) increased interferon (IFN)-γ in BALF and interleukin (IL)-10 in blood; and (f) decreased IL-4 and IL-13 in BALF. In conclusion, regular/moderate aerobic training prior to allergic asthma induction reduced inflammation and remodeling, perhaps through increased IL-10 and IFN-γ in tandem with decreased Th2 cytokines.


Subject(s)
Airway Remodeling , Asthma/immunology , Cytokines/immunology , Lung/immunology , Physical Conditioning, Animal , Animals , Asthma/chemically induced , Bronchoalveolar Lavage Fluid/immunology , Immunohistochemistry , Inflammation , Interferon-gamma/immunology , Interleukin-10/immunology , Interleukin-13/immunology , Interleukin-4/immunology , Lung/pathology , Lung/ultrastructure , Male , Mice , Mice, Inbred BALB C , Microscopy, Electron, Transmission , Ovalbumin/adverse effects , Pneumonia/chemically induced , Pneumonia/immunology , Pneumonia/pathology , Transforming Growth Factor beta/immunology
2.
Br J Pharmacol ; 173(7): 1236-47, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26989986

ABSTRACT

BACKGROUND AND PURPOSE: Asthma is characterized by chronic lung inflammation and airway hyperresponsiveness. Despite recent advances in understanding of its pathophysiology, asthma remains a major public health problem, and new therapeutic strategies are urgently needed. In this context, we sought to ascertain whether treatment with the TK inhibitor dasatinib might repair inflammatory and remodelling processes, thus improving lung function, in a murine model of asthma. EXPERIMENTAL APPROACH: Animals were sensitized and subsequently challenged, with ovalbumin (OVA) or saline. Twenty-four hours after the last challenge, animals were treated with dasatinib, dexamethasone, or saline, every 12 h for 7 consecutive days. Twenty-four hours after the last treatment, the animals were killed, and data were collected. Lung structure and remodelling were evaluated by morphometric analysis, immunohistochemistry, and transmission electron microscopy of lung sections. Inflammation was assessed by cytometric analysis and ELISA, and lung function was evaluated by invasive whole-body plethysmography. KEY RESULTS: In OVA mice, dasatinib, and dexamethasone led to significant reductions in airway hyperresponsiveness. Dasatinib was also able to attenuate alveolar collapse, contraction index, and collagen fibre deposition, as well as increasing elastic fibre content, in OVA mice. Concerning the inflammatory process, dasatinib reduced inflammatory cell influx to the airway and lung-draining mediastinal lymph nodes, without inducing the thymic atrophy promoted by dexamethasone. CONCLUSIONS AND IMPLICATIONS: In this model of allergic asthma, dasatinib effectively blunted the inflammatory and remodelling processes in asthmatic lungs, enhancing airway repair and thus improving lung mechanics.


Subject(s)
Airway Remodeling/drug effects , Asthma/drug therapy , Dasatinib/pharmacology , Lung/drug effects , Protein-Tyrosine Kinases/antagonists & inhibitors , Animals , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/therapeutic use , Asthma/immunology , Asthma/pathology , Asthma/physiopathology , Dasatinib/therapeutic use , Dexamethasone/pharmacology , Dexamethasone/therapeutic use , Female , Inflammation/drug therapy , Inflammation/immunology , Inflammation/physiopathology , Lung/pathology , Lung/physiopathology , Mice, Inbred BALB C , Ovalbumin/immunology
3.
J Fish Biol ; 85(2): 488-93, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24921946

ABSTRACT

Feeding behaviour and diet of Bryconamericus microcephalus differed between canopy conditions. At the open canopy site, a behavioural modification, grazing on algae, was observed. This was also reflected in gut content analysis and suggests behavioural plasticity in response to resource availability.


Subject(s)
Characidae/physiology , Environment , Feeding Behavior , Animals , Brazil , Diet , Gastrointestinal Contents
4.
Braz J Biol ; 72(2): 267-74, 2012 May.
Article in English | MEDLINE | ID: mdl-22735133

ABSTRACT

Spatio-temporal changes in the diet, niche breadth and niche overlap of two species of Characidium from three different sites along a Neotropical coastal stream were studied during a dry and rainy season. Seasonal changes were restricted to the occurrence of plant items in the stomach contents. The relative importance of food items in the diet of both species varied across sites, but Diptera, Ephemeroptera, Simuliidae, Trichoptera and Coleoptera larvae were always the main prey items. Contrary to the expected pattern, values of the niche breadth were higher at the site where Characidium species co-existed and niche overlapped at this site indicated 52% (p = 0.52) of feeding overlap.


Subject(s)
Characidae/physiology , Feeding Behavior/physiology , Gastrointestinal Contents , Animals , Characidae/classification , Seasons
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