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Vitamin E, γ-tocopherol, reduces airway neutrophil recruitment after inhaled endotoxin challenge in rats and in healthy volunteers

Authors :
James G. Wagner
Neil E. Alexis
Heather Wells
Qing Jiang
Hongtao Zhang
Michelle L. Hernandez
John C. Lay
Aline Kala
Katherine T. Mills
David B. Peden
Haibo Zhou
Source :
Free Radical Biology and Medicine. 60:56-62
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

Epidemiologic studies suggest that dietary vitamin E is an important candidate intervention for asthma. Our group has shown that daily consumption of vitamin E (γ-tocopherol, γT) has anti-inflammatory actions in both rodent and human phase I studies. The objective of this study was to test whether γT supplementation could mitigate a model of neutrophilic airway inflammation in rats and in healthy human volunteers. F344/N rats were randomized to oral gavage with γT versus placebo, followed by intranasal LPS (20μg) challenge. Bronchoalveolar lavage fluid and lung histology were used to assess airway neutrophil recruitment. In a phase IIa clinical study, 13 nonasthmatic subjects completed a double-blinded, placebo-controlled crossover study in which they consumed either a γT-enriched capsule or a sunflower oil placebo capsule. After 7 days of daily supplementation, they underwent an inhaled LPS challenge. Induced sputum was assessed for neutrophils 6 h after inhaled LPS. The effect of γT compared to placebo on airway neutrophils post-LPS was compared using a repeated-measures analysis of variance. In rats, oral γT supplementation significantly reduced tissue infiltration (p0.05) and accumulation of airway neutrophils (p0.05) that are elicited by intranasal LPS challenge compared to control rats. In human volunteers, γT treatment significantly decreased induced sputum neutrophils (p=0.03) compared to placebo. Oral supplementation with γT reduced airway neutrophil recruitment in both rat and human models of inhaled LPS challenge. These results suggest that γT is a potential therapeutic candidate for prevention or treatment of neutrophilic airway inflammation in diseased populations.

Details

ISSN :
08915849
Volume :
60
Database :
OpenAIRE
Journal :
Free Radical Biology and Medicine
Accession number :
edsair.doi.dedup.....a096fa27437cf4b3a754416bbda4653c
Full Text :
https://doi.org/10.1016/j.freeradbiomed.2013.02.001