Imbalance of endogenous prostanoids in moderate-to-severe asthma

Published on Jan 1, 2017in Allergology International4.806
· DOI :10.1016/J.ALIT.2016.05.013
Masaya Takemura16
Estimated H-index: 16
(Kyoto University),
Akio Niimi54
Estimated H-index: 54
(Kyoto University)
+ 6 AuthorsMichiaki Mishima76
Estimated H-index: 76
(Kyoto University)
Sources
Abstract
Abstract Background Inhalation studies suggested "protective" roles of exogenous prostaglandin E 2 , but the clinical relevance of endogenous prostanoids in asthma is poorly known. The objective of this study is to measure sputum levels of prostanoids in asthmatic patients to correlate with clinical indices. Methods Mild ( n  = 41) or moderate-to-severe (19) asthmatics and 27 normal controls were examined for pulmonary function (FEV 1 and mid-forced expiratory flow), sputum cell differentials, and sputum levels of prostaglandins D 2 , E 2 , F 2α , and thromboxane B 2 measured by sandwich enzyme immunoassay. Results Each prostanoid level did not differ among the three groups. Sputum number of bronchial epithelial cells was greater in moderate-to-severe asthmatics than in the other two groups, suggesting epithelial desquamation. Levels of prostaglandin F 2α , D 2 , and thromboxane B 2 positively correlated with the severity of airflow obstruction in the 60 asthmatic patients, whereas prostaglandin E 2 levels were unrelated to pulmonary function. The ratio of combined "contractile" prostanoids (prostaglandin D 2 /prostaglandin F 2α /thromboxane B 2 ) to prostaglandin E 2 was 2.5-fold greater in moderate-to-severe asthmatics than in controls ( p  = 0.001) or in mild asthmatics ( p  = 0.0002) but did not differ between the latter two groups. In the two asthmatic groups combined, this ratio positively correlated with the sputum number of epithelial cells. The combined "contractile" prostanoids levels positively correlated with prostaglandin E 2 levels in controls and in mild asthmatics but not in moderate-to-severe asthmatics. Conclusions An imbalance in production, breakdown, or both between prostaglandin E 2 and other prostanoids possibly due to epithelial damage may be involved in the pathogenesis of moderate-to-severe asthma.
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