Effects of vitamin E on mitochondrial dysfunction and asthma features in an experimental allergic murine model

被引:67
作者
Mabalirajan, Ulaganathan [1 ,3 ]
Aich, Jyotirmoi [1 ]
Leishangthem, Geeta Devi [2 ]
Sharma, Surendra Kumar [3 ]
Dinda, Amit Kumar [2 ]
Ghosh, Balaram [1 ]
机构
[1] Inst Genom & Integrat Biol, Immunogenet Mol Lab, Delhi 110007, India
[2] All India Inst Med Sci, Dept Pathol, Div Renal Pathol, New Delhi 110029, India
[3] All India Inst Med Sci, Dept Med, Div Pulm Crit Care & Sleep Med, New Delhi 110029, India
关键词
12/15-lipoxygenase; mitochondria; AIRWAY INFLAMMATION; ALPHA-TOCOPHEROL; MOUSE MODEL; CHILDHOOD ASTHMA; OXIDATIVE DAMAGE; MICE; INHIBITION; HYPERRESPONSIVENESS; ATHEROSCLEROSIS; LIPOXYGENASE;
D O I
10.1152/japplphysiol.00459.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Mabalirajan U, Aich J, Leishangthem GD, Sharma SK, Dinda AK, Ghosh B. Effects of vitamin E on mitochondrial dysfunction and asthma features in an experimental allergic murine model. J Appl Physiol 107: 1285-1292, 2009. First published July 23, 2009; doi:10.1152/japplphysiol.00459.2009.-We showed recently that IL-4 causes mitochondrial dysfunction in allergic asthma. IL-4 is also known to induce 12/15-lipoxygenase (12/15-LOX), a potent candidate molecule in asthma. Because vitamin E (Vit-E) reduces IL-4 and inhibits 12/15-LOX in vitro, here we tested the hypothesis that Vit-E may be effective in restoring key mitochondrial dysfunctions, thus alleviating asthma features in an experimental allergic murine model. Ovalbumin (OVA)-sensitized and challenged male BALB/c mice showed the characteristic features of asthma such as airway hyperresponsiveness (AHR), airway inflammation, and airway remodeling. In addition, these mice showed increase in the expression and metabolites of 12/15-LOX, reduction in the activity and expression of the third subunit of mitochondrial cytochrome-c oxidase, and increased cytochrome c in lung cytosol, which indicate that OVA sensitization and challenge causes mitochondrial dysfunction. Vit-E was administered orally to these mice, and 12/15-LOX expression, key mitochondrial functions, ultrastructural changes of mitochondria in bronchial epithelia, and asthmatic parameters were determined. Vit-E treatment reduced AHR, Th2 response including IL-4, IL-5, IL-13, and OVA-specific IgE, eotaxin, transforming growth factor-beta 1, airway inflammation, expression and metabolites of 12/15-LOX in lung cytosol, lipid peroxidation, and nitric oxide metabolites in the lung, restored the activity and expression of the third subunit of cytochrome-c oxidase in lung mitochondria and bronchial epithelia, respectively, reduced the appearance of cytochrome c in lung cytosol, and also restored mitochondrial ultrastructural changes of bronchial epithelia. In summary, these findings show that Vit-E reduces key mitochondrial dysfunctions and alleviates asthmatic features.
引用
收藏
页码:1285 / 1292
页数:8
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