ABSTRACT
Asthma is a chronic inflammatory disease of the airways characterized by immune cell infiltrates, bronchial hyperresponsiveness, and declining lung function. Thus, the possible effects of virgin coconut oil on a chronic allergic lung inflammation model were evaluated. Morphology of lung and airway tissue exhibited peribronchial inflammatory infiltrate, epithelial hyperplasia, and smooth muscle thickening in guinea pigs submitted to ovalbumin sensitization, which were prevented by virgin coconut oil supplementation. Additionally, in animals with lung inflammation, trachea contracted in response to ovalbumin administration, showed a greater contractile response to carbachol (CCh) and histamine, and these responses were prevented by the virgin coconut oil supplementation. Apocynin, a NADPH oxidase inhibitor, did not reduce the potency of CCh, whereas tempol, a superoxide dismutase mimetic, reduced potency only in nonsensitized animals. Catalase reduced the CCh potency in nonsensitized animals and animals sensitized and treated with coconut oil, indicating the participation of superoxide anion and hydrogen peroxide in the hypercontractility, which was prevented by virgin coconut oil. In the presence of L-NAME, a nitric oxide synthase (NOS) inhibitor, the CCh curve remained unchanged in nonsensitized animals but had increased efficacy and potency in sensitized animals, indicating an inhibition of endothelial NOS but ineffective in inhibiting inducible NOS. In animals sensitized and treated with coconut oil, the CCh curve was not altered, indicating a reduction in the release of NO by inducible NOS. These data were confirmed by peribronchiolar expression analysis of iNOS. The antioxidant capacity was reduced in the lungs of animals with chronic allergic lung inflammation, which was reversed by the coconut oil, and confirmed by analysis of peribronchiolar 8-iso-PGF2α content. Therefore, the virgin coconut oil supplementation reverses peribronchial inflammatory infiltrate, epithelial hyperplasia, smooth muscle thickening, and hypercontractility through oxidative stress and its interactions with the NO pathway.
Subject(s)
Antioxidants/therapeutic use , Bronchial Hyperreactivity/therapy , Coconut Oil/therapeutic use , Pneumonia/therapy , Animals , Antioxidants/pharmacology , Chronic Disease , Coconut Oil/pharmacology , Female , Guinea Pigs , MaleABSTRACT
Objetivos. Evaluar los efectos clínicos y preventivos de la inmunoterapia sublingual (SLIT) con respecto a la aparición de asma persistente, nuevas sensibilizaciones, síntomas clínicos e hiperreactividad bronquial (HRB). Los objetivos secundarios fueron: evaluar la magnitud del efecto clínico y el efecto sobre la HRB; ver la seguridad y adhesión a la SLIT. Material y métodos: Participaron 216 niños, de ambos sexos, entre 5 y 17 años, pacientes del Hospital Cuasso al Monte, Varese, Italia, con rinitis alérgica de al menos 2 años de evolución, con o sin síntomas de asma intermitente, y con diagnóstico de etiología alérgica confirmado para ácaros, gramíneas, árboles y malezas. Se excluyeron pacientes con asma persistente o VEF1 <80%, uso previo de inmunoterapia, anormalidades anatómicas de las vías aéreas superiores, enfermedades sistémicas crónicas (malignas o autoinmunes) y sensibilizaciones a epitelios y hongos anemófilos. Para los diagnósticos de rinitis y asma se emplearon las guías actuales (ARIA, GINA). Se realizaron prick test con panel estándar de alérgenos relevantes (ALK Abelló), histamina 1% y control negativo al principio y al final del estudio. Las pruebas de función pulmonar consistieron en espirometría computarizada con cabina pletismográfica y prueba de provocación no específica con metacolina con dosis progresivas desde 30 a 1.290 µg, durante el período de máxima exposición alérgenica según sensibilidad de cada paciente, al inicio y al final del estudio. A los pacientes con prueba negativa (descenso del VEFI <20%) se los consederaba con diagnóstico de rinitis exclusivamente. El estudi tuvo un período basal de 1 año de observación y luego una fase de aleatorización de 3 años de tratamiento abierto con dos ramas. Un grupo de pacientes utilizó drogas exclusivamente, y otro grupo drogas más SLIT (con una distribución 1/2).
Subject(s)
Asthma/therapy , Desensitization, Immunologic/adverse effects , Desensitization, Immunologic/methods , Immunotherapy/methods , Administration, Sublingual , Bronchial Hyperreactivity/therapyABSTRACT
We study the use of zafirlukast in patients with broncial hyperactivity 30 patients during 5 months, non smokers and not receiving oral or inhaled steroids, teophiline, antihistaminics or long action B2 were studied. 15 patients used zafirlukast 10 mg twice a day during 5 months, and 15 patients did not use zafirlukast. Both groups did not change significatively their spirometries and the PC 20 in the Metacholyne test
Subject(s)
Adult , Humans , Bronchial Hyperreactivity/diagnosis , Bronchial Hyperreactivity/therapy , Bronchial Provocation Tests , Spirometry , Treatment OutcomeABSTRACT
INTRODUCTION: Asthma is a worldwide disabling chronic inflammatory airway disease characterized by an intense eosinophilic inflammatory infiltrate on bronchial mucous membranes. Among the complementary therapeutic approaches to asthma, acupuncture has been widely used. OBJECTIVE: Here we used a rat pulmonary hypersensitivity experimental model that mimics human asthma in order to address whether electroacupuncture (EA) treatment could reduce the inflammatory process. MATERIALS AND METHODS: Experimental animals were divided in four groups: control (C), immobilized (I), sham-acupuncture (SA), and acupuncture (A). All rats were sensitized with heat-solidified hen egg white implant. Using clinical acupuncture points, EA treatment began 2 days after antigen priming and was repeated on alternate days for 2 weeks. Subsequently, animals were challenged by inhalation with aggregated ovalbumin and sacrificed 24 hours later when blood samples, bronchoalveolar lavage (BAL), and lungs were collected. RESULTS: Histopathologic analyses showed that peribronchial and perivascular inflammatory cell infiltrates were significantly lower in group A compared to groups SA and I (shown to be similar to group C). Furthermore, BAL total cell count and percentage of polymorphonuclears (as well as the differential counts of neutrophils and eosinophils) were significantly reduced in group A compared to group I. Corsticosterone plasma levels were similar in all groups. CONCLUSIONS: Taken together these results show that EA efficiently diminishes the bronchial immune-mediated inflammation induced in rats and that this effect is dependent on the choice of specific acupoints.
Subject(s)
Asthma/therapy , Bronchial Hyperreactivity/therapy , Bronchoalveolar Lavage Fluid/chemistry , Electroacupuncture/methods , Analysis of Variance , Animals , Asthma/immunology , Bronchial Hyperreactivity/immunology , Disease Models, Animal , Male , Ovalbumin/immunology , Rats , Rats, Wistar , Time FactorsABSTRACT
BACKGROUND: The increase of atopic disorders in developed countries has been associated with the decline of infectious diseases, including helminthic infections. We have already demonstrated that adult worm extracts from Ascaris suum (ASC) suppress the IgE antibody production against unrelated antigens. OBJECTIVE: Here we investigated the influence of ASC on the development of pulmonary eosinophilic inflammation in a murine model of asthma. METHODS: Heat-coagulated egg white alone (EWI) or mixed with ASC (EWI + ASC) was implanted subcutaneously in B10.A or C57BL/6 mice, and 14 days later they were challenged intratracheally with OVA or exposed to aerosolized OVA for 4 days. RESULTS: The suppressive effect of ASC was demonstrated on the accumulation of cells into airways, with reduction of eosinophil numbers and of eosinophil peroxidase activity in EWI + ASC-immunized mice. This effect correlated with a marked reduction of IL-5 and IL-4 levels in the BAL from C57BL/6 and B10. A mice, respectively, and of eotaxin in BAL and lung tissue from both strains. OVA-specific IgG1 and IgE levels were also impaired in serum and BAL from these mice. Airway hyper-reactivity to methacholine was obtained in B10. A mice sensitized with EWI, but the respiratory mechanical parameters returned to normal levels in EWI + ASC-immunized mice. CONCLUSION: These results indicate that ASC has a profound inhibitory effect on lung inflammation and hyper-responsiveness and that suppression of IL-5 or IL-4 and of eotaxin contributes to this effect.
Subject(s)
Antigens, Helminth/administration & dosage , Ascaris suum/immunology , Asthma/therapy , Bronchial Hyperreactivity/therapy , Eosinophilia/therapy , Immunotherapy/methods , Animals , Asthma/immunology , Bronchi/enzymology , Bronchi/immunology , Chemokine CCL11 , Chemokines, CC/metabolism , Eosinophil Peroxidase , Immunoglobulin E/blood , Immunoglobulin G/blood , Interleukin-4/analysis , Interleukin-5/analysis , Male , Mice , Mice, Inbred C57BL , Mice, Inbred Strains , Models, Animal , Peroxidases/metabolism , Rats , Rats, WistarABSTRACT
La tos es un síntoma molesto, quizás más para los circunstantes que para quien la padece, es un reflejo protector del paciente y una voz de alerta para el médico, es el síntoma más frecuente en pediatría. El centro de la tos está situado en la parte superior del tallo cerebral y protuberancia, muy cerca del centro del vómito, lo que explica que con frecuencia la tos produzca éste
Subject(s)
Child , Humans , Male , Female , Bronchial Hyperreactivity/pathology , Bronchial Hyperreactivity/therapy , Cough/diagnosis , Cough/prevention & controlABSTRACT
PURPOSE: This paper reviews the literature on the aetiology and therapy of bronchial hyperreactivity to describe the underlying pathophysiology, identify patients at risk and update knowledge on new and existing therapies. SOURCE: Information was obtained from monograms on New Drugs for Asthma, Respiratory Medicine: recent advances, Agents and Actions Supplements, Pulmonary Pharmacology, Anesth Analg, the European Journal of Respiration and a Medline literature search. PRINCIPAL FINDINGS: Reduced airway calibre, increased bronchial contractility, altered permeability of the bronchial mucosa, humoral and cellular mediators, and dysfunctional neural regulation are critical factors for bronchial hyperreactivity, a characteristic feature of hyperreactive airways which results in bronchoconstriction after exposure to varied stimuli. Preoperative anaesthetic considerations in these patients include FEV1 and PEFR testing to assess the severity and for optimal control of the condition. Bronchospasm causing hypoxaemia is the major intraoperative problem anticipated in these patients. Current therapeutic management of bronchoconstriction focuses on the beta 2 agonists, theophylline and steroids. Besides relaxing the airway smooth muscle these agents are all capable of altering bronchial inflammatory responses. Future developments of therapy are directed towards the inflammatory components of the disease. CONCLUSION: This review has presented background information on physiological mechanisms of smooth muscle contractility, pathophysiological alterations of bronchial contractility and the pharmacological basis of therapy in bronchoconstrictive disease. Information is presented to enable the prompt arrest and reversal of airway constriction, and to maintain prophylactic treatment during the perioperative period. Intraoperative bronchospasm is managed by adequate oxygenation and reversal of bronchoconstriction.
Subject(s)
Bronchial Hyperreactivity/therapy , Bronchi/blood supply , Bronchial Hyperreactivity/physiopathology , Calcium/metabolism , Calcium Channels/physiology , Glucocorticoids/therapeutic use , Humans , Potassium Channels/physiology , Receptors, Muscarinic/physiology , Sympathetic Nervous System/physiologyABSTRACT
En este estudio, 16 niños con asma alérgica recibieron inmunoterapia; con un extracto alergénico de Dermatophagoides pteronyssinus no estandarizado; durante 12 semanas hasta llegar a la mitad de la dosis de mantenimiento. Al valorarse la respuesta; la prueba de Prick mostró un descenso significativo en el área de la roncha (P<0.001); el reto con histamina no tuvo cambios significativos; mientras que cambios significativos sí fueron encontrados en el resto con el extracto alergénico (P<0.01), pero no en la reacción tardía ni en los niveles de IgE. Por lo tanto, este estudio sugiere que la inmunoterapia, con nuestro extracto alergénico no estandarizado, sí induce cambios en la hiperreactividad bronquial y cutánea específica; no afectándose la hiperreactividad bronquial inespecífica
Subject(s)
Male , Female , Adolescent , Bronchial Hyperreactivity/diagnosis , Bronchial Hyperreactivity/therapy , Desensitization, Immunologic/methods , Immunoglobulin E/analysis , Skin Tests/methodsSubject(s)
Humans , Asthma/therapy , Desensitization, Immunologic/methods , Immunotherapy , Mites/pathogenicity , Allergens/adverse effects , Allergens/therapeutic use , Asthma/immunology , Bronchial Hyperreactivity/immunology , Bronchial Hyperreactivity/therapy , Desensitization, Immunologic , Immunotherapy/trends , Meta-AnalysisSubject(s)
Humans , Asthma/therapy , Immunotherapy/methods , Desensitization, Immunologic/methods , Asthma/immunology , Meta-Analysis , Mites/pathogenicity , Allergens/adverse effects , Allergens/therapeutic use , Bronchial Hyperreactivity/immunology , Bronchial Hyperreactivity/therapy , Immunotherapy/trends , Desensitization, Immunologic/statistics & numerical dataSubject(s)
Humans , Bronchial Hyperreactivity/drug therapy , Bronchial Hyperreactivity/physiopathology , Bronchial Hyperreactivity/therapy , Methacholine Chloride , Methacholine Chloride/administration & dosage , Methacholine Chloride/adverse effects , Methacholine Chloride , Methacholine Chloride/pharmacokinetics , Methacholine Chloride/pharmacologyABSTRACT
There is not a clear definition of asthma, actually most of specialist consider to asthma how a reversible bronchial obstruction with an increased responsiveness (bronchial hyperreactivity, BHR), and inflammation. These inflammation can cause increase of the BHR and worseness the process. The new tendencies are to treat these BHR and control the two faces of asthma (early and late face). In the early or immediate face, bronchodilators are the most use full medicine meanwhile; the antiinflammatory drugs (sodium cromoglycate and inhaled steroids) are the best option for management of inflammation with reduction of BHR.
Subject(s)
Asthma/physiopathology , Bronchial Hyperreactivity/physiopathology , Bronchitis/physiopathology , Asthma/etiology , Asthma/therapy , Bronchial Hyperreactivity/complications , Bronchial Hyperreactivity/therapy , Bronchitis/complications , Bronchitis/therapy , Bronchoconstriction , Child , Chronic Disease , Humans , Terminology as TopicABSTRACT
El tratamiento del asma ha sufrido innumerables modificaciones en las últimas décadas al influjo de los cambios en la opinión científica sobre la utilidad y riesgos de medicamentos como los glucocorticoides, los beta-agonistas y los inhibidores de la fosfodiesterasa. Este excelente artículo puntualiza de manera precisa el estado del arte en la actualidad en la que al tratamiento del asma se refiere.