التفاصيل البيبلوغرافية
العنوان: |
Chronic bronchial allergic inflammation increases alveolar liquid clearance by TNF-α-dependent mechanism. |
المؤلفون: |
Tillie-Leblond, Isabelle, Guery, Benoit P.H., Janin, Anne, Leberre, Rosenn, Just, Nicolas, Pittet, Jean-Francois, Tonnel, André-Bernard, Cosset, Philippe |
المصدر: |
American Journal of Physiology: Lung Cellular & Molecular Physiology; Dec2002, Vol. 27 Issue 6, pL1303, 7p, 2 Color Photographs, 2 Charts, 4 Graphs |
مصطلحات موضوعية: |
ASTHMA, ALLERGIES, INFLAMMATION |
مستخلص: |
Bronchial inflammation in allergic asthma is associated with active exudation from the bronchial tree into the interstitial space of both mucosa and submucosa. The aim of this study was to evaluate epithelial and endothelial permeability as well as alveolar fluid movement in a model of chronic allergic inflammation in Brown-Norway rats sensitized and challenged with ovalbumin (OA). Control groups were challenged with saline solution (C), and rats were immunized by OA but not challenged (Se). Lung sections showed a marked inflammatory infiltrate associated with perivascular and peribronchiolar edema in OA. To measure alveolar liquid clearance, a 5% bovine albumin solution with 1 µCi of [sup 125]I-labeled human albumin was instilled into the air spaces. Alveolar-capillary barrier permeability was evaluated by intravascular injection of 1 µCi of [sup 131]-labeled albumin. Endothelial permeability was significantly increased in OA, from 0.08 ± 0.01 in the C group to 0.19 ± 0.03 in OA group (P < 0.05). Final-to-initial protein ratio was also statistically higher in OA (1.6 ± 0.05) compared with C (1.38 ± 0.03, P = 0.01) and Se groups (1.42 ± 0.03, P = 0.04). Administration of anti-tumor necrosis factor-α antibodies within the instillate significantly decreased this ratio (1.32 ± 0.08, P = 0.003 vs. OA). To conclude, we demonstrated a tumor necrosis factor-α-dependent increase in alveolar fluid movement in a model of severe bronchial allergic inflammation associated with endothelial and epithelial leakage. [ABSTRACT FROM AUTHOR] |
|
Copyright of American Journal of Physiology: Lung Cellular & Molecular Physiology is the property of American Physiological Society and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
قاعدة البيانات: |
Complementary Index |