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1.
Bratisl Lek Listy ; 110(8): 454-8, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19750980

RESUMEN

BACKGROUND: The anti-inflammatory, anti-allergic, antioxidant properties of flavonoids are known in the respiratory tract. We are interested in the role of Provinol during an allergic inflammation of the airway. OBJECTIVES: The aim of this study was to examine the influence of an acute administration of Provinol on tracheal smooth muscle reactivity in guinea pigs and to assess the involvement of nitric oxide in the mechanism of Provinol action. METHODS: This experiment was performed 14 days after the sensitization of animals by ovalbumin. In vivo, the specific airway conductance, as a tracheal smooth muscle reactivity parameter in response to bronchoconstrictor histamine, was evaluated after peroral administration of Provinol alone or together with L-NAME (N(omega)-nitro-L-arginine methyl ester). In vitro, Provinol alone or in combination with L-NAME were added into an organ baths before the supplement of direct bronchoconstrictor histamine, acetylcholine and the allergen ovalbumin in rising concentrations. The amplitude of the tracheal smooth muscle contraction, as a tracheal smooth muscle reactivity parameter in response to histamine, acetylcholine and ovalbumin was evaluated. RESULTS: Our results showed that a Provinol has significant bronchodilatory activities both in vivo and in vitro. CONCLUSION: Provinol alleviated the contraction of tracheal smooth muscle in guinea pigs sumin. Nitric oxide plays an important role in the mechanism of Provinol action (Fig. 2, Ref. 28n.(Fig. 2, Ref. 28).


Asunto(s)
Hiperreactividad Bronquial/tratamiento farmacológico , Flavonoides/uso terapéutico , Fenoles/uso terapéutico , Alérgenos , Animales , Hiperreactividad Bronquial/fisiopatología , Cobayas , Contracción Muscular/efectos de los fármacos , Ovalbúmina/inmunología , Polifenoles , Tráquea/efectos de los fármacos , Tráquea/fisiopatología , Vino/análisis
2.
Int J Biol Macromol ; 67: 312-7, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24680903

RESUMEN

Hemicellulose polysaccharides represent a large group of natural renewable polymers, however, their application potency is still low. In our study a hardwood 4-O-methylglucuronoxylan was isolated by alkali peroxide extraction of Fagus sylvatica sawdust and modified into sulfated water soluble derivative (MGXS). Highly sulfated MGXS was characterized by HPLC, FTIR and NMR spectroscopies, and tested in vivo on chemically induced cough reflex and smooth muscles reactivity. Farmacological tests revealed an interesting antitussive activity of MGXS. Comparative tests with drug commonly used in a clinical practice revealed that antitussive activity of MGXS was lower than that of opioid receptor agonist codeine, the strongest antitussive drug. Furthermore, the specific reactivity of airways smooth muscle was not significantly affected by MGXS, indicating thus that the polymer is not involved in the bronchodilation process.


Asunto(s)
Antitusígenos/administración & dosificación , Tos/tratamiento farmacológico , Extractos Vegetales/química , Xilanos/química , Animales , Antitusígenos/química , Codeína/administración & dosificación , Fagus/química , Cobayas , Humanos , Músculo Liso/efectos de los fármacos , Extractos Vegetales/administración & dosificación , Sulfatos/química , Xilanos/administración & dosificación , Xilanos/aislamiento & purificación
3.
Int J Biol Macromol ; 49(4): 493-7, 2011 Nov 01.
Artículo en Inglés | MEDLINE | ID: mdl-21689679

RESUMEN

A low molecular mass arabinogalactan-protein (AGP) composed of galactose and arabinose with a low protein content, isolated from the instant coffee powder of Coffea arabica beans, has been tested on antitussive (in vivo) and immunomodulating (ex vivo) activities. The results of antitussive tests revealed a significant dose dependant cough-suppressive effect of coffee AGP. It was observed 30 or 60 min after AGP administration and its efficacy lasted during the entire experiment course. Immunological tests showed that AGP affected some mediators of immunocompetent cells of immune system as TNF-α, IFN-γ and IL-2 cytokines. It seems that coffee AGP is a good inductor of both pro-inflammatory cytokines TNF-α and IFN-γ, however, less potent in TNF-α induction in comparison with that of ß-D-glucan. Evident induction of TNF-α, IL-2 and IFN-γ cytokines, pro-TH1 polarization supports our conclusion about bio-immunological efficacy of AGP with an emphasis on the cellular immunity.


Asunto(s)
Antitusígenos/farmacología , Café/química , Factores Inmunológicos/farmacología , Mucoproteínas/farmacología , Administración Oral , Resistencia de las Vías Respiratorias/efectos de los fármacos , Animales , Antitusígenos/administración & dosificación , Antitusígenos/uso terapéutico , Tos/tratamiento farmacológico , Tos/fisiopatología , Cobayas , Factores Inmunológicos/administración & dosificación , Factores Inmunológicos/uso terapéutico , Interleucina-2/metabolismo , Ratones , Mucoproteínas/administración & dosificación , Mucoproteínas/uso terapéutico , Proteínas de Plantas/administración & dosificación , Proteínas de Plantas/farmacología , Proteínas de Plantas/uso terapéutico , Polvos , Bazo/efectos de los fármacos , Bazo/metabolismo , Factor de Necrosis Tumoral alfa/metabolismo
4.
Int J Biol Macromol ; 45(1): 27-32, 2009 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-19447256

RESUMEN

The rhamnogalacturonan, isolated from the roots of medicinal plant Althaea officinalis L., showed various biological effects on the citric acid-induced cough reflex and reactivity of airways smooth muscle in vitro and in vivo conditions. It possessed dose-dependent cough suppression effect comparable with opioid agonist codeine. However, reactivity of the airways smooth muscle, measured in vitro as well as in vivo conditions was not significantly affected by rhamnogalacturonan and thus bronchodilatory activity did not participate in the cough suppression effect of polysaccharide tested. Moreover, the cough suppression effect of the polymer was not significantly modified by pretreatment of K(+)(ATP) ion channels with selective antagonist and therefore activation of this type of ion channels is not involved in the mechanism of rhamnogalacturonan cough suppressive ability. On the contrary, pretreatment of animals with selective 5-HT(2) receptors antagonist significantly decreased rhamnogalacturonan antitussive efficacy. From this point of view it seems that the cough suppression effect of the polymer is associated with the serotonergic 5-HT(2) receptor's function.


Asunto(s)
Althaea/química , Antitusígenos/farmacología , Pectinas/aislamiento & purificación , Pectinas/farmacología , Animales , Relación Dosis-Respuesta a Droga , Cobayas , Músculo Liso Vascular/efectos de los fármacos
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