Intranasal curcumin and sodium butyrate modulates airway inflammation and fibrosis via HDAC inhibition in allergic asthma

Cytokine ◽  
2022 ◽  
Vol 149 ◽  
pp. 155720
Author(s):  
Ramiya Islam ◽  
D Dash ◽  
Rashmi Singh
2021 ◽  
Vol 11 (6) ◽  
Author(s):  
Anet Laanesoo ◽  
Egon Urgard ◽  
Kapilraj Periyasamy ◽  
Martti Laan ◽  
Yury A. Bochkov ◽  
...  

2008 ◽  
Vol 31 (5) ◽  
pp. 1139-1141 ◽  
Author(s):  
A. Moreira ◽  
L. Delgado ◽  
C. Palmares ◽  
C. Lopes ◽  
T. Jacinto ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Haruka Aoki ◽  
Chihiro Mogi ◽  
Fumikazu Okajima

An acidic microenvironment has been shown to evoke a variety of airway responses, including cough, bronchoconstriction, airway hyperresponsiveness (AHR), infiltration of inflammatory cells in the lung, and stimulation of mucus hyperproduction. Except for the participation of transient receptor potential vanilloid-1 (TRPV1) and acid-sensing ion channels (ASICs) in severe acidic pH (of less than 6.0)-induced cough and bronchoconstriction through sensory neurons, the molecular mechanisms underlying extracellular acidic pH-induced actions in the airways have not been fully understood. Recent studies have revealed that ovarian cancer G protein-coupled receptor 1 (OGR1)-family G protein-coupled receptors, which sense pH of more than 6.0, are expressed in structural cells, such as airway smooth muscle cells and epithelial cells, and in inflammatory and immune cells, such as eosinophils and dendritic cells. They function in a variety of airway responses related to the pathophysiology of inflammatory diseases, including allergic asthma. In the present review, we discuss the roles of ionotropic TRPV1 and ASICs and metabotropic OGR1-family G protein-coupled receptors in the airway inflammation and AHR in asthma and respiratory diseases.


2019 ◽  
Vol 843 ◽  
pp. 251-259 ◽  
Author(s):  
Francieli Vuolo ◽  
Soraia C. Abreu ◽  
Monique Michels ◽  
Débora G. Xisto ◽  
Natália G. Blanco ◽  
...  

2017 ◽  
Vol 8 (12) ◽  
pp. 4315-4324 ◽  
Author(s):  
Sara L. Coleman ◽  
Odette M. Shaw

The potential of fruit proanthocyanidins to modulate airway inflammation through interactions with immune cells and the microbiome.


2010 ◽  
Vol 33 (3) ◽  
pp. 196 ◽  
Author(s):  
Xia Ke ◽  
Jiangju Huang ◽  
Quan Chen ◽  
Suling Hong ◽  
Daoyin Zhu

Purpose. Allergic asthma is characterized by chronic airway inflammation and airway hyperresponsiveness driven by allergen-specific T helper (Th)2 cells. Mycobacterium bovis bacillus Calmette-Guérin (BCG) vaccination has been documented to suppress Th2 responses and allergic airway inflammation in animal models. Since interleukin (IL)-12 is capable of inhibiting Th2 responses, we sought to investigate whether IL-12 could function as an adjuvant to increase the efficacy of BCG vaccination against allergic asthma. Methods. BALB/c neonatal mice (24 mice, 48-72 h old) were randomly divided into 3 subgroups (n = 8 for each group) to be immunized with PBS (control) or BCG with or without DNA plasmid-expressing IL-12. All of the mice were then sensitized and provoked with ovalbumin (OVA) to establish a model of allergic asthma. Results. Mice vaccinated with BCG alone showed a significant reduction in airway inflammation, percentage of eosinophils in bronchoalveolar lavage (BAL) fluid, and serum OVA-specific immunoglobulin E (IgE) levels in comparison with control animals. The suppressive effects of BCG were substantially augmented by the combination with IL-12. Furthermore, a decreased IL-4 and increased interferon-gamma (IFN-γ) production in BAL fluid were observed in animals inoculated with BCG alone or with IL-12 relative to control animals. Conclusion. Our data indicate that the combined vaccination with BCG and IL-12 yields a favorable outcome in prevention of experimental allergic airway inflammation, which is likely mediated through triggering a shift from a Th2 response to a Th1 response.


Author(s):  
EMANUELE CRIMI ◽  
ANTONIO SPANEVELLO ◽  
MARGHERITA NERI ◽  
PHILIP W. IND ◽  
GIOVANNI A. ROSSI ◽  
...  

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